chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1273335389273335390TG22GENICpossibly homozygous61646373
1273350121273350122AG7GENIChomozygous61224303
1273353147273353148GA11GENIChomozygous62305685
1273354226273354227TC18GENICpossibly homozygous61224306
1273355531273355532CCT1GENIChomozygous61224307
1273356159273356160GA20GENICpossibly homozygous61224309
1273364362273364363GA10GENICpossibly homozygous62305686
1273371648273371649AC6GENICheterozygous61224318
1273380053273380054CCAT1GENIChomozygous61646440
1273380152273380153A-2GENICheterozygous61333468
1273390360273390361AG24GENICheterozygous61224327
1273394919273394920TC14GENICpossibly homozygous61224328
1273410223273410224T-12GENICheterozygous61646483
1273410966273410967CT13GENICpossibly homozygous61224331
1273420131273420132T-6GENIChomozygous61646507
1273420974273420975TG10GENICpossibly homozygous62305687
1273429610273429611TC27GENIChomozygous61224334
1273436429273436430T-6GENICheterozygous61646528
1273450610273450623AGCACTGTACCTG-------------2GENIChomozygous61646544
1273453631273453632A-1GENIChomozygous62217103