| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44960366-44960555 | Common:1; Rare:68 | ||||
| chr20:44966370-44966553 | Rare:74 | ||||
| chr20:45348418-45348519 | Common:1; Rare:24 | ||||
| chr20:45362945-45363203 | Rare:83 | ||||
| chr20:45415982-45416153 | Rare:44 | ||||
| chr20:45812296-45812795 | Common:5; Rare:146 | ||||
| chr20:45834058-45834183 | Rare:42 | ||||
| chr20:45857320-45857617 | Common:3; Rare:82 | ||||
| chr20:45881041-45881254 | Common:2; Rare:51 | ||||
| chr20:45891000-45891382 | Common:4; Rare:119; Clinvar:8; Clinvar (benign):4 | ||||
| chr20:45912150-45912287 | Common:3; Rare:32 | ||||
| chr20:45934622-45934725 | Rare:52 | ||||
| chr20:45935045-45935345 | Rare:118 | ||||
| chr20:46021672-46021715 | Common:1; Rare:16 | ||||
| chr20:46364377-46364613 | Common:1; Rare:84 |