chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105362509253625093CA21GENIChomozygous51455663
105362515453625155CA27GENIChomozygous51455664
105362516053625161CA29GENIChomozygous51455665
105362516553625166GC29GENIChomozygous52376569
105362516753625168CA29GENIChomozygous52376571
105362517553625176CT29GENIChomozygous51455666
105362517953625180AG27GENIChomozygous51455667
105362519653625197GC23GENIChomozygous51455668
105362520953625210CCA18GENIChomozygous51455669
105362521153625212CA18GENIChomozygous52376573
105362521353625214CA18GENIChomozygous52376575
105362521753625218GC20GENIChomozygous51455670
105362522053625221AG20GENIChomozygous51455671
105362523753625238CA19GENIChomozygous51455672
105362524053625241AC20GENIChomozygous51455673
105362524753625248C-24GENIChomozygous51455674
105362525353625254AT29GENIChomozygous52376577
105362525553625256CA30GENIChomozygous52376579
105362526953625270CA34GENIChomozygous51455675
105362527753625278CA37GENIChomozygous51455676
105362527953625280C-38GENIChomozygous51455677
105362536453625365C-56GENIChomozygous51455681
105362528953625290TTG40GENIChomozygous51455678
105362532553625326GA53GENIChomozygous51455679
105362532653625327GA53GENIChomozygous51455680
105363990153639902TTCA8GENICheterozygous51648610
105365525053655252GT--2GENIChomozygous52248414
105365633153656332AAAG16GENIChomozygous51455818
105366181653661820ACAC----8GENICheterozygous52376581
105366303953663040GGTTGTTTTGTT8GENIChomozygous52376583
105366343053663431T-12GENIChomozygous51455831
105366347853663479AG6GENIChomozygous51455832
105367142453671425CT27GENIChomozygous51455843
105367187153671883AAGAAAGAAAGA------------21GENICheterozygous52376585