| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191245219-191245567 | Common:3; Rare:115 | ||||
| chr2:191377412-191377539 | Common:1; Rare:15 | ||||
| chr2:191677858-191678218 | Common:4; Rare:101 | ||||
| chr2:191678550-191679026 | Common:1; Rare:158 | ||||
| chr2:195656856-195657171 | Common:1; Rare:94 | ||||
| chr2:196068808-196068921 | Common:1; Rare:29 | ||||
| chr2:196639543-196639761 | Rare:75 | ||||
| chr2:196799603-196799777 | Common:1; Rare:54 | ||||
| chr2:197434970-197435198 | Rare:76 | ||||
| chr2:197453195-197453561 | Rare:128 | ||||
| chr2:197453867-197454006 | Rare:39 | ||||
| chr2:197499760-197500725 | Common:2; Rare:339; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:197515827-197516107 | Common:2; Rare:101 | ||||
| chr2:197675668-197675820 | Rare:22 | ||||
| chr2:197705196-197705430 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):2 |