| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47318723-47319114 | Common:2; Rare:119 | ||||
| chr20:47319132-47319220 | Rare:29 | ||||
| chr20:47348068-47348282 | Common:1; Rare:27 | ||||
| chr20:47351879-47351998 | Rare:18 | ||||
| chr20:47356658-47356892 | Rare:57 | ||||
| chr20:47501752-47502147 | Common:1; Rare:127 | ||||
| chr20:47659695-47659795 | Common:1; Rare:23 | ||||
| chr20:47786335-47786592 | Common:3; Rare:56 | ||||
| chr20:48921625-48921916 | Common:2; Rare:117; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:49046179-49046364 | Common:3; Rare:57 | ||||
| chr20:49219280-49219541 | Rare:118 | ||||
| chr20:49278031-49278288 | Rare:70 | ||||
| chr20:49568044-49568157 | Common:2; Rare:27 | ||||
| chr20:49812641-49812946 | Common:3; Rare:79 | ||||
| chr20:49915471-49915602 | Common:3; Rare:49 |