| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143971861-143972074 | Rare:73 | ||||
| chr3:146160975-146161320 | Common:2; Rare:113; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146251010-146251229 | Common:1; Rare:57 | ||||
| chr3:146544484-146544773 | Common:4; Rare:71 | ||||
| chr3:147393476-147393748 | Rare:76 | ||||
| chr3:147406053-147406211 | Rare:39 | ||||
| chr3:147406463-147406983 | Common:3; Rare:100 | ||||
| chr3:147409129-147409496 | Rare:102 | ||||
| chr3:149086445-149086711 | Rare:80 | ||||
| chr3:149129545-149129693 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149752408-149752566 | Common:2; Rare:56 | ||||
| chr3:149813004-149813344 | Common:2; Rare:110 | ||||
| chr3:149971126-149971354 | Common:3; Rare:109 | ||||
| chr3:150603139-150603372 | Common:2; Rare:89 | ||||
| chr3:150703364-150703587 | Rare:66 |