| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190180776-190181066 | Rare:94 | ||||
| chr2:191677856-191678140 | Common:4; Rare:79 | ||||
| chr2:196593561-196593635 | Rare:18 | ||||
| chr2:197434987-197435186 | Rare:66 | ||||
| chr2:197499820-197500427 | Common:1; Rare:237; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515968-197516118 | Rare:60 | ||||
| chr2:199911089-199911349 | Rare:72 | ||||
| chr2:200509913-200510199 | Common:1; Rare:100 | ||||
| chr2:200889243-200889445 | Common:2; Rare:76 | ||||
| chr2:200962954-200963080 | Rare:20 | ||||
| chr2:201071592-201072058 | Rare:102 | ||||
| chr2:201118207-201118496 | Common:1; Rare:53 | ||||
| chr2:201118570-201118863 | Rare:47 | ||||
| chr2:201451354-201451867 | Common:3; Rare:129 | ||||
| chr2:201642660-201642727 | Rare:35 |