| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74529673-74529952 | Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74833827-74834147 | Common:1; Rare:95 | ||||
| chr2:74958388-74958673 | Common:4; Rare:82 | ||||
| chr2:74958876-74959003 | Rare:51 | ||||
| chr2:75710648-75710739 | Common:1; Rare:37 | ||||
| chr2:75710872-75710949 | Common:1; Rare:27 | ||||
| chr2:77593194-77593379 | Common:6; Rare:60 | ||||
| chr2:84459237-84459581 | Common:3; Rare:85; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84516273-84516491 | Common:1; Rare:57 | ||||
| chr2:85327924-85328084 | Common:2; Rare:74 | ||||
| chr2:85354524-85354790 | Common:1; Rare:86 | ||||
| chr2:85538924-85539172 | Common:1; Rare:90 | ||||
| chr2:85561432-85561532 | Rare:40; Clinvar:4 | ||||
| chr2:85595558-85595764 | Common:1; Rare:65 | ||||
| chr2:85612018-85612113 | Rare:32 |