chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160332442160332443TC22INTERGENICpossibly homozygous73152490
5160333998160333999GA62INTERGENIChomozygous72905937
5160335078160335079CT61INTERGENIChomozygous72905939
5160335526160335527AG74INTERGENIChomozygous71185621
5160335852160335853CT58INTERGENIChomozygous72905941
5160336009160336010AG58INTERGENIChomozygous72905943
5160336220160336221GA72INTERGENICpossibly homozygous72905945
5160337124160337125AG47INTERGENICpossibly homozygous72905947
5160338496160338497GC47GENIChomozygous73317498
5160341300160341301AG61GENIChomozygous71185625
5160342983160342984CT42GENIChomozygous71185627
5160343323160343324GT49GENIChomozygous72905951
5160343969160343970CT62GENICpossibly homozygous72905953
5160344250160344251AG58GENIChomozygous71185629
5160346588160346589AG59GENIChomozygous71185633
5160347869160347870CT61GENIChomozygous71185635
5160348347160348348AC76GENIChomozygous71185637
5160349862160349863CT38GENICheterozygous73809767
5160349866160349867TC39GENICheterozygous71185639
5160349875160349876AG36GENICheterozygous71641114
5160355305160355306TA45GENIChomozygous73152491
5160357886160357887GA41GENIChomozygous72905955