| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:36235750-36236020 | Rare:55 | ||||
| chr20:36236372-36236540 | Common:2; Rare:47 | ||||
| chr20:36461124-36461478 | Common:1; Rare:99 | ||||
| chr20:36573220-36573690 | Common:2; Rare:177 | ||||
| chr20:36574388-36574593 | Rare:71 | ||||
| chr20:36574650-36574983 | Rare:104 | ||||
| chr20:36605487-36605814 | Common:2; Rare:117 | ||||
| chr20:36745544-36745944 | Rare:122 | ||||
| chr20:36746068-36746363 | Common:3; Rare:98 | ||||
| chr20:36773704-36773944 | Common:3; Rare:84 | ||||
| chr20:36863666-36863809 | Rare:34 | ||||
| chr20:36864048-36864165 | Common:1; Rare:41 | ||||
| chr20:36887212-36887612 | Rare:167 | ||||
| chr20:36951670-36951925 | Common:1; Rare:65; Clinvar (benign):4 | ||||
| chr20:37095578-37095803 | Common:1; Rare:72 |