chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X113564178113564179CT10GENIChomozygous585072792
X113565035113565036AAGT11GENICheterozygous722110377
X113565036113565038GT--11GENICheterozygous722110376
X113566723113566724CA7GENICheterozygous585072793
X113567128113567129AT9GENICheterozygous587736464
X113567142113567143CT10GENICheterozygous585072794
X113567157113567158TG8GENICheterozygous585072795
X113584116113584117CCA8GENICheterozygous722110379
X113592818113592820CT--7GENICheterozygous722110380
X113600881113600885TTCT----8GENICheterozygous722110382
X113607833113607834GGT10GENIChomozygous722110383
X113610388113610389CT5GENICheterozygous585072796
X113619072113619073AC7GENICpossibly homozygous587736465