chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	147805155	147805156	T	C	39	GENIC	homozygous	114047380
5	147805333	147805334	A	C	38	GENIC	homozygous	114047382
5	147805883	147805884	G	A	50	GENIC	homozygous	114047384
5	147807611	147807612	T	C	35	GENIC	homozygous	114047386
5	147809187	147809188	A	G	41	GENIC	homozygous	114047388
5	147809815	147809816	C	G	21	GENIC	heterozygous	114047390
5	147810036	147810037	A	T	33	GENIC	homozygous	114047392
5	147810187	147810188	T	G	32	GENIC	homozygous	114047394
5	147810259	147810260	T	G	36	GENIC	homozygous	114047396
5	147810358	147810359	G	A	41	GENIC	homozygous	114047398
5	147810632	147810633	A	G	13	GENIC	heterozygous	114047400
5	147810641	147810642	G	A	12	GENIC	heterozygous	114047402
5	147810747	147810748	A	G	21	GENIC	heterozygous	114047406
5	147810756	147810757	A	G	31	GENIC	heterozygous	114153115
5	147811709	147811710	T	C	22	GENIC	homozygous	114047408
5	147811735	147811736	T	C	28	GENIC	homozygous	114047410
5	147811930	147811931	C	T	26	GENIC	homozygous	114153116
5	147811962	147811963	G	A	32	GENIC	homozygous	114153117
5	147812098	147812099	C	G	30	GENIC	homozygous	114153118