chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7137148956137148957TA28GENIChomozygous602213022
7137148992137148996CTTC----26GENIChomozygous731388949
7137149091137149092TTTTCTTTCTTTCC32GENIChomozygous731388950
7137149935137149936AT19GENIChomozygous602213023
7137149953137149954GA17GENIChomozygous602213024
7137149997137149998CCTTGTTTGTTTGT13GENIChomozygous731388952
7137150134137150135T-15GENIChomozygous731388953
7137150712137150713CG38GENIChomozygous602213025
7137151560137151561CT33GENIChomozygous602213026
7137152071137152072T-13GENIChomozygous731388955
7137152103137152109CCCTTT------12GENIChomozygous731388956
7137152124137152125CCT14GENIChomozygous731388957
7137152162137152163TC22GENIChomozygous602757660
7137152231137152232TTTTTC13GENIChomozygous731388958
7137152239137152240CCT8GENICpossibly homozygous731388960
7137152239137152240CCTT8GENICheterozygous731388961
7137152282137152283GA26GENIChomozygous602213027
7137152526137152527GA18GENIChomozygous602213028
7137152728137152729AG30GENIChomozygous602213029
7137152773137152775AC--21GENIChomozygous731388962
7137152829137152830AATGTATGTGTATG6GENIChomozygous731388964
7137152913137152914CT18GENIChomozygous602213030
7137152946137152947AG20GENIChomozygous602213031
7137153342137153343GA16GENIChomozygous602213032
7137153697137153698TA13GENIChomozygous602213033
7137153739137153740AC17GENIChomozygous602213034
7137153756137153757GC14GENIChomozygous602213035
7137153959137153960AG16GENIChomozygous602213036
7137154398137154399CT26GENIChomozygous602213037
7137154438137154439TG27GENIChomozygous602213038
7137154578137154579AG27GENIChomozygous602213039
7137154663137154664GA31GENIChomozygous602213040
7137154902137154903CA28GENIChomozygous602213041
7137155045137155046TC29GENIChomozygous602213042
7137155144137155145GA27GENIChomozygous602213043
7137155198137155199CA23GENIChomozygous602213044