| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:39078767-39078902 | Common:1; Rare:54 | ||||
| chr20:39660983-39661128 | Common:4; Rare:18 | ||||
| chr20:39663550-39663704 | Common:1; Rare:28 | ||||
| chr20:40111031-40111122 | Common:1; Rare:17 | ||||
| chr20:40911893-40911974 | Common:2; Rare:18 | ||||
| chr20:41115171-41115439 | Common:2; Rare:48 | ||||
| chr20:41116018-41116373 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
| chr20:41118055-41118222 | Rare:38 | ||||
| chr20:41121458-41121735 | Common:1; Rare:57 | ||||
| chr20:41123026-41123333 | Common:1; Rare:51 | ||||
| chr20:41159320-41159623 | Common:2; Rare:56 | ||||
| chr20:41204972-41205139 | Common:1; Rare:38 | ||||
| chr20:41415616-41415883 | Rare:50 | ||||
| chr20:41693500-41693601 | Common:1; Rare:21 | ||||
| chr20:42630695-42630869 | Common:1; Rare:34 |