chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230368917230368919TG--6GENIChomozygous709614366
2230368962230368963TTTGTGTGTGTGTGTG9GENICpossibly homozygous709614367
2230370328230370329TTCTCTCTCTC5GENIChomozygous709614368
2230370879230370880CT23GENIChomozygous567090680
2230376793230376794GA19GENIChomozygous567090681
2230379604230379605TTTCATCATCA8GENIChomozygous709614370
2230379740230379741CCAAAAAAAAAAAAA4GENIChomozygous709614373
2230380529230380530CT19GENIChomozygous567090682
2230383135230383136TC18GENIChomozygous567090683
2230383623230383627AAAT----1GENIChomozygous709614374
2230384350230384351CG15GENIChomozygous567090684
2230386113230386114CCTTTTTTTTTT2GENIChomozygous709614375
2230389865230389866TTACACAC8GENICheterozygous709614378
2230389866230389868AC--8GENICheterozygous709614376
2230391218230391219CT23GENIChomozygous567090685
2230393014230393015G-7GENIChomozygous709614379
2230394024230394025AG24GENIChomozygous567090686
2230394444230394445TC15GENIChomozygous567090687
2230394477230394478TC16GENIChomozygous567090688
2230394866230394867CCA11GENIChomozygous709614382
2230395030230395034AAAA----5GENICheterozygous709614383
2230395033230395034A-5GENICheterozygous709614384
2230395393230395394GA14GENIChomozygous567090689
2230398591230398592AG33GENIChomozygous567090690