| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71331592-71331840 | Common:5; Rare:75 | ||||
| chr2:71331958-71332047 | Common:2; Rare:22 | ||||
| chr2:71332221-71332406 | Common:1; Rare:48 | ||||
| chr2:71453574-71453715 | Rare:24 | ||||
| chr2:71453839-71453870 | Rare:3 | ||||
| chr2:71466611-71466766 | Common:3; Rare:34 | ||||
| chr2:72825642-72825833 | Rare:40 | ||||
| chr2:72825865-72826108 | Rare:80 | ||||
| chr2:72887038-72887135 | Rare:15 | ||||
| chr2:72887210-72887483 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr2:72887860-72887970 | Common:1; Rare:24 | ||||
| chr2:72916013-72916356 | Common:1; Rare:106 | ||||
| chr2:72917318-72917589 | Common:2; Rare:80 | ||||
| chr2:73070515-73070779 | Common:3; Rare:66 | ||||
| chr2:73071214-73071546 | Common:3; Rare:115 |