| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9933534-9933884 | Common:2; Rare:144; Clinvar:3 | ||||
| chr3:10026329-10026465 | Rare:40 | ||||
| chr3:10115500-10115743 | Common:4; Rare:89 | ||||
| chr3:10141650-10141841 | Common:3; Rare:77; Clinvar:4; Clinvar (benign):17 | ||||
| chr3:11719438-11719620 | Rare:58 | ||||
| chr3:12004250-12004409 | Common:2; Rare:47 | ||||
| chr3:12484165-12484530 | Common:5; Rare:108; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:12664075-12664300 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12796566-12796699 | Common:5; Rare:41 | ||||
| chr3:12841482-12841882 | Common:2; Rare:129 | ||||
| chr3:13480018-13480324 | Common:2; Rare:77 | ||||
| chr3:14124736-14125145 | Common:4; Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178876 | Common:2; Rare:166; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402435-14402632 | Rare:48 | ||||
| chr3:14651486-14651824 | Rare:101 |