| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74553941-74554086 | Rare:23 | ||||
| chr2:74554406-74554755 | Common:2; Rare:102 | ||||
| chr2:74958855-74959073 | Rare:77 | ||||
| chr2:75199518-75199661 | Rare:23 | ||||
| chr2:75710669-75710779 | Common:2; Rare:42 | ||||
| chr2:84459226-84459572 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905464-84905947 | Common:2; Rare:146 | ||||
| chr2:85327916-85328080 | Common:2; Rare:74 | ||||
| chr2:85354491-85354790 | Common:1; Rare:100 | ||||
| chr2:85539068-85539185 | Common:2; Rare:47 | ||||
| chr2:85539933-85540111 | Rare:47 | ||||
| chr2:85561432-85561581 | Rare:56; Clinvar:4 | ||||
| chr2:85584326-85584478 | Common:2; Rare:45 | ||||
| chr2:85595688-85595838 | Common:1; Rare:66 | ||||
| chr2:85602618-85602904 | Rare:76 |