| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3126783-3126975 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr3:8501644-8501854 | Rare:73 | ||||
| chr3:9363020-9363091 | Rare:26 | ||||
| chr3:9933563-9933857 | Common:1; Rare:112; Clinvar:2 | ||||
| chr3:9986786-9987163 | Common:3; Rare:107 | ||||
| chr3:10026334-10026443 | Rare:31 | ||||
| chr3:14178573-14178861 | Common:2; Rare:148; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:15427478-15427616 | Common:1; Rare:50 | ||||
| chr3:15601522-15601788 | Common:4; Rare:111; Clinvar:1 | ||||
| chr3:16264899-16265234 | Common:2; Rare:103 | ||||
| chr3:23916898-23917173 | Rare:106 | ||||
| chr3:39051944-39052025 | Common:1; Rare:30 | ||||
| chr3:42804443-42804657 | Common:2; Rare:63 | ||||
| chr3:44976116-44976278 | Common:2; Rare:67 | ||||
| chr3:45842116-45842254 | Common:1; Rare:30 |