| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96208774-96208983 | Common:4; Rare:85 | ||||
| chr2:96265946-96266356 | Common:2; Rare:122; Clinvar:2 | ||||
| chr2:96305394-96305675 | Common:3; Rare:103; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96335703-96335842 | Common:2; Rare:48 | ||||
| chr2:96637185-96637293 | Rare:13 | ||||
| chr2:96638292-96638467 | Common:1; Rare:44 | ||||
| chr2:96816033-96816230 | Common:2; Rare:67 | ||||
| chr2:96857899-96858239 | Common:2; Rare:124 | ||||
| chr2:96868561-96868779 | Rare:55 | ||||
| chr2:97094810-97094980 | Common:1; Rare:42 | ||||
| chr2:97112832-97113244 | Common:1; Rare:93 | ||||
| chr2:97113373-97113681 | Common:2; Rare:73 | ||||
| chr2:97589750-97590016 | Common:5; Rare:66 | ||||
| chr2:97590265-97590616 | Common:1; Rare:65 | ||||
| chr2:97645876-97646156 | Common:3; Rare:85 |