chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	20637729	20637730	G	A	33	GENIC	homozygous	116741576
10	20641029	20641030	T	G	52	GENIC	possibly homozygous	126427508
10	20642315	20642316	G	A	47	GENIC	homozygous	116509664
10	20642377	20642378	A	G	39	GENIC	homozygous	116741577
10	20642936	20642937	C	G	45	GENIC	homozygous	116509670
10	20645530	20645531	T	A	27	GENIC	homozygous	117075365
10	20643015	20643015		G	34	GENIC	homozygous	128794286
10	20646610	20646611	T	C	9	GENIC	homozygous	116509678
10	20647103	20647104	C	G	47	GENIC	homozygous	116509682
10	20647125	20647126	G	A	46	GENIC	homozygous	116741578
10	20647521	20647522	C	T	54	GENIC	homozygous	116741579
10	20647545	20647546	C	T	51	GENIC	homozygous	116741580
10	20647558	20647559	G	A	49	GENIC	homozygous	116741581
10	20648461	20648462	C	G	33	GENIC	homozygous	116741582
10	20648765	20648765		AAAAAC	34	GENIC	homozygous	131089136
10	20649914	20649915	C	T	40	GENIC	homozygous	116509690
10	20650581	20650582	G		56	GENIC	homozygous	128794290
10	20650588	20650589	C	T	56	GENIC	homozygous	116741583
10	20650607	20650608	C	A	54	GENIC	homozygous	116741584
10	20653049	20653050	A	G	43	GENIC	homozygous	116509696
10	20654229	20654229		T	34	GENIC	homozygous	128794291
10	20654306	20654306		G	19	GENIC	homozygous	128794292
10	20654332	20654332		T	14	GENIC	homozygous	128794293
10	20654341	20654341		CTT	11	GENIC	heterozygous	132415150
10	20654343	20654343		TC	11	GENIC	heterozygous	130776447
10	20654365	20654366	C		17	GENIC	homozygous	128794295
10	20654393	20654394	G	C	21	GENIC	homozygous	123319742
10	20654394	20654395	T	A	21	GENIC	homozygous	118079832
10	20654397	20654398	T	G	21	GENIC	homozygous	123319743
10	20654398	20654399	A	C	21	GENIC	homozygous	123319744
10	20654692	20654698	CCCTCC		31	GENIC	homozygous	131089137