| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45834076-45834217 | Rare:54 | ||||
| chr20:45857320-45857634 | Common:3; Rare:89 | ||||
| chr20:45880975-45881254 | Common:2; Rare:65 | ||||
| chr20:45891252-45891387 | Common:1; Rare:48; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45896197-45896427 | Common:3; Rare:65 | ||||
| chr20:45910958-45911230 | Common:3; Rare:91 | ||||
| chr20:45912047-45912314 | Common:4; Rare:65 | ||||
| chr20:45934652-45934731 | Rare:36 | ||||
| chr20:45935048-45935358 | Rare:122 | ||||
| chr20:45971708-45971948 | Common:3; Rare:74 | ||||
| chr20:46089615-46089978 | Rare:131 | ||||
| chr20:46118131-46118321 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:46363926-46364103 | Common:1; Rare:36 | ||||
| chr20:46364360-46364551 | Rare:72 | ||||
| chr20:46406565-46406793 | Common:2; Rare:62 |