| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74482904-74483095 | Common:1; Rare:61 | ||||
| chr2:74507669-74507775 | Rare:21 | ||||
| chr2:74529662-74530020 | Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530539-74530616 | Common:1; Rare:29; Clinvar:2 | ||||
| chr2:74554666-74554750 | Common:1; Rare:32 | ||||
| chr2:74958508-74958677 | Common:3; Rare:60 | ||||
| chr2:74958877-74959032 | Rare:58 | ||||
| chr2:75560915-75561050 | Rare:31 | ||||
| chr2:75710669-75710979 | Common:3; Rare:135 | ||||
| chr2:84459228-84459581 | Common:3; Rare:90; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84905484-84905953 | Common:2; Rare:142 | ||||
| chr2:84971203-84971371 | Rare:42 | ||||
| chr2:85327936-85328084 | Common:2; Rare:69 | ||||
| chr2:85354501-85354807 | Common:1; Rare:105 | ||||
| chr2:85539033-85539168 | Common:1; Rare:53 |