| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43458253-43458422 | Common:2; Rare:66 | ||||
| chr20:43590607-43590986 | Common:1; Rare:84 | ||||
| chr20:44210697-44211102 | Common:5; Rare:146 | ||||
| chr20:44475811-44475954 | Common:1; Rare:55 | ||||
| chr20:44521979-44522233 | Common:2; Rare:82 | ||||
| chr20:44531814-44531978 | Common:1; Rare:51 | ||||
| chr20:44651670-44651839 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr20:44966383-44966571 | Common:1; Rare:70 | ||||
| chr20:45363361-45363525 | Common:1; Rare:41 | ||||
| chr20:45416035-45416170 | Rare:43 | ||||
| chr20:45791906-45792014 | Common:1; Rare:42 | ||||
| chr20:45833290-45833424 | Common:1; Rare:21 | ||||
| chr20:45857320-45857621 | Common:3; Rare:83 | ||||
| chr20:45891014-45891432 | Common:3; Rare:126; Clinvar:8; Clinvar (benign):3 | ||||
| chr20:46363930-46364064 | Common:1; Rare:23 |