chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	86922266	86922267	G	A	39	GENIC	homozygous	113607325
14	86922381	86922382	C	A	41	GENIC	homozygous	113607326
14	86922443	86922444	A	G	40	GENIC	homozygous	113607327
14	86922884	86922885	C	A	38	GENIC	homozygous	113607328
14	86922917	86922918	T	C	34	GENIC	homozygous	113607329
14	86923223	86923224	G	A	45	GENIC	homozygous	113607330
14	86923475	86923476	C	G	49	GENIC	homozygous	113607331
14	86923792	86923793	C	T	50	GENIC	homozygous	113607332
14	86923812	86923813	A	G	50	GENIC	homozygous	113607333
14	86924058	86924060	TA		31	GENIC	homozygous	132183424
14	86924646	86924647	G	A	44	GENIC	homozygous	113607334
14	86924123	86924124	A	G	42	GENIC	homozygous	118766463
14	86924161	86924162	C	T	39	GENIC	homozygous	118766464
14	86924693	86924694	G	A	51	GENIC	possibly homozygous	113680472
14	86926475	86926476	C	T	51	GENIC	homozygous	113607335
14	86931778	86931779	G	T	40	GENIC	homozygous	113607336
14	86932124	86932125	C	T	54	GENIC	homozygous	113607337
14	86932468	86932474	TCTCTG		38	GENIC	homozygous	132183425
14	86934534	86934535	C	T	64	GENIC	homozygous	113607338
14	86934715	86934716	T	C	48	GENIC	homozygous	113607339
14	86935557	86935558	G		45	GENIC	homozygous	132183426
14	86936060	86936061	C		49	GENIC	homozygous	132183427
14	86936579	86936580	A	G	42	GENIC	homozygous	113607340
14	86936732	86936733	G	A	49	GENIC	homozygous	113607341
14	86936796	86936797	T	C	47	GENIC	homozygous	113607342
14	86936892	86936916	GGGCTGTGTTTACATCGGTGGGAA		41	GENIC	homozygous	132183428
14	86936924	86936925	A	C	48	GENIC	homozygous	113607343
14	86937696	86937697	C	T	55	GENIC	homozygous	113607344
14	86937779	86937780	G	C	51	GENIC	homozygous	113607345
14	86937846	86937847	G	A	39	GENIC	homozygous	113607346
14	86938185	86938186	G	A	57	GENIC	homozygous	113607347
14	86938225	86938226	T	C	54	GENIC	homozygous	113607348
14	86938415	86938416	A	G	46	GENIC	homozygous	113607349
14	86938439	86938440	G	A	44	GENIC	homozygous	113607350
14	86939597	86939598	C	A	48	GENIC	homozygous	113607351