| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74507639-74507914 | Common:1; Rare:75 | ||||
| chr2:74525983-74526751 | Common:1; Rare:180 | ||||
| chr2:74529410-74530189 | Common:1; Rare:400; Clinvar:9; Clinvar (benign):4 | ||||
| chr2:74553856-74554778 | Common:5; Rare:328 | ||||
| chr2:74654113-74654314 | Rare:103 | ||||
| chr2:74834930-74835031 | Rare:26 | ||||
| chr2:74835124-74835324 | Rare:101 | ||||
| chr2:74958509-74958751 | Common:10; Rare:188 | ||||
| chr2:74958840-74959057 | Rare:144 | ||||
| chr2:75560746-75561194 | Common:4; Rare:163 | ||||
| chr2:75646654-75647134 | Common:4; Rare:222 | ||||
| chr2:75710600-75710837 | Common:4; Rare:196 | ||||
| chr2:84459207-84459621 | Common:6; Rare:197; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr2:84905374-84906105 | Common:5; Rare:262 | ||||
| chr2:84970320-84970850 | Common:2; Rare:190 |