chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106145689261456894GG--1GENIChomozygous52844746
106146369861463699CT9GENIChomozygous51670511
106146472661464727AT14GENIChomozygous51899796
106146621961466220GGT3GENIChomozygous51470876
106146845261468453GGGAT1GENIChomozygous51899798
106147124461471245AG15GENICpossibly homozygous51899800
106147192061471921CA10GENICheterozygous51899802
106147445061474451TG11GENICheterozygous51670529
106147488161474882CT15GENICpossibly homozygous51899804
106147797961477980CT21GENICheterozygous51470881
106153352161533522GGAAA1GENIChomozygous52379989
106153352361533524CA1GENIChomozygous52379991
106153353361533534TG1GENIChomozygous51470890
106153355761533558GC1GENIChomozygous51470891
106153355861533559AT1GENIChomozygous51470892
106153356261533563CT1GENIChomozygous51470893
106153356361533564AT1GENIChomozygous51470894
106153356761533568GA1GENIChomozygous51470895
106153358761533588CT3GENICheterozygous51470897
106153518461535185AG10GENICheterozygous51670558
106153591661535917TA3GENIChomozygous51899810
106153948461539485GGT1GENIChomozygous51470901
106154146861541469GGATT6GENICheterozygous51899814
106154537061545371AC9GENIChomozygous51899816
106154610861546109CCA7GENIChomozygous51470903
106154976561549766GA7GENIChomozygous51899820
106154989661549897TTG14GENIChomozygous51670574
106154994561549946CT5GENIChomozygous51899822
106155111961551120AG12GENIChomozygous51470904
106155222461552225AG11GENICpossibly homozygous51470905
106155306261553063CCTT5GENICheterozygous52319786
106155425461554255GT6GENIChomozygous51470908
106155684161556842CCTGTGTG6GENICheterozygous52564061
106155744061557441GA17GENIChomozygous51899826
106155849661558497GA7GENIChomozygous51899828
106156074661560747GA23GENICpossibly homozygous51899830
106156533361565334GGA2GENICheterozygous51470911
106156630361566304GA22GENIChomozygous51899834
106156791661567917GT9GENIChomozygous51470913
106156870061568701TC10GENICpossibly homozygous51470914
106157079761570798AG21GENIChomozygous51670612