| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:10430684-10430802 | Common:3; Rare:30 | ||||
| chr1:10472454-10472739 | Rare:67 | ||||
| chr1:10474819-10474984 | Rare:56; Clinvar:1 | ||||
| chr1:11099766-11099939 | Common:2; Rare:72 | ||||
| chr1:11262490-11262836 | Common:2; Rare:104 | ||||
| chr1:11691453-11691758 | Common:4; Rare:68 | ||||
| chr1:11805896-11806255 | Common:2; Rare:99; Clinvar:1 | ||||
| chr1:11934551-11934754 | Common:3; Rare:66; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:12019233-12019539 | Common:5; Rare:105 | ||||
| chr1:13749148-13749451 | Common:2; Rare:105 | ||||
| chr1:15465720-15465910 | Common:1; Rare:41 | ||||
| chr1:15526600-15526908 | Common:2; Rare:97 | ||||
| chr1:15847457-15847719 | Rare:93 | ||||
| chr1:16017224-16017688 | Common:4; Rare:111 | ||||
| chr1:16352410-16352564 | Common:2; Rare:83 |