chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105620389756203898AG25GENIChomozygous51654670
105620401256204013AG31GENICpossibly homozygous51654672
105620401856204019AG29GENICpossibly homozygous51654674
105620438756204388AG36GENIChomozygous51654676
105620446356204464AG30GENIChomozygous51654678
105620605556206056GA43GENICpossibly homozygous52059013
105620668756206688GGTTTTTT4GENICheterozygous52319089
105620692056206921GT20GENIChomozygous51654686
105620697356206974TG26GENIChomozygous51654688
105620711756207118GGC15GENIChomozygous51460011
105620712756207133TCTTAT------13GENIChomozygous52377699
105620713356207134GGAGA8GENIChomozygous52377702
105620713556207136GC8GENIChomozygous51460014
105620781156207813TA--9GENIChomozygous51654694
105620806756208068GA22GENIChomozygous52059015
105620813856208139GA19GENIChomozygous52059017
105620835456208355AG24GENIChomozygous51654696
105620879956208800AG24GENICpossibly homozygous52059019
105620881756208818TC27GENICpossibly homozygous51654698
105620917956209180TC34GENIChomozygous51654700
105620970556209706AAGAAG20GENICpossibly homozygous51654702
105620989256209893AG35GENIChomozygous51654704
105621119756211198TTACACACACACAC2GENIChomozygous52502466
105621136056211361GA26GENICpossibly homozygous52059023
105621154656211547CT22GENIChomozygous52059025
105621163056211631GA22GENIChomozygous51891274