chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14004228	14004229	C	CGAGTGAATACGAGCAAGATACAGTGATATGAAAGAG	9	GENIC	homozygous	53074817
10	14007903	14007904	C	T	26	GENIC	homozygous	51622557
10	14008199	14008200	A	G	10	GENIC	homozygous	51622558
10	14008443	14008444	A	C	31	GENIC	homozygous	51622559
10	14008631	14008632	T	C	29	GENIC	homozygous	51622560
10	14010708	14010709	G	GACACAC	7	GENIC	heterozygous	51622563
10	14012965	14012966	A	G	14	GENIC	homozygous	51622565
10	14013561	14013562	G	-	12	GENIC	homozygous	51622566
10	14013564	14013568	TTTG	----	13	GENIC	homozygous	51622568
10	14013865	14013866	T	C	23	GENIC	homozygous	51622569
10	14013945	14013946	T	C	20	GENIC	homozygous	51622570
10	14014220	14014221	A	T	6	GENIC	homozygous	51622572
10	14014236	14014237	A	ATTTTT	6	GENIC	homozygous	52481268
10	14014801	14014802	T	TA	16	GENIC	homozygous	51622574
10	14014802	14014803	T	A	16	GENIC	homozygous	51622575
10	14008220	14008221	G	GGGGC	6	GENIC	homozygous	51809980
10	14009815	14009816	T	G	27	GENIC	homozygous	51809982
10	14010222	14010223	C	T	24	GENIC	homozygous	51809984
10	14010708	14010709	G	GACACACAC	7	GENIC	possibly homozygous	51809986
10	14013746	14013747	A	G	14	GENIC	homozygous	51809988
10	14009813	14009814	G	T	25	GENIC	homozygous	52313036