| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74833843-74834212 | Rare:111 | ||||
| chr2:74834790-74835036 | Rare:64 | ||||
| chr2:74835129-74835393 | Common:1; Rare:61 | ||||
| chr2:74958456-74958944 | Common:5; Rare:203 | ||||
| chr2:75199513-75199644 | Rare:25 | ||||
| chr2:75646654-75647108 | Common:3; Rare:133 | ||||
| chr2:75647113-75647202 | Rare:30 | ||||
| chr2:75710609-75711091 | Common:3; Rare:185 | ||||
| chr2:84458639-84458887 | Common:1; Rare:61 | ||||
| chr2:84459180-84459661 | Common:4; Rare:126; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84894955-84895018 | Rare:14 | ||||
| chr2:84905427-84905702 | Common:2; Rare:90 | ||||
| chr2:84905911-84906364 | Common:3; Rare:107 | ||||
| chr2:84907162-84907333 | Rare:36 | ||||
| chr2:84970620-84970743 | Common:1; Rare:34 |