chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184734753447347535AG1GENIChomozygous46437760
184734959647349597TC20GENICpossibly homozygous46437761
184735068147350682GA21GENICpossibly homozygous46437765
184735074947350750GA23GENIChomozygous46437766
184735263747352638AG27GENICpossibly homozygous46437768
184735308547353086TTTTTTTGA1GENIChomozygous46437769
184735365947353660GA18GENIChomozygous46437770
184735375247353754TA--8GENICheterozygous46892950
184735464747354648GA26GENICheterozygous46437771
184735500147355002CT11GENIChomozygous46437772
184735557847355579G-3GENIChomozygous46437773
184735636747356368GC4GENIChomozygous46437775
184735637747356378CT5GENICheterozygous46437776
184735699947357000CT18GENICpossibly homozygous46437777
184735734447357345AAG10GENICpossibly homozygous46437778
184735862147358622GT21GENICpossibly homozygous46437779
184735906547359066AT9GENIChomozygous46437780
184735935747359358AG6GENIChomozygous46437783
184735939847359399T-2GENICheterozygous46859135
184735960647359607AG8GENICpossibly homozygous46437784
184736179447361795GA14GENICpossibly homozygous46437788
184736230947362311CT--11GENIChomozygous46437789
184736421547364219TTTG----2GENIChomozygous46437792
184736525247365253GA13GENICpossibly homozygous46437795
184736599947366000A-3GENIChomozygous46437796
184736758447367585AT23GENICpossibly homozygous46437797
184736888947368890AG9GENICpossibly homozygous46437799
184736941947369420CCA6GENIChomozygous46437800
184737178947371790CG19GENIChomozygous46437808
184737222847372229CT18GENICpossibly homozygous46437809
184737232047372321AG26GENICpossibly homozygous46437810
184737412147374122CG17GENIChomozygous46437811
184737727747377278T-26GENICheterozygous46437814
184738328047383281TC11GENIChomozygous46437820
184738490847384909AG19GENICpossibly homozygous46437821