| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6944174-6944489 | Common:3; Rare:150; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970616-6970952 | Common:3; Rare:104 | ||||
| chr12:7018431-7018584 | Common:1; Rare:46 | ||||
| chr12:7060360-7060543 | Rare:44 | ||||
| chr12:7060674-7060876 | Rare:33 | ||||
| chr12:7066972-7067056 | Rare:23 | ||||
| chr12:7091879-7091998 | Rare:27 | ||||
| chr12:7097580-7097705 | Common:3; Rare:29 | ||||
| chr12:7108468-7108701 | Common:1; Rare:64 | ||||
| chr12:7109110-7109255 | Rare:46 | ||||
| chr12:7130270-7130417 | Common:4; Rare:41 | ||||
| chr12:8066335-8066487 | Rare:20 | ||||
| chr12:8227507-8227691 | Common:1; Rare:45 | ||||
| chr12:8844922-8844965 | Rare:11 | ||||
| chr12:8949595-8949867 | Common:1; Rare:55 |