chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42191429521914296TC19GENIChomozygous975378976
42191447021914471AG15GENIChomozygous975378977
42191481221914813AG19GENIChomozygous975378978
42191494421914945GA11GENIChomozygous975378979
42191497021914971AG12GENIChomozygous975378980
42191502121915022TC11GENIChomozygous975378981
42191510921915110AG12GENIChomozygous975378982
42191526521915266AC27GENIChomozygous975378983
42191527121915272AG29GENIChomozygous975378984
42191532721915328CT21GENIChomozygous975378985
42191538121915382AG20GENIChomozygous975378986
42191550121915502GA24GENIChomozygous975378987
42191578921915790AG31GENIChomozygous975378988
42191579921915800GA30GENIChomozygous975378989
42191614221916143CG11GENIChomozygous975378990
42191620021916201AC14GENIChomozygous975378991
42191620621916207AT15GENIChomozygous975378992
42191624921916250AG22GENIChomozygous975378993
42191640121916402AT33GENIChomozygous975378994
42191645421916455CT23GENIChomozygous975378995
42191646821916469TG19GENIChomozygous975378996
42191659421916595GT14GENIChomozygous975378997
42191732121917322GA14GENIChomozygous975378998
42191845621918457TG23GENICpossibly homozygous975378999
42191865121918652CT28GENICpossibly homozygous975379000
42191895021918951TC20GENIChomozygous975379001