| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188488-49188627 | Common:2; Rare:19 | ||||
| chr12:49188981-49189087 | Rare:40; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49189114-49189171 | Rare:7 | ||||
| chr12:49264775-49265092 | Common:4; Rare:113 | ||||
| chr12:49322986-49323303 | Common:3; Rare:71 | ||||
| chr12:49367220-49367554 | Common:1; Rare:90 | ||||
| chr12:49568104-49568234 | Common:2; Rare:41 | ||||
| chr12:49623295-49623577 | Common:1; Rare:78 | ||||
| chr12:49828353-49828543 | Common:1; Rare:71 | ||||
| chr12:49843092-49843192 | Common:1; Rare:35 | ||||
| chr12:50085287-50085364 | Common:1; Rare:17 | ||||
| chr12:50283457-50283683 | Common:3; Rare:72 | ||||
| chr12:50400749-50400979 | Rare:72 | ||||
| chr12:50401309-50401432 | Common:1; Rare:29 | ||||
| chr12:50763913-50764490 | Common:3; Rare:164 |