chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157634935157634936CT29GENIChomozygous137248732
4157635472157635472GTT15GENIChomozygous136925250
4157635526157635527AG8GENIChomozygous137248733
4157635789157635790CT13GENIChomozygous137248734
4157636122157636123CT15GENIChomozygous137248735
4157636611157636612CT20GENIChomozygous137248736
4157636770157636772GA11GENICpossibly homozygous136925251
4157636774157636775GA10GENIChomozygous137248737
4157636924157636925CT16GENIChomozygous137248738
4157637116157637119CCC15GENIChomozygous136925252
4157638474157638475CG23GENIChomozygous137248739
4157637993157637994A11GENIChomozygous403125161
4157637993157637994AT11GENICheterozygous403125162
4157637992157637993A11GENIChomozygous403125159
4157637992157637993AT11GENICheterozygous403125160