chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	80383775	80383776	A	G	19	GENIC	homozygous	120144214
2	80383783	80383784	T	G	16	GENIC	homozygous	120125217
2	80384086	80384087	C	T	14	GENIC	homozygous	120125218
2	80384087	80384088	T	C	14	GENIC	homozygous	120125219
2	80384817	80384818	G	A	19	GENIC	homozygous	110713633
2	80384997	80384998	T	C	13	GENIC	homozygous	109874610
2	80384025	80384026	G	A	13	GENIC	homozygous	109874606
2	80384343	80384344	T	G	25	GENIC	homozygous	109874608
2	80388246	80388247	G	C	26	GENIC	homozygous	109874614
2	80390658	80390659	G	A	30	GENIC	homozygous	109874616
2	80392079	80392080	G	A	20	GENIC	homozygous	110713635
2	80394032	80394033	T	C	21	GENIC	homozygous	110713638
2	80394327	80394328	A	C	20	GENIC	homozygous	110713640
2	80394350	80394351	T	G	22	GENIC	homozygous	109874622
2	80395044	80395045	G	A	16	GENIC	homozygous	110713642
2	80395193	80395194	C	T	23	GENIC	homozygous	110713644
2	80395304	80395305	A	G	15	GENIC	homozygous	110713645
2	80395555	80395556	A	C	16	GENIC	homozygous	110713647
2	80396550	80396551	G	A	10	GENIC	homozygous	110713649
2	80396551	80396552	C	T	10	GENIC	homozygous	110713651
2	80398272	80398273	C	A	23	GENIC	homozygous	110713652
2	80398581	80398582	C	A	31	GENIC	homozygous	110713654
2	80399192	80399193	C	A	23	GENIC	homozygous	110713656
2	80399526	80399527	C	T	35	GENIC	homozygous	110713658
2	80399557	80399558	A	G	35	GENIC	homozygous	109874630
2	80401850	80401851	C	T	10	GENIC	homozygous	110713660
2	80402672	80402673	C	T	25	GENIC	homozygous	109874632
2	80403855	80403856	T	A	16	GENIC	possibly homozygous	110713669
2	80404628	80404629	C	T	22	GENIC	homozygous	109874636
2	80408648	80408649	T	C	11	GENIC	homozygous	109874656