| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:122655575-122655743 | Rare:43 | ||||
| chr11:123062115-123062326 | Rare:77 | ||||
| chr11:124673730-124673929 | Common:4; Rare:55 | ||||
| chr11:125625875-125625993 | Rare:39 | ||||
| chr11:125887480-125887727 | Common:2; Rare:78 | ||||
| chr11:126211644-126211804 | Rare:74 | ||||
| chr11:126268829-126269163 | Common:1; Rare:121; Clinvar:1 | ||||
| chr11:126303974-126304069 | Rare:54 | ||||
| chr11:126355526-126355778 | Common:2; Rare:71 | ||||
| chr11:131911348-131911494 | Common:1; Rare:59 | ||||
| chr11:134253310-134253586 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chr12:2877039-2877253 | Rare:64 | ||||
| chr12:4320949-4321241 | Common:4; Rare:107 | ||||
| chr12:4538715-4538896 | Common:1; Rare:36 | ||||
| chr12:6452078-6452119 | Common:1; Rare:10 |