chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40697264	40697265	G	GAA	7	GENIC	heterozygous	50204346
12	40697265	40697266	A	-	7	GENIC	heterozygous	50543733
12	40697505	40697509	ACAC	----	2	GENIC	homozygous	50543734
12	40697972	40697973	G	A	34	GENIC	homozygous	50422914
12	40698750	40698751	T	C	21	GENIC	homozygous	50204351
12	40699327	40699328	C	G	24	GENIC	homozygous	50422915
12	40699950	40699956	GAGGGG	------	4	INTERGENIC	homozygous	50422916
12	40701978	40701979	C	CA	16	INTERGENIC	homozygous	50204363
12	40701982	40701983	T	-	16	INTERGENIC	homozygous	50204364
12	40701984	40701985	T	C	15	INTERGENIC	homozygous	50204365
12	40702463	40702464	T	TAA	17	INTERGENIC	homozygous	50422917
12	40702468	40702469	G	A	17	INTERGENIC	homozygous	50543735
12	40703905	40703906	T	A	25	INTERGENIC	homozygous	50422918
12	40704330	40704331	T	G	24	INTERGENIC	homozygous	50422919
12	40704413	40704414	G	A	29	INTERGENIC	homozygous	50204375
12	40704576	40704577	C	T	12	INTERGENIC	homozygous	50422920
12	40704877	40704878	G	-	7	INTERGENIC	homozygous	50204376
12	40707206	40707207	T	TC	17	INTERGENIC	homozygous	50422921
12	40707463	40707464	G	A	25	INTERGENIC	homozygous	50422922
12	40707605	40707606	C	T	19	INTERGENIC	homozygous	50422923
12	40707622	40707623	G	A	18	INTERGENIC	homozygous	50422924
12	40707870	40707871	A	ATAGC	10	INTERGENIC	homozygous	50422926
12	40708142	40708143	C	CA	16	INTERGENIC	homozygous	50422927
12	40708783	40708784	G	C	29	INTERGENIC	homozygous	50422928
12	40708784	40708785	A	C	29	INTERGENIC	homozygous	50422929
12	40708832	40708833	T	TTTTTTTG	13	INTERGENIC	homozygous	50543736
12	40708835	40708836	C	T	20	INTERGENIC	homozygous	50512453
12	40708845	40708846	G	T	15	INTERGENIC	homozygous	50543737
12	40708941	40708942	T	C	35	INTERGENIC	homozygous	50422930
12	40709100	40709101	T	C	20	INTERGENIC	homozygous	50204379
12	40709254	40709255	C	T	27	INTERGENIC	homozygous	50422931