chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13108385130108385131A27GENIChomozygous129095015
13108385141108385141C31GENIChomozygous129095016
13108385297108385301TAGC41GENIChomozygous129095017
13108391003108391004T38GENICheterozygous130691341
13108394858108394860AC24GENICheterozygous132420858
13108398849108398849CC2GENICheterozygous130691342
13108402062108402062A47GENIChomozygous129095029
13108409769108409771CA40GENICheterozygous134067421
13108430830108430830A32GENIChomozygous129095038
13108431675108431675T29GENIChomozygous129095039
13108433592108433593C23GENIChomozygous129095040
13108433596108433596CA23GENIChomozygous129095041
13108433599108433602TAA20GENIChomozygous129095042
13108433603108433607CCTC18GENIChomozygous129095043
13108433649108433649A20GENIChomozygous129095044
13108433717108433718A3GENIChomozygous129095045
13108433739108433740G2GENIChomozygous129095046
13108433754108433755G2GENIChomozygous129095047
13108433756108433757G2GENIChomozygous129095048
13108433765108433766G2GENIChomozygous129095049
13108434383108434384G2GENIChomozygous129095050
13108434391108434392C4GENIChomozygous129095051
13108434399108434400G5GENIChomozygous129095052
13108434408108434410GA6GENIChomozygous129095053
13108408379108408379GGGG6GENIChomozygous130419850
13108434090108434091AG4GENIChomozygous132344803
13108415534108415535G11GENICheterozygous130110003
13108434404108434405GT6GENIChomozygous114602258
13108434406108434407GC6GENIChomozygous114602260
13108433607108433608CG18GENIChomozygous114699927