chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	170447018	170447019	C	T	27	GENIC	homozygous	110789071
2	170447234	170447235	T	C	30	GENIC	homozygous	110124366
2	170447913	170447914	G	A	20	GENIC	homozygous	110124368
2	170447988	170447989	A	G	28	GENIC	homozygous	110789072
2	170448125	170448126	A	G	30	GENIC	homozygous	110124369
2	170448202	170448203	C	A	24	GENIC	homozygous	110124370
2	170449617	170449618	G	A	23	GENIC	homozygous	110789073
2	170450060	170450061	C	T	21	GENIC	homozygous	110124371
2	170451114	170451115	T	C	20	GENIC	homozygous	110124372
2	170455782	170455783	T	A	26	GENIC	homozygous	110124375
2	170455958	170455959	A	G	36	GENIC	homozygous	110124376
2	170455966	170455967	A	G	36	GENIC	homozygous	110124377
2	170458385	170458386	C	T	34	GENIC	homozygous	110789074
2	170458792	170458793	C	A	27	GENIC	homozygous	110124382
2	170459464	170459465	T	C	30	GENIC	possibly homozygous	110124383
2	170461399	170461400	G	C	9	GENIC	homozygous	120179406
2	170461412	170461413	G	C	9	GENIC	homozygous	120179407
2	170461414	170461415	T	A	9	GENIC	homozygous	120179408
2	170461427	170461428	C	A	8	GENIC	homozygous	110124393
2	170461403	170461404	G	T	10	GENIC	homozygous	120128693