| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45406541-45406736 | Rare:50 | ||||
| chr20:45407087-45407314 | Rare:35 | ||||
| chr20:45407874-45408192 | Common:2; Rare:61 | ||||
| chr20:45416067-45416159 | Rare:27 | ||||
| chr20:45420338-45420604 | Rare:89; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45791920-45792014 | Common:1; Rare:35 | ||||
| chr20:45834110-45834209 | Rare:39 | ||||
| chr20:45857315-45857621 | Common:3; Rare:85 | ||||
| chr20:45890998-45891387 | Common:4; Rare:121; Clinvar:8; Clinvar (benign):4 | ||||
| chr20:45934645-45934731 | Rare:41 | ||||
| chr20:45971846-45971992 | Rare:39 | ||||
| chr20:45972179-45972304 | Rare:51 | ||||
| chr20:46364386-46364528 | Rare:55 | ||||
| chr20:46406565-46406787 | Common:2; Rare:60 | ||||
| chr20:47318731-47319106 | Common:2; Rare:114 |