chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	37308419	37308420	T	C	38	GENIC	homozygous	142063888
8	37308732	37308733	G	A	39	GENIC	homozygous	148734558
8	37310705	37310706	C	T	29	GENIC	homozygous	142063891
8	37310779	37310780	C	G	30	GENIC	homozygous	148734559
8	37311465	37311561	AGTATAAACATTTTTTTTTTCTTTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAA		23	GENIC	homozygous	142022412
8	37312982	37313009	ATATGGCCCTTAAATGAAATGACTGAA		23	GENIC	homozygous	142022413
8	37313782	37313783	T	A	39	GENIC	homozygous	148734560
8	37314858	37314859	A	G	45	GENIC	homozygous	142063892
8	37315952	37315953	A	C	48	GENIC	homozygous	142063893
8	37316792	37316794	AC		36	GENIC	homozygous	142022414
8	37316830	37316831	G	A	40	GENIC	homozygous	142063894
8	37317086	37317087	A	G	48	GENIC	homozygous	142063895
8	37317190	37317193	TTT		31	GENIC	homozygous	142022416
8	37317975	37317976	C	T	51	GENIC	possibly homozygous	142063898
8	37318176	37318177	T	A	66	GENIC	homozygous	142063899
8	37311231	37311231		A	40	GENIC	homozygous	148731604
8	37317278	37317294	CTTCCTTTCTTCCTTT		24	GENIC	homozygous	148731605
8	37317312	37317315	TTC		24	GENIC	homozygous	148731606