chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80221959	80221960	A	C	21	GENIC	homozygous	142307833
11	80221960	80221961	A	C	21	GENIC	homozygous	142307834
11	80222127	80222129	TA		27	GENIC	homozygous	142275616
11	80224915	80224916	T	C	30	GENIC	homozygous	142307835
11	80226415	80226416	T	C	28	GENIC	homozygous	142307839
11	80230751	80230753	AC		30	GENIC	homozygous	142275620
11	80230846	80230847	G	A	13	GENIC	homozygous	146250684
11	80222282	80222282		GCC	16	GENIC	homozygous	146234012
11	80230080	80230080		AGGGA	22	GENIC	possibly homozygous	146234013
11	80226681	80226682	T	A	15	GENIC	possibly homozygous	146250681
11	80229487	80229488	G	A	17	GENIC	homozygous	146250682
11	80230214	80230215	G	A	32	GENIC	homozygous	146250683
11	80232027	80232028	A	G	33	GENIC	homozygous	146250685
11	80232114	80232115	A	T	24	GENIC	homozygous	142307842
11	80234178	80234179	A	G	25	GENIC	homozygous	142307843
11	80234618	80234618		TCT	19	GENIC	homozygous	142275621
11	80238028	80238028		TG	24	GENIC	homozygous	142275622
11	80238378	80238379	G	A	23	GENIC	homozygous	142307844
11	80240070	80240071	G	A	21	GENIC	homozygous	146250686
11	80241229	80241230	C	T	7	GENIC	homozygous	142307846
11	80241688	80241689	G	A	10	GENIC	homozygous	146250687
11	80241717	80241718	A	G	14	GENIC	homozygous	142307847
11	80237154	80237155	C		13	GENIC	heterozygous	403311466
11	80237154	80237155	C	A	13	GENIC	heterozygous	403311467