| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33720205-33720500 | Common:4; Rare:77 | ||||
| chr20:33731941-33732010 | Rare:31 | ||||
| chr20:33811107-33811499 | Common:1; Rare:120 | ||||
| chr20:33993058-33993300 | Common:1; Rare:64 | ||||
| chr20:33993834-33994124 | Common:1; Rare:114 | ||||
| chr20:33994346-33994551 | Common:1; Rare:58 | ||||
| chr20:34112081-34112448 | Rare:122 | ||||
| chr20:34302941-34303399 | Common:2; Rare:177; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:34363171-34363342 | Rare:47 | ||||
| chr20:34516265-34516767 | Common:4; Rare:191 | ||||
| chr20:34558479-34559003 | Common:1; Rare:147 | ||||
| chr20:34676741-34676894 | Common:1; Rare:40 | ||||
| chr20:34677069-34677329 | Rare:69 | ||||
| chr20:34872798-34872912 | Rare:43 | ||||
| chr20:34876308-34876660 | Common:3; Rare:95 |