Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89994981-89995193 | Common:2; Rare:80 | ||||
chr1:91500568-91500881 | Common:2; Rare:74 | ||||
chr1:91886012-91886325 | Rare:127 | ||||
chr1:92298945-92299070 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92785066-92785365 | Common:6; Rare:95 | ||||
chr1:93079097-93079290 | Common:2; Rare:83 | ||||
chr1:93180079-93180151 | Rare:25 | ||||
chr1:93180229-93180699 | Common:1; Rare:183 | ||||
chr1:93345807-93345919 | Common:2; Rare:43 | ||||
chr1:93879128-93879274 | Common:1; Rare:53 | ||||
chr1:94418216-94418470 | Common:2; Rare:89 | ||||
chr1:94541730-94542006 | Rare:78 | ||||
chr1:94820186-94820432 | Common:3; Rare:63 | ||||
chr1:94927041-94927456 | Common:1; Rare:138 | ||||
chr1:95072884-95073008 | Rare:48 |