| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55974400-55974537 | Rare:26 | ||||
| chr12:55997094-55997561 | Common:2; Rare:99; Clinvar:2 | ||||
| chr12:56007318-56007526 | Rare:41 | ||||
| chr12:56007581-56008012 | Common:2; Rare:105 | ||||
| chr12:56041547-56042098 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:56042106-56042347 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):5 | ||||
| chr12:56042364-56042584 | Rare:64; Clinvar (benign):1 | ||||
| chr12:56079318-56079578 | Rare:50 | ||||
| chr12:56079914-56080145 | Common:4; Rare:56 | ||||
| chr12:56103820-56103961 | Common:2; Rare:18 | ||||
| chr12:56104117-56104703 | Common:6; Rare:195 | ||||
| chr12:56105299-56105417 | Rare:19 | ||||
| chr12:56116022-56116088 | Rare:13 | ||||
| chr12:56116252-56116346 | Rare:23 | ||||
| chr12:56116429-56116751 | Common:3; Rare:129 |