| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46363926-46364084 | Common:1; Rare:30 | ||||
| chr20:46364362-46364526 | Rare:64 | ||||
| chr20:47356664-47356892 | Rare:55 | ||||
| chr20:47501752-47501940 | Common:1; Rare:66 | ||||
| chr20:49046148-49046358 | Common:3; Rare:63 | ||||
| chr20:49188304-49188553 | Common:2; Rare:85 | ||||
| chr20:49278031-49278272 | Rare:65 | ||||
| chr20:49812573-49812925 | Common:2; Rare:81 | ||||
| chr20:49915462-49915602 | Common:3; Rare:55 | ||||
| chr20:50113112-50113239 | Common:5; Rare:61 | ||||
| chr20:50153647-50153928 | Common:2; Rare:114 | ||||
| chr20:50958408-50958896 | Common:1; Rare:190; Clinvar:5; Clinvar (benign):5 | ||||
| chr20:53593783-53593894 | Common:1; Rare:40 | ||||
| chr20:56392148-56392692 | Common:6; Rare:148 | ||||
| chr20:58309427-58309715 | Common:2; Rare:114 |