chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	207155330	207155331	C	CTGG	12	GENIC	possibly homozygous	62202680
2	207155910	207155911	G	C	36	GENIC	homozygous	62202682
2	207156238	207156239	T	C	26	GENIC	homozygous	59354874
2	207158266	207158267	A	G	28	GENIC	possibly homozygous	62202684
2	207158966	207158967	G	C	23	GENIC	homozygous	59354877
2	207159585	207159586	C	T	22	GENIC	possibly homozygous	59354879
2	207159780	207159781	G	A	30	GENIC	homozygous	59930945
2	207160329	207160330	T	-	6	GENIC	homozygous	60825865
2	207163032	207163046	TCTCTCTCTCTCTC	--------------	6	GENIC	homozygous	62202688
2	207163387	207163388	T	C	32	GENIC	homozygous	62202690
2	207164055	207164065	AGAGAGAGAG	----------	11	GENIC	homozygous	62202692
2	207165379	207165380	C	CAA	4	GENIC	homozygous	61601509
2	207165540	207165541	G	T	24	GENIC	homozygous	62202694
2	207168320	207168321	C	T	25	GENIC	homozygous	62202696
2	207168943	207168945	AA	--	9	GENIC	possibly homozygous	62202698
2	207170466	207170467	G	A	37	GENIC	homozygous	62202700
2	207171693	207171694	T	C	23	GENIC	homozygous	62202702
2	207171710	207171711	T	C	24	GENIC	homozygous	62202704
2	207171725	207171726	A	G	32	GENIC	possibly homozygous	62202706
2	207173445	207173446	T	-	10	GENIC	possibly homozygous	62202708
2	207163683	207163684	T	TG	5	GENIC	homozygous	60758773
2	207173790	207173791	A	-	16	GENIC	homozygous	60514500