chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
168115542681155427AAC16GENIChomozygous47565456
168115586981155870AAAC26GENICpossibly homozygous47565458
168115600681156007CCT33GENICpossibly homozygous47565459
168115664481156646TG--9GENICheterozygous47951876
168115784581157846AG42GENIChomozygous47565461
168115805381158054CT31GENIChomozygous47565463
168115946281159463GGTT27GENIChomozygous47565465
168115960681159608TG--24GENICpossibly homozygous47565467
168115999981160000TC29GENIChomozygous47565469
168116000981160010GGTCTCTCTCTCTCTCTCTC22GENIChomozygous47997963
168116027381160274AAT30GENIChomozygous47565471
168116047681160477GC38GENIChomozygous47565473
168116091181160912CT42GENIChomozygous47565475
168116092281160923GT44GENIChomozygous47565477
168116092381160924CCA43GENIChomozygous47565479
168116093281160933G-46GENIChomozygous47911401
168116093581160936GGA48GENIChomozygous47937377
168116094081160941GT49GENIChomozygous47565485
168116116681161167AG46GENIChomozygous47565487
168116169581161696GA42GENIChomozygous47565488
168116170581161706AC43GENIChomozygous47565490
168116201381162014TC54GENIChomozygous47565492
168116271381162714GA24GENIChomozygous47565494
168116300081163001T-21GENICheterozygous47565496
168116492781164928GA53GENIChomozygous47565500
168116538081165381CT44GENIChomozygous47565502