chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	136007913	136007914	T	C	23	GENIC	homozygous	59100513
2	136026657	136026658	T	C	11	GENIC	homozygous	60145160
2	136026658	136026659	G	A	12	GENIC	homozygous	60145162
2	136026723	136026724	C	T	17	GENIC	homozygous	59100661
2	136027276	136027277	C	T	28	GENIC	homozygous	59100663
2	136027295	136027296	C	T	29	GENIC	homozygous	59858162
2	136031021	136031025	TTTA	----	22	GENIC	possibly homozygous	59858163
2	136031251	136031252	C	T	32	GENIC	homozygous	59858164
2	136031716	136031717	T	G	26	GENIC	homozygous	59858165
2	136032209	136032210	T	TTCCTGCCAGGCA	31	GENIC	homozygous	59858166
2	136032821	136032822	G	T	19	GENIC	homozygous	59858167
2	136035053	136035054	C	T	27	GENIC	homozygous	59858168
2	136036311	136036312	A	T	22	GENIC	homozygous	59100688
2	136036554	136036555	T	C	28	GENIC	homozygous	60145164
2	136036628	136036629	A	C	27	GENIC	homozygous	59100692
2	136010609	136010617	GTGTGTGT	--------	2	GENIC	homozygous	60543637