| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:220093967-220094393 | Common:4; Rare:142; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:220094406-220094587 | Rare:58; Clinvar (benign):3 | ||||
| chr1:220271899-220272057 | Common:2; Rare:43 | ||||
| chr1:220272143-220272252 | Common:1; Rare:30 | ||||
| chr1:220272294-220272798 | Rare:134; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:220272813-220272851 | Rare:5 | ||||
| chr1:220527911-220527978 | Rare:11 | ||||
| chr1:220527982-220528781 | Common:2; Rare:259 | ||||
| chr1:220528791-220529094 | Common:2; Rare:82 | ||||
| chr1:220529197-220529308 | Rare:25 | ||||
| chr1:220748132-220748393 | Common:1; Rare:54 | ||||
| chr1:220748461-220748586 | Common:3; Rare:38 | ||||
| chr1:220786737-220787000 | Common:4; Rare:63 | ||||
| chr1:221741772-221741888 | Common:1; Rare:25 | ||||
| chr1:221741939-221742604 | Common:4; Rare:161 |