| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119067720-119067821 | Common:1; Rare:41 | ||||
| chr11:119084826-119084939 | Rare:33 | ||||
| chr11:119100367-119100479 | Rare:30; Clinvar (pathogenic):1 | ||||
| chr11:119121330-119121621 | Common:1; Rare:66 | ||||
| chr11:120123038-120123222 | Common:2; Rare:59 | ||||
| chr11:121292549-121292739 | Rare:58; Clinvar:3 | ||||
| chr11:123062403-123062672 | Common:4; Rare:124 | ||||
| chr11:124673736-124673929 | Common:4; Rare:52 | ||||
| chr11:124752159-124752370 | Common:2; Rare:45 | ||||
| chr11:124762277-124762441 | Rare:42 | ||||
| chr11:125592543-125592890 | Common:6; Rare:115 | ||||
| chr11:126211644-126211804 | Rare:74 | ||||
| chr11:126268802-126269154 | Common:1; Rare:132; Clinvar:1 | ||||
| chr11:126304027-126304083 | Rare:34 | ||||
| chr11:126355552-126355731 | Rare:43 |