chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4116261993116261994TC30GENIChomozygous113151638
4116262396116262397GA15GENIChomozygous113151639
4116262681116262682GT35GENIChomozygous113151640
4116262717116262718GT33GENIChomozygous113151641
4116262882116262882GA22GENIChomozygous132604091
4116262918116262919CA23GENIChomozygous113151642
4116263033116263034TG18GENIChomozygous113151643
4116263440116263441GA24GENIChomozygous113151644
4116263564116263565GA30GENIChomozygous113151645
4116264289116264289C7GENIChomozygous132604092
4116264467116264468AC17GENIChomozygous113151647
4116265131116265132CT26GENIChomozygous113151648
4116265249116265250TC25GENIChomozygous113151649
4116265250116265251TG25GENIChomozygous113151650
4116266462116266463AG21GENIChomozygous113151651
4116267243116267251CTCTCATC38GENIChomozygous132604093
4116267630116267631AG24GENIChomozygous113151652
4116267843116267844AT23GENIChomozygous113151653
4116267844116267845AC23GENIChomozygous113151654
4116268842116268843AT31GENIChomozygous113151655
4116268940116268941CT28GENIChomozygous113151656
4116269685116269686AG19GENIChomozygous113151657
4116270268116270269CT18GENIChomozygous113151658
4116270497116270498CT26GENIChomozygous113151659
4116270725116270726CT32GENIChomozygous113151660
4116270844116270845AG35GENIChomozygous113151661
4116271119116271120AG26GENIChomozygous113151662
4116271258116271259TC31GENICpossibly homozygous113151663
4116271459116271460GA20GENIChomozygous113151664
4116272358116272359AC19GENICpossibly homozygous113151665
4116273538116273593TTCCTTTTCTTTCCTTTTCTTTCCTTTTCTTTCCTTTCCTTTTCTTTTCTTTTCC25GENIChomozygous132604094
4116275518116275519CG21GENIChomozygous113151670
4116275846116275848CT18GENIChomozygous132604095
4116277219116277220AT21GENIChomozygous113151671
4116277382116277383AG20GENIChomozygous113151672
4116277846116277847CT15GENIChomozygous113151673
4116273612116273612T22GENIChomozygous128071614