chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14007903	14007904	C	T	21	GENIC	homozygous	51622557
10	14008199	14008200	A	G	17	GENIC	homozygous	51622558
10	14008220	14008221	G	GGGGC	20	GENIC	homozygous	51809980
10	14008443	14008444	A	C	14	GENIC	homozygous	51622559
10	14008631	14008632	T	C	22	GENIC	homozygous	51622560
10	14009815	14009816	T	G	20	GENIC	possibly homozygous	51809982
10	14010222	14010223	C	T	21	GENIC	homozygous	51809984
10	14010708	14010709	G	GACACAC	6	GENIC	heterozygous	51622563
10	14010708	14010709	G	GACACACAC	6	GENIC	heterozygous	51809986
10	14012490	14012491	C	T	5	GENIC	heterozygous	51982577
10	14012965	14012966	A	G	12	GENIC	homozygous	51622565
10	14013561	14013562	G	-	9	GENIC	homozygous	51622566
10	14013562	14013563	G	T	12	GENIC	heterozygous	51622567
10	14013564	14013568	TTTG	----	10	GENIC	heterozygous	51622568
10	14013746	14013747	A	G	12	GENIC	homozygous	51809988
10	14013865	14013866	T	C	15	GENIC	homozygous	51622569
10	14013945	14013946	T	C	12	GENIC	homozygous	51622570
10	14014220	14014221	A	T	6	GENIC	homozygous	51622572
10	14014801	14014802	T	TA	15	GENIC	homozygous	51622574