| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57556022-57556298 | Rare:64 | ||||
| chr3:57597280-57597534 | Common:3; Rare:78 | ||||
| chr3:58433799-58434171 | Common:2; Rare:111; Clinvar (benign):3 | ||||
| chr3:62318890-62319068 | Rare:73 | ||||
| chr3:63863763-63864134 | Common:7; Rare:121 | ||||
| chr3:64018681-64018964 | Common:2; Rare:77 | ||||
| chr3:67654552-67654747 | Common:2; Rare:81 | ||||
| chr3:69013588-69013719 | Rare:34 | ||||
| chr3:88058923-88059320 | Common:3; Rare:152 | ||||
| chr3:88149659-88150002 | Rare:86 | ||||
| chr3:98901644-98901990 | Common:1; Rare:131 | ||||
| chr3:99638406-99638609 | Common:1; Rare:49 | ||||
| chr3:99876129-99876278 | Common:1; Rare:37 | ||||
| chr3:100401357-100401586 | Common:1; Rare:53 | ||||
| chr3:100709228-100709686 | Common:6; Rare:141; Clinvar (benign):1 |