| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9769875-9770068 | Common:2; Rare:82 | ||||
| chr3:9792324-9793183 | Common:12; Rare:801 | ||||
| chr3:9793515-9793821 | Rare:72 | ||||
| chr3:9809659-9810000 | Common:2; Rare:187 | ||||
| chr3:9810020-9810448 | Common:7; Rare:364 | ||||
| chr3:9843847-9844229 | Common:12; Rare:391 | ||||
| chr3:9890436-9890796 | Common:6; Rare:241; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr3:9890800-9891200 | Rare:134 | ||||
| chr3:9902410-9902989 | Common:8; Rare:356 | ||||
| chr3:9916860-9917209 | Common:7; Rare:139 | ||||
| chr3:9933368-9934342 | Common:13; Rare:743; Clinvar:12; Clinvar (benign):3 | ||||
| chr3:9951850-9952250 | Common:5; Rare:157 | ||||
| chr3:9952304-9952478 | Rare:63 | ||||
| chr3:9986705-9987172 | Common:11; Rare:334 | ||||
| chr3:9987162-9987392 | Common:2; Rare:95 |