chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130262417130262418GA10GENIChomozygous54754865
7130265004130265005CCTG1GENIChomozygous54754867
7130265625130265626T-8GENIChomozygous54521321
7130265950130265951CA7GENICpossibly homozygous54110773
7130265969130265970GT9GENIChomozygous54754869
7130266187130266188CCCCCACAGCGCATGCGTGT1GENIChomozygous55408821
7130266325130266326AG7GENIChomozygous54754871
7130267224130267225C-12GENIChomozygous54754873
7130269176130269177GA3GENIChomozygous54110784
7130270455130270456TC5GENIChomozygous54110791
7130270512130270513T-5GENIChomozygous55010462
7130270959130270960TC6GENIChomozygous54110795
7130273041130273043AA--14GENICheterozygous54521337
7130273042130273043A-14GENICpossibly homozygous54521339
7130273476130273480GTGT----10GENIChomozygous54676920
7130273602130273603AATG8GENIChomozygous54110805
7130273903130273904A-10GENIChomozygous54110806
7130277321130277322CCAA5GENIChomozygous55098732
7130277711130277712GA15GENIChomozygous54754875
7130278969130278970CT9GENIChomozygous54754877
7130279760130279761GT6GENIChomozygous54754879
7130279822130279823CT13GENIChomozygous54754881
7130280018130280019AG12GENIChomozygous54110844
7130283113130283114TC11GENIChomozygous54754883
7130285433130285435GA--6GENIChomozygous54110861
7130285902130285903T-15GENIChomozygous54110863
7130286893130286894T-10GENIChomozygous54110864
7130286961130286962GA9GENIChomozygous54110865
7130287788130287789CCT3GENIChomozygous54754885
7130287873130287874A-6GENIChomozygous54110867
7130287913130287914AG6GENIChomozygous54110868
7130287954130287955GT7GENIChomozygous54110869
7130288063130288064AC9GENIChomozygous54110870
7130288174130288175A-8GENIChomozygous54110872
7130288220130288221TA6GENIChomozygous54754887
7130288272130288273A-6GENIChomozygous54110875
7130288339130288340GA13GENIChomozygous54110876
7130288503130288504CT10GENIChomozygous54110878