| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45343484-45343707 | Rare:47 | ||||
| chr20:45345499-45345784 | Common:1; Rare:52 | ||||
| chr20:45424261-45424575 | Common:3; Rare:89; Clinvar (pathogenic):1 | ||||
| chr20:45761938-45762042 | Rare:19 | ||||
| chr20:45762068-45762243 | Common:4; Rare:38 | ||||
| chr20:45894707-45894880 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:45898165-45898388 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:45899620-45899882 | Common:2; Rare:81 | ||||
| chr20:47317359-47317614 | Common:1; Rare:50 | ||||
| chr20:47352502-47352664 | Rare:28 | ||||
| chr20:47357794-47357844 | Rare:10 | ||||
| chr20:47358848-47358954 | Rare:22 | ||||
| chr20:48720180-48720293 | Common:1; Rare:24 | ||||
| chr20:48760371-48760621 | Rare:51 | ||||
| chr20:49094634-49094808 | Rare:36 |