Namespace(genes='/oak/stanford/groups/akundaje/soumyak/refs/gencode/hg38/hg38.gencode.protein_coding.tss.bed', list='/oak/stanford/groups/akundaje/projects/neuro-variants/variant_summary/rosmap/encode_2024/K562_bias/encode_2024.LV.lymphocyte.H.mean.variant_scores.tsv', out_prefix='/oak/stanford/groups/akundaje/projects/neuro-variants/variant_annotations/rosmap/encode_2024/K562_bias/encode_2024.LV.lymphocyte.H', peaks='/oak/stanford/groups/akundaje/projects/neuro-variants/data/processed/encode_2024/peaks/overlap/encode_2024.LV.lymphocyte.H.overlap.peaks.bed.gz', schema='chrombpnet') Namespace(genes='/oak/stanford/groups/akundaje/soumyak/refs/gencode/hg38/hg38.gencode.protein_coding.tss.bed', list='/oak/stanford/groups/akundaje/projects/neuro-variants/variant_summary/rosmap/encode_2024/K562_bias/encode_2024.LV.lymphocyte.H.mean.variant_scores.tsv', out_prefix='/oak/stanford/groups/akundaje/projects/neuro-variants/variant_annotations/rosmap/encode_2024/K562_bias/encode_2024.LV.lymphocyte.H', peaks='/oak/stanford/groups/akundaje/projects/neuro-variants/data/processed/encode_2024/peaks/overlap/encode_2024.LV.lymphocyte.H.overlap.peaks.bed.gz', schema='chrombpnet') chr pos end allele1 allele2 variant_id 837619 chr1 850506 850507 A T chr1:850507:A:T 837620 chr1 850562 850563 G C chr1:850563:G:C 837621 chr1 850855 850856 C T chr1:850856:C:T 837622 chr1 851095 851096 G A chr1:851096:G:A 837623 chr1 852046 852047 C T chr1:852047:C:T Variants table shape: (2531122, 6) annotating with closest genes 0 1 2 3 4 5 6 7 8 9 \ 0 chr1 850506 850507 A T chr1:850507:A:T chr1 923923 923924 SAMD11 1 chr1 850506 850507 A T chr1:850507:A:T chr1 959308 959309 NOC2L 2 chr1 850506 850507 A T chr1:850507:A:T chr1 960584 960585 KLHL17 3 chr1 850562 850563 G C chr1:850563:G:C chr1 923923 923924 SAMD11 4 chr1 850562 850563 G C chr1:850563:G:C chr1 959308 959309 NOC2L 10 11 12 13 14 0 0 + ENSG00000187634.13 protein_coding 73417 1 0 - ENSG00000188976.11 protein_coding 108802 2 0 + ENSG00000187961.15 protein_coding 110078 3 0 + ENSG00000187634.13 protein_coding 73361 4 0 - ENSG00000188976.11 protein_coding 108746 Closest genes table shape: (7593366, 15) annotating with peak overlap chr pos end allele1 allele2 variant_id 0 chr1 869815 869816 A G chr1:869816:A:G 1 chr1 869950 869951 A G chr1:869951:A:G 2 chr1 923768 923769 G A chr1:923769:G:A 3 chr1 923908 923909 G T chr1:923909:G:T 4 chr1 959351 959352 C G chr1:959352:C:G Peak overlap table shape: (25098, 6) chr pos allele1 allele2 variant_id logfc.mean \ 0 chr10 124524 T A chr10:124524:T:A 0.001657 1 chr10 124526 T A chr10:124526:T:A 0.001684 2 chr10 124528 T A chr10:124528:T:A 0.001871 3 chr10 124530 T A chr10:124530:T:A 0.001850 4 chr10 124542 T A chr10:124542:T:A 0.002590 logfc.mean.pval abs_logfc.mean abs_logfc.mean.pval jsd.mean ... \ 0 0.833791 0.001993 0.890353 0.010435 ... 1 0.833101 0.001934 0.893658 0.010195 ... 2 0.822709 0.002001 0.889055 0.010190 ... 3 0.824290 0.001850 0.896948 0.009949 ... 4 0.775527 0.002590 0.847607 0.008918 ... quantile_change.mean.pval abs_quantile_change.mean \ 0 0.883471 0.000245 1 0.881813 0.000214 2 0.873201 0.000241 3 0.868829 0.000218 4 0.837237 0.000343 abs_quantile_change.mean.pval closest_gene_1 gene_distance_1 \ 0 0.935024 ZMYND11 5565 1 0.944193 ZMYND11 5563 2 0.936904 ZMYND11 5561 3 0.942044 ZMYND11 5559 4 0.910414 ZMYND11 5547 closest_gene_2 gene_distance_2 closest_gene_3 gene_distance_3 \ 0 TUBB8 50361 DIP2C 565144 1 TUBB8 50363 DIP2C 565142 2 TUBB8 50365 DIP2C 565140 3 TUBB8 50367 DIP2C 565138 4 TUBB8 50379 DIP2C 565126 peak_overlap 0 False 1 False 2 False 3 False 4 False [5 rows x 38 columns] Annotation table shape: (2531122, 38) DONE Done Annotating