| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34876288-34876617 | Common:3; Rare:92 | ||||
| chr20:34955741-34955945 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35664880-35665003 | Common:1; Rare:33 | ||||
| chr20:35699323-35699466 | Rare:48; Clinvar (benign):2 | ||||
| chr20:36541371-36541561 | Common:2; Rare:55 | ||||
| chr20:37178924-37179173 | Rare:73 | ||||
| chr20:37289578-37289669 | Common:1; Rare:28 | ||||
| chr20:37527830-37528125 | Common:3; Rare:103 | ||||
| chr20:38033416-38033775 | Common:2; Rare:104 | ||||
| chr20:38165252-38165517 | Common:1; Rare:77 | ||||
| chr20:43590607-43590996 | Common:1; Rare:88 | ||||
| chr20:44210718-44211077 | Common:5; Rare:135 | ||||
| chr20:44885602-44885795 | Common:4; Rare:73 | ||||
| chr20:44966376-44966566 | Rare:75 | ||||
| chr20:45363106-45363221 | Rare:36 |