chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	113531956	113531957	C	G	23	GENIC	homozygous	113557222
14	113533611	113533612	G	A	32	GENIC	homozygous	113557224
14	113539309	113539310	G	A	17	GENIC	homozygous	113891600
14	113539372	113539373	G	T	23	GENIC	homozygous	113891602
14	113541006	113541007	T	C	13	GENIC	homozygous	113557228
14	113541082	113541083	G	T	20	GENIC	homozygous	113557230
14	113541309	113541310	C	T	12	GENIC	homozygous	113557232
14	113541604	113541605	G	A	17	GENIC	homozygous	113891604
14	113544101	113544102	G	A	8	GENIC	homozygous	113557234
14	113544933	113544934	A	G	17	GENIC	homozygous	113557238
14	113544941	113544942	C	A	21	GENIC	homozygous	113557240
14	113545196	113545197	A	G	24	GENIC	homozygous	113557242
14	113547706	113547707	G	A	16	GENIC	homozygous	113557244
14	113549446	113549447	A	C	33	GENIC	homozygous	113557246
14	113554774	113554775	A	G	19	GENIC	heterozygous	113891606
14	113554778	113554779	A	G	20	GENIC	heterozygous	113891608
14	113554782	113554783	A	G	20	GENIC	heterozygous	113891610
14	113558117	113558118	A	T	16	GENIC	homozygous	113557254
14	113559595	113559596	G	A	12	GENIC	homozygous	113557256
14	113555237	113555238	G	A	8	GENIC	homozygous	113699697
14	113555238	113555239	T	C	8	GENIC	homozygous	113699699