| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241637010-241637154 | Rare:60 | ||||
| chr2:241637490-241637719 | Common:1; Rare:128 | ||||
| chr2:241686709-241687133 | Common:4; Rare:136 | ||||
| chr2:241701854-241702094 | Common:1; Rare:94 | ||||
| chr2:241734472-241734702 | Common:6; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:290355-290621 | Common:13; Rare:72 | ||||
| chr20:297259-297593 | Common:6; Rare:94 | ||||
| chr20:325214-325557 | Rare:101 | ||||
| chr20:325781-325912 | Rare:34 | ||||
| chr20:347652-347947 | Common:2; Rare:81 | ||||
| chr20:380817-381792 | Common:21; Rare:316 | ||||
| chr20:407895-408098 | Common:23; Rare:54 | ||||
| chr20:408205-408345 | Common:1; Rare:32 | ||||
| chr20:408534-408934 | Common:5; Rare:142; Clinvar:2 | ||||
| chr20:462461-462698 | Common:2; Rare:111 |