chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	37040153	37040154	C	T	27	GENIC	homozygous	115319400
12	37040167	37040168	A	G	26	GENIC	homozygous	115319402
12	37040225	37040226	C	A	23	GENIC	homozygous	115319404
12	37041280	37041281	G	A	41	GENIC	homozygous	115319406
12	37041291	37041292	G	A	39	GENIC	homozygous	115319408
12	37041812	37041813	A	G	35	GENIC	homozygous	115319410
12	37042607	37042608	G	C	42	GENIC	homozygous	115319412
12	37042619	37042620	T	C	48	GENIC	homozygous	115319414
12	37042755	37042756	T	C	46	GENIC	homozygous	115319416
12	37043591	37043592	A	G	49	GENIC	homozygous	115319418
12	37044057	37044058	C	T	34	GENIC	homozygous	115319420
12	37044727	37044728	G	A	39	GENIC	homozygous	115319422
12	37044884	37044885	A	G	47	GENIC	homozygous	115319424
12	37045781	37045782	T	C	32	GENIC	homozygous	115319426
12	37045805	37045806	A	G	34	GENIC	homozygous	115319428
12	37046045	37046046	G	A	42	GENIC	homozygous	115319430
12	37046292	37046293	T	C	30	GENIC	homozygous	115319432
12	37046294	37046295	T	A	31	GENIC	homozygous	115319434
12	37046303	37046304	T	C	32	GENIC	homozygous	115319436
12	37046312	37046313	G	A	34	GENIC	homozygous	115319438
12	37046398	37046399	C	T	17	GENIC	homozygous	115319440
12	37047285	37047286	C	A	35	GENIC	homozygous	115319442
12	37047541	37047542	T	C	32	GENIC	homozygous	115319444
12	37047598	37047599	G	A	34	GENIC	homozygous	115319446
12	37047011	37047011		G	32	GENIC	homozygous	128985566
12	37041940	37041940		GA	38	GENIC	homozygous	128985564
12	37044641	37044643	CA		40	GENIC	homozygous	128985565