chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132677995126779952CT19GENIChomozygous114302942
132678020126780202AT39GENIChomozygous114302943
132678051426780515TC42GENIChomozygous114302944
132678128926781290CT26GENIChomozygous114302945
132678147226781473GA8GENIChomozygous114966856
132678537826785379AT50GENICpossibly homozygous114302946
132678726126787262AG30GENIChomozygous114302947
132678772526787726TC19GENIChomozygous114302948
132678820626788207GA30GENIChomozygous114302949
132679018426790185TG20GENIChomozygous114302950
132679135126791352TC30GENIChomozygous114302951
132679194326791944AG41GENIChomozygous114302952
132679235526792356AG28GENIChomozygous114302953
132679265226792653CA33GENIChomozygous114302954
132679287426792875TC20GENIChomozygous114302955
132679298426792985GC23GENIChomozygous114302957
132679300426793005CA21GENIChomozygous114302958
132679317026793171CG20GENIChomozygous114302959
132679393626793937GA33GENIChomozygous114302960
132679450826794509AG34GENIChomozygous114302961
132679454926794550CA32GENIChomozygous114302962
132679482426794825AG44GENIChomozygous114302963
132679490726794908CG28GENIChomozygous114302964
132679583126795832AC34GENIChomozygous114302965
132679626726796268CT39GENIChomozygous114302966
132679655826796559TC34GENIChomozygous114302967
132679692126796922AC17GENIChomozygous114302968
132679931726799318AG34GENIChomozygous114302970
132680187026801871GC45GENIChomozygous114302971
132680597726805978AG29GENICpossibly homozygous114302972
132680739526807396CT40GENIChomozygous114302973
132680755726807558CT42GENIChomozygous114302974
132680938326809384CT30GENIChomozygous114302976
132681078126810782TC43GENIChomozygous114302977
132681083926810840CG26GENIChomozygous114302978
132681097026810971GA28GENIChomozygous114302979
132679497126794972GC26GENIChomozygous114608635