| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95003605-95003652 | Rare:25; Clinvar (benign):3 | ||||
| chr12:95217438-95217859 | Common:3; Rare:113 | ||||
| chr12:95218157-95218288 | Common:2; Rare:32 | ||||
| chr12:96035523-96035764 | Common:2; Rare:51 | ||||
| chr12:98644525-98644687 | Rare:62 | ||||
| chr12:98644964-98645299 | Common:2; Rare:99 | ||||
| chr12:100266964-100267453 | Common:4; Rare:208 | ||||
| chr12:101407643-101408056 | Common:3; Rare:105 | ||||
| chr12:101877517-101877882 | Common:5; Rare:102 | ||||
| chr12:102120045-102120256 | Rare:84 | ||||
| chr12:103930302-103930564 | Common:5; Rare:109 | ||||
| chr12:103965705-103965928 | Common:2; Rare:53 | ||||
| chr12:104064068-104064220 | Rare:34 | ||||
| chr12:104064416-104064582 | Rare:39 | ||||
| chr12:104288857-104289026 | Rare:67 |