| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45363346-45363533 | Common:1; Rare:47 | ||||
| chr20:45405833-45406065 | Common:2; Rare:59 | ||||
| chr20:45406522-45406723 | Rare:54 | ||||
| chr20:45416026-45416632 | Rare:204; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr20:45791908-45792014 | Common:1; Rare:41 | ||||
| chr20:45833279-45833369 | Common:1; Rare:12 | ||||
| chr20:45833718-45833940 | Common:7; Rare:53 | ||||
| chr20:45834058-45834233 | Rare:61 | ||||
| chr20:45857311-45857621 | Common:4; Rare:85 | ||||
| chr20:45890998-45891448 | Common:4; Rare:135; Clinvar:8; Clinvar (benign):4 | ||||
| chr20:45910895-45911235 | Common:4; Rare:106 | ||||
| chr20:45911238-45911334 | Common:1; Rare:33 | ||||
| chr20:45912074-45912314 | Common:3; Rare:57 | ||||
| chr20:45934622-45934717 | Rare:49 | ||||
| chr20:45935045-45935345 | Rare:118 |