| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45363346-45363534 | Common:1; Rare:47 | ||||
| chr20:45405969-45406191 | Common:1; Rare:55 | ||||
| chr20:45406541-45406736 | Rare:50 | ||||
| chr20:45407377-45407484 | Rare:21 | ||||
| chr20:45416044-45416178 | Rare:47 | ||||
| chr20:45469664-45469869 | Rare:76 | ||||
| chr20:45791904-45792014 | Common:1; Rare:42 | ||||
| chr20:45827245-45827510 | Common:2; Rare:43 | ||||
| chr20:45827552-45827590 | Rare:5 | ||||
| chr20:45833250-45833450 | Common:1; Rare:28 | ||||
| chr20:45834092-45834281 | Rare:76 | ||||
| chr20:45857312-45857646 | Common:4; Rare:97 | ||||
| chr20:45891000-45891400 | Common:4; Rare:122; Clinvar:8; Clinvar (benign):4 | ||||
| chr20:45896147-45896409 | Common:3; Rare:73 | ||||
| chr20:45934616-45934753 | Rare:68 |