| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:5942914-5943202 | Common:2; Rare:56 | ||||
| chr12:5947040-5947152 | Rare:15 | ||||
| chr12:5948870-5949443 | Rare:132; Clinvar:6; Clinvar (benign):1 | ||||
| chr12:5949500-5949895 | Common:4; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:5951318-5951402 | Rare:16 | ||||
| chr12:5951663-5951892 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:5954624-5954992 | Common:3; Rare:62 | ||||
| chr12:5958067-5958418 | Common:6; Rare:69 | ||||
| chr12:5961516-5962170 | Common:8; Rare:98 | ||||
| chr12:5962946-5963028 | Rare:15 | ||||
| chr12:5967409-5967605 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:5971580-5971950 | Common:2; Rare:88; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:5973103-5973246 | Rare:32 | ||||
| chr12:5973440-5973740 | Common:3; Rare:49 | ||||
| chr12:5975853-5975874 | Rare:6 |