| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50958450-50958851 | Common:1; Rare:147; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:53593799-53593914 | Common:1; Rare:45 | ||||
| chr20:56392174-56392683 | Common:6; Rare:134 | ||||
| chr20:56468361-56468700 | Rare:118 | ||||
| chr20:56630629-56630793 | Common:1; Rare:42 | ||||
| chr20:58515386-58515528 | Common:2; Rare:28 | ||||
| chr20:58651144-58651305 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58888791-58888991 | Common:1; Rare:58 | ||||
| chr20:58981182-58981310 | Common:2; Rare:70 | ||||
| chr20:59042742-59043003 | Common:1; Rare:100 | ||||
| chr20:59940283-59940481 | Rare:83 | ||||
| chr20:62143265-62143807 | Common:7; Rare:227 | ||||
| chr20:62182894-62183049 | Common:1; Rare:52 | ||||
| chr20:62238253-62238581 | Common:1; Rare:93 | ||||
| chr20:62386946-62387136 | Common:3; Rare:84 |