| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:122655857-122655951 | Common:1; Rare:20 | ||||
| chr11:123062109-123062348 | Rare:93 | ||||
| chr11:123062430-123062677 | Common:3; Rare:112 | ||||
| chr11:123741632-123741799 | Common:1; Rare:48 | ||||
| chr11:124673715-124673916 | Common:4; Rare:59 | ||||
| chr11:124762287-124762447 | Rare:40 | ||||
| chr11:124800406-124800501 | Common:1; Rare:39 | ||||
| chr11:124953989-124954215 | Common:4; Rare:60 | ||||
| chr11:125111726-125112011 | Common:3; Rare:57 | ||||
| chr11:125592471-125592913 | Common:6; Rare:150 | ||||
| chr11:125625850-125626008 | Rare:52 | ||||
| chr11:125887365-125887727 | Common:3; Rare:113 | ||||
| chr11:126211638-126211804 | Rare:76 | ||||
| chr11:126268814-126269207 | Common:2; Rare:152; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126303974-126304090 | Rare:68 |