chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	130079514	130079515	G	T	29	GENIC	homozygous	111712153
3	130079915	130079916	A	C	16	GENIC	homozygous	119651648
3	130080661	130080662	T	A	24	GENIC	homozygous	111712155
3	130083042	130083043	T	C	31	GENIC	homozygous	111712157
3	130086685	130086686	A	G	18	GENIC	homozygous	111712159
3	130087161	130087162	G	A	37	GENIC	homozygous	111712161
3	130087719	130087720	C	A	21	GENIC	homozygous	111712163
3	130088608	130088609	A	C	21	GENIC	homozygous	111712165
3	130092214	130092215	A	G	39	GENIC	homozygous	111712167
3	130093077	130093078	C	T	12	GENIC	homozygous	111712169
3	130095662	130095663	G	A	34	GENIC	homozygous	111712173
3	130095689	130095690	T	G	32	GENIC	homozygous	111712175
3	130099186	130099187	T	C	44	GENIC	homozygous	111712179
3	130101150	130101151	C	T	35	GENIC	homozygous	111712185
3	130101151	130101152	C	T	35	GENIC	homozygous	111712187
3	130102225	130102226	T	C	16	GENIC	homozygous	111712189
3	130102226	130102227	G	A	17	GENIC	homozygous	111712191
3	130103570	130103571	A	C	30	GENIC	homozygous	111712193
3	130105417	130105418	T	C	27	GENIC	homozygous	111712207
3	130107784	130107785	T	G	33	GENIC	homozygous	111712209
3	130108347	130108348	C	T	34	GENIC	homozygous	111712211
3	130110536	130110537	G	A	23	GENIC	homozygous	111712213
3	130110538	130110539	G	A	24	GENIC	homozygous	111712215
3	130111565	130111566	T	G	20	GENIC	homozygous	111712217
3	130111853	130111854	G	A	19	GENIC	homozygous	111712219
3	130111949	130111950	T	G	12	GENIC	homozygous	112029020
3	130112362	130112363	C	A	39	GENIC	homozygous	111712221
3	130112531	130112532	C	G	39	GENIC	homozygous	111712223