chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17681769576817696CA69GENIChomozygous144249041
17682371076823711AC63GENIChomozygous142829694
17682671476826715TA43GENIChomozygous144249042
17682643976826439A40GENIChomozygous142787577
17682490976824919ACACACACAG31GENIChomozygous144227784
17683036276830363GA42GENIChomozygous144249043
17683404176834042AG30GENICpossibly homozygous142829706
17683908676839087AG49GENIChomozygous142829712
17684023076840240GGGGTCCCAG49GENIChomozygous144227785
17684130976841309A45GENICpossibly homozygous142787579
17684294476842946CT48GENIChomozygous144227786
17684831776848318GA37GENIChomozygous144249044
17684914976849150AG46GENIChomozygous144249045
17685025376850254C47GENIChomozygous142787586
17683248176832482AT39GENICheterozygous403792795
17683209676832097G14GENICheterozygous402951104
17683209676832097GC14GENICheterozygous402951105
17683248176832482AC39GENIChomozygous153849008
17685104776851048A14GENICheterozygous402951110
17685104776851048AT14GENICpossibly homozygous402951111