chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	53655216	53655217	G	A	13	GENIC	homozygous	49950846
13	53656420	53656421	A	G	11	GENIC	heterozygous	49950847
13	53656421	53656422	T	C	11	GENIC	heterozygous	49950848
13	53656607	53656608	G	T	26	GENIC	heterozygous	49950849
13	53656666	53656667	G	A	23	GENIC	heterozygous	49950850
13	53658161	53658162	G	A	15	GENIC	homozygous	49950854
13	53658332	53658333	C	CAA	15	GENIC	heterozygous	49950856
13	53658361	53658362	A	G	18	GENIC	heterozygous	49950857
13	53659117	53659118	C	T	11	GENIC	heterozygous	49950858
13	53659555	53659556	A	T	9	GENIC	heterozygous	49950861
13	53659894	53659895	A	T	9	GENIC	homozygous	49950864
13	53659998	53659999	G	A	13	GENIC	heterozygous	51275447
13	53655627	53655647	AAAGAAAGAAAGAAAGAAAT	--------------------	13	GENIC	heterozygous	51275437
13	53656356	53656357	A	G	17	GENIC	heterozygous	51275439
13	53656635	53656636	T	G	19	GENIC	heterozygous	51275441
13	53656636	53656637	G	A	19	GENIC	heterozygous	51275443
13	53659982	53659983	G	A	12	GENIC	heterozygous	51275445
13	53660127	53660128	A	C	9	GENIC	heterozygous	51275448
13	53662508	53662509	G	C	16	GENIC	heterozygous	49950868
13	53662881	53662882	C	T	15	GENIC	heterozygous	51275450
13	53663000	53663001	G	A	11	GENIC	homozygous	49950869
13	53664237	53664238	G	A	13	GENIC	heterozygous	49950870
13	53664429	53664430	G	A	10	GENIC	heterozygous	51275452
13	53666292	53666293	C	T	9	GENIC	heterozygous	49950874
13	53666999	53667000	G	A	18	GENIC	homozygous	49950875
13	53668144	53668145	C	CT	11	GENIC	homozygous	49950876
13	53668362	53668363	C	T	12	GENIC	heterozygous	49950877
13	53668643	53668644	G	A	16	GENIC	heterozygous	49950878
13	53669152	53669153	G	A	16	GENIC	heterozygous	51275454
13	53670664	53670665	T	G	15	GENIC	heterozygous	49950880
13	53670687	53670698	ACAAGAGTAGC	-----------	12	GENIC	heterozygous	51275456
13	53670717	53670718	A	G	13	GENIC	heterozygous	51275458
13	53663683	53663684	A	-	10	GENIC	heterozygous	50230860