chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151752995151752996TC15GENIChomozygous71220005
4151753089151753090AG17GENIChomozygous71220008
4151753484151753485CT9GENIChomozygous71220011
4151753805151753806TC17GENIChomozygous71220017
4151754161151754162TG18GENIChomozygous71220020
4151754958151754959AG29GENIChomozygous71220023
4151755214151755215TC29GENIChomozygous71220025
4151755420151755421GA23GENIChomozygous71220028
4151756412151756413GT27GENIChomozygous71220031
4151758256151758257AG14GENIChomozygous71220034
4151760501151760502AG32GENIChomozygous71220037
4151761359151761360TC19GENIChomozygous71220040
4151762544151762545TG30GENIChomozygous71220043
4151762778151762779CT29GENIChomozygous71220046
4151764650151764651CT29GENIChomozygous71220049
4151765080151765081CT16GENIChomozygous71220052
4151765510151765511AG25GENIChomozygous71220055
4151765688151765689TC21GENIChomozygous71220058
4151765775151765776TA14GENIChomozygous71220061
4151765837151765838TC15GENIChomozygous71220064
4151766136151766137GA17GENIChomozygous71220067
4151767351151767352GA16GENIChomozygous71220070
4151767902151767903GA24GENIChomozygous71220073
4151768138151768139CT23GENIChomozygous71220076
4151769231151769232TC16GENIChomozygous71220079
4151769601151769602TC8GENIChomozygous71220082
4151769765151769766CT2GENIChomozygous71220085
4151770373151770374AG32GENIChomozygous71220087
4151770438151770439GA21GENIChomozygous71220090
4151771512151771513GA25GENIChomozygous71220093
4151772177151772178TC19GENIChomozygous71220096
4151773183151773184CT23GENIChomozygous71220099
4151775307151775308AC20GENIChomozygous71220102