| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45405717-45406195 | Common:2; Rare:108 | ||||
| chr20:45406541-45406736 | Rare:50 | ||||
| chr20:45407082-45407307 | Common:1; Rare:34 | ||||
| chr20:45415982-45416207 | Rare:78; Clinvar:1 | ||||
| chr20:45834111-45834249 | Rare:53 | ||||
| chr20:45857311-45857639 | Common:4; Rare:94 | ||||
| chr20:45891252-45891387 | Common:1; Rare:48; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45896193-45896310 | Common:2; Rare:43 | ||||
| chr20:45912141-45912305 | Common:3; Rare:38 | ||||
| chr20:45934474-45934731 | Common:2; Rare:110 | ||||
| chr20:45971822-45971922 | Common:1; Rare:32 | ||||
| chr20:46363954-46364069 | Common:1; Rare:21 | ||||
| chr20:46364381-46364526 | Rare:56 | ||||
| chr20:46406566-46406787 | Common:2; Rare:60 | ||||
| chr20:46689420-46689722 | Common:1; Rare:75 |