| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39107847-39107950 | Common:1; Rare:36 | ||||
| chr3:39153497-39153843 | Common:5; Rare:108 | ||||
| chr3:39154591-39154788 | Rare:40 | ||||
| chr3:39383258-39383726 | Common:3; Rare:105; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:39406531-39406762 | Common:6; Rare:101 | ||||
| chr3:39809327-39809731 | Common:3; Rare:130 | ||||
| chr3:40309477-40309808 | Common:9; Rare:112 | ||||
| chr3:40457204-40457402 | Common:3; Rare:100 | ||||
| chr3:40524815-40524993 | Common:1; Rare:50 | ||||
| chr3:42581889-42582137 | Common:3; Rare:78 | ||||
| chr3:42582272-42582445 | Common:1; Rare:40 | ||||
| chr3:42600356-42600757 | Common:3; Rare:157 | ||||
| chr3:42773215-42773312 | Common:1; Rare:31 | ||||
| chr3:42773390-42773471 | Rare:13 | ||||
| chr3:42804204-42804677 | Common:2; Rare:138 |