chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	110604182	110604183	C	A	3	GENIC	homozygous	52802111
8	110604922	110604923	A	C	4	GENIC	homozygous	52802117
8	110605180	110605181	C	T	5	GENIC	homozygous	52802121
8	110605702	110605703	T	C	7	GENIC	homozygous	52802123
8	110606000	110606001	C	T	10	GENIC	homozygous	52802125
8	110607573	110607574	T	C	7	GENIC	homozygous	53034413
8	110607598	110607700	AATCTACTCTCTTTTTTTTTTTTCCTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC	------------------------------------------------------------------------------------------------------	7	GENIC	homozygous	53367571
8	110606913	110606914	C	G	5	GENIC	homozygous	53327969
8	110607987	110607988	T	C	13	GENIC	homozygous	53327970
8	110606135	110606136	C	T	10	GENIC	homozygous	53327967
8	110608270	110608271	G	GTT	9	GENIC	possibly homozygous	53034423
8	110608578	110608579	A	G	4	GENIC	homozygous	53034431
8	110608653	110608654	T	C	8	GENIC	homozygous	53034433
8	110609114	110609115	G	A	6	GENIC	homozygous	53327972
8	110609559	110609560	T	G	3	GENIC	homozygous	53034439
8	110609667	110609668	G	A	7	GENIC	homozygous	53327973
8	110609725	110609726	T	A	8	GENIC	homozygous	53034441
8	110610099	110610100	C	T	3	GENIC	homozygous	53327974
8	110610787	110610788	A	G	4	GENIC	homozygous	53034447
8	110611165	110611166	G	A	3	GENIC	homozygous	53327975
8	110611717	110611718	G	A	7	GENIC	homozygous	53327976
8	110612227	110612228	G	T	14	GENIC	homozygous	53034451
8	110612746	110612747	A	G	3	GENIC	homozygous	53034453
8	110613298	110613299	T	C	3	GENIC	homozygous	53034455
8	110613487	110613488	T	C	5	GENIC	homozygous	53034457
8	110613563	110613564	T	G	8	GENIC	homozygous	53034459
8	110615410	110615411	G	GC	8	GENIC	homozygous	52802156
8	110616082	110616083	C	T	6	GENIC	homozygous	53034465
8	110616432	110616433	T	C	9	GENIC	homozygous	53327977
8	110608270	110608271	G	GT	9	GENIC	heterozygous	53409054
8	110608377	110608378	T	TGTGTGC	7	GENIC	heterozygous	53409056
8	110608377	110608378	T	TGTGTGTGC	7	GENIC	heterozygous	53409058