| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:24413678-24413800 | Common:1; Rare:32 | ||||
| chr1:24415633-24415904 | Common:1; Rare:66 | ||||
| chr1:24416935-24416967 | Rare:6 | ||||
| chr1:24642971-24643365 | Common:2; Rare:121 | ||||
| chr1:24745288-24745620 | Common:2; Rare:116 | ||||
| chr1:25232460-25232654 | Rare:75 | ||||
| chr1:25247401-25247621 | Common:2; Rare:81 | ||||
| chr1:25338087-25338470 | Common:2; Rare:115 | ||||
| chr1:25800378-25800587 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:25811456-25811807 | Common:4; Rare:107; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr1:25819889-25820256 | Common:5; Rare:108 | ||||
| chr1:25892552-25892671 | Common:2; Rare:25 | ||||
| chr1:26021625-26021786 | Common:1; Rare:25 | ||||
| chr1:26279952-26280204 | Rare:138 | ||||
| chr1:26432091-26432472 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):1 |