| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:41166229-41166551 | Common:1; Rare:94 | ||||
| chr20:41169801-41170135 | Common:3; Rare:78 | ||||
| chr20:41171958-41172171 | Common:1; Rare:47 | ||||
| chr20:41173849-41174120 | Common:3; Rare:71 | ||||
| chr20:41352653-41352828 | Rare:47 | ||||
| chr20:43457800-43457907 | Rare:47 | ||||
| chr20:43458244-43458422 | Common:2; Rare:71 | ||||
| chr20:43558880-43559111 | Rare:44 | ||||
| chr20:44210718-44211105 | Common:5; Rare:141 | ||||
| chr20:44355200-44355460 | Rare:42; Clinvar:2 | ||||
| chr20:44355587-44355766 | Common:1; Rare:35; Clinvar:1 | ||||
| chr20:44531802-44531978 | Common:1; Rare:56 | ||||
| chr20:44651687-44651798 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr20:44885602-44885880 | Common:4; Rare:92 | ||||
| chr20:44966391-44966571 | Common:1; Rare:65 |