| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45306693-45306872 | Rare:37 | ||||
| chr20:45362919-45363252 | Common:1; Rare:100 | ||||
| chr20:45363357-45363534 | Common:1; Rare:46 | ||||
| chr20:45405885-45406195 | Common:2; Rare:80 | ||||
| chr20:45406538-45406760 | Rare:59 | ||||
| chr20:45407080-45407327 | Common:1; Rare:38 | ||||
| chr20:45407389-45407485 | Rare:20 | ||||
| chr20:45415973-45416252 | Rare:101; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45416385-45416693 | Rare:82; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr20:45791898-45792020 | Common:1; Rare:49 | ||||
| chr20:45812432-45812698 | Common:3; Rare:89 | ||||
| chr20:45812971-45813016 | Rare:4 | ||||
| chr20:45833271-45833633 | Common:1; Rare:62 | ||||
| chr20:45833743-45833937 | Common:7; Rare:47 | ||||
| chr20:45857315-45857633 | Common:3; Rare:90 |