| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130342104-130342244 | Rare:63; Clinvar:1 | ||||
| chr2:130342648-130342930 | Common:5; Rare:89 | ||||
| chr2:131492754-131493097 | Common:8; Rare:103 | ||||
| chr2:134918585-134918863 | Common:1; Rare:110 | ||||
| chr2:135531170-135531502 | Common:1; Rare:66 | ||||
| chr2:135985413-135985740 | Common:4; Rare:138; Clinvar (benign):1 | ||||
| chr2:138501676-138501947 | Common:2; Rare:96 | ||||
| chr2:144517460-144517739 | Common:5; Rare:80 | ||||
| chr2:144518377-144518525 | Rare:32 | ||||
| chr2:144520304-144520526 | Common:4; Rare:41; Clinvar (benign):1 | ||||
| chr2:148020692-148021023 | Common:2; Rare:69 | ||||
| chr2:148021571-148021658 | Rare:18 | ||||
| chr2:149587674-149587766 | Common:1; Rare:26; Clinvar:1 | ||||
| chr2:151289611-151289725 | Common:1; Rare:29 | ||||
| chr2:151734380-151734582 | Rare:29; Clinvar:2 |