| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134467184-134467335 | Common:1; Rare:22 | ||||
| chr12:577961-578246 | Common:1; Rare:49 | ||||
| chr12:583485-583599 | Rare:15 | ||||
| chr12:585532-585867 | Common:6; Rare:45 | ||||
| chr12:753886-754110 | Common:1; Rare:92; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:1666853-1666954 | Rare:18 | ||||
| chr12:1669074-1669483 | Common:4; Rare:84 | ||||
| chr12:3085792-3085959 | Common:2; Rare:27 | ||||
| chr12:6182473-6182568 | Common:1; Rare:27 | ||||
| chr12:6183007-6183239 | Common:1; Rare:46 | ||||
| chr12:6770189-6770523 | Rare:94 | ||||
| chr12:6818370-6818622 | Common:1; Rare:86 | ||||
| chr12:7124715-7124946 | Rare:52 | ||||
| chr12:7493184-7493331 | Rare:27 | ||||
| chr12:8242933-8243244 | Common:8; Rare:88 |