chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135578908655789094CTCTCTCT--------7GENIChomozygous708995381
135578919955789201TC--18GENICheterozygous708995383
135578922755789228TTC18GENIChomozygous708995384
135578923655789237GGTC15GENICheterozygous708995385
135578927055789271TTTCTCTCTCTGTCTTCTCTCTGTCTCTGTCTCTCTCTCTTTC10GENIChomozygous708995386
135578942255789423CG7GENICpossibly homozygous568317541
135578965455789656TC--18GENIChomozygous708995387
135578972455789725TTC17GENIChomozygous708995388
135578973155789732CCTCT16GENIChomozygous708995389
135579103355791034GA28GENIChomozygous565334225
135579200955792010GGCA14GENICheterozygous708995390
135579200955792010GGCACA14GENICheterozygous708995391
135579303055793031AG10GENIChomozygous565334226
135579307355793074T-4GENIChomozygous708995393
135579400355794004GA13GENIChomozygous568317542
135579404555794047AA--7GENICheterozygous708995394
135579446155794462CT26GENIChomozygous565334227
135579512755795128AG24GENIChomozygous565334228
135579527055795271CT22GENIChomozygous565334229
135579548355795484TC15GENIChomozygous565334230
135579568655795687GGC14GENIChomozygous708995395
135579722655797248ACACACACACACACACACACAC----------------------5GENICheterozygous708995396
135579722855797248ACACACACACACACACACAC--------------------5GENICheterozygous708995397
135579807855798079AACACCC5GENICheterozygous708995401
135579807855798079AACCCCCC5GENICheterozygous708995402
135579808655798087AG15GENIChomozygous568317543
135579830955798310TTG5GENIChomozygous708995403
135579838855798389AAGACTGACTGACTGACT11GENIChomozygous708995405
135579909955799100AC25GENIChomozygous565334231
135579987755799878AG15GENIChomozygous565334232
135580062355800624CG10GENIChomozygous565334233
135580164955801650AG23GENIChomozygous565334234
135580172555801726AG16GENIChomozygous565334235