| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74529659-74529938 | Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530434-74530628 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74554662-74554748 | Common:1; Rare:32 | ||||
| chr2:74958877-74959032 | Rare:58 | ||||
| chr2:75560923-75561165 | Common:2; Rare:65 | ||||
| chr2:84459237-84459583 | Common:3; Rare:85; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84906611-84906868 | Common:4; Rare:37 | ||||
| chr2:85327936-85328069 | Common:2; Rare:62 | ||||
| chr2:85354511-85354807 | Common:1; Rare:100 | ||||
| chr2:85410329-85410460 | Rare:31 | ||||
| chr2:85413992-85414205 | Common:2; Rare:43 | ||||
| chr2:85539017-85539168 | Common:1; Rare:60 | ||||
| chr2:85561441-85561574 | Rare:50; Clinvar:4 | ||||
| chr2:85595488-85595772 | Common:3; Rare:91 | ||||
| chr2:85602660-85602882 | Rare:56 |