chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37010820670108208AA--18GENICpossibly homozygous57435229
37010876970108772CAT---35GENIChomozygous57894466
37010908570109086TTAA24GENIChomozygous57435231
37010917270109182TGTGTGTGTG----------4GENIChomozygous59042993
37011020070110201AG3GENIChomozygous57435233
37011159170111592T-7GENICpossibly homozygous57894467
37011178770111788CCT26GENICpossibly homozygous57435241
37011224270112243T-10GENICheterozygous57894468
37011241870112419TC23GENIChomozygous57435243
37011277170112772AC30GENIChomozygous57435245
37011277270112773GA31GENIChomozygous57435247
37011289370112894CT29GENIChomozygous57894469
37011391170113912GA16GENIChomozygous57894470
37011723970117240AC20GENICpossibly homozygous57435259
37011746970117470TA23GENIChomozygous57894471
37011820270118203AAG24GENIChomozygous57894472
37011831970118325AGTTGT------34GENIChomozygous57435263
37011836070118361GA39GENIChomozygous57435265
37011847470118475TC38GENIChomozygous57435267
37011945070119451TTAA13GENICheterozygous57894473
37011945070119451TTA13GENICheterozygous57894474
37011947270119473GGA18GENIChomozygous57435271
37011968470119685CT29GENIChomozygous57435273
37012060570120606AG38GENIChomozygous57894475
37012118770121195GTCCGTCC--------1GENIChomozygous59516755
37012129170121292AG19GENIChomozygous57435283
37012198970121991AC--4GENIChomozygous58900922
37012302970123033GTGT----5GENIChomozygous58594415
37012336870123369CT28GENIChomozygous57435289
37012391270123940GGAGCGGGGCCCAGCTCACTCCTGTTAC----------------------------13GENIChomozygous58594419
37012441070124411TC28GENIChomozygous57435293
37012454070124541AG20GENIChomozygous57894480
37012508170125102CTCAGCGAGTAAGAGCACTGC---------------------17GENIChomozygous57894481
37012545970125460AG29GENIChomozygous57435297
37013013270130133AG27GENIChomozygous57435305
37013077570130776T-24GENICpossibly homozygous57894482
37013109870131099A-12GENICheterozygous58594421