chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11242283	11242284	A	G	13	GENIC	homozygous	115415349
12	11242300	11242301	G	A	13	GENIC	homozygous	115361396
12	11243043	11243044	G	A	32	GENIC	homozygous	115415351
12	11243054	11243055	A	C	32	GENIC	homozygous	115415353
12	11243893	11243894	T	G	33	GENIC	homozygous	115254912
12	11243921	11243922	T	G	36	GENIC	homozygous	115415355
12	11244353	11244354	T	C	37	GENIC	homozygous	115415357
12	11244425	11244426	C	A	43	GENIC	homozygous	115415359
12	11244561	11244562	C	T	36	GENIC	homozygous	115415361
12	11244565	11244566	C	T	34	GENIC	homozygous	115415363
12	11244773	11244774	T	C	19	GENIC	homozygous	115445087
12	11244780	11244781	A	G	19	GENIC	homozygous	115254914
12	11244793	11244794	G	T	23	GENIC	homozygous	115445089
12	11244834	11244835	G	A	31	GENIC	homozygous	115361397
12	11244840	11244841	G	A	33	GENIC	homozygous	115415365
12	11244867	11244868	T	C	32	GENIC	homozygous	115415367
12	11245458	11245459	C	T	32	GENIC	homozygous	115415369
12	11245545	11245546	C	T	17	GENIC	homozygous	115415371
12	11245623	11245624	A	G	19	GENIC	homozygous	115415373
12	11245819	11245820	A	T	48	GENIC	homozygous	115415375
12	11246666	11246667	G	A	37	GENIC	homozygous	115415377
12	11246821	11246822	G	A	21	GENIC	homozygous	115254916
12	11248048	11248049	G	T	6	GENIC	homozygous	115653331
12	11248580	11248581	A	G	21	GENIC	homozygous	115415379
12	11249902	11249903	A	T	39	GENIC	homozygous	115415381