| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33161443-33161653 | Common:6; Rare:55 | ||||
| chr11:33257152-33257427 | Common:3; Rare:93 | ||||
| chr11:34052126-34052423 | Common:4; Rare:135 | ||||
| chr11:34105493-34105682 | Common:2; Rare:62 | ||||
| chr11:34438758-34439009 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr11:34916287-34916676 | Common:10; Rare:158; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:36289399-36289505 | Common:1; Rare:41 | ||||
| chr11:36510240-36510373 | Rare:37 | ||||
| chr11:43358813-43359006 | Rare:95 | ||||
| chr11:44066110-44066349 | Common:3; Rare:59 | ||||
| chr11:46119805-46119965 | Common:2; Rare:46 | ||||
| chr11:46361466-46361566 | Rare:19 | ||||
| chr11:46846218-46846416 | Common:1; Rare:56 | ||||
| chr11:46936650-46936813 | Common:2; Rare:52 | ||||
| chr11:47176849-47177132 | Common:1; Rare:115 |