| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9843968-9844136 | Common:2; Rare:66 | ||||
| chr3:9890510-9890694 | Common:2; Rare:72 | ||||
| chr3:9933534-9933919 | Common:3; Rare:150; Clinvar:3 | ||||
| chr3:10026295-10026480 | Rare:62 | ||||
| chr3:10115540-10115713 | Common:3; Rare:65 | ||||
| chr3:10141657-10142009 | Common:2; Rare:163; Clinvar:39; Clinvar (benign):34 | ||||
| chr3:11272252-11272427 | Common:1; Rare:36 | ||||
| chr3:11643759-11644063 | Common:2; Rare:83 | ||||
| chr3:11719428-11719595 | Rare:53 | ||||
| chr3:12004254-12004404 | Common:2; Rare:46 | ||||
| chr3:12484195-12484554 | Common:5; Rare:110; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664066-12664330 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13480040-13480339 | Common:2; Rare:70 | ||||
| chr3:14124729-14125189 | Common:4; Rare:131; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:14178569-14178864 | Common:2; Rare:152; Clinvar:4; Clinvar (benign):1 |