| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34097417-34097647 | Common:1; Rare:48 | ||||
| chr20:35490909-35491141 | Rare:46 | ||||
| chr20:35605269-35605540 | Common:1; Rare:40 | ||||
| chr20:35607117-35607294 | Rare:31 | ||||
| chr20:35614657-35614843 | Common:1; Rare:36 | ||||
| chr20:35631114-35631352 | Rare:69 | ||||
| chr20:35768206-35768380 | Common:1; Rare:25 | ||||
| chr20:36050275-36050682 | Common:2; Rare:138 | ||||
| chr20:36050886-36051150 | Common:3; Rare:96 | ||||
| chr20:36914557-36914728 | Rare:29 | ||||
| chr20:40684925-40684993 | Rare:15 | ||||
| chr20:40686316-40686389 | Common:1; Rare:19; Clinvar (benign):2 | ||||
| chr20:40686515-40686661 | Rare:24; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:40686767-40687079 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:40687129-40687831 | Rare:125; Clinvar:3; Clinvar (benign):4 |