| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5112972-5113178 | Rare:87 | ||||
| chr20:5119894-5120193 | Common:1; Rare:101 | ||||
| chr20:5950410-5950689 | Common:8; Rare:86 | ||||
| chr20:10434145-10434276 | Common:1; Rare:54 | ||||
| chr20:13638904-13639048 | Common:1; Rare:42 | ||||
| chr20:13784884-13785080 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr20:16729885-16730067 | Rare:54 | ||||
| chr20:17968421-17968594 | Common:4; Rare:71 | ||||
| chr20:17968784-17969122 | Common:3; Rare:120 | ||||
| chr20:18413192-18413451 | Rare:41 | ||||
| chr20:18467137-18467428 | Rare:62 | ||||
| chr20:18497174-18497308 | Common:1; Rare:48 | ||||
| chr20:18567334-18567499 | Common:2; Rare:57 | ||||
| chr20:19934849-19935126 | Common:2; Rare:66; Clinvar (benign):2 | ||||
| chr20:21125873-21126099 | Common:3; Rare:79 |