ID: 132089728 | Neanderthal introgressed variant-containing enhancer experimental_110294 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94548498..94548667) | | |
ID: 132089727 | Neanderthal introgressed variant-containing enhancer experimental_110288 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94548013..94548182) | | |
ID: 132089726 | Neanderthal introgressed variant-containing enhancer experimental_110264 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94536374..94536543) | | |
ID: 130002118 | ATAC-STARR-seq lymphoblastoid active region 28632 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94669100..94669239) | | |
ID: 130002117 | ATAC-STARR-seq lymphoblastoid silent region 20057 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94639592..94639651) | | |
ID: 127815327 | H3K4me1 hESC enhancer GRCh37_chr9:97372257-97372756 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94609975..94610474) | | |
ID: 127815326 | NANOG hESC enhancer GRCh37_chr9:97370327-97370828 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94608045..94608546) | | |
ID: 127815325 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97353573-97354115 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94591291..94591833) | | |
ID: 127815324 | H3K4me1 hESC enhancer GRCh37_chr9:97350295-97350794 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94588013..94588512) | | |
ID: 127815323 | H3K4me1 hESC enhancer GRCh37_chr9:97349793-97350294 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94587511..94588012) | | |
ID: 127815322 | H3K4me1 hESC enhancer GRCh37_chr9:97320892-97321392 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94558610..94559110) | | |
ID: 127815321 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97316904-97317566 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94554622..94555284) | | |
ID: 127815320 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97315577-97316239 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94553295..94553957) | | |
ID: 124902219 | uncharacterized LOC124902219 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94681694..94691990) | | |
ID: 124902218 | uncharacterized LOC124902218 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94550537..94554889, complement) | | |
ID: 124310591 | Sharpr-MPRA regulatory region 4124 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94669227..94669521) | | |
ID: 107987101 | uncharacterized LOC107987101 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94690391..94700159, complement) | | |
ID: 107987100 | uncharacterized LOC107987100 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94485442..94523406, complement) | | |
ID: 101928099 | prostate cancer associated transcript 7 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94554599..94574654) | PCAN-R2 | |
ID: 54754 | NUT family member 2F [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94318198..94328644, complement) | FAM22F, NUTMF | |