chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	117625282	117625290	TTCTTTCT		16	GENIC	homozygous	128635905
8	117628346	117628347	T	C	20	GENIC	homozygous	116672088
8	117629628	117629629	G	C	25	GENIC	homozygous	116672090
8	117633092	117633093	A	G	20	GENIC	homozygous	116672092
8	117634319	117634320	G	T	23	GENIC	possibly homozygous	116672094
8	117634975	117634979	GTGA		8	GENIC	homozygous	129951233
8	117635001	117635083	GTGTTTGTGAGTGTGTGTATGTGTGCTTGTGTGTGTATGTGTGTGTGAGTGTGTATGTGTGTGAGTGTGTGTGTATGTGTGA		15	GENIC	heterozygous	129951234
8	117635159	117635159		GT	20	GENIC	homozygous	129951235
8	117636502	117636503	T	C	22	GENIC	homozygous	116672098
8	117637700	117637700		CA	31	GENIC	homozygous	128635907
8	117638887	117638888	C	T	24	GENIC	homozygous	116672100
8	117639104	117639105	T	C	25	GENIC	homozygous	116672102
8	117639162	117639163	T	C	30	GENIC	homozygous	116672104
8	117639698	117639699	C	T	16	GENIC	homozygous	116672106
8	117640268	117640269	A	G	16	GENIC	homozygous	116672108
8	117640351	117640352	C		16	GENIC	homozygous	128635908
8	117640894	117640895	G	A	19	GENIC	homozygous	116672110
8	117640915	117640916	C	T	15	GENIC	homozygous	116672112
8	117640953	117640954	T	C	15	GENIC	homozygous	116672114
8	117641100	117641101	A	G	19	GENIC	homozygous	116672116
8	117642869	117642870	G	A	23	GENIC	homozygous	116672118
8	117643636	117643637	C	T	28	GENIC	homozygous	116672120
8	117644064	117644065	G	A	22	GENIC	homozygous	116672122
8	117644937	117644938	G	A	25	GENIC	homozygous	116672124
8	117645043	117645044	C	A	24	GENIC	homozygous	116672126
8	117645653	117645654	T	C	10	GENIC	homozygous	117005931
8	117645657	117645661	CCCC		5	GENIC	homozygous	128635909
8	117645950	117645951	G	T	24	GENIC	homozygous	116672130
8	117646161	117646162	G	C	16	GENIC	homozygous	116672132