| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:77040001-77040155 | Rare:36 | ||||
| chr3:79018999-79019085 | Rare:30 | ||||
| chr3:81761437-81761821 | Common:8; Rare:138; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:86991085-86991236 | Rare:39 | ||||
| chr3:87227172-87227477 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058515-88058723 | Common:1; Rare:69 | ||||
| chr3:88058923-88059326 | Common:3; Rare:152 | ||||
| chr3:88149613-88149764 | Common:1; Rare:34 | ||||
| chr3:88149856-88150049 | Common:5; Rare:77 | ||||
| chr3:93973807-93974067 | Rare:62; Clinvar:5 | ||||
| chr3:93979885-93980236 | Common:4; Rare:132; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94028408-94028562 | Rare:21 | ||||
| chr3:94028564-94028650 | Rare:13 | ||||
| chr3:94028652-94028716 | Rare:12 | ||||
| chr3:94062877-94063117 | Rare:63 |