| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45896832-45897037 | Rare:57; Clinvar:1 | ||||
| chr20:45897478-45897720 | Common:1; Rare:40 | ||||
| chr20:45897723-45898060 | Common:2; Rare:88; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:45912143-45912273 | Common:3; Rare:32 | ||||
| chr20:45934557-45934731 | Common:1; Rare:84 | ||||
| chr20:46406565-46406814 | Common:2; Rare:66 | ||||
| chr20:46513532-46513592 | Common:1; Rare:19 | ||||
| chr20:46689130-46689213 | Rare:20; Clinvar (pathogenic):1 | ||||
| chr20:46689319-46689445 | Common:3; Rare:59 | ||||
| chr20:46689491-46689525 | Rare:10 | ||||
| chr20:46689536-46689637 | Rare:21 | ||||
| chr20:46709536-46709695 | Rare:47; Clinvar:1 | ||||
| chr20:47318731-47318854 | Rare:34 | ||||
| chr20:47319011-47319135 | Common:1; Rare:36 | ||||
| chr20:47356661-47356888 | Rare:53 |