chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186227907162279072AG34GENIChomozygous971287983
186227928462279285CT34GENIChomozygous971287984
186227939462279395AG27GENIChomozygous971287985
186227943562279436CT22GENIChomozygous971287986
186227944662279447CT26GENIChomozygous971287987
186227954462279545TC34GENIChomozygous971287988
186227958962279590AG39GENIChomozygous971287989
186227960862279609CA38GENIChomozygous971287990
186227962962279630GA38GENIChomozygous971287991
186227967662279677TC35GENIChomozygous971287992
186227971562279716TC41GENIChomozygous971287993
186228055362280554TA13GENIChomozygous971287994
186228060362280604CT18GENIChomozygous971287995
186228069762280698CT13GENIChomozygous971287996
186228074362280744CT14GENIChomozygous971287997
186228079562280796TC24GENIChomozygous971287998
186228080162280802AG25GENIChomozygous971287999
186228082462280825TC27GENIChomozygous971288000
186228089062280891TC32GENIChomozygous971288001
186228105962281060GC18GENIChomozygous971288002
186228133462281335CT17GENIChomozygous971288003
186228160862281609AT28GENIChomozygous971288004
186228226062282261AG11GENIChomozygous971288005
186228711162287112TA32GENIChomozygous971288006
186228727462287275AG18GENIChomozygous971288007
186228730062287301TC19GENIChomozygous971288008
186228735662287357CT18GENIChomozygous971288009