| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44885602-44885875 | Common:4; Rare:90 | ||||
| chr20:44966376-44966560 | Rare:73 | ||||
| chr20:45348418-45348497 | Common:1; Rare:16 | ||||
| chr20:45363346-45363525 | Common:1; Rare:43 | ||||
| chr20:45405933-45406191 | Common:2; Rare:65 | ||||
| chr20:45407423-45407487 | Rare:14 | ||||
| chr20:45408136-45408359 | Common:1; Rare:57 | ||||
| chr20:45416049-45416181 | Rare:49; Clinvar:1 | ||||
| chr20:45791906-45792005 | Common:1; Rare:40 | ||||
| chr20:45857320-45857646 | Common:3; Rare:95 | ||||
| chr20:45881018-45881241 | Common:2; Rare:51 | ||||
| chr20:45891020-45891387 | Common:3; Rare:109; Clinvar:8; Clinvar (benign):3 | ||||
| chr20:45912079-45912329 | Common:4; Rare:57 | ||||
| chr20:45934558-45934731 | Common:1; Rare:84 | ||||
| chr20:46089885-46090124 | Common:1; Rare:81 |