| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6970515-6970966 | Common:4; Rare:139; Clinvar (benign):1 | ||||
| chr12:7091798-7091965 | Rare:43 | ||||
| chr12:7108468-7108654 | Common:1; Rare:56 | ||||
| chr12:7109124-7109359 | Rare:70 | ||||
| chr12:7189563-7189731 | Rare:63; Clinvar:4 | ||||
| chr12:8914396-8914735 | Common:6; Rare:104 | ||||
| chr12:9115820-9116292 | Common:3; Rare:95 | ||||
| chr12:9869347-9869457 | Common:1; Rare:17 | ||||
| chr12:10613484-10613686 | Common:1; Rare:80 | ||||
| chr12:11171190-11171237 | Rare:23 | ||||
| chr12:11171553-11171659 | Common:2; Rare:34 | ||||
| chr12:12357004-12357151 | Common:2; Rare:78 | ||||
| chr12:12611816-12611945 | Common:1; Rare:44 | ||||
| chr12:12725655-12725929 | Common:2; Rare:59 | ||||
| chr12:12891306-12891583 | Common:1; Rare:54 |