chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	110220848	110220849	A	G	39	GENIC	homozygous	138413351
8	110220964	110220965	G	A	14	GENIC	homozygous	144829719
8	110221947	110221948	C	A	52	GENIC	homozygous	144829720
8	110222409	110222410	T	C	69	GENIC	possibly homozygous	138413353
8	110222430	110222431	C	T	64	GENIC	possibly homozygous	144829721
8	110222634	110222635	C	T	58	GENIC	homozygous	138413355
8	110223608	110223609	G	A	41	GENIC	homozygous	154541831
8	110223900	110223901	A	G	53	GENIC	homozygous	138413356
8	110225490	110225491	A	G	48	GENIC	homozygous	138413359
8	110225561	110225562	G	A	55	GENIC	homozygous	142100502
8	110222858	110222859	G	A	76	GENIC	homozygous	142100499
8	110223608	110223609	G		41	GENIC	heterozygous	403248977
8	110223608	110223609	G	C	41	GENIC	heterozygous	403248978
8	110226367	110226368	C	T	59	GENIC	homozygous	138413360
8	110227163	110227164	A	C	61	GENIC	homozygous	138413361
8	110227457	110227458	A	G	60	GENIC	homozygous	138413362
8	110227473	110227474	C	T	58	GENIC	homozygous	142100503
8	110228816	110228817	G	A	49	GENIC	homozygous	144829722
8	110229101	110229102	A	G	50	GENIC	homozygous	138413364
8	110229343	110229344	A	G	51	GENIC	homozygous	138413365
8	110229448	110229449	T	A	39	GENIC	heterozygous	154541840
8	110229448	110229449	T		39	GENIC	possibly homozygous	403248979
8	110230481	110230482	A	G	62	GENIC	homozygous	138413367
8	110223348	110223348		TCCT	21	GENIC	possibly homozygous	138264322
8	110223569	110223571	TT		41	GENIC	homozygous	144814406
8	110229447	110229449	AT		37	GENIC	homozygous	142030621
8	110229839	110229840	T	C	65	GENIC	homozygous	142100505
8	110230216	110230217	T	C	62	GENIC	homozygous	138413366
8	110234599	110234599		G	48	GENIC	homozygous	144814407
8	110234638	110234638		G	48	GENIC	homozygous	144814408
8	110234644	110234645	G	T	50	GENIC	homozygous	138413370