| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:23490998-23491115 | Common:4; Rare:29 | ||||
| chr20:23568224-23568635 | Common:4; Rare:117 | ||||
| chr20:23568643-23568794 | Common:2; Rare:37 | ||||
| chr20:23637951-23638071 | Common:2; Rare:43 | ||||
| chr20:23988626-23988688 | Common:1; Rare:17 | ||||
| chr20:23988748-23988990 | Common:4; Rare:59 | ||||
| chr20:24469414-24469640 | Common:1; Rare:58 | ||||
| chr20:24992678-24992839 | Common:5; Rare:75 | ||||
| chr20:25032175-25032370 | Common:2; Rare:51 | ||||
| chr20:25057829-25058106 | Common:5; Rare:83 | ||||
| chr20:25195542-25196024 | Common:10; Rare:142 | ||||
| chr20:25247967-25248371 | Common:2; Rare:162 | ||||
| chr20:25290241-25290622 | Common:3; Rare:129 | ||||
| chr20:25390699-25391042 | Common:5; Rare:136; Clinvar:4; Clinvar (benign):3 | ||||
| chr20:25407495-25407906 | Common:4; Rare:158; Clinvar (pathogenic):1 |