| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135531159-135531644 | Common:2; Rare:203 | ||||
| chr2:135741591-135741983 | Common:5; Rare:137 | ||||
| chr2:135742460-135742910 | Common:3; Rare:155 | ||||
| chr2:135876367-135876663 | Common:2; Rare:148 | ||||
| chr2:135985404-135985795 | Common:10; Rare:310; Clinvar (benign):2 | ||||
| chr2:137964003-137964816 | Common:11; Rare:313 | ||||
| chr2:138501471-138502060 | Common:8; Rare:353 | ||||
| chr2:142877416-142877716 | Common:2; Rare:85 | ||||
| chr2:144332449-144332649 | Rare:80 | ||||
| chr2:147844199-147844837 | Common:13; Rare:340 | ||||
| chr2:148020653-148021135 | Common:4; Rare:216; Clinvar (benign):4 | ||||
| chr2:148644780-148645130 | Common:2; Rare:156 | ||||
| chr2:149587159-149587615 | Common:4; Rare:127 | ||||
| chr2:149587675-149587836 | Common:2; Rare:84; Clinvar:2 | ||||
| chr2:151409814-151410010 | Common:2; Rare:71 |