| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:53593797-53593894 | Common:1; Rare:35 | ||||
| chr20:56392197-56392695 | Common:6; Rare:131 | ||||
| chr20:56411881-56412099 | Common:1; Rare:38 | ||||
| chr20:56468478-56468734 | Rare:93 | ||||
| chr20:58309421-58309715 | Common:2; Rare:115 | ||||
| chr20:58388984-58389319 | Common:4; Rare:167; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:58651053-58651332 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:58839682-58839760 | Rare:19 | ||||
| chr20:58840343-58840764 | Common:1; Rare:160; Clinvar:3 | ||||
| chr20:58888788-58889132 | Common:1; Rare:102 | ||||
| chr20:58892159-58892190 | Common:3; Rare:15 | ||||
| chr20:59042711-59043015 | Common:1; Rare:113 | ||||
| chr20:59940297-59940486 | Rare:78 | ||||
| chr20:62143238-62143823 | Common:8; Rare:239 | ||||
| chr20:62182909-62183049 | Rare:49 |