chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	180938789	180938790	T	C	5	GENIC	heterozygous	110155247
2	180943237	180943238	A	G	9	GENIC	homozygous	110155252
2	180943890	180943891	T	G	8	GENIC	homozygous	110155253
2	180946612	180946613	T	C	11	GENIC	homozygous	110155255
2	180949860	180949861	G	A	6	GENIC	homozygous	110155256
2	180950178	180950179	G	C	10	GENIC	homozygous	110155257
2	180950477	180950478	T	C	20	GENIC	homozygous	110155258
2	180950646	180950647	T	C	6	GENIC	homozygous	110155259
2	180952509	180952510	G	A	10	GENIC	homozygous	110155263
2	180952924	180952925	A	G	12	GENIC	homozygous	110155264
2	180953164	180953165	G	T	19	GENIC	homozygous	110155267
2	180953254	180953255	C	T	23	GENIC	homozygous	110155268
2	180953487	180953488	T	C	14	GENIC	homozygous	110155269
2	180953787	180953788	A	G	11	GENIC	possibly homozygous	110155270
2	180956099	180956100	G	A	14	GENIC	homozygous	110155271
2	180957492	180957493	A	G	16	GENIC	homozygous	110155272
2	180957645	180957646	C	A	15	GENIC	homozygous	110155273
2	180959216	180959217	G	T	8	GENIC	homozygous	110155274
2	180959329	180959330	T	G	11	GENIC	homozygous	110155275
2	180959579	180959580	C	T	13	GENIC	homozygous	110155277
2	180959593	180959594	T	C	13	GENIC	homozygous	110155278
2	180960122	180960123	C	T	10	GENIC	homozygous	110155279
2	180960358	180960359	A	G	5	GENIC	homozygous	110155280
2	180962348	180962349	A	C	7	GENIC	possibly homozygous	110155284
2	180962817	180962818	T	C	12	GENIC	homozygous	110155286
2	180962859	180962860	T	C	10	GENIC	homozygous	110155287
2	180962999	180963000	A	G	15	GENIC	homozygous	110155288
2	180963174	180963175	C	G	9	GENIC	homozygous	110155289
2	180963205	180963206	A	G	7	GENIC	homozygous	110155290
2	180963558	180963559	A	G	9	GENIC	homozygous	110155291
2	180963559	180963560	C	T	9	GENIC	homozygous	110155292
2	180963598	180963599	C	T	8	GENIC	homozygous	110155293
2	180963731	180963732	C	T	9	GENIC	homozygous	110155294
2	180963739	180963740	G	A	9	GENIC	homozygous	110155295