| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:192917836-192918023 | Common:2; Rare:84 | ||||
| chr3:193593101-193593303 | Rare:61; Clinvar:1 | ||||
| chr3:196082080-196082259 | Common:2; Rare:70 | ||||
| chr3:196318163-196318340 | Common:1; Rare:77 | ||||
| chr3:196568527-196568842 | Common:5; Rare:94 | ||||
| chr3:196712228-196712311 | Common:1; Rare:27 | ||||
| chr3:196867788-196867938 | Rare:52 | ||||
| chr3:197029780-197029948 | Common:1; Rare:55 | ||||
| chr3:197949885-197950251 | Common:4; Rare:112; Clinvar (benign):2 | ||||
| chr3:197959989-197960252 | Common:1; Rare:93 | ||||
| chr4:337632-337837 | Rare:51 | ||||
| chr4:499149-499324 | Common:2; Rare:61 | ||||
| chr4:663616-663748 | Rare:44 | ||||
| chr4:673842-673920 | Rare:30 | ||||
| chr4:674246-674542 | Rare:138 |