chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4697896546978966GT16GENIChomozygous810241048
X4699037246990373GT7GENIChomozygous810241049
X4699041646990417TG5GENIChomozygous810241050
X4699846146998462AC32GENICheterozygous810241051
X4699846946998470AT33GENICheterozygous810241052
X4699851546998516GA32GENICheterozygous810241053
X4699856646998567GT30GENICheterozygous810241054
X4699952746999528TA26GENICheterozygous810241055
X4699953346999534AT26GENICheterozygous810241056
X4700349947003500TA7GENIChomozygous810241057
X4700354147003542TA12GENIChomozygous810241058
X4700358147003582CT14GENIChomozygous810241059
X4700361047003611GT6GENIChomozygous810241060
X4700365247003653CA12GENIChomozygous810241061
X4701675447016755TA12GENIChomozygous810241062
X4701927347019274AC121GENICheterozygous810241063
X4701929247019293AC132GENICheterozygous810241064
X4701930247019303TC127GENICheterozygous810241065
X4702017447020175GA12GENICheterozygous810241066