chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50140469	50140470	G	A	32	GENIC	homozygous	116815382
8	50140919	50140920	A	T	19	GENIC	homozygous	116815384
8	50141637	50141638	A	G	20	GENIC	homozygous	116815386
8	50144282	50144283	C	T	23	GENIC	homozygous	116815388
8	50145831	50145832	T		16	GENIC	homozygous	130361719
8	50145832	50145833	T	G	16	GENIC	homozygous	117927958
8	50145835	50145835		CCT	16	GENIC	homozygous	130361720
8	50145904	50145905	A	G	22	GENIC	homozygous	116815392
8	50147252	50147253	C	T	26	GENIC	homozygous	116815394
8	50147870	50147871	A	G	31	GENIC	homozygous	116815396
8	50151350	50151351	G	A	20	GENIC	homozygous	116815398
8	50151558	50151559	C	T	24	GENIC	homozygous	116815400
8	50151949	50151950	C	A	15	GENIC	homozygous	116815402
8	50151955	50151956	C	G	14	GENIC	homozygous	116815404
8	50153184	50153264	TGGGGTACACTCTAGGATGAAATGTTAGAACTCTGGCTCCTGGGGTACACTCTAGGAGGAGATATTAGAACTGTGGCTCT		4	GENIC	homozygous	130361721
8	50153611	50153612	G	A	22	GENIC	homozygous	116815414
8	50153978	50153979	G	A	26	GENIC	homozygous	116815416
8	50154824	50154825	A	G	24	GENIC	homozygous	116815418
8	50156314	50156315	A	G	26	GENIC	homozygous	116815420
8	50158325	50158326	T	C	32	GENIC	homozygous	116815422
8	50159066	50159067	G	A	24	GENIC	homozygous	116815424
8	50159196	50159197	G	C	16	GENIC	homozygous	116815426
8	50159318	50159319	C	T	21	GENIC	homozygous	116815428
8	50160037	50160038	C	T	28	GENIC	homozygous	116815430