chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103634641336346414CT15INTERGENICheterozygous51413705
103634650136346502CT14INTERGENICheterozygous52139311
103634700836347009CT21INTERGENICheterozygous51413707
103634706736347068AG23INTERGENICheterozygous52139313
103634853236348533G-8INTERGENIChomozygous51413713
103634862736348628TC13INTERGENICheterozygous51413715
103634937436349375AG19INTERGENICheterozygous51413717
103635004636350047TC11INTERGENICheterozygous51413719
103635005036350051GA10INTERGENICheterozygous51413721
103635207336352074TC18INTERGENICheterozygous51413723
103635219736352198CT14INTERGENIChomozygous51413725
103635223536352236CT19INTERGENICheterozygous51413727
103635224936352250TC19INTERGENICheterozygous51413729
103635233736352338AG10INTERGENICheterozygous51413731
103635258036352581GGA14INTERGENICheterozygous51413733
103635281036352811CT7INTERGENICheterozygous51413735
103635327936353280TA11INTERGENICheterozygous52139315
103635460936354610AC11INTERGENICheterozygous51413751
103635491236354913AT14INTERGENIChomozygous51413753
103635514936355150AG23INTERGENICheterozygous51413755
103635528936355290AAG15INTERGENICheterozygous51413757
103635533336355334CT15INTERGENICheterozygous51413759
103635540536355406TA16INTERGENICheterozygous51413761
103635728936357290GA7GENIChomozygous51413770
103635738636357387AG12GENICheterozygous51413772
103635757136357572CT12GENICheterozygous51413774
103635901036359018CTGGGCTA--------8GENICheterozygous51413784
103635903436359035T-8GENICheterozygous52040293
103635934136359342GA11GENICheterozygous51413786
103636008236360083AATG17GENICheterozygous51413788