chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85911087059110871AC14GENIChomozygous117108083
85911183159111832GA21GENIChomozygous117184656
85911194659111947GT25GENIChomozygous116510932
85911195159111952TC27GENIChomozygous116510934
85911233659112337GA23GENIChomozygous117184657
85911245459112455CT22GENIChomozygous117184658
85911261859112619GA18GENIChomozygous116510938
85911309359113094CT11GENIChomozygous116510940
85911320659113207CG13GENIChomozygous116510942
85911351659113517CT23GENIChomozygous116510944
85911356259113563AG22GENIChomozygous116510946
85911375759113758TG26GENIChomozygous116510950
85911595459115955CT13GENIChomozygous117184660
85911611659116117AG20GENIChomozygous116510962
85911662959116630CT15GENIChomozygous117184661
85911674159116742AT10GENIChomozygous116510966
85911715759117158CT23GENIChomozygous116510969
85911721659117217CT20GENIChomozygous116510971
85911730559117306CT20GENIChomozygous116510973
85911793859117939CT27GENIChomozygous116510975
85911794559117946GA27GENIChomozygous116510977
85911796259117963AT22GENIChomozygous116510979
85911808359118084CT29GENIChomozygous117184662
85911921359119214GA12GENIChomozygous116511015
85911944959119450AG13GENIChomozygous116511017
85911960859119609CT15GENIChomozygous116511019
85911976059119761CG21GENIChomozygous116511021
85911987859119879CT13GENIChomozygous116511023
85912080259120803AG10GENIChomozygous116511027
85912092659120927CT10GENIChomozygous116511029
85912099759120998CT7GENIChomozygous116511033
85912110759121108GA20GENIChomozygous116511035
85912123859121239CG12GENIChomozygous116511037
85912156659121567AG15GENIChomozygous116511039
85912182659121827CT14GENIChomozygous116511041
85912188259121883GA21GENIChomozygous116511043
85912231659122317CT13GENIChomozygous116511045
85912232459122325GA13GENIChomozygous116511047
85912254359122544TC17GENIChomozygous116511049
85912269759122698TA11GENIChomozygous116511051