| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45891206-45891379 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45897519-45897770 | Rare:47; Clinvar (pathogenic):1 | ||||
| chr20:45910931-45911192 | Common:4; Rare:80 | ||||
| chr20:45912149-45912273 | Common:3; Rare:31 | ||||
| chr20:45934407-45934730 | Common:2; Rare:136 | ||||
| chr20:45935053-45935351 | Rare:115 | ||||
| chr20:45971822-45971993 | Common:1; Rare:52 | ||||
| chr20:45972172-45972495 | Common:1; Rare:118 | ||||
| chr20:46363920-46364074 | Common:1; Rare:28 | ||||
| chr20:46364324-46364544 | Common:1; Rare:79 | ||||
| chr20:46406565-46406779 | Common:2; Rare:54 | ||||
| chr20:46689141-46689172 | Rare:6 | ||||
| chr20:46689536-46689844 | Rare:64 | ||||
| chr20:47356660-47356899 | Rare:60 | ||||
| chr20:47501710-47502009 | Common:1; Rare:105 |