chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	51528126	51528127	C	CT	16	GENIC	homozygous	48307220
15	51528809	51528810	A	G	14	GENIC	homozygous	48825955
15	51528988	51528989	A	G	11	GENIC	homozygous	48825957
15	51529831	51529833	CC	--	17	GENIC	homozygous	48601765
15	51530327	51530328	T	G	18	GENIC	homozygous	48307221
15	51530568	51530569	A	G	18	GENIC	homozygous	48825959
15	51530676	51530677	C	T	14	GENIC	homozygous	48825961
15	51531010	51531011	G	C	25	GENIC	homozygous	48307222
15	51531694	51531695	T	C	14	GENIC	homozygous	48825963
15	51532201	51532202	T	TACAC	4	GENIC	homozygous	48307224
15	51532616	51532617	G	-	17	GENIC	homozygous	48307227
15	51532628	51532629	G	T	22	GENIC	homozygous	48307228
15	51532644	51532645	C	-	23	GENIC	homozygous	48307229
15	51534649	51534650	T	TGC	28	GENIC	possibly homozygous	48307245
15	51534669	51534670	T	A	32	GENIC	possibly homozygous	48825965
15	51534704	51534705	C	CTG	22	GENIC	possibly homozygous	48825967
15	51534715	51534716	C	T	25	GENIC	possibly homozygous	48958031
15	51537718	51537719	G	A	18	GENIC	homozygous	48825969
15	51539301	51539302	T	C	31	GENIC	homozygous	48825971
15	51540135	51540136	A	C	12	GENIC	homozygous	48307255
15	51541671	51541672	A	G	17	GENIC	homozygous	48307259