| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45348381-45348519 | Common:1; Rare:38 | ||||
| chr20:45362934-45363213 | Rare:84 | ||||
| chr20:45363357-45363542 | Common:2; Rare:51 | ||||
| chr20:45405861-45406205 | Common:2; Rare:86 | ||||
| chr20:45406533-45406747 | Rare:60 | ||||
| chr20:45407082-45407312 | Common:1; Rare:34 | ||||
| chr20:45407823-45408370 | Common:3; Rare:115 | ||||
| chr20:45415882-45416159 | Rare:67 | ||||
| chr20:45791927-45792017 | Common:1; Rare:34 | ||||
| chr20:45833743-45833852 | Common:3; Rare:25 | ||||
| chr20:45834068-45834207 | Rare:50 | ||||
| chr20:45857343-45857639 | Common:3; Rare:80 | ||||
| chr20:45881031-45881241 | Common:2; Rare:48 | ||||
| chr20:45890107-45890330 | Common:1; Rare:79 | ||||
| chr20:45890994-45891387 | Common:4; Rare:124; Clinvar:8; Clinvar (benign):4 |