| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127811121-127811306 | Common:1; Rare:66 | ||||
| chr2:127858090-127858341 | Common:4; Rare:99 | ||||
| chr2:127885878-127885972 | Rare:20 | ||||
| chr2:128091034-128091347 | Common:8; Rare:103 | ||||
| chr2:130181528-130181709 | Common:2; Rare:71 | ||||
| chr2:130342127-130342281 | Rare:60 | ||||
| chr2:130342686-130342930 | Common:3; Rare:79 | ||||
| chr2:131105192-131105375 | Common:1; Rare:84 | ||||
| chr2:131493033-131493118 | Common:1; Rare:24 | ||||
| chr2:134918718-134918898 | Rare:79 | ||||
| chr2:135052167-135052310 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr2:135531170-135531514 | Common:1; Rare:72 | ||||
| chr2:135741611-135741937 | Common:4; Rare:119 | ||||
| chr2:135876277-135876633 | Common:1; Rare:107 | ||||
| chr2:135985407-135985816 | Common:5; Rare:162; Clinvar (benign):1 |