| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9397434-9397670 | Rare:79 | ||||
| chr3:9749850-9749983 | Rare:41 | ||||
| chr3:9792364-9792610 | Rare:68 | ||||
| chr3:9792726-9793144 | Common:3; Rare:149 | ||||
| chr3:9890457-9890702 | Common:3; Rare:102 | ||||
| chr3:9933514-9933895 | Common:3; Rare:153; Clinvar:3 | ||||
| chr3:10026252-10026476 | Common:1; Rare:67 | ||||
| chr3:10026503-10026696 | Rare:44 | ||||
| chr3:10115517-10115784 | Common:4; Rare:89 | ||||
| chr3:10141694-10141871 | Common:1; Rare:83; Clinvar:15; Clinvar (benign):18 | ||||
| chr3:10321045-10321292 | Common:2; Rare:99 | ||||
| chr3:12484218-12484554 | Common:5; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664088-12664351 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:13480063-13480345 | Common:1; Rare:68 | ||||
| chr3:14124733-14125054 | Common:4; Rare:89; Clinvar:3; Clinvar (benign):1 |