| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125887513-125887740 | Common:2; Rare:68 | ||||
| chr11:126211634-126211807 | Rare:78 | ||||
| chr11:126268555-126268624 | Common:2; Rare:17 | ||||
| chr11:126268779-126269207 | Common:2; Rare:165; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:128693956-128694174 | Rare:39 | ||||
| chr11:134253278-134253586 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr12:389297-389389 | Rare:32 | ||||
| chr12:991101-991245 | Common:1; Rare:53 | ||||
| chr12:2877065-2877262 | Rare:62 | ||||
| chr12:4538431-4538764 | Rare:72 | ||||
| chr12:4648988-4649149 | Common:2; Rare:52; Clinvar (benign):1 | ||||
| chr12:6451775-6452148 | Common:4; Rare:68 | ||||
| chr12:6493239-6493386 | Common:5; Rare:41 | ||||
| chr12:6568255-6568347 | Rare:35 | ||||
| chr12:6723855-6724317 | Common:2; Rare:98 |