| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47318731-47318874 | Rare:42 | ||||
| chr20:47318993-47319114 | Common:1; Rare:32 | ||||
| chr20:47356672-47356908 | Rare:60 | ||||
| chr20:47501710-47501993 | Common:1; Rare:98 | ||||
| chr20:49046173-49046363 | Common:3; Rare:59 | ||||
| chr20:49219258-49219464 | Common:1; Rare:101 | ||||
| chr20:49278026-49278266 | Rare:65 | ||||
| chr20:49812767-49812925 | Common:2; Rare:43 | ||||
| chr20:49915496-49915548 | Rare:17 | ||||
| chr20:50113118-50113223 | Common:5; Rare:52 | ||||
| chr20:50115926-50116087 | Common:2; Rare:38 | ||||
| chr20:50510071-50510427 | Common:3; Rare:138 | ||||
| chr20:50794863-50795099 | Common:1; Rare:87 | ||||
| chr20:50958490-50958843 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:53593775-53593914 | Common:1; Rare:52 |