chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107074001270740013TC22INTERGENIChomozygous51489128
107074032070740321AG16INTERGENIChomozygous51489130
107074044470740445GA16INTERGENIChomozygous52199884
107074095070740951TG29INTERGENIChomozygous52251440
107074095770740958AG31INTERGENIChomozygous51489131
107074117070741171AC28INTERGENIChomozygous51489132
107074128570741286GGTGTGA17INTERGENIChomozygous51489133
107074172770741728TA38INTERGENIChomozygous51489134
107074235470742355TTA22INTERGENICpossibly homozygous51489135
107074249970742500TTC28INTERGENIChomozygous51489136
107074250170742502AC27INTERGENIChomozygous52384057
107074250270742503AT28INTERGENIChomozygous52384059
107074280770742808GC26INTERGENIChomozygous51489137
107074283070742831G-14INTERGENIChomozygous51489139
107074423870744274ACACACACACACACACACACACACACACACACACAC------------------------------------15INTERGENIChomozygous52384061