chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106611712106611713TC29GENIChomozygous51766321
10106611846106611847GA32GENIChomozygous52407559
10106612130106612131GA24GENIChomozygous51766323
10106614044106614045AG21GENICpossibly homozygous52407564
10106614987106614988TA23GENIChomozygous51766329
10106615335106615347GGAGAGGGAGAG------------7GENICheterozygous51766333
10106616041106616042TC19GENIChomozygous53176857
10106616303106616304GT22GENIChomozygous52407565
10106616344106616345CT27GENIChomozygous52407568
10106616413106616414TC28GENIChomozygous53176858