chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122552135122552135G15GENIChomozygous128513472
7122552152122552153G12GENIChomozygous128513473
7122562200122562201TG43GENICheterozygous132482007
7122562202122562203GA43GENICheterozygous132482008
7122563133122563133G40GENICheterozygous132478777
7122564587122564588A22GENIChomozygous128513477
7122568574122568575TA54GENIChomozygous115860930
7122570444122570445CT29GENIChomozygous118322292
7122571369122571370CT49GENICpossibly homozygous118322294
7122573650122573651AG57GENIChomozygous115860933
7122574999122574999CTC47GENIChomozygous128513480
7122577597122577598AG53GENIChomozygous115860941
7122578861122578861TGGTGATGGTGTTGTTGG5GENIChomozygous128513481
7122578961122578963TC10GENIChomozygous128513486
7122578966122578966G10GENIChomozygous128513487
7122578975122578975A15GENIChomozygous128513488
7122578981122578981A15GENIChomozygous128513489
7122578986122578986G15GENIChomozygous128513490
7122578994122578995A17GENIChomozygous128513491
7122579026122579027T22GENIChomozygous128513492
7122579037122579038A25GENIChomozygous128513493
7122579044122579044CC27GENIChomozygous128513494
7122579456122579457AG38GENIChomozygous115860943
7122580221122580222AG54GENIChomozygous115860945
7122581619122581620AG55GENIChomozygous115860949
7122568855122568855CACGCACA47GENIChomozygous131024259
7122570875122570875A43GENIChomozygous131024260
7122575155122575155TCCTCT11GENIChomozygous131024261