chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90958090	90958091	A	AG	23	GENIC	homozygous	51538783
10	90960440	90960441	C	T	36	GENIC	homozygous	52207218
10	90963310	90963311	G	C	22	GENIC	homozygous	52207220
10	90963374	90963375	G	C	32	GENIC	homozygous	51738354
10	90964012	90964016	AAAA	----	23	GENIC	homozygous	51538785
10	90964062	90964063	T	G	22	GENIC	homozygous	51538787
10	90965092	90965093	G	A	28	GENIC	homozygous	52207222
10	90965149	90965150	T	C	34	GENIC	homozygous	52207224
10	90965236	90965240	TTGT	----	26	GENIC	homozygous	52207226
10	90965577	90965578	T	TCA	21	GENIC	homozygous	52207228
10	90965616	90965617	T	TACACACACACACACACACAC	15	GENIC	homozygous	52397123
10	90964015	90964016	A	AGTG	12	GENIC	homozygous	52397115
10	90964017	90964018	A	T	23	GENIC	homozygous	52397117
10	90965013	90965014	C	CTGTGTG	11	GENIC	heterozygous	52397119
10	90965013	90965014	C	CTGTGTGTG	11	GENIC	heterozygous	52397121
10	90966365	90966366	G	GT	8	GENIC	possibly homozygous	52323279
10	90966431	90966432	C	CT	2	GENIC	heterozygous	51538788
10	90966997	90966998	A	-	9	GENIC	homozygous	51738378
10	90967787	90967788	G	A	26	GENIC	homozygous	52207232
10	90967887	90967888	T	C	35	GENIC	homozygous	52207234
10	90967951	90967952	T	G	26	GENIC	homozygous	51538789
10	90968077	90968078	A	G	28	GENIC	homozygous	51738381