| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71068015-71068315 | Rare:79 | ||||
| chr2:71068534-71068679 | Rare:66 | ||||
| chr2:71130220-71130662 | Common:6; Rare:123; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276450-71276641 | Rare:69 | ||||
| chr2:71453641-71453686 | Rare:7 | ||||
| chr2:72887309-72887427 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr2:73071680-73071841 | Common:2; Rare:67 | ||||
| chr2:73214172-73214279 | Common:1; Rare:38 | ||||
| chr2:73233162-73233499 | Common:3; Rare:101 | ||||
| chr2:73234189-73234361 | Common:2; Rare:51 | ||||
| chr2:73234549-73234694 | Rare:51 | ||||
| chr2:73385641-73386076 | Common:4; Rare:204; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73737286-73737490 | Common:2; Rare:63 | ||||
| chr2:73828804-73829037 | Common:1; Rare:54 | ||||
| chr2:73926695-73926934 | Common:2; Rare:114; Clinvar:7; Clinvar (benign):3 |