chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230368917230368919TG--15GENICpossibly homozygous59431827
2230368962230368963TTTGTGTGTGTGTGTG4GENIChomozygous60520636
2230370303230370304TTTC8GENICpossibly homozygous59431828
2230370879230370880CT29GENIChomozygous59431830
2230376793230376794GA31GENIChomozygous59431831
2230377252230377253AC26GENIChomozygous61940667
2230379604230379605TTTCATCATCA10GENIChomozygous59431832
2230379740230379741CCAAAAAAAAAAAAA11GENICpossibly homozygous60458944
2230380529230380530CT22GENIChomozygous59431834
2230383135230383136TC30GENIChomozygous59431835
2230383548230383549TTA10GENICheterozygous61976793
2230383623230383627AAAT----3GENIChomozygous59431836
2230384350230384351CG25GENIChomozygous59431837
2230386113230386114CCTTTTTTTTTT7GENIChomozygous60520637
2230389865230389866TTACACAC6GENICheterozygous60550455
2230389866230389868AC--6GENICheterozygous60550456
2230391218230391219CT26GENIChomozygous59431842
2230393014230393015G-25GENIChomozygous59431843
2230394024230394025AG29GENICpossibly homozygous59431844
2230394444230394445TC21GENIChomozygous59431845
2230394477230394478TC28GENIChomozygous59431846
2230394866230394867CCA16GENIChomozygous59431847
2230395393230395394GA22GENIChomozygous59431848
2230398591230398592AG25GENIChomozygous59431849