chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207867832207867833CCCA6GENICheterozygous59356617
2207868353207868354A-28GENIChomozygous59356619
2207868952207868953TTTC6GENICheterozygous59356620
2207869356207869357CT31GENICpossibly homozygous59356623
2207869592207869593CT36GENIChomozygous59356624
2207871200207871201AG29GENIChomozygous59356626
2207871595207871596GGCCTGGCT20GENIChomozygous59356627
2207872461207872462TG23GENICheterozygous59356628
2207872469207872470G-21GENICheterozygous59356629
2207872469207872470GGTTTGTTT15GENICpossibly homozygous59356630
2207873593207873594TTTC26GENIChomozygous59356631
2207873609207873610CCTCTT30GENICheterozygous59356632
2207873609207873610CCT30GENICheterozygous59931781