| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101628819-101629037 | Rare:24 | ||||
| chr12:102120058-102120229 | Rare:66 | ||||
| chr12:103930033-103930536 | Common:9; Rare:167 | ||||
| chr12:103957123-103957352 | Common:7; Rare:63 | ||||
| chr12:103965664-103965941 | Common:2; Rare:73 | ||||
| chr12:104064465-104064633 | Rare:50 | ||||
| chr12:104138164-104138392 | Common:1; Rare:60 | ||||
| chr12:104288817-104288932 | Rare:57 | ||||
| chr12:105107609-105107803 | Common:1; Rare:92; Clinvar:1 | ||||
| chr12:105236035-105236304 | Common:2; Rare:116 | ||||
| chr12:105353360-105353556 | Rare:43 | ||||
| chr12:106955656-106955850 | Rare:62 | ||||
| chr12:107093514-107093679 | Rare:61 | ||||
| chr12:108515052-108515319 | Common:1; Rare:79 | ||||
| chr12:109098128-109098582 | Common:2; Rare:183; Clinvar:4; Clinvar (benign):1 |