chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84506079545060796GA20GENIChomozygous138325553
84506126545061266GA39GENIChomozygous138325554
84506236745062368AG10GENIChomozygous138325555
84506308145063082AG48GENIChomozygous146465607
84506442445064425GA41GENIChomozygous138325556
84506458745064588TC47GENIChomozygous138325557
84506460245064603CT50GENIChomozygous138325558
84506506645065067TC45GENIChomozygous138325559
84506604545066046GC53GENIChomozygous138325560
84506791345067914AG38GENIChomozygous138325561
84506832045068321AG14GENICheterozygous154505163
84506832145068322CT14GENICheterozygous154505164
84507000145070002AT45GENICpossibly homozygous138325562
84507045745070458TC37GENIChomozygous138325563
84507082245070823GA36GENIChomozygous138325564
84507110045071101TA59GENIChomozygous138325565
84507125345071254GT41GENIChomozygous138325566
84507278145072782TC55GENIChomozygous138325567
84507321745073218TC46GENIChomozygous138325568
84507399445073995TC41GENIChomozygous138325569
84507565445075655TC33GENIChomozygous138325575
84507661145076612CT41GENIChomozygous138325576
84506814845068148A20GENICheterozygous144389557
84507308345073083A43GENIChomozygous138243555
84507407445074080TATCTC33GENIChomozygous138243556
84507635745076362TTTAC34GENIChomozygous138243560
84506832045068321A14GENICheterozygous403236313
84506832145068322C14GENICheterozygous403236314
84508006945080070AT34GENIChomozygous138325578
84508178945081790TA43GENIChomozygous138325579