| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45971734-45972036 | Common:3; Rare:88 | ||||
| chr20:45972172-45972475 | Common:1; Rare:114 | ||||
| chr20:46089621-46089956 | Rare:117 | ||||
| chr20:46118155-46118344 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:46363940-46364085 | Common:1; Rare:28 | ||||
| chr20:46364362-46364565 | Common:1; Rare:77 | ||||
| chr20:46406565-46406790 | Common:2; Rare:61 | ||||
| chr20:46513506-46513592 | Common:1; Rare:30 | ||||
| chr20:46709583-46709689 | Rare:32; Clinvar:1 | ||||
| chr20:47318703-47319118 | Common:2; Rare:127 | ||||
| chr20:47319122-47319212 | Rare:34 | ||||
| chr20:47356657-47356887 | Rare:54 | ||||
| chr20:47501764-47502019 | Common:1; Rare:88 | ||||
| chr20:48921588-48921854 | Common:3; Rare:108; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:49046214-49046358 | Common:3; Rare:43 |