| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:18137782-18137932 | Common:1; Rare:52 | ||||
| chr20:18288496-18288559 | Rare:18 | ||||
| chr20:18466994-18467131 | Rare:37 | ||||
| chr20:18467183-18467444 | Common:1; Rare:48 | ||||
| chr20:18507460-18507652 | Rare:50; Clinvar:1 | ||||
| chr20:18567329-18567513 | Common:2; Rare:66 | ||||
| chr20:19889289-19889552 | Common:2; Rare:48 | ||||
| chr20:20017215-20017410 | Rare:71 | ||||
| chr20:21125867-21126107 | Common:3; Rare:83 | ||||
| chr20:21303223-21303470 | Rare:78 | ||||
| chr20:21303571-21303870 | Common:1; Rare:89 | ||||
| chr20:23049627-23049939 | Common:3; Rare:101; Clinvar (pathogenic):1 | ||||
| chr20:23085776-23085887 | Common:2; Rare:38 | ||||
| chr20:23086188-23086534 | Common:1; Rare:87 | ||||
| chr20:23350488-23350928 | Common:4; Rare:136 |