| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70087433-70088027 | Rare:196 | ||||
| chr2:70248503-70248809 | Common:5; Rare:120 | ||||
| chr2:71068526-71068672 | Rare:71 | ||||
| chr2:71129780-71129951 | Rare:35 | ||||
| chr2:71130220-71130662 | Common:6; Rare:123; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276448-71276608 | Rare:52 | ||||
| chr2:73071701-73071848 | Common:2; Rare:57 | ||||
| chr2:73233200-73233476 | Common:1; Rare:77 | ||||
| chr2:73234567-73234770 | Rare:62 | ||||
| chr2:73385673-73386059 | Common:4; Rare:183; Clinvar:16; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr2:73828896-73829037 | Rare:39 | ||||
| chr2:74002574-74002721 | Common:2; Rare:59 | ||||
| chr2:74147862-74148140 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74343391-74343626 | Common:1; Rare:41 | ||||
| chr2:74391795-74392100 | Common:2; Rare:148 |