chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2056545315654532AT9GENICheterozygous830190349
2056550655655066TC13GENIChomozygous830190350
2056555755655576CT9GENICheterozygous830190351
2056565375656538G-8GENICheterozygous830190352
2056567935656794GA12GENICheterozygous830190353
2056574425657443AG10GENICheterozygous830190354
2056582755658276CT12GENICheterozygous830190355
2056583765658377AG14GENIChomozygous830190356
2056589015658902TG18GENICheterozygous830190357
2056597355659736CT8GENICheterozygous830190358
2056597365659737CT8GENICheterozygous830190359
2056614195661420TC12GENICheterozygous830190360
2056616765661677CT15GENICheterozygous830190361
2056626995662700GT12GENICheterozygous830190362
2056629025662903CT15GENICheterozygous830190363
2056642555664256GA8GENICheterozygous830190364
2056646225664623AG13GENICheterozygous830190365
2056653085665309TG13GENICheterozygous830190366
2056662905666291AATG9GENIChomozygous830190367
2056665285666529AAT10GENICheterozygous830190368
2056672565667257TC11GENICheterozygous830190369
2056673785667379AG11GENICheterozygous830190370
2056693135669314GT12GENICheterozygous830190371
2056699945669995TG12GENICheterozygous830190372
2056702125670215CTC---11GENICheterozygous830190373
2056702855670286CA11GENICheterozygous830190374
2056706325670633GA16GENIChomozygous830190375
2056708145670815GA14GENICheterozygous830190376
2056709145670915CT15GENICheterozygous830190377
2056711975671198CT10GENICheterozygous830190378