| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25789987-25790118 | Common:3; Rare:50 | ||||
| chr3:28348784-28349188 | Common:4; Rare:126 | ||||
| chr3:29280875-29281073 | Common:2; Rare:38 | ||||
| chr3:32502795-32502909 | Rare:28 | ||||
| chr3:32570763-32570966 | Common:1; Rare:90 | ||||
| chr3:33097098-33097285 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33218795-33218944 | Common:3; Rare:42 | ||||
| chr3:33277295-33277476 | Common:2; Rare:45 | ||||
| chr3:33440904-33441105 | Rare:43 | ||||
| chr3:33798435-33798634 | Common:2; Rare:53 | ||||
| chr3:36993108-36993569 | Common:2; Rare:149; Clinvar:28; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr3:37243152-37243348 | Common:1; Rare:53 | ||||
| chr3:39051909-39052052 | Common:1; Rare:47 | ||||
| chr3:39107612-39107716 | Common:2; Rare:26 | ||||
| chr3:39383582-39383676 | Rare:20; Clinvar:1 |