| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35771847-35772051 | Common:2; Rare:67 | ||||
| chr20:36236447-36236493 | Rare:8 | ||||
| chr20:36573273-36573616 | Common:1; Rare:145 | ||||
| chr20:36746051-36746215 | Common:2; Rare:70 | ||||
| chr20:36951621-36951726 | Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:36951771-36951792 | Rare:3 | ||||
| chr20:37178875-37179213 | Rare:99 | ||||
| chr20:37179519-37179602 | Rare:35 | ||||
| chr20:37344524-37344735 | Common:3; Rare:47 | ||||
| chr20:37527818-37528168 | Common:3; Rare:121 | ||||
| chr20:38033408-38033905 | Common:3; Rare:141 | ||||
| chr20:38962145-38962382 | Common:1; Rare:98 | ||||
| chr20:41028624-41028890 | Rare:106 | ||||
| chr20:44210710-44211105 | Common:5; Rare:143 | ||||
| chr20:44311144-44311256 | Common:1; Rare:41 |