| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70900350-70900665 | Common:6; Rare:97 | ||||
| chr2:71068539-71068654 | Rare:52 | ||||
| chr2:71130225-71130662 | Common:6; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73828804-73828999 | Common:1; Rare:43 | ||||
| chr2:74147870-74148052 | Common:1; Rare:47; Clinvar:2 | ||||
| chr2:74440407-74440651 | Rare:63 | ||||
| chr2:74441882-74442056 | Common:2; Rare:31 | ||||
| chr2:74482954-74483095 | Common:1; Rare:49 | ||||
| chr2:74507668-74507790 | Rare:25 | ||||
| chr2:74529674-74529964 | Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74958872-74959003 | Rare:53 | ||||
| chr2:84459237-84459554 | Common:3; Rare:79; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:85327945-85328080 | Common:2; Rare:63 | ||||
| chr2:85354526-85354786 | Common:1; Rare:83 | ||||
| chr2:85561463-85561581 | Rare:37; Clinvar:3 |