| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11136860-11137168 | Rare:55 | ||||
| chr3:11154396-11154542 | Common:3; Rare:38 | ||||
| chr3:11582328-11582692 | Rare:97 | ||||
| chr3:11643592-11644179 | Common:5; Rare:127 | ||||
| chr3:11846515-11846588 | Common:2; Rare:19 | ||||
| chr3:12484333-12484586 | Common:5; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556741-12557161 | Common:5; Rare:115 | ||||
| chr3:12663375-12664055 | Common:8; Rare:183; Clinvar:6; Clinvar (benign):6 | ||||
| chr3:12664067-12664351 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:14124717-14125196 | Common:4; Rare:144; Clinvar:8; Clinvar (benign):2 | ||||
| chr3:14134842-14135260 | Common:1; Rare:130; Clinvar:9; Clinvar (benign):8 | ||||
| chr3:14136539-14136812 | Common:1; Rare:55 | ||||
| chr3:14178436-14178879 | Common:3; Rare:212; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:14402405-14402756 | Common:4; Rare:81 | ||||
| chr3:14651471-14651828 | Rare:108 |