chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124497813124497814AT2GENIChomozygous588491267
7124497822124497823GGA3GENICheterozygous722602368
7124499530124499531G-2GENICheterozygous722602369
7124499764124499765CCG5GENICheterozygous722602371
7124508120124508121CCA2GENIChomozygous722602372
7124519871124519872GA9GENICheterozygous588471831
7124523401124523402T-3GENICheterozygous722602373
7124551017124551018GGT4GENIChomozygous722602374
7124551019124551020GGC4GENIChomozygous722602375
7124554059124554060GGATGGACCATATCTGGGAAAAAGAATTAGACTGACT1GENIChomozygous722602376
7124554104124554105T-2GENIChomozygous722602377
7124562472124562473G-3GENICheterozygous722602378
7124565416124565417C-7GENIChomozygous722602379
7124565428124565429G-5GENIChomozygous722602380
7124565441124565442GC10GENIChomozygous588491268
7124565491124565492A-4GENICheterozygous722602381
7124565501124565502G-4GENIChomozygous722602382
7124565502124565503AC4GENIChomozygous588491269
7124566603124566604C-2GENIChomozygous722602383
7124566607124566608C-2GENIChomozygous722602384
7124566675124566676AC2GENIChomozygous588491270
7124566711124566712T-5GENIChomozygous722602385
7124566725124566726T-6GENIChomozygous722602386
7124566749124566750A-1GENIChomozygous722602387
7124566752124566753C-1GENIChomozygous722602388
7124566788124566789G-1GENIChomozygous722602389
7124566793124566794G-2GENIChomozygous722602390
7124566816124566817G-2GENIChomozygous722602391
7124577154124577155GC4GENIChomozygous588471832
7124580866124580867A-10GENICheterozygous722602392
7124582222124582223T-5GENICheterozygous722602394
7124585947124585948AC9GENICheterozygous588491271
7124588392124588393T-8GENICheterozygous722602395
7124600924124600925AAG2GENICheterozygous722602398
7124600931124600932CCA1GENIChomozygous722602399