chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85409011754090118GA19GENIChomozygous52636155
85409025054090251GA29GENIChomozygous52636157
85409107954091080T-31GENIChomozygous52636159
85409215854092159AAG33GENIChomozygous52636161
85409240454092405TG27GENIChomozygous52636163
85409439054094391CCAT10GENICpossibly homozygous52636165
85409530454095305AC22GENIChomozygous52636167
85409540554095406AAT23GENIChomozygous52636169
85409548754095488TC23GENIChomozygous52636171
85409608154096082AG20GENIChomozygous52636173
85409697054096971AG32GENIChomozygous52636175
85409703354097034AG39GENICpossibly homozygous52636177
85409756554097584TCTATCTCAGTGGCCTCTT-------------------1GENIChomozygous53387439
85409792154097922TTG31GENIChomozygous52636179
85409911954099120CT20GENIChomozygous52636181
85409944154099442TC9GENIChomozygous52636183
85409968554099686CT19GENIChomozygous52636185
85410001354100029ACACACACACACACAC----------------13GENIChomozygous52636187
85410027654100277TTA29GENICpossibly homozygous52636189
85410027654100277TTAA29GENICheterozygous53119798
85410033554100336T-23GENIChomozygous52636191
85410089654100897CT27GENIChomozygous52636193
85410107954101080TTC25GENIChomozygous52636195
85410108754101088CCAA26GENIChomozygous52636197
85410110854101112AAAC----12GENIChomozygous52636201
85410166354101664CCAAA5GENIChomozygous53431420
85410209654102097TA31GENIChomozygous52636203
85410249554102496T-22GENIChomozygous52636205
85410265754102658TC21GENIChomozygous52636207
85410278154102791GTTGTGTGCA----------18GENIChomozygous52636209
85410282854102829CG23GENIChomozygous52636211
85410305754103058AG24GENIChomozygous52636213
85410317554103176AG20GENIChomozygous52636215
85410327854103279CCTTTT6GENIChomozygous52636217
85410422054104221GA23GENICpossibly homozygous52636219