ID: 132090579 | Neanderthal introgressed variant-containing enhancer experimental_60428 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45810250..45810419) | | |
ID: 132090578 | Neanderthal introgressed variant-containing enhancer experimental_60411 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45783843..45784012) | | |
ID: 132090577 | Neanderthal introgressed variant-containing enhancer experimental_60389 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45775577..45775746) | | |
ID: 130065968 | ATAC-STARR-seq lymphoblastoid silent region 12962 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45812447..45812636) | | |
ID: 130065967 | ATAC-STARR-seq lymphoblastoid silent region 12961 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45792517..45792656) | | |
ID: 130065966 | ATAC-STARR-seq lymphoblastoid silent region 12960 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45792037..45792306) | | |
ID: 127893429 | H3K27ac hESC enhancer GRCh37_chr20:44449199-44449846 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45820560..45821207) | | |
ID: 127893428 | H3K27ac hESC enhancer GRCh37_chr20:44447254-44447902 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45818615..45819263) | | |
ID: 127893427 | H3K4me1 hESC enhancer GRCh37_chr20:44408579-44409079 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45779940..45780440) | | |
ID: 127893426 | H3K27ac hESC enhancer GRCh37_chr20:44400300-44400892 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45771661..45772253) | | |
ID: 127893425 | H3K27ac hESC enhancer GRCh37_chr20:44399706-44400299 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45771067..45771660) | | |
ID: 127893424 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr20:44394305-44395236 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45765666..45766597) | | |
ID: 127893423 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr20:44393372-44394304 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45764733..45765665) | | |
ID: 127893422 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:44391506-44392438 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45762867..45763799) | | |
ID: 125387277 | Sharpr-MPRA regulatory region 6194 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45781290..45781584) | | |
ID: 124904915 | uncharacterized LOC124904915 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45762061..45767580) | | |
ID: 121627906 | Sharpr-MPRA regulatory region 12827 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45777950..45778244) | | |
ID: 106479559 | RNA, U6atac small nuclear 38, pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45778698..45778822) | | |
ID: 140863 | serine peptidase inhibitor, Kunitz type 5, pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45749920..45750074) | C20orf168, dJ447F3.6 | |
ID: 140686 | WAP four-disulfide core domain 3 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45774213..45791883, complement) | WAP14, dJ447F3.3 | |