chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 111698989 111698990 G A 36 GENIC homozygous 929627843 8 111700490 111700491 T C 48 GENIC homozygous 929627844 8 111700575 111700576 T C 50 GENIC homozygous 929627845 8 111702284 111702285 G A 27 GENIC homozygous 929627846 8 111706168 111706169 G A 28 GENIC homozygous 929627847 8 111706234 111706235 G A 25 GENIC homozygous 929627848 8 111706261 111706262 G A 26 GENIC homozygous 929627849 8 111706952 111706953 C T 42 GENIC homozygous 929627850 8 111708179 111708180 G A 38 GENIC homozygous 929627851 8 111708481 111708482 T C 37 GENIC homozygous 929627852 8 111709172 111709173 G C 51 GENIC homozygous 929627853 8 111709376 111709377 G A 57 GENIC homozygous 929627854 8 111711762 111711763 G T 35 GENIC homozygous 929627855 8 111713977 111713978 A G 41 GENIC homozygous 929627856 8 111714595 111714596 A G 29 GENIC homozygous 929627857 8 111716278 111716279 T G 32 GENIC homozygous 929627858 8 111717640 111717641 G A 36 GENIC homozygous 929627859 8 111719885 111719886 A G 37 GENIC homozygous 929627860 8 111720114 111720115 G A 52 GENIC homozygous 929627861 8 111720827 111720828 C T 40 GENIC homozygous 929627862