chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116581804116581805CT39GENIChomozygous52828381
8116582097116582098A-16GENIChomozygous53291240
8116583144116583145GT21GENIChomozygous52828382
8116583369116583370AG34GENIChomozygous52828383
8116584154116584158GTTC----13GENICheterozygous53411376
8116584195116584196AG21GENIChomozygous52828384
8116584398116584399TC31GENIChomozygous52828385
8116585731116585737GGCACT------22GENIChomozygous52828398
8116585893116585894TC21GENIChomozygous53291242
8116586144116586145GGC19GENIChomozygous52828399
8116586307116586308GA35GENIChomozygous52828401
8116586711116586712CCA13GENICheterozygous52828402
8116586712116586713CCA12GENICheterozygous53411378
8116586712116586713CCACA12GENICheterozygous53411379
8116586993116586994GGTGTGTGTGTCTGTC35GENICpossibly homozygous53411380
8116587456116587457TA31GENIChomozygous52828405
8116587624116587625AC23GENIChomozygous52828406
8116587743116587744AAC23GENIChomozygous52828407
8116588180116588181CT36GENIChomozygous52828408
8116588490116588492AT--23GENIChomozygous52828410
8116588496116588498AA--23GENIChomozygous52828411
8116588540116588541CT32GENICpossibly homozygous52828412
8116588594116588606TTTTTTTTTTTT------------23GENIChomozygous52828413
8116595831116595855CTGCCTCCGCCTCTGCCTCCGCCT------------------------6GENICheterozygous53411382