| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33277312-33277495 | Common:1; Rare:50 | ||||
| chr3:33440373-33440483 | Rare:30 | ||||
| chr3:33717959-33718295 | Rare:120 | ||||
| chr3:33798499-33798770 | Common:2; Rare:96 | ||||
| chr3:33798985-33799058 | Rare:26 | ||||
| chr3:36944863-36945141 | Common:1; Rare:61 | ||||
| chr3:36993057-36993557 | Common:2; Rare:171; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:36993663-36993830 | Rare:68; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:37176237-37176393 | Rare:51 | ||||
| chr3:37242884-37243604 | Common:6; Rare:201 | ||||
| chr3:37683445-37683709 | Common:1; Rare:51 | ||||
| chr3:37994096-37994175 | Rare:23 | ||||
| chr3:38024458-38024671 | Common:1; Rare:82 | ||||
| chr3:38029591-38029904 | Common:1; Rare:65 | ||||
| chr3:38165443-38165580 | Rare:49 |