chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	13609615	13609616	G		16	GENIC	homozygous	144102609
14	13609911	13609912	G	A	30	GENIC	homozygous	144115369
14	13610187	13610188	C	T	26	GENIC	homozygous	144115370
14	13610195	13610196	C	T	26	GENIC	homozygous	144115371
14	13610200	13610201	G	A	26	GENIC	homozygous	144115372
14	13610584	13610585	G		19	GENIC	homozygous	139380186
14	13610687	13610688	T	A	32	GENIC	homozygous	139452652
14	13611490	13611491	C	T	28	GENIC	homozygous	139452654
14	13611515	13611516	G	A	28	GENIC	homozygous	139452655
14	13611533	13611534	G	T	28	GENIC	homozygous	144115373
14	13611679	13611680	C	T	25	GENIC	homozygous	144115374
14	13611743	13611744	C	G	24	GENIC	homozygous	139452658
14	13611853	13611854	C	T	22	GENIC	homozygous	144115375
14	13612588	13612589	G	A	17	GENIC	homozygous	144115376
14	13612973	13612974	T	C	26	GENIC	homozygous	139452661
14	13612995	13612996	C	T	23	GENIC	homozygous	144115377
14	13613143	13613144	C	T	26	GENIC	homozygous	144115378
14	13613365	13613365		CATCTTGC	19	GENIC	homozygous	139380187
14	13613464	13613465	C	T	19	GENIC	possibly homozygous	144115379
14	13613662	13613662		A	21	GENIC	homozygous	139380188