chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185799019857990199CG25GENICheterozygous140327687
185799020557990206GA25GENICheterozygous140327688
185799021157990212TG25GENICheterozygous140327689
185799021557990216GA26GENICheterozygous140327690
185799022157990222GC26GENICheterozygous140327691
185799023157990232CT26GENICheterozygous140327692
185799026857990269GA29GENICheterozygous140327693
185799029157990292CT25GENICheterozygous140327694
185799029357990294GA25GENICheterozygous140327695
185799029757990298G27GENICheterozygous140225950
185799488157994881A28GENICheterozygous140926522
185799489757994898GA28GENICheterozygous140927635
185799307757993078GA26GENICheterozygous140927628
185799307857993079GA26GENICheterozygous140927629
185799308757993088TA26GENICheterozygous140927630
185799489657994897CT28GENICheterozygous140927634
185799310857993109CT29GENICheterozygous145060632
185799492757994928GA24GENICheterozygous140927636
185799492957994930CT25GENICheterozygous140927637
185799493357994934TC25GENICheterozygous140927638
185799494357994944G24GENICheterozygous140926523
185799495257994953CA24GENICheterozygous140927639
185799495957994960GT26GENICheterozygous140927640
185800102758001028TA19GENICheterozygous140927641
185800103258001033TC18GENICheterozygous140927642
185800106958001070TC20GENICheterozygous140327707