chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3177015193177015194GC16GENIChomozygous111843010
3177015478177015479GT14GENIChomozygous111843012
3177016773177016774AG19GENIChomozygous111843014
3177017850177017851AG22GENIChomozygous111843016
3177019326177019327AC10GENIChomozygous111843018
3177019372177019375CAC8GENIChomozygous127965528
3177020639177020640T11GENIChomozygous127965529
3177023243177023244T28GENICpossibly homozygous127965530
3177024104177024105AC14GENIChomozygous119653220
3177025987177025988AG21GENIChomozygous111843020
3177027334177027335AG13GENIChomozygous111843022
3177033894177033895CG31GENIChomozygous111843024
3177039682177039683GC26GENIChomozygous111843028
3177042791177042791G16GENIChomozygous127965537
3177024103177024103C13GENIChomozygous127965531
3177033054177033066CCACCATCACCA7GENIChomozygous127965532
3177033351177033401TTTAAAGACAATATTTACTGTAAGTAGAATGATCAAAAGATGTGCCTATA10GENIChomozygous127965533
3177035790177035794TTTC14GENIChomozygous127965534
3177038352177038352T22GENICpossibly homozygous127965535
3177038745177038748CAA13GENIChomozygous127965536
3177043355177043356TC18GENIChomozygous111843030
3177045519177045520TC13GENIChomozygous111843032