| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58908855-58909216 | Common:3; Rare:84; Clinvar:1 | ||||
| chr20:58910331-58910936 | Common:3; Rare:146; Clinvar (pathogenic):2 | ||||
| chr20:58981182-58981361 | Common:2; Rare:87 | ||||
| chr20:59032218-59032560 | Common:3; Rare:147; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59042711-59043073 | Common:1; Rare:130 | ||||
| chr20:59300008-59300189 | Common:1; Rare:41 | ||||
| chr20:59933609-59933798 | Common:4; Rare:75 | ||||
| chr20:59940297-59940514 | Rare:82 | ||||
| chr20:62139077-62139354 | Common:1; Rare:80 | ||||
| chr20:62143269-62143748 | Common:6; Rare:198 | ||||
| chr20:62182886-62183049 | Common:1; Rare:56 | ||||
| chr20:62302796-62303058 | Common:2; Rare:81 | ||||
| chr20:62386946-62387371 | Common:3; Rare:157 | ||||
| chr20:62427498-62427735 | Common:1; Rare:42 | ||||
| chr20:62926455-62926638 | Common:2; Rare:57 |