chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147745072147745073CT45GENIChomozygous112874961
4147745246147745247GT25GENICheterozygous119348269
4147745447147745448AG24GENIChomozygous112874962
4147746422147746423AG24GENIChomozygous112874964
4147746759147746760CT29GENIChomozygous112874965
4147746881147746882AC28GENIChomozygous112874966
4147747002147747003TC17GENIChomozygous112874967
4147747117147747118GA31GENIChomozygous112874968
4147747310147747311CT24GENIChomozygous112874969
4147748124147748125TC26GENIChomozygous112874970
4147748297147748298TC19GENIChomozygous112874971
4147749508147749509TC36GENICpossibly homozygous112874972
4147749643147749644AG26GENIChomozygous112874973
4147749856147749857AG31GENIChomozygous112874974
4147750735147750736CG39GENIChomozygous112874975
4147751820147751821CT24GENIChomozygous112874976
4147752908147752909AG28GENIChomozygous112874977
4147754040147754041CA29GENIChomozygous112874979
4147754966147754967GA16GENIChomozygous112874980
4147756091147756092TC22GENIChomozygous112874981