chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1503757615037580CCCA9GENIChomozygous129722345
X1504077115040772G10GENIChomozygous129722346
X1504183115041832CT7GENIChomozygous108233018
X1504231415042315AG4GENIChomozygous108233020
X1504267115042672AG5GENIChomozygous108233022
X1504534515045345GA12GENIChomozygous129722347
X1504535315045354C11GENIChomozygous129722348
X1504537115045371T11GENIChomozygous129722349
X1504542615045427A7GENIChomozygous129722350
X1504543615045436A6GENIChomozygous129722351
X1504545315045454T6GENIChomozygous129722352
X1504545515045456CG6GENIChomozygous120536135
X1504549315045493G6GENIChomozygous129722353
X1504558515045585C10GENIChomozygous129722354
X1504560415045605C10GENIChomozygous129722355
X1504562015045621T9GENIChomozygous129722356
X1504566215045663A10GENIChomozygous129722357
X1504567115045672T11GENIChomozygous129722358
X1504569115045692A11GENIChomozygous129722359
X1504570615045707C13GENIChomozygous129722360
X1504571715045718C10GENIChomozygous129722361
X1504572915045730GT8GENIChomozygous108471978
X1504575915045760GA8GENIChomozygous108233024
X1504576015045761AG8GENIChomozygous108233026
X1504576415045765G7GENIChomozygous129722362
X1504578415045785GC4GENIChomozygous108233028
X1504578615045787TG4GENIChomozygous108233030
X1504578715045788GC4GENIChomozygous108233032
X1504650015046500A4GENIChomozygous129722363
X1504719015047191TG9GENIChomozygous108233034
X1504728215047283CG16GENIChomozygous108233036
X1504729015047291CA15GENIChomozygous108233038
X1504731615047317AG16GENIChomozygous108233040
X1504737415047375GA7GENIChomozygous108233042
X1504738415047385CA6GENIChomozygous108233044
X1504738515047386GA6GENIChomozygous108233046
X1504739215047393CA6GENIChomozygous108233048
X1504480915044810AG7GENIChomozygous108369814
X1504724815047249C17GENIChomozygous129722364
X1504539815045399GA11GENIChomozygous119905696
X1504551615045517TG7GENIChomozygous119905697
X1504544915045450AT6GENIChomozygous108766286
X1504564015045641GT11GENIChomozygous108618320