| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33097104-33097258 | Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277331-33277489 | Common:1; Rare:41 | ||||
| chr3:33798412-33798723 | Common:2; Rare:103 | ||||
| chr3:36993117-36993569 | Common:2; Rare:143; Clinvar:28; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr3:37176094-37176395 | Common:1; Rare:84 | ||||
| chr3:37243193-37243578 | Common:1; Rare:104 | ||||
| chr3:38024501-38024660 | Common:1; Rare:61 | ||||
| chr3:38138365-38138680 | Common:2; Rare:88 | ||||
| chr3:39051942-39052028 | Common:1; Rare:32 | ||||
| chr3:39107562-39107680 | Common:2; Rare:39 | ||||
| chr3:39153517-39153737 | Common:3; Rare:73 | ||||
| chr3:40309471-40309711 | Common:6; Rare:65 | ||||
| chr3:40457208-40457470 | Common:6; Rare:121 | ||||
| chr3:41199231-41199632 | Common:1; Rare:167 | ||||
| chr3:41224298-41224548 | Rare:60; Clinvar (benign):1 |