ID: 132089642 | Neanderthal introgressed variant-containing enhancer experimental_105469 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110932203..110932372) | | |
ID: 132089641 | Neanderthal introgressed variant-containing enhancer experimental_105449 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110915390..110915559) | | |
ID: 132089640 | Neanderthal introgressed variant-containing enhancer experimental_105435 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110915043..110915212) | | |
ID: 132089639 | Neanderthal introgressed variant-containing enhancer experimental_105418 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110902625..110902794) | | |
ID: 130002354 | ATAC-STARR-seq lymphoblastoid active region 28792 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111078426..111078475) | | |
ID: 130002353 | ATAC-STARR-seq lymphoblastoid silent region 20176 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111037900..111038239) | | |
ID: 130002352 | ATAC-STARR-seq lymphoblastoid silent region 20175 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110952717..110952766) | | |
ID: 130002351 | ATAC-STARR-seq lymphoblastoid active region 28791 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110935991..110936060) | | |
ID: 130002350 | ATAC-STARR-seq lymphoblastoid active region 28790 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110933790..110934159) | | |
ID: 130002349 | ATAC-STARR-seq lymphoblastoid active region 28789 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110933560..110933769) | | |
ID: 130002348 | ATAC-STARR-seq lymphoblastoid active region 28788 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110821262..110821471) | | |
ID: 130002347 | ATAC-STARR-seq lymphoblastoid active region 28787 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110808723..110808772) | | |
ID: 127815588 | H3K4me1 hESC enhancer GRCh37_chr9:113715081-113715580 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110952801..110953300) | | |
ID: 127815587 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:113553096-113553668 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110790816..110791388) | | |
ID: 126860730 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:113544666-113545865 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110782386..110783585) | | |
ID: 124902248 | uncharacterized LOC124902248 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111036928..111042959) | | |
ID: 107987115 | uncharacterized LOC107987115 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110761058..110785691, complement) | | |
ID: 106479757 | RNA, U6 small nuclear 432, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110903337..110903445) | | |
ID: 100379298 | RNY4 pseudogene 18 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111097327..111097413, complement) | | |
ID: 4593 | muscle associated receptor tyrosine kinase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (110668791..110806558) | CMS9, FADS, FADS1 | 601296 |