chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4139701279139701280A25GENIChomozygous136916815
4139702029139702030GA27GENIChomozygous137213130
4139702394139702394TTA21GENIChomozygous136916816
4139705228139705229GT31GENIChomozygous137213131
4139705472139705473GT31GENIChomozygous137213132
4139705793139705794AC21GENIChomozygous137213133
4139707090139707091TC22GENIChomozygous137213134
4139707371139707372TC24GENIChomozygous137213135
4139708218139708223GAAAA18GENIChomozygous136916817
4139708547139708548TC29GENIChomozygous137213136
4139708823139708826CAC14GENIChomozygous136916818
4139708841139708841CT7GENIChomozygous136916819
4139709479139709480TA24GENIChomozygous137213137
4139710069139710069A20GENIChomozygous136916820
4139711695139711696T20GENIChomozygous136916821
4139717934139717936TG21GENIChomozygous136916822
4139718962139718963TC28GENIChomozygous137213143
4139709601139709602AT32GENIChomozygous137213138
4139710715139710716TC15GENIChomozygous137213139
4139713896139713897GA29GENIChomozygous137213140
4139717045139717046CA23GENIChomozygous137213141
4139717936139717937TC21GENIChomozygous137213142
4139710465139710466GA24GENIChomozygous149218046