| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68903784-68903938 | Common:4; Rare:74; Clinvar (benign):6 | ||||
| chr11:69640970-69641195 | Rare:49 | ||||
| chr11:69675307-69675519 | Rare:56 | ||||
| chr11:70203195-70203313 | Common:1; Rare:46 | ||||
| chr11:70398421-70398614 | Common:2; Rare:73 | ||||
| chr11:71448327-71448690 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928930-71929061 | Common:1; Rare:44 | ||||
| chr11:72041058-72041320 | Common:1; Rare:47 | ||||
| chr11:72041534-72041746 | Rare:32 | ||||
| chr11:72041846-72041889 | Common:1; Rare:9 | ||||
| chr11:72041935-72042044 | Rare:20 | ||||
| chr11:72080471-72080819 | Common:1; Rare:76; Clinvar:5 | ||||
| chr11:72752396-72752558 | Common:2; Rare:49 | ||||
| chr11:73598049-73598254 | Common:3; Rare:53 | ||||
| chr11:73760158-73760300 | Rare:25 |