| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45415955-45416168 | Rare:61 | ||||
| chr20:45791816-45791999 | Common:1; Rare:63 | ||||
| chr20:45812281-45812683 | Common:3; Rare:117 | ||||
| chr20:45833489-45833672 | Common:1; Rare:35 | ||||
| chr20:45833709-45833838 | Common:2; Rare:31 | ||||
| chr20:45834012-45834209 | Rare:70 | ||||
| chr20:45834239-45834639 | Common:1; Rare:173 | ||||
| chr20:45857320-45857646 | Common:3; Rare:95 | ||||
| chr20:45881015-45881283 | Common:2; Rare:63 | ||||
| chr20:45891110-45891440 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:45910893-45911205 | Common:4; Rare:95 | ||||
| chr20:45911649-45911866 | Rare:43 | ||||
| chr20:45912149-45912329 | Common:4; Rare:38 | ||||
| chr20:45934510-45934753 | Common:1; Rare:112 | ||||
| chr20:45934938-45935045 | Common:1; Rare:48 |