| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:236833550-236833824 | Rare:61 | ||||
| chr2:236968133-236968398 | Rare:39 | ||||
| chr2:236988953-236989115 | Common:2; Rare:35 | ||||
| chr2:236989128-236989165 | Common:1; Rare:7 | ||||
| chr2:240870065-240870266 | Common:3; Rare:33 | ||||
| chr2:240870402-240870631 | Common:1; Rare:64 | ||||
| chr2:240873975-240874317 | Common:6; Rare:99; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):8 | ||||
| chr2:240986119-240986264 | Rare:33 | ||||
| chr20:371892-372063 | Common:2; Rare:38 | ||||
| chr20:1164472-1164684 | Common:1; Rare:42 | ||||
| chr20:2301376-2301605 | Common:2; Rare:30 | ||||
| chr20:4961820-4962067 | Common:3; Rare:43 | ||||
| chr20:4967678-4967704 | Rare:4 | ||||
| chr20:4967707-4967748 | Common:1; Rare:5 | ||||
| chr20:6704282-6704482 | Rare:25 |