| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45833752-45833832 | Common:1; Rare:19 | ||||
| chr20:45857330-45857621 | Common:3; Rare:78 | ||||
| chr20:45891247-45891382 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45935045-45935329 | Rare:113 | ||||
| chr20:45971503-45971818 | Common:1; Rare:83 | ||||
| chr20:45971838-45971981 | Common:1; Rare:45 | ||||
| chr20:46363655-46364083 | Common:1; Rare:87 | ||||
| chr20:46364366-46364514 | Rare:54 | ||||
| chr20:46406565-46406787 | Common:2; Rare:60 | ||||
| chr20:47319015-47319059 | Rare:9 | ||||
| chr20:47356658-47356899 | Rare:60 | ||||
| chr20:47501710-47502121 | Common:1; Rare:135 | ||||
| chr20:48921642-48921736 | Rare:40 | ||||
| chr20:49046166-49046398 | Common:3; Rare:73 | ||||
| chr20:49219200-49219538 | Common:1; Rare:142 |