chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42061086	42061087	A		40	GENIC	heterozygous	128991299
12	42107615	42107617	AG		19	GENIC	heterozygous	128991301
12	42115316	42115318	CG		18	GENIC	homozygous	128991302
12	42115324	42115325	A		18	GENIC	homozygous	128991303
12	42115327	42115327		T	18	GENIC	homozygous	128991304
12	42115332	42115333	C		18	GENIC	homozygous	128991305
12	42121034	42121034		G	14	GENIC	homozygous	128991306
12	42121066	42121067	T		13	GENIC	homozygous	128991307
12	42121074	42121075	A		14	GENIC	homozygous	128991308
12	42121086	42121086		A	14	GENIC	homozygous	128991309
12	42126535	42126535		T	33	GENIC	homozygous	128991311
12	42126550	42126550		T	36	GENIC	homozygous	128991312
12	42129449	42129451	CC		38	GENIC	homozygous	128991313
12	42129510	42129512	CC		43	GENIC	homozygous	128991314
12	42083614	42083615	G		16	GENIC	heterozygous	130688032
12	42117031	42117035	ACCC		8	GENIC	heterozygous	130688033
12	42117054	42117055	T	C	10	GENIC	heterozygous	130689646