chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85785931557859316CT6GENIChomozygous53271484
85786052857860529AC15GENIChomozygous52656823
85786065357860654GA14GENIChomozygous53271485
85786076157860762AG20GENIChomozygous52656825
85786093157860932GA22GENIChomozygous52656827
85786114557861146TTAA9GENICheterozygous53207947
85786160357861604CT22GENIChomozygous52656835
85786201657862017GA39GENIChomozygous52656837
85786215457862155AG12GENIChomozygous53271486
85786267957862680TTTG24GENICpossibly homozygous53271487
85786355857863561CTT---7GENIChomozygous53271488
85786380157863802GGTT12GENICheterozygous52656843
85786380357863804T-12GENICheterozygous53432368
85786610657866107AC18GENIChomozygous52656847
85786670457866706GT--26GENIChomozygous53461145
85786673957866740TG28GENIChomozygous53271489
85786708657867087AC31GENIChomozygous53271490
85786728257867283C-15GENIChomozygous53271491
85786878257868783AG5GENIChomozygous52656855
85786915557869156AC20GENIChomozygous52656857
85786920757869208TC24GENIChomozygous52656859
85787111757871133GCAGCTGGAGTTCCGG----------------18GENIChomozygous53271493
85787124457871245AATTTTTTT6GENIChomozygous52656863
85787277657872777AG23GENIChomozygous52656865
85787281857872819TC23GENIChomozygous52656867
85787474957874750CT25GENIChomozygous53271494