chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39258286	39258287	G	A	25	GENIC	homozygous	53268612
8	39262327	39262328	G	A	32	GENIC	possibly homozygous	53268613
8	39263035	39263036	T	C	29	GENIC	homozygous	53363195
8	39263278	39263282	AAAA	----	10	GENIC	heterozygous	53363196
8	39263279	39263282	AAA	---	10	GENIC	heterozygous	53377774
8	39263355	39263356	A	G	22	GENIC	homozygous	52590733
8	39263652	39263653	G	A	13	GENIC	homozygous	53268614
8	39264450	39264451	G	GT	20	GENIC	homozygous	52590756
8	39264469	39264470	T	C	12	GENIC	homozygous	52590757
8	39265392	39265393	A	G	21	GENIC	homozygous	52590769
8	39265890	39265891	C	CCGCG	16	GENIC	homozygous	53610683
8	39266256	39266257	C	T	32	GENIC	homozygous	53101557
8	39266876	39266877	A	G	38	GENIC	homozygous	52961991
8	39266899	39266900	G	GAA	17	GENIC	possibly homozygous	52961997
8	39267538	39267539	T	C	36	GENIC	homozygous	53268616
8	39268032	39268035	AAA	---	7	GENIC	homozygous	52962007
8	39268048	39268049	C	-	2	GENIC	homozygous	53377777
8	39269258	39269259	G	A	29	GENIC	possibly homozygous	53268618
8	39270255	39270256	G	GACAGACAC	12	GENIC	homozygous	53363197
8	39270849	39270850	G	A	28	GENIC	homozygous	53268619
8	39272797	39272798	C	T	28	GENIC	possibly homozygous	53268620
8	39269254	39269255	T	TTGAGGG	26	GENIC	heterozygous	53902216
8	39269255	39269256	C	CAGCCTGTACTTTCCTGA	26	GENIC	heterozygous	53902218
8	39269261	39269262	C	CCAGGCA	31	GENIC	heterozygous	53902220
8	39269265	39269266	C	CTTGGTTACAAG	32	GENIC	heterozygous	53902222