| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348806-28348890 | Common:1; Rare:18 | ||||
| chr3:32570766-32570970 | Common:1; Rare:90 | ||||
| chr3:33798520-33798672 | Common:2; Rare:55 | ||||
| chr3:36993171-36993553 | Common:2; Rare:114; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr3:37243166-37243310 | Common:1; Rare:34 | ||||
| chr3:39051977-39052031 | Common:1; Rare:21 | ||||
| chr3:40309460-40309803 | Common:9; Rare:116 | ||||
| chr3:40457215-40457379 | Common:3; Rare:82 | ||||
| chr3:42581913-42582137 | Common:3; Rare:69 | ||||
| chr3:42600425-42600741 | Common:2; Rare:119 | ||||
| chr3:44338065-44338152 | Common:2; Rare:30 | ||||
| chr3:44477633-44477758 | Common:1; Rare:24 | ||||
| chr3:44510588-44510653 | Common:2; Rare:22 | ||||
| chr3:44761590-44761829 | Common:3; Rare:86 | ||||
| chr3:44861763-44861925 | Common:2; Rare:73 |