| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74178800-74179002 | Common:2; Rare:54 | ||||
| chr2:74421639-74421759 | Rare:39 | ||||
| chr2:74440413-74440683 | Rare:70 | ||||
| chr2:74465354-74465527 | Common:2; Rare:46 | ||||
| chr2:74482919-74483098 | Common:1; Rare:60 | ||||
| chr2:74507669-74507781 | Rare:24 | ||||
| chr2:74529662-74529788 | Rare:51; Clinvar:1 | ||||
| chr2:74958866-74959071 | Rare:75 | ||||
| chr2:75710669-75710802 | Common:2; Rare:58 | ||||
| chr2:84459229-84459567 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84971192-84971371 | Rare:43 | ||||
| chr2:85327945-85328066 | Common:1; Rare:57 | ||||
| chr2:85354526-85354792 | Common:1; Rare:85 | ||||
| chr2:85538869-85539168 | Common:1; Rare:97 | ||||
| chr2:85561431-85561590 | Rare:60; Clinvar:4 |