chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4077649140776492AT3GENIChomozygous540544192
X4078266640782667AG6GENIChomozygous537197538
X4082084540820846GC22GENICheterozygous540544193
X4083551640835517AT2GENIChomozygous540544194
X4083551840835519AC2GENIChomozygous540544195
X4085334940853350AAC2GENIChomozygous698239081
X4085703940857041TG--7GENICheterozygous698239082
X4086647740866478AG13GENICheterozygous540544196
X4087556540875566GT5GENIChomozygous540544197
X4087556740875568C-5GENIChomozygous698239083
X4087568840875689GA8GENIChomozygous537197539
X4087569640875697TA10GENIChomozygous537197540
X4087569840875699AT11GENIChomozygous537197541
X4088176740881768GGAATATTAA6GENIChomozygous698239084
X4088391440883915T-6GENICheterozygous698239085
X4090325640903257CCA10GENIChomozygous698239086
X4090327140903272A-10GENIChomozygous698239087
X4090590440905905TTG10GENIChomozygous698239088
X4092570440925705AG17GENICheterozygous540544198
X4093228340932284AAGTT5GENIChomozygous698239089
X4093651540936516GT8GENICheterozygous540544199
X4094140040941401TC11GENIChomozygous540544200
X4094140740941408AAC10GENIChomozygous698239090
X4095497640954977TG4GENICheterozygous540544201
X4095584340955844GC15GENICheterozygous540544202
X4095588840955889GT10GENICheterozygous540544203
X4095589040955891GA10GENICheterozygous540544204
X4095589640955897TG10GENICheterozygous540544205
X4096906140969062CCT3GENIChomozygous698239091
X4097461040974611TC8GENICheterozygous540544206
X4097879540978796T-1GENIChomozygous698239092
X4098327040983271CCA2GENIChomozygous698239093
X4099425940994260CT7GENIChomozygous537197542
X4099426240994263CT7GENIChomozygous537197543
X4100597841005979GGC2GENIChomozygous698239094
X4101723241017233GT10GENIChomozygous537197544
X4101725641017257GT6GENIChomozygous537197545
X4101728041017281CCT7GENIChomozygous698239095
X4101731541017316C-8GENIChomozygous698239096