| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46069850-46070056 | Rare:44 | ||||
| chr22:46085882-46086030 | Common:1; Rare:37 | ||||
| chr22:47631584-47631886 | Common:2; Rare:81 | ||||
| chr3:9396037-9396322 | Common:1; Rare:88 | ||||
| chr3:14125743-14125928 | Common:1; Rare:46 | ||||
| chr3:39411659-39411960 | Common:1; Rare:80; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:40453172-40453417 | Common:5; Rare:53 | ||||
| chr3:42906729-42906928 | Rare:28 | ||||
| chr3:46991284-46991525 | Rare:68; Clinvar:1 | ||||
| chr3:48583576-48583737 | Rare:39; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:75435106-75435403 | Common:3; Rare:95 | ||||
| chr3:100522556-100522748 | Rare:32 | ||||
| chr3:101576825-101577082 | Common:2; Rare:66 | ||||
| chr3:101676256-101676468 | Common:2; Rare:71 | ||||
| chr3:101680936-101681157 | Common:2; Rare:48 |