| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9843958-9844137 | Common:2; Rare:75 | ||||
| chr3:9890457-9890655 | Common:3; Rare:78 | ||||
| chr3:9916960-9917158 | Common:2; Rare:43 | ||||
| chr3:9933507-9933857 | Common:2; Rare:140; Clinvar:3 | ||||
| chr3:10026334-10026484 | Rare:42 | ||||
| chr3:10115520-10115737 | Common:3; Rare:80 | ||||
| chr3:11137001-11137250 | Rare:47 | ||||
| chr3:11846843-11847008 | Common:1; Rare:46 | ||||
| chr3:12484334-12484548 | Common:5; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556912-12557139 | Common:5; Rare:80 | ||||
| chr3:12664058-12664352 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:12759189-12759684 | Common:6; Rare:90 | ||||
| chr3:13480018-13480330 | Common:2; Rare:77 | ||||
| chr3:14124690-14125184 | Common:4; Rare:145; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178881 | Common:2; Rare:166; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 |