chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99420965394209655TT--23GENIChomozygous52280347
99420983494209835A-21GENICpossibly homozygous52280349
99421006994210070TG30GENIChomozygous52280351
99421047894210479T-5GENIChomozygous52280353
99421048494210486TT--6GENICheterozygous52280354
99421099994211000TA24GENIChomozygous52280356
99421100894211009CA23GENIChomozygous52280357
99421115694211159AGA---28GENIChomozygous52280359
99421168394211684A-12GENIChomozygous52052440
99421250994212510AT18GENIChomozygous52280361
99421281594212816GA25GENIChomozygous52280362
99421505694215057GA30GENIChomozygous52280364
99421509194215092AG30GENIChomozygous52280366
99421516294215163GT33GENIChomozygous52280367
99421571094215711T-20GENIChomozygous52280369
99421574794215748TTTTTTTCCC30GENIChomozygous52052442
99421605494216055CT21GENIChomozygous52052446
99421646894216469GA13GENIChomozygous52280370
99421656994216570GA11GENIChomozygous52280372
99421688394216884AG23GENIChomozygous52280374
99421907394219074A-4GENIChomozygous52052448
99421909294219093CCAAAA4GENIChomozygous52052450
99422021394220214CCCCCCCT1GENIChomozygous52915528
99422133394221334GA7GENIChomozygous52280377
99422139394221394CT18GENIChomozygous52280378
99422155694221557TC29GENIChomozygous52052452
99422316694223194TGTGTGTGTGTGTGTGTGTGTGTGTGTT----------------------------6GENICheterozygous52915529
99422320694223207TC6GENIChomozygous52915530
99422320894223209TC6GENIChomozygous52052454
99422404294224043GC31GENIChomozygous52280380
99422445094224451TG24GENIChomozygous52280382
99422459194224592CG26GENIChomozygous52052460