chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84413730944137310AC24GENIChomozygous117155337
84413765444137655TC15GENIChomozygous117155338
84413883244138833TC17GENIChomozygous116949115
84414052544140526GA18GENIChomozygous116949117
84414092344140924AG33GENIChomozygous116949119
84414183844141839TA21GENIChomozygous116949123
84414290044142901AT16GENIChomozygous117155339
84414330744143308AG6GENIChomozygous116949125
84414411844144119TC22GENIChomozygous116949127
84414438644144387CG24GENIChomozygous116949131
84414502844145029AG29GENIChomozygous116949133
84414531944145320TG26GENIChomozygous117155340
84414545044145451AG37GENIChomozygous116949135
84414547744145478TC35GENIChomozygous116949137
84414564044145641AG26GENIChomozygous116949139
84414576544145766AG25GENIChomozygous116949141
84414634544146346TC21GENICpossibly homozygous117155341
84414673444146735GA16GENIChomozygous117927752
84414858644148587GA22GENIChomozygous117155344
84414956244149563CT24GENIChomozygous117155345
84415016444150165TC20GENIChomozygous117155346
84415085844150859TC27GENIChomozygous117155347
84415125744151258AC24GENIChomozygous117155348
84415182044151821TA23GENIChomozygous117155349
84415192744151928GA22GENIChomozygous117155350
84415213344152134CG23GENIChomozygous117155351
84415215044152151AG22GENIChomozygous117155352
84415317944153180CT29GENIChomozygous117155356
84415358244153583TC36GENIChomozygous117155357
84415363844153639TC33GENIChomozygous117155358
84415375844153759AG32GENIChomozygous117155359
84415391344153914GA29GENIChomozygous117155360
84415401144154012GC22GENIChomozygous117155361
84415419444154195CT15GENIChomozygous117155362
84415420444154205TC14GENIChomozygous117155363
84415421144154212CT14GENIChomozygous117155364
84415421244154213AG13GENIChomozygous117155365
84415450344154504GA16GENICpossibly homozygous117155369
84415561544155616AG24GENIChomozygous117155370
84415564744155648AC32GENIChomozygous117155371
84415753944157540AC28GENIChomozygous116949147