chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76922749169227492C-21GENIChomozygous53952274
76922804469228047AAA---16GENICpossibly homozygous54442285
76922804669228047A-16GENICheterozygous55082614
76922842969228430GT30GENIChomozygous54442287
76922867469228675AG15GENIChomozygous54442289
76922921769229218CT32GENIChomozygous54442291
76923211669232117CG23GENIChomozygous54442296
76922986869229869CCTTT16GENIChomozygous54442294
76923128469231285CCAGT14GENICpossibly homozygous53952289
76923182169231822AG38GENIChomozygous53952294
76923202569232028TGT---8GENICheterozygous53952295
76923245169232452TC28GENIChomozygous53952301
76923350369233504CT13GENIChomozygous54442298
76923411769234118GT32GENIChomozygous54442300
76923411869234119GA31GENIChomozygous53952312
76923480969234810AAT24GENIChomozygous53952316
76923481269234813GGAGAGAGGA24GENIChomozygous53952318
76923573869235739AAAGGGGTTGTTTC31GENIChomozygous53952320
76923609569236096GA52GENIChomozygous54442304
76923638869236389GC29GENIChomozygous54442306
76923778469237785TC12GENIChomozygous54442308
76923802369238024GA16GENIChomozygous53952321
76923805669238057AG19GENIChomozygous53952322
76923898769238988GA38GENICpossibly homozygous54442320
76923953169239539ACACACGT--------4GENICheterozygous54442322
76924028869240289T-16GENICpossibly homozygous54442326
76924067169240672AG32GENIChomozygous54442328
76924086869240869CG28GENIChomozygous54442330
76924151669241517AAT17GENIChomozygous54442332
76924188169241882GA27GENIChomozygous53952329
76924244769242448TC38GENIChomozygous54442334
76924441569244416GT33GENIChomozygous54442336
76924026169240263TT--19GENIChomozygous54906871
76923785769237879ATATATATATATATATATACAC----------------------4GENIChomozygous54981051
76923789769237898A-8GENIChomozygous54981053
76923790069237903TTC---9GENIChomozygous54981055
76923952969239539ACACACACGT----------4GENICheterozygous54981057
76924027669240277GGGA22GENIChomozygous54981059