| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44210208-44210256 | Rare:11 | ||||
| chr20:44210585-44211106 | Common:5; Rare:180 | ||||
| chr20:44355261-44355455 | Rare:32; Clinvar:1 | ||||
| chr20:44521910-44522233 | Common:2; Rare:102 | ||||
| chr20:44531790-44531969 | Rare:59 | ||||
| chr20:44651594-44651831 | Common:1; Rare:74; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:44885645-44885884 | Common:4; Rare:82 | ||||
| chr20:44960251-44960481 | Common:1; Rare:93 | ||||
| chr20:44966357-44966577 | Common:2; Rare:88 | ||||
| chr20:45348395-45348519 | Common:1; Rare:33 | ||||
| chr20:45406541-45406720 | Rare:46 | ||||
| chr20:45415958-45416165 | Rare:57 | ||||
| chr20:45416366-45416652 | Rare:81; Clinvar (pathogenic):2 | ||||
| chr20:45791854-45791991 | Rare:50 | ||||
| chr20:45812339-45813122 | Common:7; Rare:205 |