| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:17680011-17680120 | Common:2; Rare:22 | ||||
| chr20:18793969-18794089 | Rare:39 | ||||
| chr20:19757517-19757697 | Common:3; Rare:51 | ||||
| chr20:19757929-19758322 | Common:5; Rare:129 | ||||
| chr20:19823921-19823972 | Rare:14 | ||||
| chr20:21326360-21326545 | Common:1; Rare:53 | ||||
| chr20:23358114-23358234 | Common:1; Rare:36 | ||||
| chr20:25281746-25282076 | Common:5; Rare:74 | ||||
| chr20:25854008-25854116 | Common:3; Rare:42 | ||||
| chr20:35490957-35491136 | Rare:34 | ||||
| chr20:36049959-36050281 | Common:1; Rare:68 | ||||
| chr20:36050330-36050729 | Common:1; Rare:140 | ||||
| chr20:36050920-36051132 | Common:3; Rare:75 | ||||
| chr20:36064743-36064843 | Rare:27 | ||||
| chr20:40686522-40686671 | Rare:26; Clinvar:2; Clinvar (benign):3 |