| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:36573267-36573740 | Common:6; Rare:755 | ||||
| chr20:36574157-36574274 | Rare:27 | ||||
| chr20:36574758-36574922 | Rare:63 | ||||
| chr20:36605428-36605860 | Common:12; Rare:768 | ||||
| chr20:36700584-36700698 | Rare:28 | ||||
| chr20:36745830-36746400 | Common:20; Rare:716 | ||||
| chr20:36773432-36774046 | Common:12; Rare:399 | ||||
| chr20:36773995-36774395 | Common:2; Rare:113 | ||||
| chr20:36863393-36864073 | Rare:358 | ||||
| chr20:36864042-36864165 | Common:1; Rare:42 | ||||
| chr20:36864098-36864498 | Common:3; Rare:93 | ||||
| chr20:36951616-36952033 | Common:7; Rare:637; Clinvar:5; Clinvar (benign):28 | ||||
| chr20:37095282-37095890 | Common:4; Rare:422 | ||||
| chr20:37095902-37096512 | Common:12; Rare:698 | ||||
| chr20:37178104-37178602 | Common:5; Rare:196 |