chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101419619314196195CA--11GENICpossibly homozygous712926168
101419645714196458GC30GENIChomozygous575253290
101419645814196459TTG30GENIChomozygous712926170
101421459614214597GGT15GENICheterozygous712926171
101421459614214597GGTTT15GENICheterozygous712926172
101421860014218601TC36GENIChomozygous573473263
101423561914235625CACACA------12GENIChomozygous712926173
101424054514240546TC24GENIChomozygous573473264
101425364514253646TTTAA1GENIChomozygous712926178
101426204914262050CCT18GENICheterozygous712926180
101426205014262051T-18GENICheterozygous712926179
101426636514266366G-12GENIChomozygous712926181
101426636614266367GA13GENIChomozygous575253291
101427222114272222TTACACAC6GENIChomozygous712926182
101427492614274927TTTG6GENIChomozygous712926183
101427492914274930CCTTGCT6GENIChomozygous712926184
101427493314274934CCAAGCGCTCTACCACTGAGCTAAAT5GENIChomozygous712926185