chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	163130223	163130224	C		43	GENIC	homozygous	131364397
4	163130238	163130238		A	40	GENIC	homozygous	131364398
4	163130246	163130246		G	40	GENIC	homozygous	131364399
4	163130254	163130255	G		38	GENIC	homozygous	131364400
4	163130269	163130270	T		38	GENIC	homozygous	131364401
4	163130282	163130283	G	A	39	GENIC	homozygous	131376380
4	163130283	163130284	A	G	39	GENIC	homozygous	113308463
4	163130305	163130305		G	44	GENIC	homozygous	129905246
4	163130309	163130310	T		42	GENIC	homozygous	129905247
4	163130352	163130353	G		28	GENIC	homozygous	128099483
4	163130363	163130363		C	27	GENIC	homozygous	128099484
4	163130367	163130368	G		26	GENIC	homozygous	128099485
4	163130372	163130373	T		23	GENIC	homozygous	128099486
4	163130386	163130388	AG		22	GENIC	homozygous	128099487
4	163130408	163130408		A	18	GENIC	homozygous	128099488
4	163130416	163130416		T	16	GENIC	homozygous	128099489
4	163130419	163130420	C		14	GENIC	homozygous	128099490
4	163130426	163130426		A	13	GENIC	homozygous	128099491
4	163130639	163130639		G	26	GENIC	homozygous	129905248
4	163130647	163130647		T	26	GENIC	homozygous	129905249
4	163130662	163130665	CGT		22	GENIC	homozygous	128099492
4	163130706	163130707	G		16	GENIC	homozygous	129905250
4	163130712	163130714	TG		14	GENIC	homozygous	129905251