chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2237728716237728717AG28GENIChomozygous110324942
2237729519237729520AT29GENIChomozygous110324944
2237730217237730218AG26GENIChomozygous110324948
2237733400237733401CA14GENIChomozygous110324954
2237733941237733942TC18GENIChomozygous110324956
2237734407237734408TC18GENIChomozygous111379767
2237736226237736227CT25GENIChomozygous111379769
2237737553237737554AG4GENIChomozygous111379770
2237737557237737558AG6GENICheterozygous111379772
2237738804237738805GA13GENIChomozygous111379778
2237738932237738933TC21GENIChomozygous110324978
2237740195237740196TC31GENIChomozygous110324980
2237741273237741274CT28GENICpossibly homozygous110324982
2237741351237741352AT27GENIChomozygous110324984
2237741390237741391CT26GENIChomozygous111379780
2237742201237742202GA25GENIChomozygous111379782
2237743139237743140CT27GENIChomozygous111379784
2237743309237743310TC28GENIChomozygous110324990
2237743457237743458TC22GENIChomozygous111379786
2237744343237744344AG22GENIChomozygous110324994
2237745428237745429AG28GENIChomozygous111180787
2237746346237746347CT35GENIChomozygous110325000
2237746655237746656GA23GENIChomozygous111379788
2237747306237747307AG26GENIChomozygous110325002
2237749016237749017TC23GENIChomozygous110325004
2237751077237751078CT26GENIChomozygous110325006
2237751216237751217GA26GENIChomozygous111379789