| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39051883-39052109 | Common:3; Rare:171 | ||||
| chr3:39107142-39107300 | Common:4; Rare:58 | ||||
| chr3:39107467-39107776 | Common:12; Rare:231 | ||||
| chr3:39153501-39153783 | Common:11; Rare:256 | ||||
| chr3:39383227-39383794 | Common:8; Rare:307; Clinvar:18; Clinvar (benign):7 | ||||
| chr3:39406358-39406776 | Common:15; Rare:326 | ||||
| chr3:39406800-39407140 | Common:8; Rare:181 | ||||
| chr3:39809305-39809766 | Common:6; Rare:242 | ||||
| chr3:40309448-40309910 | Common:27; Rare:420 | ||||
| chr3:40457127-40457455 | Common:13; Rare:344 | ||||
| chr3:40457420-40457690 | Common:5; Rare:122 | ||||
| chr3:40477038-40477269 | Common:5; Rare:136 | ||||
| chr3:40505900-40506170 | Rare:148 | ||||
| chr3:40506240-40506570 | Rare:75 | ||||
| chr3:40524738-40525098 | Common:4; Rare:247 |