chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	104197576	104197577	A	C	21	GENIC	homozygous	52780671
8	104197620	104197621	T	TA	16	GENIC	homozygous	52780672
8	104197622	104197623	T	C	16	GENIC	homozygous	53367133
8	104197624	104197625	T	G	15	GENIC	homozygous	53367134
8	104197628	104197629	G	A	15	GENIC	homozygous	53406545
8	104197629	104197630	A	G	15	GENIC	homozygous	53406546
8	104197639	104197640	G	-	13	GENIC	homozygous	52780673
8	104197644	104197645	T	C	9	GENIC	homozygous	53406547
8	104197646	104197647	G	T	8	GENIC	homozygous	53406548
8	104197650	104197651	G	-	8	GENIC	homozygous	52780674
8	104197664	104197665	C	-	2	GENIC	homozygous	52780675
8	104197671	104197672	A	AT	1	GENIC	homozygous	53406549
8	104197672	104197673	G	GTGTGTGTGTGT	1	GENIC	homozygous	53406550
8	104197674	104197675	G	T	1	GENIC	homozygous	52780676
8	104209672	104209673	T	-	16	GENIC	heterozygous	53023366
8	104213611	104213612	A	T	6	GENIC	homozygous	52780738
8	104213612	104213613	A	G	17	GENIC	homozygous	52780739