| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49219261-49219496 | Common:1; Rare:110 | ||||
| chr20:49278039-49278278 | Rare:67 | ||||
| chr20:49812731-49812925 | Common:2; Rare:52 | ||||
| chr20:49915496-49915607 | Common:3; Rare:34 | ||||
| chr20:50113106-50113221 | Common:5; Rare:57 | ||||
| chr20:50794821-50795106 | Common:2; Rare:97 | ||||
| chr20:50958481-50958875 | Common:1; Rare:148; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:53593797-53593894 | Common:1; Rare:35 | ||||
| chr20:54070620-54070942 | Common:5; Rare:53 | ||||
| chr20:56392156-56392704 | Common:6; Rare:149 | ||||
| chr20:58388975-58389281 | Common:3; Rare:140; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58515436-58515528 | Common:1; Rare:19 | ||||
| chr20:58651144-58651305 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58651597-58651788 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:58651811-58652090 | Rare:65; Clinvar (benign):2 |