chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	69069789	69069790	T	C	18	GENIC	homozygous	52846245
10	69069823	69069824	C	A	21	GENIC	homozygous	53156208
10	69070072	69070073	T	C	43	GENIC	homozygous	53156210
10	69070107	69070108	C	G	12	GENIC	homozygous	51484288
10	69070119	69070120	G	C	20	GENIC	homozygous	53156212
10	69070329	69070330	G	A	31	GENIC	homozygous	53156214
10	69070514	69070515	G	C	30	GENIC	homozygous	53156216
10	69071508	69071509	T	G	39	GENIC	homozygous	51484292
10	69071544	69071545	T	C	35	GENIC	homozygous	53156218
10	69071635	69071636	T	A	29	GENIC	homozygous	51484293
10	69072268	69072269	T	TTGTGTG	11	GENIC	homozygous	52846255
10	69072498	69072499	T	C	34	GENIC	homozygous	53156220
10	69072597	69072598	A	G	43	GENIC	homozygous	51484296
10	69073021	69073022	A	G	37	GENIC	homozygous	51484297
10	69073248	69073249	C	CCACACA	1	GENIC	homozygous	51484298
10	69073486	69073487	A	C	36	GENIC	homozygous	51484299
10	69073487	69073488	T	C	36	GENIC	homozygous	51484300
10	69073644	69073645	T	G	42	GENIC	homozygous	51484301
10	69073985	69073986	A	T	39	GENIC	homozygous	51484302
10	69074030	69074031	T	G	28	GENIC	homozygous	51484303
10	69074050	69074051	A	G	31	GENIC	homozygous	51484304
10	69074143	69074144	T	G	39	GENIC	homozygous	51484306