chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	143897818	143897819	A	G	6	GENIC	homozygous	126541605
7	143898110	143898111	C	T	9	GENIC	homozygous	126541606
7	143898896	143898897	T	A	11	GENIC	homozygous	126541608
7	143899130	143899131	T	G	2	GENIC	homozygous	126541609
7	143908992	143908993	C	T	12	GENIC	homozygous	126541628
7	143909021	143909022	G	A	13	GENIC	homozygous	126541629
7	143910312	143910313	C		13	GENIC	homozygous	128531515
7	143911772	143911772		AGAG	39	GENIC	homozygous	128531516
7	143913006	143913007	A	G	60	GENIC	homozygous	115944785
7	143911536	143911537	C	A	34	GENIC	homozygous	115944784
7	143909402	143909403	T	C	24	GENIC	homozygous	115944782
7	143909478	143909479	T	C	31	GENIC	homozygous	115944783
7	143913815	143913816	A	G	44	GENIC	homozygous	115944786
7	143914697	143914698	T		28	GENIC	homozygous	128531517
7	143916696	143916696		AGTGCCTCCAT	37	GENIC	homozygous	128531518
7	143919631	143919631		ATTA	44	GENIC	homozygous	128531519
7	143921070	143921070		TT	37	GENIC	homozygous	128531520