| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126268381-126268618 | Common:3; Rare:54 | ||||
| chr11:126268800-126269199 | Common:1; Rare:156; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:126355526-126355725 | Common:2; Rare:51 | ||||
| chr11:134224542-134224695 | Rare:57 | ||||
| chr11:134253285-134253586 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr12:389238-389385 | Rare:57 | ||||
| chr12:401446-401677 | Rare:61 | ||||
| chr12:991120-991229 | Common:1; Rare:44 | ||||
| chr12:2812638-2812724 | Rare:33 | ||||
| chr12:2877018-2877260 | Rare:71 | ||||
| chr12:2959784-2959951 | Common:2; Rare:46 | ||||
| chr12:4538431-4538933 | Common:3; Rare:115 | ||||
| chr12:4648974-4649171 | Common:2; Rare:64; Clinvar (benign):2 | ||||
| chr12:5431929-5432118 | Common:4; Rare:75 | ||||
| chr12:6451791-6452141 | Common:4; Rare:66 |