chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	221152841	221152842	A	G	11	GENIC	homozygous	136482013
2	221153641	221153642	G	A	19	GENIC	homozygous	141443602
2	221154342	221154343	A	G	25	GENIC	homozygous	136482016
2	221155950	221155951	G	A	12	GENIC	homozygous	141443603
2	221154544	221154545	T		9	GENIC	possibly homozygous	141338720
2	221157527	221157528	C	A	18	GENIC	homozygous	136482024
2	221158068	221158069	T	C	22	GENIC	homozygous	136482025
2	221159686	221159687	G	C	23	GENIC	homozygous	141443604
2	221160963	221160964	A		17	GENIC	homozygous	141338721
2	221163059	221163060	T	C	9	GENIC	homozygous	136482026
2	221164104	221164114	GGCTGCTGCA		17	GENIC	homozygous	141338722
2	221164322	221164323	T	C	17	GENIC	homozygous	136482027
2	221164374	221164375	C	T	16	GENIC	homozygous	141443605
2	221165478	221165479	A	T	17	GENIC	homozygous	136482029
2	221166248	221166249	C	T	22	GENIC	homozygous	141443606
2	221166601	221166602	T	C	8	GENIC	homozygous	136482031
2	221167156	221167157	G	A	7	GENIC	homozygous	141443607
2	221167436	221167437	T	C	14	GENIC	homozygous	136482032
2	221168470	221168471	A	G	13	GENIC	homozygous	136482034
2	221170477	221170478	C	T	15	GENIC	homozygous	136482037
2	221171437	221171438	A	G	15	GENIC	homozygous	136482038
2	221173147	221173148	T	C	16	GENIC	homozygous	136482039
2	221173206	221173207	A	G	18	GENIC	homozygous	141443608
2	221174337	221174338	G	A	13	GENIC	homozygous	141443609
2	221174632	221174633	T	A	16	GENIC	homozygous	141443610
2	221175033	221175034	C	G	11	GENIC	homozygous	141443611
2	221175208	221175209	C	T	14	GENIC	homozygous	136482040
2	221175248	221175249	T		16	GENIC	homozygous	141338723
2	221175249	221175250	C	A	16	GENIC	homozygous	141443612