chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728373617283737GA6GENIChomozygous1001530527
141728481617284817CT7GENIChomozygous1001530528
141728505217285053TA3GENIChomozygous1001530529
141728505817285059CT4GENIChomozygous1001530530
141728520317285204GC2GENIChomozygous1001530531
141728587617285877CG3GENIChomozygous1001530532
141728588117285882CT3GENIChomozygous1001530533
141728604017286041GA2GENIChomozygous1001530534
141728610817286109AC4GENIChomozygous1001530535
141728669517286696CT6GENIChomozygous1001530536
141728676817286769TA3GENIChomozygous1001530537
141728677617286777TC3GENIChomozygous1001530538
141728685817286859TC5GENIChomozygous1001530539
141728703617287037CA3GENIChomozygous1001530540
141728704817287049CT3GENIChomozygous1001530541
141728710317287104CT5GENIChomozygous1001530542
141728766817287669TA3GENIChomozygous1001530543
141728781917287820TG6GENIChomozygous1001530544
141728792417287925CT3GENIChomozygous1001530545
141728817517288176GA5GENIChomozygous1001530546
141728961817289619GA5GENIChomozygous1001530547
141728963217289633AG5GENIChomozygous1001530548
141728977417289775GA4GENIChomozygous1001530549
141728978717289788AG4GENIChomozygous1001530550
141729025017290251TC6GENIChomozygous1001530551
141729108717291088CT3GENIChomozygous1001530552
141729122717291228CA5GENIChomozygous1001530553
141729125217291253TC8GENIChomozygous1001530554
141729141717291418CG9GENIChomozygous1001530555
141729148217291483GC4GENIChomozygous1001530556
141729201917292020CT2GENIChomozygous1001530557
141729228617292287GC5GENIChomozygous1001530558
141729231617292317CT2GENIChomozygous1001530559
141729294717292948GT5GENIChomozygous1001530560
141729295017292951CT5GENIChomozygous1001530561
141729329117293292TC4GENIChomozygous1001530562
141729339117293392AG13GENIChomozygous1001530563
141729348817293489AG3GENIChomozygous1001530564
141729502417295025TC8GENIChomozygous1001530565
141729696617296967GA3GENIChomozygous1001530566