| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:65947783-65947971 | Common:1; Rare:30 | ||||
| chr12:65948691-65948955 | Rare:47 | ||||
| chr12:65950385-65950617 | Rare:34 | ||||
| chr12:65958886-65958943 | Rare:9 | ||||
| chr12:65959828-65959882 | Rare:12 | ||||
| chr12:66479066-66479103 | Rare:8 | ||||
| chr12:66979028-66979139 | Rare:15 | ||||
| chr12:67031830-67031885 | Common:1; Rare:9 | ||||
| chr12:67920491-67920822 | Common:1; Rare:56 | ||||
| chr12:68647372-68647564 | Common:4; Rare:29 | ||||
| chr12:68815462-68815705 | Common:2; Rare:44 | ||||
| chr12:68820275-68820379 | Rare:30 | ||||
| chr12:69543880-69544099 | Common:2; Rare:34 | ||||
| chr12:69588527-69588644 | Rare:27 | ||||
| chr12:69597617-69598067 | Common:5; Rare:105; Clinvar:2 |