| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7128880-7128984 | Rare:15 | ||||
| chr12:7189519-7189750 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:7444144-7444202 | Common:1; Rare:13 | ||||
| chr12:8032589-8032766 | Rare:62 | ||||
| chr12:8066335-8066550 | Rare:30 | ||||
| chr12:8227584-8227686 | Rare:28 | ||||
| chr12:8697791-8698043 | Rare:106 | ||||
| chr12:8949923-8950097 | Common:2; Rare:50 | ||||
| chr12:9089987-9090098 | Common:1; Rare:24 | ||||
| chr12:9607435-9607496 | Rare:8 | ||||
| chr12:9760883-9761008 | Common:1; Rare:16 | ||||
| chr12:10505844-10505897 | Rare:25 | ||||
| chr12:10613508-10613646 | Common:1; Rare:55 | ||||
| chr12:10723150-10723459 | Common:5; Rare:100 | ||||
| chr12:11170917-11171250 | Common:3; Rare:87 |