| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32106408-32106674 | Common:4; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502763-32502924 | Rare:50 | ||||
| chr3:32570759-32570984 | Common:1; Rare:96 | ||||
| chr3:33097106-33097285 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33798499-33798635 | Common:2; Rare:40 | ||||
| chr3:36908489-36908605 | Rare:22 | ||||
| chr3:36944863-36945165 | Common:1; Rare:67 | ||||
| chr3:36993124-36993525 | Common:2; Rare:120; Clinvar:21; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr3:36993663-36993829 | Rare:68; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:37243146-37243310 | Common:1; Rare:43 | ||||
| chr3:38138527-38138698 | Common:2; Rare:62; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051944-39052042 | Common:1; Rare:35 | ||||
| chr3:39383269-39383432 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383582-39383680 | Rare:23; Clinvar:1 | ||||
| chr3:40309463-40309709 | Common:6; Rare:65 |