| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35284552-35284848 | Common:2; Rare:77 | ||||
| chr20:35664862-35665042 | Common:1; Rare:50 | ||||
| chr20:35699183-35699260 | Rare:9 | ||||
| chr20:35699354-35699429 | Rare:22 | ||||
| chr20:35713020-35713186 | Common:2; Rare:34 | ||||
| chr20:35742145-35742582 | Common:4; Rare:129 | ||||
| chr20:36236436-36236510 | Rare:14 | ||||
| chr20:37289570-37289674 | Common:1; Rare:31 | ||||
| chr20:38033420-38033753 | Common:2; Rare:96 | ||||
| chr20:43590643-43590996 | Rare:80 | ||||
| chr20:44210701-44211111 | Common:5; Rare:148 | ||||
| chr20:45791884-45792006 | Common:1; Rare:49 | ||||
| chr20:45857315-45857624 | Common:3; Rare:87 | ||||
| chr20:45891252-45891420 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45935051-45935326 | Rare:106 |