chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107424117974241180CT36GENICheterozygous116636663
107424131874241319GT55GENICheterozygous116636667
107424173074241731AG46GENICheterozygous116636671
107424187174241872CG38GENICheterozygous116636675
107424253874242539GT26GENICheterozygous116636677
107424265974242660GT26GENICheterozygous116636681
107424336374243364CA20GENICheterozygous116636687
107424345874243459TC33GENICheterozygous116636689
107424372974243730GA57GENICheterozygous116636693
107424373274243733CT55GENICheterozygous116636695
107424373374243734GC54GENICheterozygous116636697
107424396374243964AG85GENICheterozygous116636699
107424408674244087TC49GENICheterozygous116636703
107424410774244108CG55GENICheterozygous116636705
107424420174244202GA36GENICheterozygous116636711
107424429774244298GT51GENICheterozygous116636713
107424443974244440CA50GENICheterozygous116800144
107424444174244442GT48GENICheterozygous116636715
107424449874244499GC47GENICheterozygous116636717
107424456274244563GT48GENICheterozygous116636719
107424486774244868CT46GENICheterozygous116636721
107424498274244983AG24GENICheterozygous116636723
107424504174245042GC19GENICheterozygous116636725
107424507874245079AG43GENICheterozygous116800146
107424518374245184TC35GENICheterozygous116636727
107424536274245363CA26GENICheterozygous116893544
107424938974249390CG43GENICheterozygous116636745
107425050774250508TC21GENIChomozygous116800152
107425051174250512TC20GENIChomozygous116800154
107425051274250513CA18GENIChomozygous116893546
107427746174277462CT23GENICheterozygous116636837
107427748574277486CA25GENICheterozygous116636838
107429848474298485AG8GENICheterozygous116800158
107429851874298519GA6GENICheterozygous116636896