| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58433506-58433627 | Common:1; Rare:44; Clinvar (benign):2 | ||||
| chr3:58433755-58434042 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:59049942-59050120 | Rare:60 | ||||
| chr3:61251352-61251644 | Common:4; Rare:70 | ||||
| chr3:61561097-61561230 | Rare:38 | ||||
| chr3:61561412-61561581 | Common:1; Rare:65 | ||||
| chr3:62318871-62319044 | Rare:73 | ||||
| chr3:63863398-63863496 | Rare:23 | ||||
| chr3:63863548-63863951 | Common:2; Rare:129 | ||||
| chr3:63864220-63864595 | Common:2; Rare:110 | ||||
| chr3:63911889-63912172 | Rare:84 | ||||
| chr3:63912226-63912741 | Common:4; Rare:212; Clinvar (benign):1 | ||||
| chr3:63968263-63968384 | Rare:21 | ||||
| chr3:64023385-64023651 | Common:3; Rare:111 | ||||
| chr3:66220787-66221105 | Common:4; Rare:102 |