| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32570666-32570994 | Common:1; Rare:140 | ||||
| chr3:33097104-33097272 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277313-33277509 | Common:2; Rare:59 | ||||
| chr3:33645405-33645563 | Rare:18 | ||||
| chr3:33659071-33659443 | Common:3; Rare:62 | ||||
| chr3:33659570-33659723 | Rare:42 | ||||
| chr3:33798499-33798669 | Common:2; Rare:63 | ||||
| chr3:35638860-35638963 | Rare:19 | ||||
| chr3:35639427-35639852 | Common:4; Rare:93 | ||||
| chr3:35639854-35640076 | Common:2; Rare:49 | ||||
| chr3:35642225-35642382 | Rare:22 | ||||
| chr3:36993071-36993553 | Common:2; Rare:162; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr3:37176131-37176393 | Rare:73 | ||||
| chr3:37242924-37243364 | Common:6; Rare:118 | ||||
| chr3:38165115-38165236 | Common:1; Rare:20 |