| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:57391098-57391546 | Common:29; Rare:400 | ||||
| chr20:57391840-57393091 | Common:11; Rare:386 | ||||
| chr20:57709838-57710320 | Common:3; Rare:373 | ||||
| chr20:57710474-57710681 | Common:1; Rare:124 | ||||
| chr20:58309399-58310000 | Common:11; Rare:606 | ||||
| chr20:58309988-58310217 | Common:1; Rare:57 | ||||
| chr20:58388970-58389463 | Common:8; Rare:404; Clinvar:10; Clinvar (benign):5 | ||||
| chr20:58389470-58389740 | Rare:138; Clinvar:1 | ||||
| chr20:58650440-58651011 | Common:11; Rare:216 | ||||
| chr20:58651002-58652026 | Common:10; Rare:405; Clinvar:8; Clinvar (benign):10 | ||||
| chr20:58652310-58652570 | Common:4; Rare:133 | ||||
| chr20:58688765-58690260 | Common:20; Rare:415 | ||||
| chr20:58692527-58693074 | Common:10; Rare:404 | ||||
| chr20:58693010-58693220 | Common:2; Rare:102 | ||||
| chr20:58693240-58693860 | Common:5; Rare:217 |