| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062438-123062663 | Common:2; Rare:102 | ||||
| chr11:123654570-123654748 | Common:2; Rare:44 | ||||
| chr11:123741636-123741746 | Rare:28 | ||||
| chr11:124673704-124673935 | Common:4; Rare:72 | ||||
| chr11:124762129-124762436 | Rare:93 | ||||
| chr11:124954031-124954215 | Common:4; Rare:46 | ||||
| chr11:125164558-125164762 | Rare:37 | ||||
| chr11:125496198-125496465 | Rare:60 | ||||
| chr11:125592506-125592917 | Common:6; Rare:132 | ||||
| chr11:125625886-125626003 | Rare:32 | ||||
| chr11:125887436-125887727 | Common:2; Rare:89 | ||||
| chr11:126211641-126211809 | Rare:77 | ||||
| chr11:126268779-126269209 | Common:2; Rare:166; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126303979-126304081 | Rare:58 | ||||
| chr11:126355526-126355763 | Common:2; Rare:66 |