chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13108385130108385131A8GENIChomozygous129095015
13108385141108385141C10GENIChomozygous129095016
13108385297108385301TAGC12GENIChomozygous129095017
13108402062108402062A7GENIChomozygous129095029
13108415499108415500GC11GENIChomozygous132178412
13108423267108423268G3GENIChomozygous130110005
13108423299108423299C6GENIChomozygous130110006
13108423326108423326T8GENIChomozygous130110008
13108430830108430830A26GENIChomozygous129095038
13108431675108431675T14GENIChomozygous129095039
13108433592108433593C6GENIChomozygous129095040
13108433596108433596CA6GENIChomozygous129095041
13108433599108433602TAA6GENIChomozygous129095042
13108433603108433607CCTC6GENIChomozygous129095043
13108433649108433649A9GENIChomozygous129095044
13108433717108433718A1GENIChomozygous129095045
13108433739108433740G1GENIChomozygous129095046
13108433754108433755G1GENIChomozygous129095047
13108433756108433757G1GENIChomozygous129095048
13108433765108433766G1GENIChomozygous129095049
13108434383108434384G1GENIChomozygous129095050
13108434391108434392C1GENIChomozygous129095051
13108434399108434400G3GENIChomozygous129095052
13108434404108434405GT5GENIChomozygous114602258
13108434406108434407GC6GENIChomozygous114602260
13108434408108434410GA6GENIChomozygous129095053
13108433607108433608CG6GENIChomozygous114699927