chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139784733139784734GGTTTTGTTTTGT25GENIChomozygous54150648
7139785310139785311A-27GENIChomozygous54529204
7139786412139786413GA15GENIChomozygous54150650
7139788646139788650GTGT----15GENICheterozygous54150652
7139788648139788650GT--15GENICpossibly homozygous54150654
7139788695139788696GGGT19GENIChomozygous54150656
7139788856139788857TTTG30GENICpossibly homozygous54150658
7139789828139789829TC37GENIChomozygous54150664
7139789894139789895AC24GENIChomozygous54150666
7139790523139790524CT32GENIChomozygous54150668