chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151752705151752706CG4GENIChomozygous73678260
4151753518151753519GT6GENIChomozygous71220014
4151752995151752996TC16GENIChomozygous71220005
4151753089151753090AG17GENIChomozygous71220008
4151753484151753485CT16GENIChomozygous71220011
4151753805151753806TC15GENIChomozygous71220017
4151754161151754162TG12GENIChomozygous71220020
4151754958151754959AG14GENIChomozygous71220023
4151755052151755052G9GENICheterozygous73678262
4151755214151755215TC24GENIChomozygous71220025
4151755420151755421GA25GENIChomozygous71220028
4151756412151756413GT9GENIChomozygous71220031
4151758256151758257AG10GENIChomozygous71220034
4151760501151760502AG26GENIChomozygous71220037
4151761359151761360TC13GENIChomozygous71220040
4151761250151761251A20GENICheterozygous72884367
4151762544151762545TG19GENIChomozygous71220043
4151762778151762779CT17GENIChomozygous71220046
4151764650151764651CT28GENIChomozygous71220049
4151765080151765081CT17GENIChomozygous71220052
4151765510151765511AG28GENIChomozygous71220055
4151765688151765689TC19GENIChomozygous71220058
4151765775151765776TA16GENIChomozygous71220061
4151765837151765838TC20GENIChomozygous71220064
4151766136151766137GA20GENICpossibly homozygous71220067
4151767351151767352GA19GENIChomozygous71220070
4151767880151767880AC27GENICheterozygous73678264
4151767902151767903GA22GENIChomozygous71220073
4151768138151768139CT20GENIChomozygous71220076
4151769231151769232TC22GENIChomozygous71220079
4151769601151769602TC9GENIChomozygous71220082
4151769788151769789GA6GENIChomozygous72884378
4151770373151770374AG26GENIChomozygous71220087
4151770438151770439GA15GENIChomozygous71220090
4151771512151771513GA21GENIChomozygous71220093
4151772177151772178TC23GENIChomozygous71220096
4151773183151773184CT8GENIChomozygous71220099
4151775307151775308AC16GENIChomozygous71220102