| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:134120034-134120240 | Common:1; Rare:73 | ||||
| chr2:134918209-134918242 | Rare:11 | ||||
| chr2:134918580-134918904 | Common:1; Rare:133 | ||||
| chr2:135052217-135052320 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr2:135052630-135052676 | Rare:10 | ||||
| chr2:135530548-135530983 | Common:4; Rare:99 | ||||
| chr2:135531160-135531526 | Common:1; Rare:79 | ||||
| chr2:135741611-135741984 | Common:4; Rare:134 | ||||
| chr2:135876343-135876652 | Common:1; Rare:90 | ||||
| chr2:135985262-135985340 | Rare:14 | ||||
| chr2:135985413-135985685 | Common:4; Rare:122; Clinvar (benign):1 | ||||
| chr2:135985687-135985721 | Rare:8 | ||||
| chr2:138501652-138502022 | Common:3; Rare:133 | ||||
| chr2:144332440-144332658 | Rare:85 | ||||
| chr2:144514916-144514931 | Rare:2 |