| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125592520-125592933 | Common:6; Rare:135 | ||||
| chr11:125887501-125887727 | Common:2; Rare:69 | ||||
| chr11:126211641-126211804 | Rare:75 | ||||
| chr11:126268802-126269192 | Common:1; Rare:152; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126303974-126304083 | Rare:63 | ||||
| chr11:126355532-126355747 | Common:1; Rare:56 | ||||
| chr11:128522269-128522546 | Common:1; Rare:88 | ||||
| chr11:129815719-129815877 | Common:1; Rare:39 | ||||
| chr11:129895516-129895687 | Common:2; Rare:68 | ||||
| chr11:134253306-134253584 | Common:2; Rare:89; Clinvar (benign):1 | ||||
| chr12:401446-401655 | Rare:55 | ||||
| chr12:2876959-2877272 | Rare:99 | ||||
| chr12:3077261-3077406 | Common:4; Rare:59 | ||||
| chr12:4320961-4321250 | Common:5; Rare:107 | ||||
| chr12:4538444-4538907 | Common:1; Rare:102 |