chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59165087	59165088	C	T	17	GENIC	homozygous	126704279
8	59166333	59166334	C	T	15	GENIC	homozygous	126704280
8	59166457	59166457		AA	11	GENIC	homozygous	130363041
8	59166589	59166590	G	T	20	GENIC	homozygous	126704281
8	59166932	59166933	A	G	24	GENIC	homozygous	126704282
8	59167202	59167209	GAGATGG		5	GENIC	heterozygous	131693691
8	59167388	59167388		C	15	GENIC	homozygous	128595532
8	59168799	59168800	A	G	17	GENIC	homozygous	130372306
8	59169560	59169560		AAAC	15	GENIC	homozygous	130363042
8	59170941	59170942	A	G	35	GENIC	homozygous	118145807
8	59177022	59177023	T	A	4	GENIC	homozygous	130372307
8	59171782	59171783	T	C	16	GENIC	homozygous	116511157
8	59175024	59175025	C	T	22	GENIC	homozygous	116511161
8	59175320	59175321	G	A	24	GENIC	homozygous	126704283
8	59176662	59176663	C	T	21	GENIC	homozygous	126704284
8	59177240	59177241	A	T	16	GENIC	homozygous	130372308
8	59177588	59177589	G	A	27	GENIC	homozygous	130372309
8	59177717	59177718	C	T	23	GENIC	homozygous	126704285
8	59179908	59179909	G	C	21	GENIC	homozygous	126704286
8	59180323	59180324	A		17	GENIC	homozygous	130363043
8	59180681	59180682	G	A	17	GENIC	homozygous	126704287
8	59180744	59180745	G	T	12	GENIC	homozygous	126704288
8	59180868	59180869	G	A	12	GENIC	homozygous	126704289
8	59181073	59181074	A	T	18	GENIC	homozygous	126704290
8	59181213	59181214	C	A	18	GENIC	homozygous	126704291
8	59181364	59181365	G	A	13	GENIC	homozygous	126704292
8	59181527	59181528	T	A	23	GENIC	homozygous	118145819
8	59181975	59181991	CTCTCTCTCTCTCTCC		17	GENIC	possibly homozygous	130363044
8	59182994	59182995	G	A	26	GENIC	homozygous	126704293
8	59183457	59183458	A	G	24	GENIC	homozygous	116511173