| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74958560-74958677 | Common:2; Rare:42 | ||||
| chr2:74958872-74959038 | Rare:62 | ||||
| chr2:75560884-75561154 | Common:1; Rare:68 | ||||
| chr2:80303846-80304118 | Rare:48 | ||||
| chr2:84459219-84459581 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84516315-84516546 | Rare:60 | ||||
| chr2:84905506-84905859 | Common:1; Rare:112 | ||||
| chr2:84906611-84906734 | Rare:18 | ||||
| chr2:85327916-85328080 | Common:2; Rare:74 | ||||
| chr2:85354501-85354807 | Common:1; Rare:105 | ||||
| chr2:85539012-85539168 | Common:1; Rare:61 | ||||
| chr2:85561424-85561636 | Common:1; Rare:72; Clinvar:4 | ||||
| chr2:85595555-85595814 | Common:2; Rare:91 | ||||
| chr2:85602629-85602900 | Rare:70 | ||||
| chr2:85612030-85612113 | Rare:24 |