chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1117724258117724259TA23GENICheterozygous60813114
1117724302117724304TT--19GENICheterozygous60813120
1117724305117724306GC21GENICheterozygous61508012
1117724309117724310TC22GENICheterozygous61508013
1117724318117724319GA26GENICheterozygous61508014
1117724321117724322AC26GENICheterozygous61508015
1117724330117724331CA31GENICheterozygous61508016
1117724332117724333TC31GENICheterozygous61508017
1117724341117724342TC33GENICheterozygous61508018
1117724354117724355TTGTACAACA35GENICheterozygous60813121
1117724367117724368GT39GENICheterozygous61508019
1117724371117724372GA41GENICheterozygous61508020
1117724413117724414CA42GENICheterozygous62834813
1117724425117724426CT44GENICheterozygous62834814
1117724433117724434TG43GENICheterozygous62834815
1117724539117724540CT54GENICheterozygous61671385
1117724548117724549AC57GENICheterozygous62879728
1117724552117724553CT59GENICheterozygous62879729
1117724561117724562CG61GENICheterozygous62865213
1117724568117724569CG59GENICheterozygous62865214
1117724569117724570CG59GENICheterozygous62865215
1117724600117724601TC51GENICheterozygous62766007
1117724607117724608AC51GENICheterozygous60813122
1117724636117724637CT58GENICheterozygous60813124
1117724650117724651CT80GENICheterozygous60813125
1117724687117724688AG90GENICheterozygous62766008
1117724688117724689CA90GENICheterozygous62766009
1117724689117724690CT90GENICheterozygous62766010
1117724757117724758CT96GENICheterozygous60813127
1117724758117724759GA96GENICheterozygous60813128
1117724767117724768TTC94GENICheterozygous60813129
1117724795117724796TG56GENICheterozygous61508021
1117725598117725599CT5GENICheterozygous60813131
1117725611117725612CA5GENICheterozygous60813132
1117725612117725613CG5GENICheterozygous61300979
1117725614117725615GA5GENICheterozygous61300980
1117725639117725640CT7GENICheterozygous60813134
1117725645117725646CT7GENICheterozygous60813135
1117725656117725657GA7GENICheterozygous60813136