chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12182156421821565GGT21GENIChomozygous60638649
12182708721827089CA--1GENIChomozygous62121177
12185810921858110G-8GENICheterozygous60638653
12187085621870857TTTGTG7GENICpossibly homozygous60638654
12187291821872919GGGT7GENICheterozygous61391809
12184879221848793AG30GENIChomozygous61391801
12185623221856233AAAC12GENICheterozygous61391803
12185392021853922AT--5GENICheterozygous62550597
12187291821872919GGGTGTGTGT7GENICheterozygous62323655
12187412321874124TTTTTTGTTTTG18GENIChomozygous61391811
12187905921879060GGGT4GENICheterozygous62121198
12187906021879062GT--4GENICheterozygous62224969
12188397621883977CT16GENIChomozygous60638656
12188398821883989CT14GENIChomozygous60638657
12188399321883994CG13GENIChomozygous60638658
12188400821884009CT16GENIChomozygous60638659
12188402521884026CG17GENIChomozygous60638660
12188403921884040CG15GENIChomozygous62072463
12188404021884041TC15GENIChomozygous62072465
12188404421884045TA16GENIChomozygous61271259
12188404821884049CT19GENIChomozygous60638661
12188405321884054CG19GENIChomozygous60638662
12188410121884102AAG17GENIChomozygous60638663
12188412221884123TC16GENIChomozygous60638664
12188414521884146CCA17GENIChomozygous60638665
12188414921884150TTC21GENIChomozygous60638666
12188415621884157TTC21GENIChomozygous60638667
12189204721892048TC26GENIChomozygous61271261
12189204921892050CT28GENIChomozygous61271262
12189225721892261CTTT----14GENICheterozygous62121208
12189287921892880T-9GENICheterozygous62252836
12189312021893122TG--23GENICheterozygous62243991