chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	39623959	39623960	G	A	21	GENIC	homozygous	112483797
15	39624297	39624298	C	T	28	GENIC	homozygous	112483799
15	39625884	39625885	C	G	35	GENIC	homozygous	112483801
15	39627886	39627887	A	T	26	GENIC	homozygous	112483803
15	39635573	39635574	T	A	10	GENIC	homozygous	112483807
15	39640764	39640765	T	G	30	GENIC	homozygous	112672830
15	39642994	39642995	A	T	18	GENIC	homozygous	112483813
15	39645113	39645114	T	C	28	GENIC	homozygous	112483815
15	39645755	39645756	T	C	33	GENIC	homozygous	112483817
15	39647672	39647673	C	A	26	GENIC	homozygous	112483819
15	39651595	39651596	C	T	23	GENIC	homozygous	112483821
15	39652277	39652278	C	T	31	GENIC	homozygous	112483823
15	39654009	39654010	A	G	23	GENIC	homozygous	112483825
15	39658687	39658688	A	G	17	GENIC	homozygous	112483827
15	39659561	39659562	C	A	27	GENIC	possibly homozygous	112483829
15	39664529	39664530	G	A	21	GENIC	heterozygous	112483831
15	39640823	39640824	A	G	14	GENIC	homozygous	112808142
15	39651631	39651632	G	A	15	GENIC	homozygous	112808144