chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150366194150366195CA3GENICheterozygous126292116
5150366668150366669TG15GENIChomozygous114056068
5150366695150366696GC11GENIChomozygous114056069
5150368826150368827AT4GENIChomozygous114451095
5150369249150369250AG16GENIChomozygous114056077
5150369382150369383AG14GENIChomozygous114451097
5150369534150369535TC21GENIChomozygous114056079
5150371883150371884GA12GENIChomozygous114056081
5150372944150372945TC17GENIChomozygous126241218
5150375415150375416AG8GENIChomozygous114451101
5150375467150375468TC9GENIChomozygous114056085
5150375472150375473CA6GENIChomozygous114056087
5150376116150376117TC15GENIChomozygous114056089
5150376911150376912GC13GENIChomozygous114451103
5150377210150377211CT14GENIChomozygous114056091
5150377808150377809AG16GENIChomozygous114056093
5150378151150378152TC4GENICheterozygous126241220
5150378500150378501TC13GENIChomozygous114056095
5150378996150378997GC24GENIChomozygous114451105
5150379516150379517GT7GENIChomozygous114056097
5150380919150380920GA13GENIChomozygous114451109
5150382171150382172CT21GENIChomozygous114056100
5150382239150382240AC20GENIChomozygous114056102
5150382642150382643TA20GENIChomozygous114451111
5150384424150384425AG21GENIChomozygous114056108
5150384936150384937CT7GENIChomozygous114056114
5150384971150384972CA15GENIChomozygous114056116
5150385891150385892GC12GENIChomozygous114056124
5150385969150385970TC12GENIChomozygous114056126
5150386227150386228GA11GENIChomozygous114451115
5150387156150387157CA11GENIChomozygous126206114
5150388934150388935AT17GENIChomozygous114451117