| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50958464-50958874 | Common:2; Rare:298; Clinvar:3; Clinvar (benign):7 | ||||
| chr20:51801279-51801444 | Rare:28 | ||||
| chr20:51801374-51801964 | Common:11; Rare:167 | ||||
| chr20:52191243-52191366 | Common:5; Rare:49 | ||||
| chr20:52191704-52191815 | Rare:20 | ||||
| chr20:52191716-52191819 | Rare:18 | ||||
| chr20:52192135-52192281 | Common:2; Rare:57 | ||||
| chr20:52192300-52192710 | Common:6; Rare:137 | ||||
| chr20:52972430-52972920 | Common:6; Rare:168 | ||||
| chr20:53593797-53593909 | Common:2; Rare:83 | ||||
| chr20:53594120-53594900 | Common:2; Rare:417 | ||||
| chr20:53609800-53610260 | Common:2; Rare:131 | ||||
| chr20:54207827-54208149 | Rare:83 | ||||
| chr20:56358686-56359006 | Common:3; Rare:102 | ||||
| chr20:56392131-56392695 | Common:12; Rare:294 |