| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:53583089-53583222 | Common:1; Rare:25 | ||||
| chr20:53593573-53593882 | Common:3; Rare:119 | ||||
| chr20:56392149-56392699 | Common:6; Rare:150 | ||||
| chr20:56468398-56468757 | Rare:115 | ||||
| chr20:56516724-56516931 | Rare:53 | ||||
| chr20:56629124-56629311 | Rare:56 | ||||
| chr20:58389000-58389281 | Common:3; Rare:134; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58651102-58651307 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58652316-58652581 | Common:2; Rare:89 | ||||
| chr20:58981038-58981364 | Common:3; Rare:144 | ||||
| chr20:58990738-58991044 | Common:1; Rare:75 | ||||
| chr20:59032218-59032575 | Common:3; Rare:152; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59042696-59042987 | Common:1; Rare:99 | ||||
| chr20:59933597-59933798 | Common:4; Rare:80 | ||||
| chr20:59940283-59940523 | Rare:90 |