| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:53593803-53593902 | Common:1; Rare:38 | ||||
| chr20:53609775-53609832 | Rare:13 | ||||
| chr20:56392101-56392694 | Common:6; Rare:156 | ||||
| chr20:56468504-56468727 | Rare:87 | ||||
| chr20:58388987-58389312 | Common:4; Rare:164; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:58651056-58651311 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58981098-58981318 | Common:2; Rare:106 | ||||
| chr20:59032217-59032633 | Common:5; Rare:185; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59042711-59043073 | Common:1; Rare:130 | ||||
| chr20:59300353-59300621 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:59940213-59940518 | Rare:112 | ||||
| chr20:62143265-62143812 | Common:7; Rare:230 | ||||
| chr20:62182915-62183049 | Rare:47 | ||||
| chr20:62302762-62303035 | Common:2; Rare:82 | ||||
| chr20:62386915-62387136 | Common:3; Rare:100 |