chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214123574214123575TG8GENIChomozygous931211790
1214130365214130366GA13GENIChomozygous931211791
1214131140214131141CT10GENIChomozygous931211792
1214132380214132381AG15GENIChomozygous931211793
1214132531214132532GA11GENIChomozygous931211794
1214134376214134377AG20GENIChomozygous931211795
1214141343214141344AG7GENIChomozygous931211796
1214141591214141592TC7GENIChomozygous931211797
1214146027214146028TC6GENIChomozygous931211798
1214147043214147044GA13GENICpossibly homozygous931211799