Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26432087-26432429 | Common:10; Rare:177; Clinvar:4; Clinvar (benign):2 | ||||
chr1:26472290-26472565 | Common:6; Rare:181 | ||||
chr1:26472670-26473370 | Common:7; Rare:495 | ||||
chr1:26529576-26529831 | Common:3; Rare:91 | ||||
chr1:26695413-26695764 | Common:1; Rare:173 | ||||
chr1:26695921-26696116 | Rare:111 | ||||
chr1:26786800-26787108 | Rare:101 | ||||
chr1:26787851-26788255 | Common:6; Rare:224; Clinvar:4; Clinvar (benign):4 | ||||
chr1:26826575-26826749 | Rare:62 | ||||
chr1:26862974-26863177 | Rare:75 | ||||
chr1:26899880-26900350 | Rare:258 | ||||
chr1:26900393-26900559 | Rare:121 | ||||
chr1:26914250-26914580 | Common:4; Rare:90 | ||||
chr1:26921529-26921904 | Common:6; Rare:221 | ||||
chr1:26960330-26960890 | Common:2; Rare:142 |