chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71188210811882109CT49GENIChomozygous53789579
71188356911883570CCCTGT52GENIChomozygous53789580
71188483811884839AG21GENICpossibly homozygous53789581
71188485911884860AG16GENICheterozygous54853521
71188490611884907T-9GENICheterozygous53789582
71188490811884910GA--9GENICheterozygous54710880
71188491611884917AAG10GENICheterozygous53789583
71188495711884960AGA---10GENIChomozygous53789584
71188501011885011TC4GENIChomozygous53789585
71188508111885082GGGAA3GENICheterozygous53789586
71188509911885102GAT---3GENICheterozygous53789587
71188510111885106TGGAG-----3GENICheterozygous53789588
71188515211885155AGA---3GENIChomozygous53789592
71188520511885206TC18GENIChomozygous53789593
71188588811885889GA36GENIChomozygous53789594
71188591511885916GC34GENIChomozygous53789595
71188596111885962GC37GENIChomozygous53789596
71188597211885973CT38GENIChomozygous53789597
71188703011887031TC36GENIChomozygous53789598
71188776911887770AT32GENIChomozygous53789599
71188779611887797GT45GENIChomozygous53789600
71188801711888018A-17GENICheterozygous53789601
71188801711888018AACACAGCCGCGGCCCAG19GENIChomozygous53789602
71188858311888584TTAC38GENIChomozygous53789603
71188865411888655CT49GENIChomozygous53789604
71188882411888825GA50GENIChomozygous53789605
71188890011888901AG53GENIChomozygous53789606
71188912511889126GT40GENIChomozygous53789607
71188969111889693CA--36GENIChomozygous53789608
71189064711890648TG36GENIChomozygous53789609
71189128511891286GGAA7GENICheterozygous53789611
71189128511891286GGAAA7GENICpossibly homozygous53789612
71189146411891465AG43GENIChomozygous53789613
71189177211891773CT41GENIChomozygous53789614
71189185211891853TC39GENIChomozygous53789615
71189197611891977TC46GENIChomozygous53789616