| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:41340694-41340853 | Rare:51 | ||||
| chr20:41618340-41618747 | Common:2; Rare:121 | ||||
| chr20:43457807-43457907 | Rare:45 | ||||
| chr20:43590585-43591029 | Common:1; Rare:111 | ||||
| chr20:44210710-44211119 | Common:5; Rare:150 | ||||
| chr20:44475821-44475947 | Rare:50 | ||||
| chr20:44521940-44522243 | Common:2; Rare:96 | ||||
| chr20:44531830-44532065 | Common:2; Rare:67 | ||||
| chr20:44532238-44532580 | Common:2; Rare:66 | ||||
| chr20:44582441-44582686 | Rare:35 | ||||
| chr20:44651662-44651831 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr20:44715011-44715168 | Common:2; Rare:29 | ||||
| chr20:44885602-44885885 | Common:4; Rare:93 | ||||
| chr20:44960340-44960531 | Common:1; Rare:75 | ||||
| chr20:44966351-44966581 | Common:2; Rare:90 |