chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	69069806	69069807	C	-	14	GENIC	possibly homozygous	51484285
10	69070105	69070106	C	CTG	3	GENIC	heterozygous	51484286
10	69070105	69070106	C	CTGTG	3	GENIC	heterozygous	51484287
10	69070107	69070108	C	G	4	GENIC	heterozygous	51484288
10	69070121	69070122	C	G	11	GENIC	heterozygous	51484289
10	69071336	69071337	G	A	14	GENIC	heterozygous	51484291
10	69071508	69071509	T	G	20	GENIC	possibly homozygous	51484292
10	69071635	69071636	T	A	7	GENIC	possibly homozygous	51484293
10	69071946	69071947	G	C	11	GENIC	possibly homozygous	51484294
10	69072597	69072598	A	G	24	GENIC	possibly homozygous	51484296
10	69073021	69073022	A	G	19	GENIC	possibly homozygous	51484297
10	69073486	69073487	A	C	9	GENIC	homozygous	51484299
10	69073487	69073488	T	C	9	GENIC	homozygous	51484300
10	69073644	69073645	T	G	17	GENIC	possibly homozygous	51484301
10	69073985	69073986	A	T	28	GENIC	homozygous	51484302
10	69074030	69074031	T	G	14	GENIC	homozygous	51484303
10	69074050	69074051	A	G	15	GENIC	homozygous	51484304
10	69074090	69074091	T	C	15	GENIC	possibly homozygous	51484305
10	69074143	69074144	T	G	20	GENIC	possibly homozygous	51484306
10	69074338	69074339	G	A	8	GENIC	homozygous	51484307