chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17681769576817696CA41GENICpossibly homozygous144249041
17682371076823711AC42GENIChomozygous142829694
17682671476826715TA24GENIChomozygous144249042
17683036276830363GA38GENIChomozygous144249043
17682643976826439A31GENIChomozygous142787577
17682490976824919ACACACACAG29GENIChomozygous144227784
17682977376829774AT41GENIChomozygous146344140
17683209876832099GC16GENICheterozygous402951107
17683209676832097G16GENICheterozygous402951104
17683209676832097GC16GENICheterozygous402951105
17683209876832099G16GENICheterozygous402951106
17683248176832482AC32GENICpossibly homozygous153849008
17683404176834042AG30GENIChomozygous142829706
17683908676839087AG43GENIChomozygous142829712
17684023076840240GGGGTCCCAG33GENIChomozygous144227785
17684831776848318GA39GENIChomozygous144249044
17684914976849150AG33GENIChomozygous144249045
17685104776851048A7GENICheterozygous402951110
17685104776851048AT7GENICheterozygous402951111
17683248176832482AT32GENICheterozygous403792795
17684130976841309A24GENIChomozygous142787579
17684294476842946CT24GENIChomozygous144227786
17685025376850254C44GENIChomozygous142787586