chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4241028263241028264TC29GENICpossibly homozygous57161842
4241045620241045621G-18GENIChomozygous57162135
4241054550241054551AAT3GENICheterozygous57162228
4241054579241054580CCA2GENICheterozygous57162231
4241054582241054583CCA1GENIChomozygous57162233
4241054609241054610GGA4GENIChomozygous57162235
4241054614241054615AAT6GENIChomozygous57162238
4241064363241064364AG11GENICheterozygous57162336
4241086276241086277G-3GENIChomozygous57162419
4241086277241086278GC3GENIChomozygous58308350
4241086280241086281AC3GENIChomozygous57162422
4241098449241098450A-1GENIChomozygous57162456
4241100460241100461TTCCGCTGA2GENIChomozygous57162506
4241109772241109773CA11GENICheterozygous57162909
4241109794241109795CA2GENIChomozygous57162912
4241109823241109824C-6GENIChomozygous57162914
4241111605241111606GT15GENIChomozygous57162946
4241116941241116942C-14GENIChomozygous57162989
4241117009241117010CG13GENICpossibly homozygous57162991
4241117044241117045TA9GENIChomozygous57162994
4241117076241117077G-8GENIChomozygous57162997
4241117192241117193TC9GENICpossibly homozygous57162999
4241129472241129589AAAAATGACTGTTTACGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAAGCCCTGGGTTCAGTCCCCAGCTCCGGAAAAAAAAAGAACCAAAAAAAAAAA---------------------------------------------------------------------------------------------------------------------23GENICheterozygous58308372