| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45833677-45833858 | Common:6; Rare:64 | ||||
| chr20:45834073-45834200 | Rare:47 | ||||
| chr20:45857326-45857829 | Common:7; Rare:226 | ||||
| chr20:45881037-45881271 | Common:4; Rare:107 | ||||
| chr20:45890079-45890344 | Common:2; Rare:140 | ||||
| chr20:45891000-45891413 | Common:6; Rare:207; Clinvar:11; Clinvar (benign):6 | ||||
| chr20:45910873-45911181 | Common:8; Rare:168 | ||||
| chr20:45934373-45934748 | Common:3; Rare:258 | ||||
| chr20:45935031-45935368 | Rare:252 | ||||
| chr20:45971719-45972071 | Common:5; Rare:153 | ||||
| chr20:45972140-45972680 | Common:4; Rare:273 | ||||
| chr20:46363854-46364119 | Common:2; Rare:89 | ||||
| chr20:46364331-46364559 | Common:2; Rare:149 | ||||
| chr20:46406010-46406460 | Common:3; Rare:119 | ||||
| chr20:46406539-46406827 | Common:6; Rare:142 |