chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10530550	10530551	T	C	32	GENIC	homozygous	116493186
10	10530607	10530608	G	T	23	GENIC	homozygous	116493188
10	10532561	10532562	C	T	27	GENIC	homozygous	116493190
10	10532748	10532749	G	A	30	GENIC	homozygous	116493192
10	10533526	10533527	G	A	14	GENIC	homozygous	116493194
10	10534499	10534500	C	T	15	GENIC	homozygous	116493196
10	10534522	10534523	G	A	19	GENIC	homozygous	116493198
10	10535172	10535173	T	G	40	GENIC	possibly homozygous	116493200
10	10536347	10536348	G	C	39	GENIC	homozygous	116493202
10	10537247	10537248	C	T	39	GENIC	homozygous	116493204
10	10538149	10538150	C	T	47	GENIC	homozygous	116493206
10	10538829	10538830	G	A	39	GENIC	homozygous	116493208
10	10540177	10540178	G	C	36	GENIC	homozygous	116493210