| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45406537-45406723 | Rare:49 | ||||
| chr20:45407860-45407995 | Common:2; Rare:23 | ||||
| chr20:45416086-45416171 | Rare:34 | ||||
| chr20:45416374-45416603 | Rare:67; Clinvar (pathogenic):2 | ||||
| chr20:45791879-45792014 | Common:1; Rare:51 | ||||
| chr20:45833288-45833360 | Common:1; Rare:9 | ||||
| chr20:45834060-45834209 | Rare:53 | ||||
| chr20:45857299-45857635 | Common:4; Rare:96 | ||||
| chr20:45891227-45891393 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45897430-45897777 | Common:2; Rare:63; Clinvar (pathogenic):1 | ||||
| chr20:45934391-45934731 | Common:2; Rare:143 | ||||
| chr20:45935048-45935345 | Rare:116 | ||||
| chr20:45971832-45971981 | Common:1; Rare:47 | ||||
| chr20:46363962-46364081 | Common:1; Rare:24 | ||||
| chr20:46364362-46364511 | Rare:57 |