chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107087100470871005GA28GENIChomozygous52199900
107087439870874399CA20GENIChomozygous51689612
107087280470872805AG30GENIChomozygous51489542
107087387570873876AG13GENIChomozygous51489543
107087387870873879TC12GENIChomozygous51489544
107087473370874734CA14GENIChomozygous52199902
107087497670874977AG14GENIChomozygous51489546
107087519270875193T-16GENIChomozygous52199904
107087616670876167GA26GENIChomozygous51689620
107087630770876308AG20GENIChomozygous51489555
107087637770876378CCAGG30GENIChomozygous51489556
107087658870876589TA16GENIChomozygous51489557
107087679170876792AAG22GENIChomozygous51489558
107087727970877280GA26GENIChomozygous51489559
107087770770877708AT22GENIChomozygous51689624
107087899270878993GT19GENIChomozygous52160622
107087556570875577TGTGTGTGTGTA------------13GENICheterozygous53310326
107087824670878247CT26GENIChomozygous52160621
107088013970880140A-4GENIChomozygous52384150
107088016170880162AG8GENIChomozygous51489567
107088152770881528GA15GENIChomozygous52160623
107088175670881757AG13GENIChomozygous52160624
107088263970882640GA10GENIChomozygous52160625
107088297670882977GA16GENIChomozygous52160626
107088350270883503TA8GENIChomozygous52160627
107088356170883562CCTTTTTT2GENIChomozygous52384152
107088531070885311TC14GENIChomozygous51689636