chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108487523084875231AG17GENIChomozygous116664676
108487559084875707AACAAAGGCAAAGGCAATGGGCGGGTTGGGGATTTGGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGTCCTGGGTTCAGTCCCCAGCCCCGAAGGAAAAAAAAAAAAAAAAA7GENICheterozygous128841114
108487577184875771C17GENIChomozygous128841115
108487627284876273TC20GENIChomozygous116664680
108487642984876430CG30GENIChomozygous116664684
108487698384876984AG25GENIChomozygous116664686
108487714084877141AG22GENIChomozygous116664688
108487775184877752AG36GENIChomozygous116664690
108487832384878324CT19GENIChomozygous116664694
108487882284878823CA15GENICpossibly homozygous131712152
108487994684879947GT23GENIChomozygous116664696
108488053284880533TC21GENIChomozygous116664698
108488072684880727GA24GENIChomozygous117018662
108488076684880767TC19GENIChomozygous116664700
108488082584880826AG16GENIChomozygous116664702