chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	118404266	118404267	G	C	23	GENIC	homozygous	52832247
8	118404612	118404615	GGT	---	28	GENIC	homozygous	52832248
8	118405006	118405007	T	-	9	GENIC	possibly homozygous	52832249
8	118405022	118405023	C	CT	6	GENIC	homozygous	52832250
8	118405111	118405112	T	A	20	GENIC	possibly homozygous	52832251
8	118405599	118405600	C	T	21	GENIC	homozygous	52832252
8	118405662	118405663	G	T	25	GENIC	possibly homozygous	52832253
8	118406400	118406401	G	A	25	GENIC	homozygous	52832254
8	118406572	118406573	A	G	32	GENIC	homozygous	52832255
8	118406689	118406690	A	T	30	GENIC	homozygous	52832256
8	118407154	118407155	G	A	23	GENIC	homozygous	52832257
8	118407302	118407303	T	C	27	GENIC	homozygous	52832258
8	118407392	118407393	T	C	25	GENIC	homozygous	52832259
8	118407458	118407459	A	G	30	GENIC	homozygous	52832260
8	118407464	118407465	C	A	35	GENIC	homozygous	52832261
8	118408057	118408058	A	G	21	GENIC	homozygous	52832262
8	118408583	118408584	C	CCAGGGTCTG	14	GENIC	homozygous	52832263
8	118408613	118408614	C	A	19	GENIC	homozygous	52832264
8	118408662	118408663	C	T	20	GENIC	homozygous	52832265
8	118409235	118409236	T	C	34	GENIC	homozygous	52832266