| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401350-67401730 | Common:3; Rare:197 | ||||
| chr11:67401734-67402164 | Common:23; Rare:873 | ||||
| chr11:67403660-67404126 | Common:2; Rare:245 | ||||
| chr11:67420380-67420780 | Rare:162 | ||||
| chr11:67420836-67420996 | Common:2; Rare:35 | ||||
| chr11:67421104-67421504 | Common:16; Rare:503 | ||||
| chr11:67428217-67428617 | Common:2; Rare:421 | ||||
| chr11:67428926-67429526 | Common:2; Rare:372 | ||||
| chr11:67440174-67440578 | Rare:195 | ||||
| chr11:67443313-67443811 | Common:11; Rare:500 | ||||
| chr11:67443753-67444014 | Rare:110 | ||||
| chr11:67464539-67465006 | Common:1; Rare:849 | ||||
| chr11:67469100-67469500 | Common:15; Rare:578 | ||||
| chr11:67482687-67483197 | Common:3; Rare:385; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):6 | ||||
| chr11:67483109-67483336 | Rare:86; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):3 |