chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	80141999	80142000	A	G	57	GENIC	homozygous	109298279
1	80142658	80142659	C	T	69	GENIC	homozygous	109298281
1	80143876	80143877	G	A	53	GENIC	homozygous	109298283
1	80145242	80145243	C	T	52	GENIC	homozygous	109298285
1	80146189	80146190	G	A	47	GENIC	homozygous	109298287
1	80146818	80146818		C	36	GENIC	homozygous	131258295
1	80146955	80146956	C	A	25	GENIC	homozygous	108140126
1	80147005	80147006	C	A	21	GENIC	homozygous	108140127
1	80147387	80147389	TC		29	GENIC	homozygous	131258296
1	80147768	80147769	C	G	53	GENIC	homozygous	109298289
1	80147986	80147987	G	C	48	GENIC	homozygous	109298291
1	80148038	80148039	G	A	45	GENIC	homozygous	109298293
1	80150788	80150789	A	C	51	GENIC	homozygous	109298297
1	80150882	80150882		AT	40	GENIC	homozygous	131258298
1	80153053	80153054	A	C	60	GENIC	homozygous	109298299
1	80153111	80153112	G		45	GENIC	homozygous	131258299
1	80155869	80155870	G	A	60	GENIC	homozygous	109298301
1	80156047	80156048	G	A	45	GENIC	homozygous	109298303
1	80157395	80157396	G	C	61	GENIC	homozygous	109298305
1	80157793	80157799	AGAGGC		49	GENIC	homozygous	131258300
1	80158951	80158952	A		38	GENIC	homozygous	131258301
1	80159443	80159444	C	T	13	GENIC	homozygous	109298307
1	80159707	80159708	G	A	48	GENIC	homozygous	109298309
1	80159949	80159950	T	C	45	GENIC	homozygous	109298311
1	80144383	80144397	TGTGTGTGTGTGTC		18	GENIC	homozygous	131778832
1	80146566	80146567	T	C	55	GENIC	homozygous	120481167
1	80155250	80155251	A		4	GENIC	homozygous	130619272