chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101664691101664692GA16GENIChomozygous61485454
1101666029101666030A-9GENICheterozygous60779875
1101666031101666032C-7GENIChomozygous60779876
1101666483101666484AG15GENIChomozygous61485455
1101666983101666984AG16GENIChomozygous61485456
1101670610101670611AT13GENIChomozygous61485457
1101670752101670753AC15GENICpossibly homozygous61485458
1101671083101671084GC17GENIChomozygous61485459
1101671645101671646C-6GENICheterozygous60779877
1101672448101672450CC--14GENIChomozygous61485460
1101672802101672803TTG11GENIChomozygous61485461