chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121160732116074TC52GENIChomozygous135482811
121170342117035GA47GENIChomozygous142803567
121178872117888CT58GENIChomozygous135482813
121181312118132TC50GENIChomozygous142803568
121185392118540CT59GENIChomozygous135482815
121207112120712GA56GENIChomozygous142803569
121218342121835GA59GENIChomozygous135482822
121218352121836AC58GENIChomozygous135482823
121253452125346GA64GENIChomozygous142803570
121261272126128CT72GENIChomozygous142803571
121303922130393GA44GENICpossibly homozygous142803572
121312942131295AG54GENIChomozygous135482846
121323402132341TC45GENIChomozygous142803573
121325162132517GC45GENIChomozygous142803574
121391102139111GA44GENIChomozygous135482868
121403802140381CT61GENIChomozygous135482872
121409792140980AG58GENIChomozygous135482873
121419122141913TG47GENIChomozygous135482875
121449072144908GA62GENIChomozygous142803575
121453842145385CA35GENIChomozygous135482880
121453862145387CT35GENIChomozygous135482881
121179352117936A56GENIChomozygous135390211
121237332123733TTG59GENIChomozygous142782013
121288032128805AC56GENIChomozygous142782014
121389142138914T56GENICpossibly homozygous142782015
121453932145394AC29GENICheterozygous402938832
121453962145397C29GENICheterozygous404048456
121453932145394A29GENICheterozygous402938830
121453932145394AT29GENICheterozygous402938831
121354802135485ACACA13GENIChomozygous143732365
121354872135488CT13GENIChomozygous143747902
121354872135488C13GENICheterozygous404048454
121453962145397CT29GENICheterozygous404048455
121475922147597AATAA58GENIChomozygous142782016
121478092147810CT43GENIChomozygous135482887
121545642154565GT68GENIChomozygous142803576
121546652154666AC39GENIChomozygous142803577
121550392155040GA42GENIChomozygous135482898
121562372156238AG54GENIChomozygous135482903
121570282157029CT53GENIChomozygous142803578
121453972145398CT29GENICheterozygous147243504