Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:706813-707213 | Common:3; Rare:120 | ||||
chr11:747249-747507 | Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
chr11:776477-776877 | Common:6; Rare:128 | ||||
chr11:777020-777300 | Common:1; Rare:79 | ||||
chr11:777465-777617 | Common:1; Rare:67 | ||||
chr11:789947-790347 | Common:6; Rare:131 | ||||
chr11:797255-797481 | Common:2; Rare:64 | ||||
chr11:797587-797792 | Rare:58 | ||||
chr11:804336-804518 | Common:1; Rare:53 | ||||
chr11:805187-805466 | Common:7; Rare:101 | ||||
chr11:809156-809317 | Common:4; Rare:40 | ||||
chr11:809483-809651 | Common:2; Rare:48 | ||||
chr11:809767-809978 | Rare:90 | ||||
chr11:826787-827614 | Common:16; Rare:325 | ||||
chr11:827863-828263 | Common:11; Rare:108 |