chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108514904985149050CCCTTGTG16GENIChomozygous52392031
108514906785149068AAG19GENIChomozygous51723356
108514906985149070GGCTCTACCACTGAGCT19GENIChomozygous52392033
108514907185149072AAATCC19GENIChomozygous52392035
108515277885152780GA--9GENICheterozygous52444470
108515546285155464AC--6GENICheterozygous52392037
108515736285157363G-8GENIChomozygous51525264
108515737585157376A-11GENIChomozygous51525265
108515738785157388CT17GENIChomozygous51525266
108515739385157394C-16GENIChomozygous51525267
108516121685161218GT--3GENICheterozygous52392043
108516340185163402GGTGCTTGCTA9GENIChomozygous52392045
108516340385163404GGCA9GENIChomozygous52392047
108516340585163406GGCGC8GENIChomozygous52392049
108516340985163410AACCACTG6GENIChomozygous52392051
108516341185163412GGCTAAATCCCCA6GENIChomozygous52392053
108516448585164486GGTTTTTTT11GENICheterozygous52392055
108516534385165344CCTGAGCAA11GENIChomozygous51525288
108516546785165468CT3GENIChomozygous51525289
108516606885166069CCCCAAAACAAAGGAGAACAAAG19GENIChomozygous51525290
108518563185185633TG--1GENIChomozygous52392057
108519301585193016GT8GENIChomozygous52996575
108519348185193482CCA1GENIChomozygous52444476
108519806085198061A-14GENICheterozygous51920297
108520062085200622TC--6GENICheterozygous52444478
108520064585200647CT--13GENICheterozygous52603614
108520074385200744A-30GENIChomozygous51525294
108520802785208028AAGT7GENICpossibly homozygous53064476
108521026885210270CC--39GENIChomozygous51525299
108522596685225968AG--13GENICheterozygous51525326
108522952285229524GT--3GENICheterozygous52392059
108522983185229832GGA1GENIChomozygous52444480