chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	110220848	110220849	A	G	30	GENIC	homozygous	138413351
8	110221410	110221411	C	T	44	GENIC	homozygous	138413352
8	110222409	110222410	T	C	39	GENIC	homozygous	138413353
8	110222619	110222620	A	T	43	GENIC	homozygous	138413354
8	110222634	110222635	C	T	41	GENIC	homozygous	138413355
8	110223348	110223348		TCCT	14	GENIC	possibly homozygous	138264322
8	110223900	110223901	A	G	29	GENIC	homozygous	138413356
8	110224267	110224268	A	G	26	GENIC	homozygous	138413357
8	110224371	110224372	C	A	23	GENIC	homozygous	138413358
8	110225490	110225491	A	G	36	GENIC	homozygous	138413359
8	110226367	110226368	C	T	52	GENIC	homozygous	138413360
8	110227163	110227164	A	C	50	GENIC	homozygous	138413361
8	110227457	110227458	A	G	38	GENIC	homozygous	138413362
8	110229069	110229070	G	T	40	GENIC	homozygous	138413363
8	110229101	110229102	A	G	48	GENIC	homozygous	138413364
8	110229343	110229344	A	G	45	GENIC	homozygous	138413365
8	110229441	110229441		AA	27	GENIC	homozygous	138264325
8	110230216	110230217	T	C	42	GENIC	homozygous	138413366
8	110230481	110230482	A	G	32	GENIC	homozygous	138413367
8	110232268	110232284	AACCATGCACACCTGT		33	GENIC	homozygous	138264326
8	110232390	110232391	A	G	37	GENIC	homozygous	138413368
8	110232952	110232953	G	A	43	GENIC	homozygous	138413369
8	110234644	110234645	G	T	18	GENIC	homozygous	138413370
8	110229448	110229449	T		36	GENIC	heterozygous	403248979
8	110229448	110229449	T	A	36	GENIC	homozygous	154541840