chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X152416096152416097AG5GENIChomozygous119963220
X152416101152416102CT5GENIChomozygous119963222
X152416218152416219CT6GENIChomozygous119963224
X152416242152416243AC8GENIChomozygous108429330
X152416483152416484CT2GENIChomozygous119963226
X152429691152429692AT38GENICheterozygous119963228
X152457378152457379AT24GENICheterozygous119963240
X152457594152457595GA14GENICheterozygous119963242
X152457716152457717AC43GENICheterozygous120015168
X152471406152471407GA27GENICheterozygous120015169
X152471411152471412GA28GENICheterozygous119963244
X152471464152471465TC21GENICheterozygous120015170
X152489748152489749TC26GENICheterozygous119963252
X152489755152489756AC24GENICheterozygous119963254
X152457228152457229TG14GENICheterozygous120038054
X152523834152523835GC142GENICheterozygous120038055
X152528303152528304GA6GENIChomozygous108353672
X152528305152528306AC6GENIChomozygous108353674
X152538823152538824CA29GENICheterozygous120015184
X152539037152539038GT40GENICheterozygous120038056
X152542838152542839AT112GENICheterozygous120038057
X152543042152543043TC56GENICheterozygous119963304
X152551419152551420GC18GENICpossibly homozygous108353678
X152553670152553671CA125GENICheterozygous120015197
X152553702152553703GT118GENICheterozygous120038058
X152553730152553731GC118GENICheterozygous120038059
X152553739152553740CT116GENICheterozygous120038060
X152554466152554467CT44GENICheterozygous119963318
X152555047152555048GA26GENICheterozygous120038061
X152555061152555062CT28GENICheterozygous120038062
X152555081152555082TC29GENICheterozygous119963322
X152548244152548245AT9GENIChomozygous108600072
X152551441152551442GT16GENIChomozygous108461904
X152628623152628624CT8GENICheterozygous120038063
X152628655152628656TC15GENICheterozygous119963326
X152628663152628664CT19GENICheterozygous120038064