chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153921783153921784CT41GENIChomozygous56989520
4153921928153921929A-1GENIChomozygous56989521
4153922217153922218CT52GENIChomozygous56989522
4153923011153923012TC15GENICpossibly homozygous56989523
4153923022153923025TTT---11GENICheterozygous56989524
4153923023153923025TT--11GENICheterozygous56989525
4153923203153923204GA33GENIChomozygous56989526
4153924866153924867AG51GENIChomozygous56989527
4153925267153925268CT67GENIChomozygous56989528
4153925311153925312CT57GENIChomozygous56989529
4153925838153925839GA24GENIChomozygous56989530
4153925876153925877AG31GENIChomozygous56989531
4153925904153925905AC36GENIChomozygous56989532
4153925922153925923AC38GENIChomozygous56989533
4153927956153927957CT43GENIChomozygous56989534
4153928180153928181GGTAA29GENIChomozygous56989535
4153929259153929261AA--1GENIChomozygous56989536
4153929869153929870TTAC18GENICheterozygous56989537
4153929874153929878ACAC----18GENICheterozygous56989538
4153930161153930162CT38GENICpossibly homozygous56989539
4153930347153930348TTTG4GENICheterozygous56989540
4153932761153932762CT26GENIChomozygous56989541
4153936462153936463A-7GENIChomozygous56989542
4153936887153936888CG51GENIChomozygous56989543
4153938083153938084TG26GENICpossibly homozygous56989544
4153940599153940600T-46GENIChomozygous56989545
4153941224153941225G-6GENICheterozygous56989546