chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3166739132166739133TC30GENIChomozygous57770390
3166739436166739437GA32GENIChomozygous57770391
3166739575166739576CA37GENIChomozygous57770392
3166739771166739772CG29GENIChomozygous57770393
3166740357166740358TC36GENIChomozygous57770394
3166740709166740710AG19GENIChomozygous57770395
3166741254166741255CT17GENIChomozygous57770396
3166741838166741839CG31GENIChomozygous57770397
3166741865166741866AG26GENIChomozygous57770398
3166742009166742010AG25GENICpossibly homozygous57770399
3166742344166742345AAT6GENICheterozygous57770400
3166742366166742367TTTGG5GENICheterozygous57770401
3166742406166742407GA7GENICheterozygous57770402
3166742409166742410CT8GENICheterozygous57770403
3166742412166742413CG8GENICheterozygous57770404
3166742418166742419TC10GENICheterozygous57770405
3166742474166742475AAT6GENIChomozygous57770406
3166742504166742505TC15GENIChomozygous57770408
3166742720166742721AAT7GENICheterozygous57770409
3166742720166742721AATT7GENICheterozygous57770410
3166742740166742743TTT---10GENICpossibly homozygous57770411
3166742933166742934TC26GENIChomozygous57770412
3166743473166743474GA50GENIChomozygous57770413
3166744739166744740CCCTAT5GENIChomozygous57770414
3166745488166745489TC31GENIChomozygous57770415