chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109055965990559660CT6GENIChomozygous588191128
109056012390560124GT8GENIChomozygous586307197
109056017790560178CT8GENIChomozygous588191129
109056035790560360CCC---1GENIChomozygous720407247
109056037490560375TC4GENIChomozygous588191130
109056094090560941AAC2GENIChomozygous720407248
109056094190560942AAC5GENIChomozygous720407250
109056144490561445TTTG3GENIChomozygous720407252
109056166290561663CT6GENIChomozygous588191131
109056223990562240GT6GENIChomozygous586307198
109056272390562724TC9GENICpossibly homozygous588191132
109056272990562730T-7GENIChomozygous720407256
109056460190564602AG3GENIChomozygous588191133
109056464790564648CT5GENIChomozygous588191134
109056468190564682AG7GENIChomozygous588191135
109056474790564748TC9GENIChomozygous588191136
109056480390564804GGGGGAATTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC4GENIChomozygous720407257
109056483290564833CT9GENIChomozygous588191137
109056510390565104CT8GENIChomozygous588191138
109056510590565106TC8GENIChomozygous588191139
109056511690565117AG10GENIChomozygous588191140
109056512590565129GCTG----10GENIChomozygous720407258
109056519890565199GA13GENIChomozygous588191141
109056524390565244TC7GENIChomozygous588191142
109056527790565278CT6GENIChomozygous588191143
109056529990565300CT4GENIChomozygous588191144
109056542690565427AT3GENIChomozygous588191145
109056547590565476CT3GENIChomozygous588191146
109056586990565870GA7GENIChomozygous588191147