| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58841453-58841691 | Common:2; Rare:50 | ||||
| chr20:58888761-58888991 | Common:1; Rare:69 | ||||
| chr20:58895456-58895689 | Common:2; Rare:40 | ||||
| chr20:58909141-58909415 | Common:3; Rare:66; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr20:58909858-58910401 | Common:1; Rare:129 | ||||
| chr20:58981097-58981354 | Common:2; Rare:115 | ||||
| chr20:58991141-58991422 | Common:1; Rare:71 | ||||
| chr20:59032219-59032578 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59042734-59043030 | Common:1; Rare:111 | ||||
| chr20:59933299-59933418 | Common:2; Rare:43 | ||||
| chr20:59933573-59933834 | Common:5; Rare:106 | ||||
| chr20:59940344-59940481 | Rare:56 | ||||
| chr20:62065819-62065991 | Common:1; Rare:78 | ||||
| chr20:62122954-62123172 | Rare:72 | ||||
| chr20:62143249-62143818 | Common:7; Rare:236 |