| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241734399-241734739 | Common:9; Rare:140; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:241734812-241734938 | Common:5; Rare:43 | ||||
| chr2:241735390-241735642 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:241858825-241859067 | Common:1; Rare:58 | ||||
| chr20:290357-290857 | Common:18; Rare:138 | ||||
| chr20:297214-297495 | Common:4; Rare:77 | ||||
| chr20:325196-325434 | Rare:64 | ||||
| chr20:346981-347199 | Common:1; Rare:66 | ||||
| chr20:347636-347953 | Common:2; Rare:85 | ||||
| chr20:347991-348311 | Common:1; Rare:74 | ||||
| chr20:380674-380706 | Common:1; Rare:5 | ||||
| chr20:380721-381354 | Common:6; Rare:164 | ||||
| chr20:381762-382168 | Common:22; Rare:104 | ||||
| chr20:407846-408098 | Common:24; Rare:65 | ||||
| chr20:408187-408529 | Common:1; Rare:78 |