chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	97160123	97160125	AC		18	GENIC	heterozygous	141163544
1	97170719	97170720	A	C	27	GENIC	homozygous	141220313
1	97168285	97168286	T	C	22	GENIC	homozygous	141220308
1	97168560	97168561	T	A	18	GENIC	homozygous	141220309
1	97170129	97170130	A	G	31	GENIC	homozygous	141220310
1	97170378	97170379	A	T	30	GENIC	homozygous	141220311
1	97170571	97170572	G	A	32	GENIC	homozygous	141220312
1	97171386	97171387	A	G	28	GENIC	homozygous	141220314
1	97171893	97171894	A	G	20	GENIC	homozygous	141220315
1	97172661	97172662	G	T	27	GENIC	homozygous	141220316
1	97172837	97172837		CCA	24	GENIC	homozygous	141163545
1	97172912	97172912		TCAGCTCCAT	25	GENIC	homozygous	141163546
1	97173112	97173113	C	T	28	GENIC	homozygous	141220317
1	97173701	97173702	G	A	27	GENIC	homozygous	141220318
1	97174417	97174418	A	G	29	GENIC	homozygous	141220319
1	97174775	97174776	C	T	32	GENIC	homozygous	141220320
1	97175283	97175283		A	31	GENIC	homozygous	141163547
1	97176092	97176093	T	C	30	GENIC	homozygous	141220321
1	97176416	97176417	C	T	25	GENIC	homozygous	141220322
1	97176618	97176619	C	T	25	GENIC	homozygous	141220323
1	97176859	97176863	CTTC		22	GENIC	homozygous	141163548
1	97177867	97177868	T	C	21	GENIC	homozygous	141220324