chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151752995151752996TC16GENIChomozygous71220005
4151753089151753090AG15GENIChomozygous71220008
4151753484151753485CT4GENIChomozygous71220011
4151753805151753806TC8GENIChomozygous71220017
4151754161151754162TG7GENIChomozygous71220020
4151754958151754959AG16GENIChomozygous71220023
4151755214151755215TC12GENIChomozygous71220025
4151755420151755421GA22GENIChomozygous71220028
4151756412151756413GT8GENIChomozygous71220031
4151758256151758257AG3GENIChomozygous71220034
4151760501151760502AG5GENIChomozygous71220037
4151761359151761360TC12GENIChomozygous71220040
4151762544151762545TG11GENIChomozygous71220043
4151762778151762779CT10GENIChomozygous71220046
4151764650151764651CT11GENIChomozygous71220049
4151765080151765081CT5GENIChomozygous71220052
4151765510151765511AG2GENIChomozygous71220055
4151766136151766137GA8GENIChomozygous71220067
4151765688151765689TC21GENIChomozygous71220058
4151765775151765776TA12GENICpossibly homozygous71220061
4151765837151765838TC18GENIChomozygous71220064
4151767351151767352GA7GENIChomozygous71220070
4151767902151767903GA3GENIChomozygous71220073
4151768138151768139CT8GENIChomozygous71220076
4151769231151769232TC4GENIChomozygous71220079
4151769601151769602TC5GENIChomozygous71220082
4151769765151769766CT1GENIChomozygous71220085
4151770373151770374AG10GENIChomozygous71220087
4151770438151770439GA14GENIChomozygous71220090
4151771512151771513GA5GENIChomozygous71220093
4151772177151772178TC13GENIChomozygous71220096
4151773183151773184CT4GENIChomozygous71220099
4151775307151775308AC11GENIChomozygous71220102