| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10511649-10511699 | Rare:10 | ||||
| chr20:10670736-10670963 | Rare:51 | ||||
| chr20:10672014-10672300 | Common:1; Rare:58 | ||||
| chr20:10672659-10672879 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:10674860-10674942 | Common:1; Rare:14 | ||||
| chr20:11261588-11261712 | Rare:21 | ||||
| chr20:11267396-11267474 | Rare:15 | ||||
| chr20:11455062-11455225 | Rare:31 | ||||
| chr20:11455391-11455424 | Rare:4 | ||||
| chr20:11456425-11456640 | Common:1; Rare:37 | ||||
| chr20:13220108-13220235 | Rare:50 | ||||
| chr20:13260693-13260872 | Common:2; Rare:31 | ||||
| chr20:13264978-13265181 | Rare:43 | ||||
| chr20:13336516-13336555 | Rare:8 | ||||
| chr20:13336855-13336934 | Rare:13 |