| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:57351316-57351716 | Rare:123 | ||||
| chr20:57391081-57392088 | Common:86; Rare:1430 | ||||
| chr20:57523551-57523951 | Common:3; Rare:136 | ||||
| chr20:57523934-57524082 | Common:2; Rare:80 | ||||
| chr20:57524745-57525370 | Common:13; Rare:618 | ||||
| chr20:57525323-57525938 | Common:17; Rare:149 | ||||
| chr20:57560825-57561225 | Common:1; Rare:151; Clinvar:1 | ||||
| chr20:57709843-57710463 | Common:4; Rare:400 | ||||
| chr20:57710427-57710827 | Common:2; Rare:106 | ||||
| chr20:58308832-58309232 | Common:2; Rare:109 | ||||
| chr20:58309361-58309941 | Common:16; Rare:993 | ||||
| chr20:58309952-58310352 | Common:1; Rare:119 | ||||
| chr20:58388840-58389280 | Common:16; Rare:702; Clinvar:14; Clinvar (benign):5 | ||||
| chr20:58389267-58389913 | Common:3; Rare:462; Clinvar:6; Clinvar (benign):3 | ||||
| chr20:58650750-58651511 | Common:18; Rare:507; Clinvar:9; Clinvar (benign):8 |