| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8612716-8613058 | Rare:62; Clinvar (benign):1 | ||||
| chr12:8914831-8914937 | Rare:23 | ||||
| chr12:8949362-8949538 | Common:1; Rare:24 | ||||
| chr12:8949552-8950211 | Common:4; Rare:153 | ||||
| chr12:9669527-9669846 | Common:4; Rare:78 | ||||
| chr12:9673515-9673756 | Common:4; Rare:41 | ||||
| chr12:9673813-9674031 | Common:1; Rare:36 | ||||
| chr12:9732944-9733109 | Common:1; Rare:53 | ||||
| chr12:9733147-9733420 | Common:5; Rare:69 | ||||
| chr12:9760776-9761003 | Common:2; Rare:37 | ||||
| chr12:9869349-9869467 | Common:1; Rare:20 | ||||
| chr12:9869618-9869941 | Common:4; Rare:62 | ||||
| chr12:10612820-10613110 | Common:1; Rare:84 | ||||
| chr12:10613169-10613349 | Common:1; Rare:47 | ||||
| chr12:10613442-10613744 | Common:1; Rare:112 |