chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	170447234	170447235	T	C	25	GENIC	homozygous	110124366
2	170447491	170447492	G	T	19	GENIC	homozygous	110124367
2	170447913	170447914	G	A	17	GENIC	homozygous	110124368
2	170448125	170448126	A	G	11	GENIC	homozygous	110124369
2	170448202	170448203	C	A	16	GENIC	homozygous	110124370
2	170450060	170450061	C	T	23	GENIC	homozygous	110124371
2	170451114	170451115	T	C	19	GENIC	homozygous	110124372
2	170452068	170452069	A	G	10	GENIC	homozygous	110124373
2	170452213	170452214	A	C	6	GENIC	homozygous	125595662
2	170455782	170455783	T	A	12	GENIC	homozygous	110124375
2	170455958	170455959	A	G	12	GENIC	homozygous	110124376
2	170455966	170455967	A	G	12	GENIC	homozygous	110124377
2	170456141	170456142	A	T	19	GENIC	homozygous	110124378
2	170456884	170456885	A	G	18	GENIC	homozygous	110124379
2	170457905	170457906	A	T	6	GENIC	homozygous	110124380
2	170458632	170458633	G	A	17	GENIC	homozygous	110124381
2	170458792	170458793	C	A	12	GENIC	homozygous	110124382
2	170459464	170459465	T	C	21	GENIC	homozygous	110124383
2	170459732	170459733	G	T	11	GENIC	homozygous	110124384
2	170452574	170452575	C	A	4	GENIC	heterozygous	125663433