| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131105193-131105375 | Common:1; Rare:84 | ||||
| chr2:131492762-131492959 | Common:4; Rare:64 | ||||
| chr2:131493034-131493107 | Common:1; Rare:21 | ||||
| chr2:134918597-134918907 | Common:1; Rare:131 | ||||
| chr2:135531182-135531508 | Common:1; Rare:66 | ||||
| chr2:135985407-135985685 | Common:4; Rare:123; Clinvar (benign):1 | ||||
| chr2:138501638-138502088 | Common:4; Rare:163 | ||||
| chr2:144517331-144517685 | Common:5; Rare:104; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144520320-144520528 | Common:4; Rare:38; Clinvar (benign):1 | ||||
| chr2:147925825-147926090 | Rare:48 | ||||
| chr2:148020694-148021100 | Common:2; Rare:93; Clinvar (benign):2 | ||||
| chr2:148021571-148021625 | Rare:13 | ||||
| chr2:149038588-149038786 | Common:3; Rare:66 | ||||
| chr2:149587093-149587370 | Common:3; Rare:65; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:149587672-149587816 | Common:1; Rare:41; Clinvar:1 |