chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109008484590084846C10GENIChomozygous131469323
109008491690085046AGGAGTACCAGGTTTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC10GENICheterozygous131469324
109008512590085126CT10GENIChomozygous116904189
109008612390086123GT21GENIChomozygous131469325
109008664890086649GA17GENIChomozygous116904191
109008714990087150CT14GENIChomozygous116904193
109008735090087351GA20GENIChomozygous116904195
109008854690088558AAACAAACAAAC16GENIChomozygous131469326
109008868390088684T13GENIChomozygous131469327
109008927590089276TC17GENIChomozygous116904197
109008960090089601GA12GENIChomozygous116904199