| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70257978-70258266 | Common:2; Rare:102 | ||||
| chr2:70293644-70293828 | Common:2; Rare:66 | ||||
| chr2:70978477-70978637 | Rare:42 | ||||
| chr2:71068533-71068686 | Rare:68 | ||||
| chr2:71129812-71129932 | Rare:26 | ||||
| chr2:71130201-71130666 | Common:6; Rare:132; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71453471-71453500 | Rare:6 | ||||
| chr2:71453503-71453883 | Common:2; Rare:71 | ||||
| chr2:72147449-72147558 | Rare:28 | ||||
| chr2:73071322-73071474 | Common:1; Rare:44 | ||||
| chr2:73071674-73071857 | Common:2; Rare:75 | ||||
| chr2:73233196-73233451 | Common:1; Rare:66 | ||||
| chr2:73234244-73234368 | Common:1; Rare:43 | ||||
| chr2:73234532-73234598 | Rare:20 | ||||
| chr2:73385620-73386090 | Common:4; Rare:219; Clinvar:17; Clinvar (benign):9; Clinvar (pathogenic):1 |