chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152416790224167902TATACCCT25GENIChomozygous132193875
152417136024171361TC31GENIChomozygous112469066
152417259524172595ATAAA28GENIChomozygous129238388
152417262124172621T31GENIChomozygous129238389
152417467924174680CT17GENIChomozygous112799991
152417371224173713CT26GENIChomozygous112799989
152417258824172589CG28GENIChomozygous112799985
152417323224173233AG35GENIChomozygous112799987
152417556124175562AG18GENIChomozygous112469068
152417679824176798G29GENIChomozygous132193876
152417699124176992AT22GENIChomozygous119042253
152417789824177899TC23GENIChomozygous119042258
152417909324179094TA23GENIChomozygous112799993
152418175624181757CT28GENIChomozygous112469072
152418337824183379CA5GENICheterozygous132352043
152418532724185328GA26GENIChomozygous112799995
152418590224185903CT19GENIChomozygous112799997
152418717724187178AT22GENIChomozygous112799999
152418821924188220T16GENIChomozygous129238395
152419051924190519AC21GENIChomozygous129238397
152419109424191095AT30GENIChomozygous112800001
152419383324193834CT35GENIChomozygous112800003
152419404324194044CT33GENIChomozygous112800005
152419612024196121TC27GENIChomozygous112469184
152419645924196460C19GENIChomozygous129238405
152419900624199007T8GENIChomozygous129238406
152419919324199193A2GENIChomozygous129238407