| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783597-50783822 | Common:2; Rare:74 | ||||
| chr22:50784097-50784266 | Rare:24 | ||||
| chr3:196702-196806 | Rare:35 | ||||
| chr3:197002-197371 | Common:3; Rare:129 | ||||
| chr3:198201-198427 | Common:1; Rare:88 | ||||
| chr3:3126660-3127232 | Common:10; Rare:220; Clinvar (benign):4 | ||||
| chr3:3179636-3179891 | Common:2; Rare:100; Clinvar:4 | ||||
| chr3:4303252-4303439 | Common:1; Rare:72 | ||||
| chr3:4303484-4303720 | Common:2; Rare:88 | ||||
| chr3:4303975-4303997 | Rare:3 | ||||
| chr3:4467004-4467350 | Common:2; Rare:156; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:4493117-4493363 | Common:2; Rare:93; Clinvar:1 | ||||
| chr3:4978551-4978933 | Common:4; Rare:117 | ||||
| chr3:4979135-4979534 | Common:2; Rare:95 | ||||
| chr3:4980215-4980530 | Rare:79 |