| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9933514-9933863 | Common:2; Rare:142; Clinvar:3 | ||||
| chr3:10026300-10026496 | Rare:62 | ||||
| chr3:10115552-10115817 | Common:2; Rare:83 | ||||
| chr3:10141673-10141825 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):11 | ||||
| chr3:11137014-11137257 | Rare:48 | ||||
| chr3:11225884-11226027 | Rare:17 | ||||
| chr3:12158732-12158819 | Rare:50 | ||||
| chr3:12503191-12503350 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:13480040-13480354 | Common:2; Rare:75 | ||||
| chr3:14124659-14125193 | Common:4; Rare:158; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:14178464-14178876 | Common:3; Rare:200; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402465-14402716 | Rare:58 | ||||
| chr3:14651468-14651828 | Rare:109 | ||||
| chr3:14947082-14947587 | Common:5; Rare:213 | ||||
| chr3:14948319-14948662 | Common:2; Rare:106 |