ID: 132090440 | Neanderthal introgressed variant-containing enhancer experimental_46374 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88850174..88850343) | | |
ID: 130059763 | ATAC-STARR-seq lymphoblastoid active region 11373 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88871228..88871367) | | |
ID: 130059762 | ATAC-STARR-seq lymphoblastoid silent region 7883 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88856680..88857079) | | |
ID: 130059761 | ATAC-STARR-seq lymphoblastoid silent region 7882 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88854941..88855010) | | |
ID: 130059760 | ATAC-STARR-seq lymphoblastoid silent region 7879 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88811681..88812080) | | |
ID: 130059759 | ATAC-STARR-seq lymphoblastoid silent region 7878 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88803871..88803980) | | |
ID: 129663928 | ReSE screen-validated silencer GRCh37_chr16:88940900-88941052 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88874492..88874644) | | |
ID: 127885154 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:88930168-88930918 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88863760..88864510) | | |
ID: 127885153 | H3K4me1 hESC enhancer GRCh37_chr16:88883099-88883598 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88816691..88817190) | | |
ID: 127885152 | H3K4me1 hESC enhancer GRCh37_chr16:88882597-88883098 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88816157..88816690) | | |
ID: 127885151 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:88879396-88880079 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88812988..88813671) | | |
ID: 127885150 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:88878711-88879395 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88812303..88812987) | | |
ID: 127885149 | H3K4me1 hESC enhancer GRCh37_chr16:88876670-88877205 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88810262..88810797) | | |
ID: 127885148 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:88873249-88873762 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88806841..88807354) | | |
ID: 127885147 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:88871629-88872511 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88805221..88806103) | | |
ID: 127885146 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:88870745-88871628 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88804337..88805220) | | |
ID: 127885145 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:88869451-88870026 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88803043..88803790) | | |
ID: 126862447 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr16:88884193-88885392 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88817785..88818984) | | |
ID: 107983950 | uncharacterized LOC107983950 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88855128..88856580, complement) | | |
ID: 101927793 | uncharacterized LOC101927793 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (88883515..88887136) | | |