| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46118147-46118317 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:46363940-46364061 | Common:1; Rare:20 | ||||
| chr20:46364369-46364556 | Common:1; Rare:71 | ||||
| chr20:46406571-46406788 | Common:2; Rare:57 | ||||
| chr20:46433063-46433250 | Common:3; Rare:27 | ||||
| chr20:46513495-46513620 | Common:1; Rare:41 | ||||
| chr20:46651456-46651584 | Rare:31 | ||||
| chr20:47318703-47319027 | Common:1; Rare:102 | ||||
| chr20:47319040-47319233 | Common:1; Rare:67 | ||||
| chr20:47351708-47351782 | Rare:12 | ||||
| chr20:47351895-47352190 | Common:1; Rare:49 | ||||
| chr20:47356664-47356900 | Rare:59 | ||||
| chr20:47501764-47502086 | Common:1; Rare:107 | ||||
| chr20:49046166-49046354 | Common:3; Rare:55 | ||||
| chr20:49219211-49219524 | Common:1; Rare:134 |