chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151752995151752996TC29GENIChomozygous71220005
4151753089151753090AG25GENIChomozygous71220008
4151753484151753485CT20GENIChomozygous71220011
4151753805151753806TC24GENIChomozygous71220017
4151754161151754162TG18GENIChomozygous71220020
4151754958151754959AG13GENIChomozygous71220023
4151755214151755215TC36GENIChomozygous71220025
4151755420151755421GA29GENIChomozygous71220028
4151756412151756413GT22GENIChomozygous71220031
4151758256151758257AG37GENIChomozygous71220034
4151760501151760502AG38GENIChomozygous71220037
4151761359151761360TC19GENIChomozygous71220040
4151762544151762545TG36GENIChomozygous71220043
4151762778151762779CT27GENIChomozygous71220046
4151764650151764651CT25GENIChomozygous71220049
4151765080151765081CT26GENIChomozygous71220052
4151765510151765511AG31GENIChomozygous71220055
4151765688151765689TC27GENIChomozygous71220058
4151765775151765776TA30GENIChomozygous71220061
4151765837151765838TC29GENIChomozygous71220064
4151766136151766137GA32GENIChomozygous71220067
4151767351151767352GA25GENIChomozygous71220070
4151767902151767903GA31GENIChomozygous71220073
4151768138151768139CT33GENIChomozygous71220076
4151769231151769232TC16GENIChomozygous71220079
4151769601151769602TC10GENIChomozygous71220082
4151769765151769766CT6GENIChomozygous71220085
4151770373151770374AG27GENICpossibly homozygous71220087
4151770438151770439GA29GENIChomozygous71220090
4151771512151771513GA25GENIChomozygous71220093
4151772177151772178TC31GENIChomozygous71220096
4151773183151773184CT40GENIChomozygous71220099
4151775307151775308AC30GENIChomozygous71220102