chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	106480929	106480930	C	G	24	GENIC	homozygous	146263920
13	106481037	106481038	A	T	17	GENIC	homozygous	146263921
13	106482444	106482445	A	G	14	GENIC	homozygous	139371534
13	106482798	106482799	A		15	GENIC	homozygous	141096281
13	106483758	106483759	A	G	11	GENIC	homozygous	139371536
13	106483844	106483845	T	C	13	GENIC	homozygous	139371537
13	106484181	106484182	A	G	12	GENIC	homozygous	139371539
13	106484393	106484394	G	A	11	GENIC	homozygous	146263922
13	106484417	106484418	G	A	13	GENIC	homozygous	146263923
13	106484422	106484423	T	C	13	GENIC	homozygous	139371540
13	106487342	106487343	A	G	19	GENIC	homozygous	146263924
13	106487694	106487695	T	C	22	GENIC	homozygous	143597150
13	106487820	106487821	C	G	20	GENIC	homozygous	139371541
13	106487863	106487864	G	C	18	GENIC	homozygous	146263925
13	106488178	106488179	A	G	18	GENIC	homozygous	146263926
13	106488349	106488350	T	C	23	GENIC	homozygous	139371542
13	106488892	106488893	A	G	22	GENIC	homozygous	139371543
13	106489013	106489014	G	T	21	GENIC	homozygous	146263927
13	106489781	106489782	A	G	16	GENIC	homozygous	139371544
13	106489888	106489889	T	C	15	GENIC	homozygous	139371545
13	106484773	106484791	CCTCTCCCTCTTCCTCTT		10	GENIC	homozygous	146259643
13	106484784	106484785	T	C	10	GENIC	heterozygous	154796685
13	106487879	106487884	CCAGG		16	GENIC	homozygous	146259644
13	106484784	106484785	T		10	GENIC	homozygous	403849888
13	106493393	106493402	ATTAGGAAC		17	GENIC	homozygous	139192224
13	106494425	106494426	T		17	GENIC	homozygous	139192225