| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9933511-9933863 | Common:2; Rare:142; Clinvar:3 | ||||
| chr3:10026304-10026453 | Rare:50 | ||||
| chr3:10115530-10115761 | Common:3; Rare:84 | ||||
| chr3:11137025-11137250 | Rare:42 | ||||
| chr3:11154285-11154542 | Common:4; Rare:65 | ||||
| chr3:11643610-11643746 | Common:1; Rare:20 | ||||
| chr3:11719427-11719593 | Rare:52 | ||||
| chr3:11846843-11846994 | Common:1; Rare:42 | ||||
| chr3:12287750-12287970 | Common:6; Rare:38 | ||||
| chr3:12484323-12484564 | Common:5; Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664075-12664315 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13480018-13480339 | Common:2; Rare:80 | ||||
| chr3:14124723-14125156 | Common:4; Rare:125; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178879 | Common:2; Rare:167; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402437-14402700 | Rare:62 |