chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71922858	71922859	A	G	21	GENIC	homozygous	115985484
11	71922902	71922903	G	A	27	GENIC	homozygous	115985486
11	71922955	71922956	G	A	23	GENIC	homozygous	115985488
11	71923390	71923391	A	T	19	GENIC	homozygous	115985490
11	71924074	71924075	A	G	19	GENIC	homozygous	116051476
11	71933277	71933278	A	G	30	GENIC	homozygous	115985500
11	71933465	71933466	C	T	28	GENIC	homozygous	115985502
11	71933662	71933663	C	G	29	GENIC	homozygous	115985504
11	71933674	71933675	G	A	27	GENIC	homozygous	116051480
11	71933737	71933738	C	T	22	GENIC	homozygous	116051482
11	71934630	71934631	G	A	39	GENIC	homozygous	116051484
11	71935389	71935390	C	T	28	GENIC	homozygous	115985506
11	71935437	71935438	C	T	35	GENIC	homozygous	115985508
11	71935814	71935815	T	A	27	GENIC	homozygous	115985512
11	71936104	71936105	C	T	40	GENIC	homozygous	115985514
11	71936727	71936728	C	T	31	GENIC	homozygous	116051486
11	71936878	71936879	T	A	25	GENIC	homozygous	115985516
11	71937863	71937864	A	T	20	GENIC	homozygous	116051488
11	71938257	71938258	T	C	11	GENIC	homozygous	115985518