| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58651596-58651850 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:58888754-58889151 | Common:1; Rare:123 | ||||
| chr20:58891182-58891426 | Common:4; Rare:97 | ||||
| chr20:58891906-58892183 | Common:7; Rare:140 | ||||
| chr20:58908870-58909662 | Common:5; Rare:199; Clinvar:2; Clinvar (pathogenic):4 | ||||
| chr20:58981098-58981349 | Common:2; Rare:114 | ||||
| chr20:59007020-59007084 | Rare:23 | ||||
| chr20:59007264-59007331 | Rare:12 | ||||
| chr20:59032270-59032568 | Common:3; Rare:124; Clinvar (benign):4 | ||||
| chr20:59940295-59940446 | Rare:61 | ||||
| chr20:62065823-62066055 | Common:2; Rare:100 | ||||
| chr20:62143243-62143792 | Common:7; Rare:221 | ||||
| chr20:62182887-62183046 | Common:1; Rare:55 | ||||
| chr20:62302625-62303045 | Common:3; Rare:118 | ||||
| chr20:62386932-62387131 | Common:3; Rare:89 |