| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71453503-71453934 | Common:2; Rare:81 | ||||
| chr2:71466527-71466781 | Common:5; Rare:61 | ||||
| chr2:73233177-73233494 | Common:1; Rare:94 | ||||
| chr2:73234193-73234380 | Common:2; Rare:59 | ||||
| chr2:73737300-73737520 | Common:3; Rare:70 | ||||
| chr2:74147862-74148052 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74421585-74421759 | Rare:61 | ||||
| chr2:74454880-74455150 | Rare:79 | ||||
| chr2:74458113-74458509 | Common:1; Rare:122 | ||||
| chr2:74465339-74465461 | Common:1; Rare:33; Clinvar:1 | ||||
| chr2:74482958-74483117 | Common:1; Rare:61 | ||||
| chr2:74503307-74503454 | Rare:36 | ||||
| chr2:74507334-74507518 | Rare:52 | ||||
| chr2:74507669-74507775 | Rare:21 | ||||
| chr2:74529662-74529918 | Rare:72; Clinvar:2; Clinvar (benign):1 |