chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101816116101816117CT24GENIChomozygous51585580
10101816125101816126CG22GENIChomozygous51585582
10101816363101816364AAG20GENIChomozygous52327269
10101816397101816398GA35GENIChomozygous51585584
10101816412101816413TC33GENIChomozygous51585586
10101817204101817208GTGT----5GENICheterozygous52813562
10101817932101817933CG36GENIChomozygous51585588
10101818019101818020CT21GENIChomozygous51585590
10101818177101818178CA25GENIChomozygous51585592
10101818371101818372CG18GENIChomozygous51585594
10101818373101818374GA18GENIChomozygous51585596
10101818380101818381GC17GENIChomozygous51585598
10101818384101818385GA15GENIChomozygous51585600
10101818595101818596GA25GENIChomozygous51585602
10101818701101818705CGCG----28GENIChomozygous51585604
10101818719101818720CT28GENIChomozygous51585606
10101819141101819142A-17GENIChomozygous51585608
10101819145101819146GA17GENIChomozygous51585610
10101819260101819261TTGGA1GENIChomozygous52447242
10101819366101819367AAG17GENIChomozygous51585612
10101819401101819402AAGCTGGGAGAAGAAGGAAGATGAGGAG3GENIChomozygous52447244
10101819410101819411AG5GENIChomozygous52403594
10101819584101819604TGATGTTGTTCCCTCAGTAA--------------------2GENIChomozygous52403596
10101819613101819629ATGCCTATGAGCGCTC----------------6GENIChomozygous52403598
10101820721101820722TC19GENIChomozygous51585614
10101820731101820732AC16GENIChomozygous51585616
10101820861101820862TG16GENICpossibly homozygous51585618
10101820864101820876ACACACACACAT------------19GENICpossibly homozygous52327273
10101820955101820956CCACACACACACATACACACAA16GENIChomozygous52447246
10101820979101820980CCACACACAT19GENICpossibly homozygous52447248
10101821372101821374AC--22GENIChomozygous51585654
10101817206101817208GT--5GENICheterozygous52514105