| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7189519-7189733 | Rare:73; Clinvar:4 | ||||
| chr12:8032568-8032775 | Common:4; Rare:70 | ||||
| chr12:8914366-8914764 | Common:6; Rare:115 | ||||
| chr12:8949563-8950154 | Common:4; Rare:138 | ||||
| chr12:10212241-10212454 | Rare:55 | ||||
| chr12:10613473-10613731 | Common:1; Rare:99 | ||||
| chr12:10722785-10723017 | Common:3; Rare:76 | ||||
| chr12:11171098-11171261 | Common:2; Rare:61 | ||||
| chr12:11171551-11171733 | Common:2; Rare:62 | ||||
| chr12:12356981-12357204 | Common:4; Rare:111 | ||||
| chr12:12611814-12611955 | Common:1; Rare:48 | ||||
| chr12:12696148-12696286 | Rare:38 | ||||
| chr12:12717242-12717492 | Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725625-12725929 | Common:3; Rare:67 | ||||
| chr12:12891285-12891623 | Common:1; Rare:70 |