chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	70164834	70164835	T	C	10	GENIC	possibly homozygous	113750444
14	70165380	70165381	T	C	27	GENIC	homozygous	113750446
14	70167327	70167328	T	C	13	GENIC	possibly homozygous	118785420
14	70167774	70167775	C	T	15	GENIC	homozygous	113750448
14	70168489	70168490	C	T	32	GENIC	homozygous	113750450
14	70169287	70169288	A	C	22	GENIC	homozygous	113750452
14	70169357	70169358	T	C	19	GENIC	homozygous	113750454
14	70169384	70169385	T	G	23	GENIC	homozygous	113750456
14	70169709	70169710	T	A	27	GENIC	homozygous	113750458
14	70170736	70170737	C	T	31	GENIC	homozygous	113750460
14	70170809	70170810	C	T	30	GENIC	homozygous	113750462
14	70171672	70171673	T	C	29	GENIC	homozygous	113750464
14	70172285	70172286	T	G	24	GENIC	homozygous	113750466
14	70172572	70172573	G	A	25	GENIC	homozygous	113750468
14	70172834	70172835	C	T	22	GENIC	homozygous	113750470
14	70173112	70173113	G	A	20	GENIC	homozygous	113750472
14	70173149	70173150	C	T	23	GENIC	homozygous	113750474
14	70173720	70173721	G	C	23	GENIC	homozygous	113750476
14	70173998	70173999	G	T	22	GENIC	homozygous	113750478
14	70174669	70174670	G	A	20	GENIC	homozygous	113750480
14	70175052	70175053	A	G	26	GENIC	homozygous	113750482
14	70175432	70175433	G	A	31	GENIC	homozygous	118785421
14	70175626	70175627	G	A	19	GENIC	homozygous	113750484
14	70175778	70175779	C	T	17	GENIC	homozygous	113750486
14	70175825	70175826	A	G	16	GENIC	homozygous	113750488
14	70175899	70175900	C	T	18	GENIC	homozygous	113750490
14	70176610	70176611	C	T	24	GENIC	homozygous	113750492
14	70176724	70176725	A	G	25	GENIC	homozygous	113750494
14	70176957	70176958	A	G	18	GENIC	homozygous	113750496
14	70177103	70177104	T	C	23	GENIC	homozygous	113750498
14	70177225	70177226	G	C	19	GENIC	homozygous	113750500
14	70177780	70177781	A	G	25	GENIC	homozygous	113750502
14	70176093	70176094	A	C	23	GENIC	possibly homozygous	113788295