chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	105207175	105207176	G	-	19	GENIC	heterozygous	61737349
1	105207176	105207177	G	A	33	GENIC	heterozygous	61737351
1	105207223	105207224	G	GACA	19	GENIC	heterozygous	61491696
1	105207226	105207227	T	TA	16	GENIC	heterozygous	61491697
1	105207501	105207502	A	T	26	GENIC	homozygous	61491699
1	105207707	105207710	GGG	---	16	GENIC	homozygous	61491702
1	105207707	105207708	G	GT	19	GENIC	homozygous	61491703
1	105207713	105207714	G	GTAT	18	GENIC	heterozygous	61491704
1	105207883	105207884	T	C	35	GENIC	homozygous	61737353
1	105212116	105212117	C	T	25	GENIC	homozygous	61737355
1	105212957	105212958	A	G	20	GENIC	homozygous	61491720
1	105213674	105213675	C	T	42	GENIC	homozygous	61737357
1	105213758	105213759	G	A	38	GENIC	homozygous	61737359
1	105213915	105213916	T	G	19	GENIC	homozygous	61737361
1	105214154	105214155	A	-	16	GENIC	possibly homozygous	61737363
1	105214252	105214253	A	G	12	GENIC	homozygous	61737365
1	105214153	105214155	AA	--	16	GENIC	heterozygous	61954492
1	105214335	105214336	G	A	14	GENIC	homozygous	61737367
1	105214416	105214417	C	T	26	GENIC	homozygous	61737369
1	105214436	105214437	T	G	29	GENIC	homozygous	61737371
1	105214809	105214821	GTGTGTGTGTGT	------------	19	GENIC	heterozygous	61491722
1	105215229	105215230	G	A	13	GENIC	homozygous	61737373
1	105218072	105218073	C	CA	7	GENIC	heterozygous	61954501
1	105219382	105219383	A	G	28	GENIC	homozygous	61737375
1	105219473	105219474	A	AGTGTGT	4	GENIC	heterozygous	61491734
1	105219473	105219474	A	AGTGT	4	GENIC	heterozygous	61491735
1	105221107	105221108	T	TGACA	41	GENIC	homozygous	61491736
1	105222652	105222653	T	C	48	GENIC	homozygous	61491739
1	105222773	105222774	G	C	28	GENIC	homozygous	61737377
1	105224362	105224363	T	C	36	GENIC	homozygous	61737379
1	105212876	105212880	GATA	----	8	GENIC	homozygous	61299740