| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:5254230-5255823 | Common:33; Rare:639; Clinvar:23; Clinvar (pathogenic):3 | ||||
| chr11:5269760-5270450 | Common:3; Rare:437 | ||||
| chr11:5441670-5442100 | Common:4; Rare:101 | ||||
| chr11:5505557-5506003 | Common:11; Rare:306 | ||||
| chr11:5595991-5596391 | Common:1; Rare:298 | ||||
| chr11:5596310-5596610 | Common:11; Rare:64 | ||||
| chr11:5596615-5596761 | Common:4; Rare:53 | ||||
| chr11:5596691-5597119 | Common:11; Rare:326 | ||||
| chr11:5624762-5625162 | Rare:250 | ||||
| chr11:5684600-5684900 | Common:1; Rare:85 | ||||
| chr11:5684895-5685652 | Common:26; Rare:308 | ||||
| chr11:5690242-5691104 | Common:11; Rare:276 | ||||
| chr11:6234401-6235636 | Common:24; Rare:907 | ||||
| chr11:6390025-6390577 | Common:15; Rare:575; Clinvar (benign):1 | ||||
| chr11:6418907-6419307 | Common:8; Rare:176 |