| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52280880-52281244 | Common:3; Rare:58 | ||||
| chr12:52286721-52286842 | Rare:42 | ||||
| chr12:52286846-52287308 | Common:4; Rare:118; Clinvar (pathogenic):2 | ||||
| chr12:52287328-52288093 | Common:10; Rare:247; Clinvar (pathogenic):1 | ||||
| chr12:52288126-52288374 | Common:3; Rare:69; Clinvar:1 | ||||
| chr12:52288505-52288778 | Common:6; Rare:58 | ||||
| chr12:52305161-52305256 | Common:2; Rare:25 | ||||
| chr12:52898415-52898513 | Common:2; Rare:29; Clinvar:1 | ||||
| chr12:52898924-52898942 | Rare:8 | ||||
| chr12:52899384-52899396 | Rare:3 | ||||
| chr12:52945578-52945901 | Rare:62 | ||||
| chr12:53179692-53179714 | Rare:5 | ||||
| chr12:53307160-53307541 | Common:4; Rare:100; Clinvar (benign):2 | ||||
| chr12:53479369-53479442 | Common:1; Rare:15 | ||||
| chr12:53665083-53665190 | Rare:16 |