ID: 132090792 | Neanderthal introgressed variant-containing enhancer experimental_109489 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91974441..91974610) | | |
ID: 132089710 | Neanderthal introgressed variant-containing enhancer experimental_109450 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91719711..91719880) | | |
ID: 130002063 | ATAC-STARR-seq lymphoblastoid silent region 20028 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91950214..91950393) | | |
ID: 130002062 | ATAC-STARR-seq lymphoblastoid silent region 20027 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91714627..91714676) | | |
ID: 127815202 | H3K4me1 hESC enhancer GRCh37_chr9:94711803-94712302 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91949521..91950020) | | |
ID: 127815201 | H3K4me1 hESC enhancer GRCh37_chr9:94711301-94711802 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91949019..91949520) | | |
ID: 127815200 | NANOG hESC enhancer GRCh37_chr9:94707493-94707994 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91945211..91945712) | | |
ID: 127815199 | NANOG-H3K4me1 hESC enhancer GRCh37_chr9:94702261-94702775 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91939979..91940493) | | |
ID: 127815198 | H3K4me1 hESC enhancer GRCh37_chr9:94696982-94697815 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91934700..91935533) | | |
ID: 127815197 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:94683912-94684752 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91921630..91922470) | | |
ID: 127815196 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:94683071-94683911 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91920789..91921629) | | |
ID: 127815195 | NANOG-H3K4me1 hESC enhancer GRCh37_chr9:94670331-94670937 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91908049..91908655) | | |
ID: 127815194 | H3K4me1 hESC enhancer GRCh37_chr9:94667938-94668501 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91905656..91906278) | | |
ID: 127815193 | NANOG hESC enhancer GRCh37_chr9:94656806-94657388 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91894524..91895106) | | |
ID: 127815192 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:94648927-94649508 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91886645..91887226) | | |
ID: 127815191 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:94648343-94648926 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91886061..91886644) | | |
ID: 127815190 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:94647759-94648342 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91885477..91886060) | | |
ID: 127815189 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:94619807-94620466 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91857525..91858184) | | |
ID: 127815188 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:94619147-94619806 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91856865..91857524) | | |
ID: 127815187 | H3K4me1 hESC enhancer GRCh37_chr9:94605877-94606451 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91843595..91844169) | | |