ID: 129664759 | ReSE screen-validated silencer GRCh37_chr21:47560109-47560298 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46140195..46140384) | | |
ID: 127895136 | H3K4me1 hESC enhancer GRCh37_chr21:47612079-47612691 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46192165..46192777) | | |
ID: 127895135 | H3K4me1 hESC enhancer GRCh37_chr21:47611464-47612078 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46191550..46192164) | | |
ID: 127895134 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:47603039-47603642 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46183125..46183728) | | |
ID: 127895133 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:47602435-47603038 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46182521..46183124) | | |
ID: 127895132 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:47600015-47600618 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46180101..46180704) | | |
ID: 127895131 | H3K27ac hESC enhancer GRCh37_chr21:47590605-47591105 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46170691..46171191) | | |
ID: 127895130 | H3K27ac hESC enhancer GRCh37_chr21:47590104-47590604 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46170190..46170690) | | |
ID: 127895129 | H3K4me1 hESC enhancer GRCh37_chr21:47574563-47575266 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46154649..46155352) | | |
ID: 127895128 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:47573859-47574562 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46153945..46154648) | | |
ID: 127895127 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:47573155-47573858 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46153241..46153944) | | |
ID: 127895126 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:47572449-47573154 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46152535..46153240) | | |
ID: 127895125 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:47571745-47572448 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46151831..46152534) | | |
ID: 127895124 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:47556247-47557020 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46136333..46137106) | | |
ID: 127895123 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:47551971-47552475 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46132057..46132561) | | |
ID: 127895122 | OCT4-NANOG hESC enhancer GRCh37_chr21:47527125-47527884 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46107211..46107970) | | |
ID: 125418088 | Sharpr-MPRA regulatory region 3768 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46141942..46142509) | | |
ID: 124908236 | uncharacterized LOC124908236 [Homo sapiens (human)] | | | |
ID: 124905045 | uncharacterized LOC124905045 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46184547..46189173) | | |
ID: 124905043 | uncharacterized LOC124905043 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46108915..46112031, complement) | | |