chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	105207175	105207176	G	-	16	GENIC	heterozygous	61737349
1	105207501	105207502	A	T	9	GENIC	heterozygous	61491699
1	105207883	105207884	T	C	11	GENIC	heterozygous	61737353
1	105212116	105212117	C	T	16	GENIC	heterozygous	61737355
1	105212957	105212958	A	G	19	GENIC	heterozygous	61491720
1	105213674	105213675	C	T	10	GENIC	heterozygous	61737357
1	105213758	105213759	G	A	22	GENIC	heterozygous	61737359
1	105213915	105213916	T	G	11	GENIC	heterozygous	61737361
1	105214153	105214154	A	-	10	GENIC	heterozygous	62763278
1	105214252	105214253	A	G	15	GENIC	heterozygous	61737365
1	105214335	105214336	G	A	12	GENIC	heterozygous	61737367
1	105214416	105214417	C	T	8	GENIC	heterozygous	61737369
1	105214436	105214437	T	G	10	GENIC	heterozygous	61737371
1	105215229	105215230	G	A	14	GENIC	heterozygous	61737373
1	105219382	105219383	A	G	17	GENIC	heterozygous	61737375
1	105221107	105221108	T	TGACA	12	GENIC	heterozygous	61491736
1	105222120	105222121	C	CCTG	21	GENIC	heterozygous	62085484
1	105222652	105222653	T	C	25	GENIC	homozygous	61491739
1	105222773	105222774	G	C	17	GENIC	homozygous	61737377
1	105224362	105224363	T	C	20	GENIC	homozygous	61737379