chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X135053167135053168TC35GENIChomozygous45315624
X135053275135053276TC45GENICpossibly homozygous45315625
X135053442135053443G-39GENIChomozygous45315626
X135055523135055526TTT---3GENIChomozygous45315627
X135055673135055674AC36GENIChomozygous45315628
X135055817135055818CT33GENIChomozygous45315629
X135056047135056048AT45GENIChomozygous45315630
X135056998135056999CT31GENIChomozygous45315631
X135057718135057719GA43GENIChomozygous45315632
X135057919135057920TC35GENIChomozygous45315633
X135058265135058280TAATAATAATAATAA---------------20GENIChomozygous45315634
X135058283135058284TC37GENICheterozygous45315635
X135058314135058315CT32GENIChomozygous45315636
X135059145135059146AG33GENIChomozygous45315637
X135059168135059169CT34GENIChomozygous45315638
X135059192135059193TC32GENIChomozygous45315639
X135059832135059833GGA24GENIChomozygous45315640
X135061762135061763GA34GENIChomozygous45315641
X135061902135061903CCGT26GENICheterozygous45315642
X135061903135061904AG30GENIChomozygous45315643
X135062245135062246CG10GENICheterozygous45315644
X135062247135062248CG10GENICheterozygous45315645
X135062249135062250CG10GENICheterozygous45315646
X135062251135062252CG11GENICheterozygous45315647
X135062313135062314AT30GENICpossibly homozygous45315648
X135062541135062542TG36GENIChomozygous45315649
X135062947135062948GA30GENIChomozygous45315651
X135063148135063149CG28GENICpossibly homozygous45315652
X135064261135064262CT40GENIChomozygous45315653
X135065206135065207AACC2GENIChomozygous45315654
X135065869135065871AG--35GENIChomozygous45315655
X135066274135066275GA26GENIChomozygous45315656
X135066471135066472AG22GENIChomozygous45315657
X135067273135067274AG39GENIChomozygous45315658
X135067540135067541C-28GENIChomozygous45315659