chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4139701279139701280A54GENICpossibly homozygous136916815
4139702029139702030GA61GENIChomozygous137213130
4139702394139702394TTA63GENIChomozygous136916816
4139705228139705229GT69GENIChomozygous137213131
4139705472139705473GT63GENIChomozygous137213132
4139705793139705794AC48GENIChomozygous137213133
4139707090139707091TC62GENIChomozygous137213134
4139707371139707372TC54GENIChomozygous137213135
4139708218139708223GAAAA49GENIChomozygous136916817
4139708547139708548TC67GENIChomozygous137213136
4139708823139708826CAC26GENIChomozygous136916818
4139708841139708841CT19GENIChomozygous136916819
4139709479139709480TA42GENIChomozygous137213137
4139709601139709602AT61GENIChomozygous137213138
4139710069139710069A47GENIChomozygous136916820
4139710715139710716TC60GENIChomozygous137213139
4139711695139711696T63GENIChomozygous136916821
4139713896139713897GA78GENIChomozygous137213140
4139717045139717046CA63GENIChomozygous137213141
4139717934139717936TG57GENIChomozygous136916822
4139714371139714372CA56GENIChomozygous143938924
4139717936139717937TC57GENIChomozygous137213142
4139718962139718963TC50GENIChomozygous137213143