chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121532503115325032CT10GENICheterozygous50072230
121532510915325110TTC14GENIChomozygous50072232
121532515915325160TC12GENICpossibly homozygous50072234
121532530315325304CT24GENIChomozygous50072236
121532534515325346AG24GENICpossibly homozygous50072238
121532571315325714CT23GENICheterozygous50072240
121532582415325825TTTTTTTCTTTCCTTTTTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTATGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCTGTTAATAGTTTCTA9GENICheterozygous50504030
121532688215326892GAGAATGAAT----------3GENICheterozygous50504031
121532777315327774AG6GENIChomozygous50072254
121532911615329117TG17GENICpossibly homozygous50072260
121532964415329645TC16GENIChomozygous50072262
121533037515330376AG22GENIChomozygous50072264
121533130815331309GA28GENICpossibly homozygous50072266
121533148415331485CT22GENICheterozygous50072272
121533204915332050AG17GENIChomozygous50072278
121533205815332059TC13GENICpossibly homozygous50072280
121533230915332310GA31GENICpossibly homozygous50072282
121533267915332680AAGT18GENICpossibly homozygous50072284
121533297015332976CACACA------3GENICheterozygous50533650
121533644115336451AAATAATAAC----------2GENIChomozygous50072355
121533715515337156TC21GENIChomozygous50072361
121533844815338449CT20GENIChomozygous50072363