chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	117574602	117574603	G	A	20	GENIC	homozygous	116672000
8	117574873	117574874	C	T	16	GENIC	homozygous	116988178
8	117575608	117575609	G	A	16	GENIC	homozygous	116672002
8	117576152	117576153	C	T	20	GENIC	homozygous	116672004
8	117579060	117579061	T	C	26	GENIC	homozygous	116988179
8	117579086	117579087	T	C	21	GENIC	homozygous	116672006
8	117580189	117580190	A	C	22	GENIC	homozygous	116672008
8	117580267	117580268	G	A	23	GENIC	homozygous	116672010
8	117581875	117581876	T	C	30	GENIC	homozygous	116672012
8	117582039	117582044	TCTAC		21	GENIC	homozygous	128635893
8	117582166	117582167	C	T	19	GENIC	homozygous	116672014
8	117584809	117584810	A	T	7	GENIC	possibly homozygous	116672016
8	117586169	117586170	C		23	GENIC	homozygous	128635894
8	117590581	117590582	T	G	22	GENIC	homozygous	116672018
8	117593787	117593787		ACGT	12	GENIC	homozygous	128635896
8	117596175	117596175		T	30	GENIC	homozygous	128635897
8	117596942	117596943	A	C	17	GENIC	homozygous	116672022
8	117597825	117597826	A	G	34	GENIC	homozygous	116672026
8	117597914	117597914		AT	19	GENIC	homozygous	129951232
8	117597975	117597976	C	T	7	GENIC	homozygous	117059134
8	117599006	117599007	A	G	20	GENIC	homozygous	116672028
8	117599030	117599031	A	G	24	GENIC	homozygous	116672030
8	117583254	117583255	G	A	24	GENIC	homozygous	117969001