chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
168115542681155427AAC17GENIChomozygous47565456
168115586981155870AAAC19GENICpossibly homozygous47565458
168115600681156007CCT24GENICpossibly homozygous47565459
168115664481156646TG--11GENICheterozygous47951876
168115784581157846AG34GENIChomozygous47565461
168115805381158054CT26GENIChomozygous47565463
168115946281159463GGTT15GENIChomozygous47565465
168115960681159608TG--24GENIChomozygous47565467
168115999981160000TC18GENIChomozygous47565469
168116000981160010GGTCTCTCTCTCTCTCTCTC13GENIChomozygous47997963
168116027381160274AAT35GENIChomozygous47565471
168116047681160477GC24GENIChomozygous47565473
168116091181160912CT28GENIChomozygous47565475
168116092281160923GT26GENIChomozygous47565477
168116092381160924CCA27GENIChomozygous47565479
168116094081160941GT26GENIChomozygous47565485
168116116681161167AG27GENIChomozygous47565487
168116169581161696GA22GENIChomozygous47565488
168116170581161706AC21GENIChomozygous47565490
168116201381162014TC30GENIChomozygous47565492
168116271381162714GA15GENIChomozygous47565494
168116300081163001T-15GENICheterozygous47565496
168116492781164928GA34GENIChomozygous47565500
168116538081165381CT25GENIChomozygous47565502
168116093281160933G-25GENIChomozygous47911401
168116093581160936GGA26GENIChomozygous47937377