chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	37040153	37040154	C	T	30	GENIC	homozygous	115319400
12	37040167	37040168	A	G	27	GENIC	homozygous	115319402
12	37040225	37040226	C	A	28	GENIC	homozygous	115319404
12	37041280	37041281	G	A	33	GENIC	homozygous	115319406
12	37041291	37041292	G	A	30	GENIC	homozygous	115319408
12	37041812	37041813	A	G	31	GENIC	homozygous	115319410
12	37042607	37042608	G	C	22	GENIC	homozygous	115319412
12	37042619	37042620	T	C	32	GENIC	homozygous	115319414
12	37042755	37042756	T	C	33	GENIC	homozygous	115319416
12	37043591	37043592	A	G	19	GENIC	homozygous	115319418
12	37044057	37044058	C	T	34	GENIC	homozygous	115319420
12	37044727	37044728	G	A	31	GENIC	homozygous	115319422
12	37044884	37044885	A	G	29	GENIC	homozygous	115319424
12	37045781	37045782	T	C	29	GENIC	homozygous	115319426
12	37045805	37045806	A	G	27	GENIC	homozygous	115319428
12	37046045	37046046	G	A	31	GENIC	homozygous	115319430
12	37046292	37046293	T	C	32	GENIC	homozygous	115319432
12	37046294	37046295	T	A	32	GENIC	homozygous	115319434
12	37046303	37046304	T	C	34	GENIC	homozygous	115319436
12	37046312	37046313	G	A	33	GENIC	homozygous	115319438
12	37046398	37046399	C	T	36	GENIC	possibly homozygous	115319440
12	37047285	37047286	C	A	24	GENIC	homozygous	115319442
12	37047541	37047542	T	C	22	GENIC	homozygous	115319444
12	37047598	37047599	G	A	18	GENIC	homozygous	115319446