chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
61572664815726649TA18GENIChomozygous115048150
61572718615727187CT14GENIChomozygous118650064
61572841415728415AG23GENIChomozygous118650065
61573116315731164AG9GENICheterozygous115048154
61573147815731479CT19GENIChomozygous118650066
61573181115731812CT16GENIChomozygous118650067
61573476915734770AC15GENIChomozygous115048159
61573562615735627TC15GENIChomozygous115048160
61573575615735757AG23GENIChomozygous115048161
61574141315741414CA8GENIChomozygous118650068
61574198415741985GA9GENIChomozygous115048163
61574861815748619GC19GENIChomozygous118650069
61574991615749917TC18GENIChomozygous115048166
61575137115751372CA17GENIChomozygous115048167
61575941815759419AG12GENIChomozygous115048170
61576016615760167GA9GENIChomozygous115048171
61576026315760264GT18GENIChomozygous118650071
61576185015761851CA7GENIChomozygous118650072
61576217815762179TC17GENIChomozygous118650073
61576332815763329GA26GENIChomozygous118650074
61576663615766637AC12GENIChomozygous115048179
61574122415741225TC11GENICheterozygous126394262