| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47319040-47319114 | Common:1; Rare:22 | ||||
| chr20:47351730-47351754 | Rare:5 | ||||
| chr20:47351895-47352076 | Common:1; Rare:29 | ||||
| chr20:47356656-47356882 | Rare:52 | ||||
| chr20:47501752-47502111 | Common:1; Rare:117 | ||||
| chr20:47786539-47786813 | Common:6; Rare:41 | ||||
| chr20:49046185-49046354 | Common:3; Rare:48 | ||||
| chr20:49219245-49219481 | Common:1; Rare:111 | ||||
| chr20:49278039-49278266 | Rare:64 | ||||
| chr20:49812772-49812925 | Common:2; Rare:43 | ||||
| chr20:49915491-49915545 | Rare:19 | ||||
| chr20:50113112-50113239 | Common:5; Rare:61 | ||||
| chr20:50958502-50958834 | Common:1; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:54070498-54070636 | Rare:21 | ||||
| chr20:56392193-56392397 | Rare:52 |