| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45891010-45891394 | Common:3; Rare:116; Clinvar:8; Clinvar (benign):3 | ||||
| chr20:45897556-45897770 | Rare:43; Clinvar (pathogenic):1 | ||||
| chr20:45912132-45912303 | Common:3; Rare:39 | ||||
| chr20:45934471-45934731 | Common:2; Rare:111 | ||||
| chr20:45935056-45935345 | Rare:111 | ||||
| chr20:45971828-45971985 | Common:1; Rare:49 | ||||
| chr20:46118125-46118330 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:46364369-46364551 | Rare:69 | ||||
| chr20:46406565-46406787 | Common:2; Rare:60 | ||||
| chr20:46513546-46513629 | Common:1; Rare:29 | ||||
| chr20:47318718-47319030 | Common:1; Rare:96 | ||||
| chr20:47319040-47319125 | Common:1; Rare:28 | ||||
| chr20:47356646-47356943 | Rare:70 | ||||
| chr20:47501796-47502016 | Common:1; Rare:74 | ||||
| chr20:47786290-47786581 | Common:3; Rare:68 |