chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	14178096	14178096		C	12	GENIC	homozygous	129662156
20	14178104	14178104		C	12	GENIC	homozygous	129662157
20	14178135	14178136	T	C	13	GENIC	homozygous	119771297
20	14178194	14178195	A		15	GENIC	homozygous	129662158
20	14178268	14178268		T	6	GENIC	homozygous	129662159
20	14178280	14178280		CG	6	GENIC	homozygous	129662160
20	14178575	14178576	A		6	GENIC	homozygous	129662161
20	14178595	14178595		C	8	GENIC	homozygous	129662162
20	14178632	14178633	C		9	GENIC	homozygous	129662163
20	14178661	14178661		G	9	GENIC	homozygous	129662164
20	14178676	14178676		G	11	GENIC	homozygous	129662165
20	14178693	14178693		G	13	GENIC	homozygous	129662166
20	14178719	14178719		C	15	GENIC	homozygous	129662167
20	14178726	14178726		G	15	GENIC	homozygous	129662168
20	14178734	14178734		A	14	GENIC	homozygous	129662169
20	14178736	14178736		A	13	GENIC	homozygous	129662170
20	14188634	14188635	T	C	30	GENIC	heterozygous	109101033
20	14188693	14188694	G	C	37	GENIC	heterozygous	109101035
20	14189333	14189334	G		33	GENIC	heterozygous	129662182
20	14189334	14189335	C	T	33	GENIC	heterozygous	109101041
20	14189379	14189380	G	C	27	GENIC	heterozygous	109101043