ID: 132090223 | Neanderthal introgressed variant-containing enhancer experimental_34518 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (57943732..57943901) | | |
ID: 132090222 | Neanderthal introgressed variant-containing enhancer experimental_34475 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (57904012..57904181) | | |
ID: 130055724 | ATAC-STARR-seq lymphoblastoid active region 8442 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58200342..58200531) | | |
ID: 130055723 | ATAC-STARR-seq lymphoblastoid silent region 5797 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58199792..58200181) | | |
ID: 130055722 | ATAC-STARR-seq lymphoblastoid active region 8441 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58199592..58199721) | | |
ID: 130055721 | ATAC-STARR-seq lymphoblastoid active region 8440 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58171184..58171243) | | |
ID: 130055720 | ATAC-STARR-seq lymphoblastoid silent region 5794 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58151748..58151937) | | |
ID: 127827655 | NANOG hESC enhancer GRCh37_chr14:58595390-58595891 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58128672..58129173) | | |
ID: 127827654 | NANOG hESC enhancer GRCh37_chr14:58587185-58587752 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58120467..58121034) | | |
ID: 127827653 | H3K27ac hESC enhancer GRCh37_chr14:58418179-58418679 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (57951461..57951961) | | |
ID: 127827652 | NANOG hESC enhancer GRCh37_chr14:58282822-58283323 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (57816104..57816605) | | |
ID: 127827651 | H3K4me1 hESC enhancer GRCh37_chr14:58266137-58266636 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (57799419..57799918) | | |
ID: 127827650 | NANOG hESC enhancer GRCh37_chr14:58220473-58221005 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (57753755..57754287) | | |
ID: 127827649 | OCT4-NANOG hESC enhancer GRCh37_chr14:58181078-58182074 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (57714360..57715356) | | |
ID: 126861957 | MED14-independent group 3 enhancer GRCh37_chr14:58252116-58253315 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (57785398..57786597) | | |
ID: 125024491 | Sharpr-MPRA regulatory region 2203 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58152038..58152445) | | |
ID: 121838593 | Sharpr-MPRA regulatory region 5436 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58072611..58072905) | | |
ID: 106481759 | RNA, 7SL, cytoplasmic 598, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58179771..58180064) | | |
ID: 106479138 | RN7SK pseudogene 99 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (57837354..57837660, complement) | | |
ID: 100420347 | polycomb group ring finger 3 pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58100985..58101572) | | |