| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25428107-25428311 | Rare:40 | ||||
| chr3:25783392-25783640 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chr3:25790008-25790118 | Common:3; Rare:42 | ||||
| chr3:28348626-28348704 | Rare:16 | ||||
| chr3:28348779-28348890 | Common:1; Rare:29 | ||||
| chr3:28349041-28349208 | Common:3; Rare:51 | ||||
| chr3:29280831-29280911 | Common:1; Rare:16 | ||||
| chr3:29280991-29281374 | Common:13; Rare:70 | ||||
| chr3:32106431-32106712 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277325-33277490 | Common:1; Rare:43 | ||||
| chr3:33798479-33798666 | Common:2; Rare:68 | ||||
| chr3:35639725-35639877 | Common:1; Rare:34 | ||||
| chr3:36993064-36993559 | Common:2; Rare:167; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:39051944-39052063 | Common:1; Rare:44 | ||||
| chr3:39192564-39192752 | Common:1; Rare:32 |