chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12692978	12692979	C	A	49	GENIC	homozygous	115570347
7	12693100	12693101	C	T	31	GENIC	homozygous	115570348
7	12693960	12693961	C	T	28	GENIC	homozygous	115570349
7	12694259	12694260	A	G	28	GENIC	homozygous	115570350
7	12694669	12694670	A	G	31	GENIC	homozygous	115570351
7	12695414	12695415	T	C	29	GENIC	homozygous	115570353
7	12695577	12695578	T	A	15	GENIC	homozygous	115570354
7	12695606	12695607	C	T	12	GENIC	homozygous	115570355
7	12696130	12696131	A	G	29	GENIC	homozygous	115570356
7	12696420	12696421	T	C	19	GENIC	homozygous	115570357
7	12696678	12696679	G	A	25	GENIC	homozygous	115570358
7	12697038	12697039	A	G	40	GENIC	homozygous	115570359
7	12697499	12697500	A	G	36	GENIC	homozygous	115570360
7	12698397	12698398	G	A	23	GENIC	homozygous	115570361
7	12698484	12698485	T	C	17	GENIC	homozygous	115570362
7	12699269	12699270	G	A	32	GENIC	homozygous	115570366
7	12699816	12699817	C	T	37	GENIC	homozygous	115570368
7	12700520	12700521	C	T	30	GENIC	homozygous	115570369
7	12701138	12701139	T	C	28	GENIC	homozygous	115570370
7	12702500	12702501	A	G	27	GENIC	homozygous	115570371
7	12702674	12702675	A	G	32	GENIC	homozygous	115570372
7	12702680	12702681	T	C	33	GENIC	homozygous	115570373
7	12702899	12702900	G	A	23	GENIC	homozygous	115570374
7	12703096	12703097	T	C	29	GENIC	homozygous	115570375
7	12703442	12703443	C	T	25	GENIC	homozygous	115570376
7	12704778	12704779	C	T	31	GENIC	homozygous	115570377
7	12705309	12705310	T	C	15	GENIC	homozygous	115570378
7	12706479	12706480	C	T	19	GENIC	homozygous	115570379
7	12706499	12706500	C	T	19	GENIC	homozygous	115570380
7	12706653	12706654	C	A	15	GENIC	homozygous	115570381
7	12707555	12707556	G	A	26	GENIC	homozygous	115570382