| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45971555-45971911 | Common:3; Rare:100 | ||||
| chr20:46363771-46364049 | Common:1; Rare:54 | ||||
| chr20:46364362-46364511 | Rare:57 | ||||
| chr20:46406571-46406790 | Common:2; Rare:58 | ||||
| chr20:46709583-46709662 | Rare:19 | ||||
| chr20:47318716-47318874 | Rare:44 | ||||
| chr20:47318953-47319184 | Common:1; Rare:75 | ||||
| chr20:47356657-47356887 | Rare:54 | ||||
| chr20:47501548-47502009 | Common:2; Rare:146 | ||||
| chr20:48921572-48921850 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:49046207-49046354 | Common:3; Rare:44 | ||||
| chr20:49278031-49278291 | Rare:71 | ||||
| chr20:49278436-49278713 | Common:9; Rare:109 | ||||
| chr20:49568058-49568155 | Common:2; Rare:23 | ||||
| chr20:49812569-49812925 | Common:2; Rare:82 |