chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135578908655789094CTCTCTCT--------24GENIChomozygous759545213
135578919955789201TC--13GENICheterozygous759545215
135578922755789228TTC13GENIChomozygous759545216
135578923655789237GGTC11GENICheterozygous759545217
135578927055789271TTTCTCTCTCTGTCTTCTCTCTGTCTCTGTCTCTCTCTCTTTC10GENIChomozygous759545218
135578942255789423CG4GENIChomozygous654136031
135578965455789656TC--22GENIChomozygous759545219
135578972455789725TTC21GENIChomozygous759545220
135578973155789732CCTCT26GENICpossibly homozygous759545221
135579103355791034GA26GENIChomozygous654136032
135579200955792010GGCA22GENICheterozygous759545222
135579200955792010GGCACA22GENICheterozygous759545223
135579200955792010GGCACACA22GENICheterozygous759545224
135579303055793031AG20GENIChomozygous654136033
135579307355793074T-22GENIChomozygous759545225
135579400355794004GA31GENIChomozygous654136034
135579446155794462CT41GENIChomozygous654136035
135579512755795128AG34GENIChomozygous654136036
135579527055795271CT23GENIChomozygous654136037
135579548355795484TC28GENIChomozygous654136038
135579568655795687GGC27GENIChomozygous759545226
135579722655797248ACACACACACACACACACACAC----------------------13GENICheterozygous759545227
135579722855797248ACACACACACACACACACAC--------------------13GENICpossibly homozygous759545228
135579807855798079AACACC11GENICheterozygous759545230
135579807855798079AACACCC11GENICheterozygous759545232
135579807855798079AACCCCCC11GENICheterozygous759545233
135579808655798087AG16GENIChomozygous654136039
135579830955798310TTG12GENIChomozygous759545234
135579838855798389AAGACTGACTGACTGACT16GENIChomozygous759545236
135579909955799100AC21GENIChomozygous654136040
135579987755799878AG31GENIChomozygous654136041
135580062355800624CG25GENIChomozygous654136042
135580164955801650AG16GENIChomozygous654136043
135580172555801726AG30GENIChomozygous654136044