| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:25250852-25251206 | Rare:118; Clinvar:5; Clinvar (benign):4 | ||||
| chr12:25251209-25251376 | Rare:40 | ||||
| chr12:25251435-25251529 | Rare:17 | ||||
| chr12:26832327-26832522 | Rare:45 | ||||
| chr12:26832994-26833579 | Common:3; Rare:156 | ||||
| chr12:26937887-26938593 | Common:11; Rare:228 | ||||
| chr12:27014164-27014574 | Common:1; Rare:136 | ||||
| chr12:27014780-27014916 | Rare:23 | ||||
| chr12:27022391-27022624 | Common:3; Rare:72 | ||||
| chr12:27243948-27244388 | Common:2; Rare:143 | ||||
| chr12:27332257-27332372 | Rare:18 | ||||
| chr12:27332643-27332936 | Common:3; Rare:84 | ||||
| chr12:27333029-27333255 | Common:3; Rare:49 | ||||
| chr12:27333354-27333559 | Rare:51 | ||||
| chr12:27523216-27523517 | Rare:49 |