chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136729540136729541CT16GENIChomozygous114245994
5136730375136730376GA20GENIChomozygous114245995
5136730844136730845TC29GENIChomozygous114245997
5136733149136733150TC21GENIChomozygous114245999
5136733687136733688TC17GENIChomozygous114020631
5136734329136734330TC30GENIChomozygous114246000
5136734522136734523CA34GENIChomozygous114246002
5136735041136735042GA25GENIChomozygous114246004
5136737561136737562CT29GENIChomozygous114246005
5136738047136738048AG23GENIChomozygous114020642
5136739230136739231AC24GENIChomozygous114020644
5136739411136739412CT35GENIChomozygous114020646
5136740341136740342TC25GENIChomozygous114020648
5136740572136740573AG24GENIChomozygous114020650
5136740810136740811CT20GENIChomozygous114020652
5136740912136740913GA15GENIChomozygous114020654
5136742263136742264CA22GENICheterozygous114020656
5136742275136742276CA21GENIChomozygous114145406
5136744274136744275CT18GENICheterozygous114246007
5136744283136744284GA19GENICheterozygous114246009
5136744294136744295CT16GENICheterozygous114246011
5136744307136744308TC13GENICheterozygous114246012
5136744959136744960GA27GENIChomozygous114020662
5136745359136745360GA27GENIChomozygous114246014
5136746896136746897GA22GENIChomozygous114020664
5136746903136746904GA24GENICpossibly homozygous114246015
5136747100136747101AG31GENIChomozygous114246017
5136747767136747768AG17GENIChomozygous114020668
5136748497136748498CA19GENIChomozygous114020670