ID: 132090536 | Neanderthal introgressed variant-containing enhancer experimental_50884 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29430078..29430247) | | |
ID: 132090535 | Neanderthal introgressed variant-containing enhancer experimental_50793 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29398143..29398312) | | |
ID: 132090534 | Neanderthal introgressed variant-containing enhancer experimental_50790 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29393770..29393939) | | |
ID: 132090533 | Neanderthal introgressed variant-containing enhancer experimental_50764 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29318340..29318509) | | |
ID: 130064123 | ATAC-STARR-seq lymphoblastoid active region 14409 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29624008..29624057) | | |
ID: 130064122 | ATAC-STARR-seq lymphoblastoid active region 14408 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29622192..29622251) | | |
ID: 130064121 | ATAC-STARR-seq lymphoblastoid silent region 10463 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29621051..29621100) | | |
ID: 130064120 | ATAC-STARR-seq lymphoblastoid active region 14407 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29605936..29606425) | | |
ID: 130064119 | ATAC-STARR-seq lymphoblastoid active region 14406 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29277426..29277475) | | |
ID: 130064118 | ATAC-STARR-seq lymphoblastoid active region 14405 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29213095..29213334) | | |
ID: 129664409 | ReSE screen-validated silencer GRCh37_chr19:29763000-29763195 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29272093..29272288) | | |
ID: 129391090 | MPRA-validated peak3428 silencer [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29329579..29329779) | | |
ID: 127891124 | H3K27ac hESC enhancer GRCh37_chr19:30156127-30156680 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29665029..29665773) | | |
ID: 127891123 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:30100801-30101312 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29609894..29610405) | | |
ID: 127891122 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr19:30087367-30087867 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29596460..29596960) | | |
ID: 127891121 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr19:30086866-30087366 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29595959..29596459) | | |
ID: 127891120 | H3K4me1 hESC enhancer GRCh37_chr19:30059413-30059913 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29568506..29569006) | | |
ID: 127891119 | H3K4me1 hESC enhancer GRCh37_chr19:30055952-30056800 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29565045..29565893) | | |
ID: 127891118 | H3K4me1 hESC enhancer GRCh37_chr19:30053547-30054047 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29562640..29563140) | | |
ID: 127891117 | H3K4me1 hESC enhancer GRCh37_chr19:30030691-30031191 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29539784..29540284) | | |