| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207166163-207166440 | Common:3; Rare:125 | ||||
| chr2:207166811-207167000 | Common:2; Rare:81 | ||||
| chr2:207529710-207530131 | Common:3; Rare:121 | ||||
| chr2:207625267-207625616 | Common:1; Rare:101 | ||||
| chr2:207711582-207711932 | Rare:108 | ||||
| chr2:208025417-208025588 | Common:2; Rare:42 | ||||
| chr2:208189842-208190098 | Rare:67 | ||||
| chr2:208190187-208190322 | Common:1; Rare:20 | ||||
| chr2:208254421-208254544 | Common:1; Rare:30 | ||||
| chr2:208255019-208255238 | Common:2; Rare:58 | ||||
| chr2:208266015-208266101 | Common:3; Rare:30 | ||||
| chr2:208266104-208266390 | Common:6; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423975-209424552 | Common:5; Rare:144 | ||||
| chr2:209579231-209579731 | Common:9; Rare:92 | ||||
| chr2:209661332-209661564 | Common:2; Rare:38 |