chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123941568139415682AG20GENIChomozygous50199117
123941621539416216TTG8GENIChomozygous50199119
123941622239416223GGTGTGT9GENIChomozygous50543003
123941715739417169CCAAAAAAAAAA------------12GENIChomozygous50571292
123941718439417185A-17GENIChomozygous50571293
123941720339417204C-16GENIChomozygous50199147
123941749539417507TATTATTATTAT------------4GENIChomozygous50199149
123941777039417771CG23GENIChomozygous50199155
123941787239417873CG21GENIChomozygous50199159
123941843239418444GATTGATTGATT------------13GENIChomozygous50571295
123941863139418632GGT11GENIChomozygous50511674
123941894839418949TTGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCA5GENIChomozygous50543016
123941901139419012GGT2GENIChomozygous50511676
123941945539419456CG35GENIChomozygous50511678
123941984939419850TA18GENIChomozygous50511681
123942019539420196TTA8GENIChomozygous50511683
123942085039420851CCTTTT1GENIChomozygous50571296
123942120839421209AG7GENIChomozygous50199173
123942125139421252G-7GENICheterozygous50543017
123942126939421271GG--9GENICheterozygous50543018
123942347639423477CCT9GENICheterozygous50199177
123942348439423610TTTTTTTCGGAGCTGGGGACTGAACCCAGGACCTTGCGCTTGCTAGGCAAGTGCTCTACCACTGAGCTAAATCCCCAACCCCCCCCCCCCCCCGTTTAGTTTTTTTTTTTTTTTTTTTCCCGGTTC------------------------------------------------------------------------------------------------------------------------------12GENICheterozygous50558895
123942401439424015T-10GENIChomozygous50199187
123942417139424172TTAC5GENICheterozygous50571298
123942492939424930AG22GENIChomozygous50199193
123942548839425489CCT19GENIChomozygous50199195
123942549539425496TC22GENIChomozygous50199197