chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	105207175	105207176	G	-	31	GENIC	heterozygous	61737349
1	105207176	105207177	G	A	55	GENIC	heterozygous	61737351
1	105207223	105207224	G	GACA	28	GENIC	heterozygous	61491696
1	105207501	105207502	A	T	40	GENIC	possibly homozygous	61491699
1	105207707	105207710	GGG	---	19	GENIC	homozygous	61491702
1	105207707	105207708	G	GT	23	GENIC	homozygous	61491703
1	105207713	105207714	G	GTAT	17	GENIC	homozygous	61491704
1	105207883	105207884	T	C	57	GENIC	homozygous	61737353
1	105209930	105209931	T	G	37	GENIC	heterozygous	62016717
1	105212116	105212117	C	T	48	GENIC	homozygous	61737355
1	105212957	105212958	A	G	43	GENIC	homozygous	61491720
1	105213674	105213675	C	T	41	GENIC	possibly homozygous	61737357
1	105213758	105213759	G	A	41	GENIC	possibly homozygous	61737359
1	105213915	105213916	T	G	28	GENIC	homozygous	61737361
1	105214154	105214155	A	-	18	GENIC	homozygous	61737363
1	105214252	105214253	A	G	41	GENIC	homozygous	61737365
1	105214335	105214336	G	A	39	GENIC	homozygous	61737367
1	105214416	105214417	C	T	41	GENIC	homozygous	61737369
1	105221107	105221108	T	TGACA	43	GENIC	homozygous	61491736
1	105214436	105214437	T	G	38	GENIC	homozygous	61737371
1	105215229	105215230	G	A	54	GENIC	homozygous	61737373
1	105219382	105219383	A	G	53	GENIC	homozygous	61737375
1	105219473	105219474	A	AGTGTGT	13	GENIC	heterozygous	61491734
1	105219473	105219474	A	AGTGT	13	GENIC	heterozygous	61491735
1	105212876	105212880	GATA	----	16	GENIC	homozygous	61299740
1	105214117	105214118	T	G	25	GENIC	heterozygous	60780738
1	105221125	105221126	G	A	58	GENIC	heterozygous	61491737
1	105222652	105222653	T	C	40	GENIC	possibly homozygous	61491739
1	105222773	105222774	G	C	46	GENIC	homozygous	61737377
1	105224362	105224363	T	C	51	GENIC	homozygous	61737379