| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6946347-6946583 | Common:1; Rare:62 | ||||
| chr12:6970583-6971028 | Common:5; Rare:143; Clinvar (benign):2 | ||||
| chr12:6971146-6971183 | Rare:11 | ||||
| chr12:6971343-6971403 | Rare:15 | ||||
| chr12:7018244-7019065 | Common:6; Rare:230 | ||||
| chr12:7060602-7060735 | Rare:23 | ||||
| chr12:7092430-7092665 | Rare:42 | ||||
| chr12:7109165-7109323 | Rare:51 | ||||
| chr12:7130000-7130038 | Rare:5 | ||||
| chr12:7130248-7130435 | Common:5; Rare:51 | ||||
| chr12:7189056-7189199 | Common:2; Rare:29 | ||||
| chr12:7189498-7189974 | Common:6; Rare:158; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:7935880-7936475 | Common:6; Rare:102 | ||||
| chr12:8032394-8032504 | Rare:27 | ||||
| chr12:8032522-8032874 | Common:5; Rare:103 |