Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44213348-44213548 | Common:1; Rare:40 | ||||
chr1:44642818-44642912 | Common:1; Rare:20 | ||||
chr1:44643109-44643155 | Rare:7 | ||||
chr1:44674406-44674755 | Common:3; Rare:94 | ||||
chr1:44739648-44739881 | Common:2; Rare:89 | ||||
chr1:44775452-44775620 | Common:1; Rare:67 | ||||
chr1:44775838-44776140 | Common:2; Rare:109 | ||||
chr1:44777604-44778067 | Common:2; Rare:114 | ||||
chr1:44800143-44800379 | Common:1; Rare:54 | ||||
chr1:44808444-44808585 | Rare:42 | ||||
chr1:45010910-45011241 | Common:2; Rare:95 | ||||
chr1:45011884-45012262 | Common:5; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45339937-45340045 | Common:1; Rare:41; Clinvar (benign):1 | ||||
chr1:45340114-45340217 | Rare:49; Clinvar:4; Clinvar (benign):4 | ||||
chr1:45340386-45340559 | Common:1; Rare:44; Clinvar:1 |