chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2174552087174552088GA59GENIChomozygous142964991
2174552617174552618AG64GENIChomozygous136373306
2174554627174554628AG61GENIChomozygous136373307
2174554939174554940GA61GENIChomozygous142964992
2174557431174557432AT46GENIChomozygous142964993
2174557308174557320AGAAGGAGGAGG54GENIChomozygous142901010
2174557451174557466TAGTAGTAGTAGTAA47GENIChomozygous142901011
2174557465174557466A47GENIChomozygous403028004
2174557453174557454GA47GENICheterozygous154018974
2174557465174557466AG47GENICheterozygous154018975
2174557453174557454G47GENIChomozygous403028003
2174557456174557457GA47GENICheterozygous403707951
2174557456174557457G47GENIChomozygous403707952
2174559402174559403TC63GENIChomozygous142964994
2174559647174559649AC40GENICpossibly homozygous142901012
2174559654174559655CG44GENICpossibly homozygous154018980
2174559654174559655C44GENICheterozygous403028006
2174559658174559659CG45GENICpossibly homozygous154018982
2174559658174559659C45GENICheterozygous403028008
2174559662174559663CG48GENICpossibly homozygous142964995
2174561613174561614T45GENICpossibly homozygous141135572
2174562327174562327T34GENICpossibly homozygous142901013
2174559639174559641AG37GENIChomozygous135961219
2174563685174563685TTGTTTTGTAATTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC13GENICheterozygous147248355