Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:67428340-67428532 | Rare:66 | ||||
chr11:67443451-67443733 | Common:2; Rare:91 | ||||
chr11:67469130-67469436 | Common:3; Rare:103 | ||||
chr11:67482910-67483188 | Rare:61; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr11:67508048-67508454 | Common:1; Rare:90 | ||||
chr11:67583634-67583851 | Common:1; Rare:71 | ||||
chr11:68010130-68010390 | Common:1; Rare:63 | ||||
chr11:68030378-68030744 | Common:3; Rare:103; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68121374-68121573 | Common:1; Rare:55 | ||||
chr11:68271966-68272134 | Common:2; Rare:67 | ||||
chr11:68460560-68460773 | Common:3; Rare:79 | ||||
chr11:68841802-68841876 | Common:1; Rare:31; Clinvar (benign):2 | ||||
chr11:68903779-68903930 | Common:4; Rare:72; Clinvar (benign):6 | ||||
chr11:69675251-69675482 | Rare:74 | ||||
chr11:70203141-70203358 | Common:3; Rare:82 |