chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	225165330	225165331	C	G	14	GENIC	homozygous	108556567
1	225166399	225166400	G	A	9	GENIC	homozygous	108556568
1	225166759	225166760	C	T	22	GENIC	homozygous	108556569
1	225166828	225166829	A	G	15	GENIC	homozygous	108556570
1	225166884	225166885	A	C	14	GENIC	homozygous	108556571
1	225166916	225166917	A	G	14	GENIC	homozygous	108556572
1	225167312	225167313	T		27	GENIC	possibly homozygous	127487517
1	225167606	225167607	G	A	25	GENIC	homozygous	108556573
1	225167947	225167948	T	A	23	GENIC	possibly homozygous	108556574
1	225168879	225168880	G	T	29	GENIC	homozygous	108556575
1	225168895	225168896	G	A	32	GENIC	homozygous	108556576
1	225170443	225170443		T	13	GENIC	possibly homozygous	127487518
1	225171390	225171390		TTA	18	GENIC	homozygous	127487519
1	225171763	225171764	C	A	10	GENIC	homozygous	108556577
1	225171920	225171920		AA	19	GENIC	homozygous	127487520
1	225172293	225172294	G	A	18	GENIC	homozygous	108556578
1	225172339	225172339		TGTGCT	19	GENIC	homozygous	127487521
1	225173060	225173061	C	T	31	GENIC	homozygous	108556579
1	225173061	225173062	C	G	30	GENIC	homozygous	108556580
1	225170344	225170345	A	T	5	GENIC	heterozygous	129861055