chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	5859920	5859921	A	G	17	GENIC	homozygous	51798967
10	5860588	5860589	T	C	18	GENIC	homozygous	51611044
10	5860943	5860944	A	AGT	15	GENIC	homozygous	51798970
10	5862036	5862037	G	GA	13	GENIC	homozygous	51312362
10	5862207	5862208	T	C	25	GENIC	homozygous	51611045
10	5862263	5862264	T	C	27	GENIC	homozygous	51798972
10	5862301	5862302	A	G	30	GENIC	homozygous	51611046
10	5862501	5862502	G	A	20	GENIC	homozygous	51798975
10	5864418	5864419	A	G	9	GENIC	homozygous	51798977
10	5865143	5865144	C	CTCAT	10	GENIC	homozygous	51312365
10	5865679	5865680	A	G	19	GENIC	homozygous	51611049
10	5866194	5866195	G	A	18	GENIC	homozygous	51798980
10	5866269	5866270	G	A	13	GENIC	homozygous	51798982
10	5866416	5866417	C	T	22	GENIC	homozygous	51312367
10	5866791	5866792	G	GTA	17	GENIC	homozygous	51798984
10	5866982	5866983	A	G	13	GENIC	homozygous	51312369
10	5868386	5868392	AAAAAA	------	12	GENIC	possibly homozygous	51798986
10	5869310	5869311	C	-	18	GENIC	homozygous	51798988
10	5869746	5869747	T	C	17	GENIC	homozygous	51611052
10	5869848	5869849	C	T	16	GENIC	homozygous	51798991
10	5871464	5871465	C	A	21	GENIC	homozygous	51798994
10	5872426	5872427	T	G	16	GENIC	homozygous	51312372
10	5872698	5872699	G	A	23	GENIC	homozygous	51798996
10	5873050	5873051	A	T	20	GENIC	homozygous	51798998
10	5873570	5873571	T	C	25	GENIC	homozygous	51611054
10	5876277	5876278	C	A	19	GENIC	homozygous	51312374
10	5876278	5876279	C	A	19	GENIC	homozygous	51312375
10	5876281	5876282	C	G	18	GENIC	homozygous	51312377
10	5876282	5876283	C	A	18	GENIC	homozygous	51312379
10	5876286	5876287	C	G	17	GENIC	homozygous	51312380
10	5877681	5877682	A	G	31	GENIC	homozygous	51611055
10	5877811	5877826	GTGTGTGTGTGTGTG	---------------	15	GENIC	heterozygous	52457809
10	5877815	5877826	GTGTGTGTGTG	-----------	15	GENIC	possibly homozygous	51611057
10	5877955	5877956	G	-	11	GENIC	homozygous	52294959
10	5878618	5878619	C	CCTTACGGCGGTCTGGGGCAGCAAG	13	GENIC	homozygous	51312382