chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122604494122604495TC18GENIChomozygous116226277
7122604569122604570CA18GENIChomozygous115860975
7122606274122606275CG21GENIChomozygous116226278
7122606836122606837CT20GENIChomozygous116226279
7122607733122607734TC28GENIChomozygous116226281
7122608102122608103GA24GENIChomozygous115860977
7122608157122608158TA26GENIChomozygous115860979
7122609735122609736TC31GENIChomozygous115860983
7122611371122611372AC21GENIChomozygous115860989
7122612344122612345TC27GENIChomozygous116226282
7122612625122612626AC20GENIChomozygous116226283
7122612930122612931GA28GENIChomozygous116226284
7122613437122613438AG10GENIChomozygous116226285
7122613518122613519CA18GENIChomozygous116226286
7122613601122613602CT20GENIChomozygous116226287
7122614783122614784CT19GENIChomozygous115860991
7122614953122614954CT14GENIChomozygous116226288
7122616079122616080TA33GENIChomozygous115860993
7122618006122618007TG22GENIChomozygous115860997
7122623363122623364AG18GENIChomozygous115860999
7122623392122623393TC23GENIChomozygous116226292
7122623666122623667GA29GENIChomozygous116226293
7122624872122624873CA26GENIChomozygous118286390
7122625154122625155CA17GENIChomozygous116226294
7122625551122625552TC36GENIChomozygous116226295
7122626169122626170CT21GENIChomozygous116226296
7122627284122627285CT26GENIChomozygous115861007
7122628376122628377CT29GENIChomozygous116226297
7122628559122628560CT18GENIChomozygous115861009
7122628870122628871GT33GENIChomozygous116226298
7122629063122629064TC25GENIChomozygous115861011
7122629068122629069AT22GENIChomozygous115861013
7122629071122629072GA20GENIChomozygous115861015
7122629426122629427GA28GENIChomozygous116226299
7122630384122630385TC23GENIChomozygous116226300
7122630844122630845TC30GENIChomozygous115861019
7122631057122631058AG21GENIChomozygous115861023
7122632986122632987GT33GENIChomozygous115861029
7122633199122633200TA24GENIChomozygous116226305
7122633265122633266CA14GENIChomozygous115861031
7122633557122633558AG30GENIChomozygous116226306