| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45388436-45388604 | Rare:40 | ||||
| chr3:45689180-45689464 | Common:1; Rare:96 | ||||
| chr3:45943298-45943477 | Rare:32 | ||||
| chr3:45944865-45945052 | Common:1; Rare:38 | ||||
| chr3:45995743-45995943 | Common:2; Rare:42; Clinvar:1 | ||||
| chr3:46693499-46693828 | Common:3; Rare:73 | ||||
| chr3:46979459-46979857 | Common:3; Rare:99; Clinvar:2 | ||||
| chr3:46981981-46982121 | Rare:22 | ||||
| chr3:47005234-47005537 | Common:1; Rare:90; Clinvar (benign):1 | ||||
| chr3:47163929-47164244 | Common:1; Rare:87 | ||||
| chr3:47380792-47381090 | Rare:100 | ||||
| chr3:47381421-47381615 | Rare:47 | ||||
| chr3:47475801-47476058 | Common:3; Rare:105 | ||||
| chr3:47513672-47513788 | Rare:34 | ||||
| chr3:47802879-47803212 | Common:1; Rare:98 |