| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74421565-74421781 | Rare:72 | ||||
| chr2:74458100-74458534 | Common:1; Rare:130 | ||||
| chr2:74465377-74465439 | Rare:13 | ||||
| chr2:74482937-74483109 | Common:1; Rare:62 | ||||
| chr2:74507652-74507795 | Rare:31 | ||||
| chr2:74529668-74530189 | Rare:154; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74553948-74554086 | Rare:22 | ||||
| chr2:74654083-74654295 | Common:1; Rare:58 | ||||
| chr2:74958509-74958732 | Common:5; Rare:91 | ||||
| chr2:74958876-74959011 | Rare:53 | ||||
| chr2:75646694-75646828 | Rare:42 | ||||
| chr2:75710692-75710769 | Common:1; Rare:33 | ||||
| chr2:75710872-75710955 | Common:1; Rare:31 | ||||
| chr2:80304182-80304311 | Rare:32 | ||||
| chr2:80304395-80304651 | Common:2; Rare:55 |