chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69627658796276588GA11GENICheterozygous54592060
69627722196277222TG25GENICpossibly homozygous54592061
69627820296278203GA26GENIChomozygous54592062
69627922296279224CT--4GENIChomozygous54592065
69627934196279342A-6GENIChomozygous54592066
69627988996279894ATATG-----8GENICpossibly homozygous54592067
69628104996281050TTAAACA4GENIChomozygous54592068
69628114896281149AATG9GENIChomozygous54592069
69628352596283526TG7GENICpossibly homozygous54592070
69628405196284052AG6GENIChomozygous54592073
69628483096284831TTCTTC1GENIChomozygous54592074
69628527596285276GT1GENIChomozygous55522124
69628631196286312A-2GENIChomozygous54592077
69628644796286448AG9GENIChomozygous54592078
69628665096286651AG5GENIChomozygous54592079
69628698096286981AG17GENICpossibly homozygous54592080
69628861496288615AT13GENIChomozygous54592082
69628891796288918TC24GENICpossibly homozygous54592083
69628921796289218TG11GENICpossibly homozygous54592084
69629029596290296AAGTGTCAGC5GENICheterozygous54592085
69629032996290330GA8GENIChomozygous54592086
69629089696290897AG6GENIChomozygous54592087
69629103496291035AG10GENIChomozygous54592088
69629172196291722CT7GENIChomozygous54592089
69629227796292278GA23GENICpossibly homozygous54592090
69629278296292783CCT3GENICheterozygous54592091
69629306796293068TC2GENIChomozygous54592092
69629365796293658TC14GENIChomozygous54592093
69629490896294909GGGTT13GENICheterozygous54592094
69629637296296373AT14GENIChomozygous54592095
69629680896296809AG7GENIChomozygous54592096
69629687496296875AC10GENIChomozygous54592097
69629758496297585TG6GENIChomozygous54592099
69629777696297777CT1GENIChomozygous54592100
69629837996298380TC9GENIChomozygous54592101
69629892096298921CT14GENIChomozygous54592102
69629903096299032TA--11GENIChomozygous54592103
69628526596285273AGGGGGGG--------4GENIChomozygous55417273