| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062067-123062326 | Common:4; Rare:108 | ||||
| chr11:123062393-123062628 | Common:4; Rare:105 | ||||
| chr11:123741612-123741815 | Common:2; Rare:63 | ||||
| chr11:124673715-124673940 | Common:4; Rare:66 | ||||
| chr11:124876539-124876877 | Common:4; Rare:68 | ||||
| chr11:124953980-124954213 | Common:4; Rare:64 | ||||
| chr11:125111731-125112004 | Common:3; Rare:54 | ||||
| chr11:125569196-125569545 | Common:2; Rare:101 | ||||
| chr11:125592506-125592933 | Common:6; Rare:138 | ||||
| chr11:125625874-125626008 | Rare:43 | ||||
| chr11:125887495-125887727 | Common:2; Rare:72 | ||||
| chr11:125903179-125903326 | Rare:34 | ||||
| chr11:126211635-126211827 | Rare:88 | ||||
| chr11:126268779-126269214 | Common:2; Rare:169; Clinvar:3; Clinvar (benign):4 | ||||
| chr11:126303959-126304081 | Rare:69 |