| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:88035257-88036005 | Common:8; Rare:481 | ||||
| chr12:88141847-88142428 | Common:1; Rare:784; Clinvar:33; Clinvar (benign):1 | ||||
| chr12:88142430-88142830 | Common:3; Rare:62 | ||||
| chr12:89524532-89525049 | Common:10; Rare:331 | ||||
| chr12:89525194-89525652 | Common:6; Rare:370 | ||||
| chr12:89525803-89526450 | Common:5; Rare:635 | ||||
| chr12:89708772-89709099 | Common:2; Rare:528 | ||||
| chr12:89709020-89709125 | Rare:34 | ||||
| chr12:89709190-89709850 | Common:14; Rare:985 | ||||
| chr12:92144346-92145444 | Common:16; Rare:692 | ||||
| chr12:92145799-92146380 | Common:20; Rare:836 | ||||
| chr12:92146384-92146505 | Common:1; Rare:37 | ||||
| chr12:92928695-92929095 | Common:2; Rare:117 | ||||
| chr12:92929101-92929677 | Common:10; Rare:858 | ||||
| chr12:93377643-93378043 | Rare:411 |