| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35664756-35665170 | Common:10; Rare:450 | ||||
| chr20:35699040-35699673 | Rare:703; Clinvar (benign):20 | ||||
| chr20:35741210-35741741 | Common:7; Rare:213 | ||||
| chr20:35742018-35742800 | Common:44; Rare:1419 | ||||
| chr20:35771720-35772125 | Common:11; Rare:455 | ||||
| chr20:35772129-35772537 | Common:3; Rare:313 | ||||
| chr20:35954157-35955123 | Common:23; Rare:1064 | ||||
| chr20:35967825-35968225 | Common:7; Rare:101 | ||||
| chr20:36092440-36092900 | Common:1; Rare:128 | ||||
| chr20:36154160-36154660 | Common:1; Rare:96 | ||||
| chr20:36236170-36236667 | Common:10; Rare:330 | ||||
| chr20:36461077-36461878 | Common:48; Rare:913 | ||||
| chr20:36472292-36473200 | Common:5; Rare:210 | ||||
| chr20:36541272-36541672 | Common:10; Rare:242 | ||||
| chr20:36572725-36573125 | Common:2; Rare:118 |