chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184060816540608166GT30GENIChomozygous594701604
184060825240608253G-4GENICheterozygous725036322
184060864040608660ACATACATATATATATATAC--------------------2GENIChomozygous725036323
184060913440609135AG31GENIChomozygous594701605
184060922040609221AG40GENIChomozygous594701606
184060963040609631AG27GENIChomozygous594701607
184061014540610146CT30GENIChomozygous594701608
184061107540611076GGTTT26GENICpossibly homozygous725036324
184061107540611076GGTTTGTTT26GENICheterozygous725036325
184061194540611946AG32GENIChomozygous591982471
184061213440612137TTT---37GENIChomozygous725036326
184061214040612141TTAAAA40GENIChomozygous725036327
184061304940613050CA26GENIChomozygous594701609
184061710140617102GA34GENIChomozygous594701610
184061763240617633CCT19GENICheterozygous725036328
184061763240617633CCTTTT19GENICpossibly homozygous725036329
184061773440617735TC39GENIChomozygous594701611
184061774840617749GT32GENIChomozygous594701612
184061833040618331GA30GENIChomozygous594701613
184061875240618753GA39GENIChomozygous594701614
184061904140619042AG39GENIChomozygous594701615
184061928940619290AG14GENIChomozygous594701616
184062017040620171AG35GENIChomozygous594701617
184062099840620999GA28GENIChomozygous594701618
184062283840622839AG38GENIChomozygous594701619
184062301440623015GA36GENIChomozygous594701620
184062434140624342CCGTGT10GENICheterozygous725036330
184062450740624508TTTC22GENIChomozygous725036331
184062465840624659GC38GENIChomozygous594701621
184062598440625985GGA4GENIChomozygous725036332
184062819840628199GA30GENIChomozygous591982472
184062860140628602CT32GENIChomozygous594701622
184063096340630973CACACACACA----------19GENIChomozygous725036333
184063123440631235GA41GENIChomozygous594701623
184063172440631725GA28GENIChomozygous594701624
184063333540633336AC29GENIChomozygous594701625
184063387540633876GA23GENIChomozygous594701626