| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792376-9792596 | Rare:62 | ||||
| chr3:9792699-9793129 | Common:3; Rare:150 | ||||
| chr3:9933517-9933884 | Common:2; Rare:151; Clinvar:3 | ||||
| chr3:10026329-10026457 | Rare:39 | ||||
| chr3:10115520-10115765 | Common:3; Rare:86 | ||||
| chr3:10321035-10321330 | Common:2; Rare:114 | ||||
| chr3:11719419-11719589 | Rare:53 | ||||
| chr3:12663826-12663961 | Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:12664105-12664310 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124725-14125145 | Common:4; Rare:119; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178873 | Common:2; Rare:164; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402433-14402628 | Rare:48 | ||||
| chr3:14651463-14651828 | Rare:110 | ||||
| chr3:14947159-14947583 | Common:5; Rare:177 | ||||
| chr3:14948412-14948648 | Common:2; Rare:73 |