| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130181561-130181760 | Common:2; Rare:90 | ||||
| chr2:130342127-130342244 | Rare:47 | ||||
| chr2:130342642-130342930 | Common:5; Rare:90 | ||||
| chr2:130355913-130356085 | Common:2; Rare:50 | ||||
| chr2:130836781-130836944 | Common:2; Rare:70 | ||||
| chr2:131104992-131105356 | Common:2; Rare:112 | ||||
| chr2:131492734-131492963 | Common:4; Rare:74 | ||||
| chr2:131493013-131493097 | Common:1; Rare:23 | ||||
| chr2:134918706-134918908 | Rare:85 | ||||
| chr2:135531172-135531508 | Common:1; Rare:70 | ||||
| chr2:135985404-135985721 | Common:4; Rare:134; Clinvar (benign):1 | ||||
| chr2:136118126-136118288 | Rare:41 | ||||
| chr2:138501664-138502026 | Common:2; Rare:128 | ||||
| chr2:144517324-144517732 | Common:5; Rare:125; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:148020686-148021113 | Common:2; Rare:97; Clinvar (benign):2 |