chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182931776029317763TGT---17GENIChomozygous46812491
182931776329317764CA16GENIChomozygous46812492
182931776429317765CCAAA16GENIChomozygous46812493
182931924029319241C-6GENIChomozygous46410407
182931961229319613TC13GENIChomozygous46756383
182932004229320043CCT25GENIChomozygous46410412
182932104229321043TC19GENIChomozygous46756384
182932307729323078A-8GENIChomozygous46756385
182932361929323620AT15GENIChomozygous46756386
182932380129323802CCT11GENIChomozygous46410440
182932380829323809TTACAC2GENICheterozygous46812494
182932409629324097AG21GENIChomozygous46756387
182932459629324597TC7GENIChomozygous46410444
182932583729325838TTA5GENIChomozygous46410452
182932623429326258TCCTTCCTTCCTTCCTTCCTTCCT------------------------6GENIChomozygous46812496
182932642029326421GGTTTTTTTT4GENICheterozygous46812497
182932644529326460CGGAGCTGGGTGTTG---------------13GENICheterozygous46812498
182932765129327652GGT8GENIChomozygous46857930
182932861329328614G-14GENIChomozygous46410469
182932895229328953TC2GENIChomozygous46410475
182932899429328995GGAAAA4GENICheterozygous46410479
182932901629329029TTCTCGCTATGCT-------------13GENICheterozygous46812499
182932941429329415GA32GENIChomozygous46756389