chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	57601931	57601932	A	G	1	GENIC	homozygous	49956459
13	57601985	57601986	C	A	4	GENIC	heterozygous	49956460
13	57602551	57602552	G	T	9	GENIC	heterozygous	49956461
13	57604327	57604328	A	G	15	GENIC	homozygous	49956462
13	57604415	57604416	G	A	17	GENIC	possibly homozygous	49956463
13	57604900	57604903	CCT	---	7	GENIC	heterozygous	49956464
13	57604932	57604933	C	-	14	GENIC	homozygous	49956465
13	57604987	57604988	G	A	15	GENIC	possibly homozygous	49956466
13	57605098	57605099	A	G	9	GENIC	possibly homozygous	49956467
13	57605177	57605178	T	C	16	GENIC	homozygous	49956468
13	57605477	57605483	CTCTGG	------	1	GENIC	homozygous	49956469
13	57607321	57607322	A	G	7	GENIC	possibly homozygous	49956470
13	57607419	57607420	T	C	6	GENIC	heterozygous	49956471
13	57609602	57609603	C	T	24	GENIC	homozygous	49956472
13	57610694	57610695	G	T	21	GENIC	possibly homozygous	49956473
13	57616009	57616010	T	C	23	GENIC	homozygous	49956475
13	57616495	57616496	C	T	12	GENIC	heterozygous	49956476
13	57618252	57618253	T	-	3	GENIC	heterozygous	50431681
13	57618964	57618965	T	C	19	GENIC	possibly homozygous	49956478
13	57619780	57619781	A	AACATCTCT	1	GENIC	homozygous	49956479
13	57622879	57622880	T	C	12	GENIC	heterozygous	49956480
13	57619782	57619783	G	T	1	GENIC	homozygous	50495595