chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157634935157634936CT65GENIChomozygous137248732
4157635472157635472GTT41GENIChomozygous136925250
4157635526157635527AG36GENIChomozygous137248733
4157635789157635790CT69GENIChomozygous137248734
4157636122157636123CT31GENIChomozygous137248735
4157636611157636612CT64GENIChomozygous137248736
4157636770157636772GA38GENIChomozygous136925251
4157636774157636775GA38GENIChomozygous137248737
4157636924157636925CT55GENIChomozygous137248738
4157637116157637119CCC39GENIChomozygous136925252
4157637993157637994AT24GENICheterozygous403125162
4157637992157637993A24GENICheterozygous403125159
4157637992157637993AT24GENICheterozygous403125160
4157637993157637994A24GENICheterozygous403125161
4157638474157638475CG35GENIChomozygous137248739