| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38378105-38378259 | Rare:35 | ||||
| chr20:38378591-38378631 | Rare:6 | ||||
| chr20:38379579-38379649 | Rare:18 | ||||
| chr20:40008537-40008722 | Rare:28 | ||||
| chr20:40687299-40687563 | Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:40687650-40687803 | Rare:30; Clinvar (benign):2 | ||||
| chr20:44357218-44357322 | Rare:13 | ||||
| chr20:44358993-44359081 | Rare:10 | ||||
| chr20:44359085-44359283 | Common:3; Rare:23 | ||||
| chr20:44359750-44359909 | Common:1; Rare:27 | ||||
| chr20:44395469-44395700 | Common:1; Rare:28 | ||||
| chr20:44447955-44448252 | Common:1; Rare:54 | ||||
| chr20:44467207-44467528 | Common:1; Rare:60 | ||||
| chr20:45344190-45344516 | Common:1; Rare:71 | ||||
| chr20:45419362-45419586 | Common:2; Rare:88; Clinvar:1; Clinvar (pathogenic):1 |