| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6792691-6792875 | Common:1; Rare:38 | ||||
| chr12:6872534-6872681 | Rare:63 | ||||
| chr12:6890969-6891568 | Common:5; Rare:186 | ||||
| chr12:6927498-6927720 | Rare:63 | ||||
| chr12:6936783-6937130 | Common:1; Rare:138; Clinvar (benign):1 | ||||
| chr12:6947572-6947584 | Rare:4 | ||||
| chr12:6952031-6952108 | Rare:12 | ||||
| chr12:6953319-6953736 | Common:1; Rare:96 | ||||
| chr12:6953933-6954284 | Common:2; Rare:64 | ||||
| chr12:6961810-6961913 | Common:2; Rare:21 | ||||
| chr12:7752642-7752765 | Common:2; Rare:26 | ||||
| chr12:7933378-7933505 | Common:3; Rare:30 | ||||
| chr12:7933728-7933889 | Common:1; Rare:40 | ||||
| chr12:7934783-7934868 | Common:2; Rare:13 | ||||
| chr12:7959624-7959884 | Common:1; Rare:53 |