chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3114218778114218779CT63GENIChomozygous112140012
3114218996114218997C57GENIChomozygous127920053
3114219743114219744CG39GENIChomozygous121964739
3114219744114219745TC39GENIChomozygous121964740
3114219746114219747GC37GENIChomozygous121964741
3114219755114219756CT38GENIChomozygous112140013
3114221077114221078CT65GENIChomozygous112140014
3114224219114224220GT66GENIChomozygous112140015
3114219255114219256TC58GENIChomozygous111678488
3114220255114220256CT66GENIChomozygous111678489
3114223074114223075AG73GENIChomozygous111678490
3114223634114223635TC90GENIChomozygous111678491
3114223670114223671AG89GENIChomozygous111678492
3114224482114224483TC55GENIChomozygous111678494
3114219738114219739CT38GENIChomozygous112428890
3114223338114223338CAGCTTCCCCATGAGGG58GENIChomozygous130908375
3114225556114225557TC60GENIChomozygous112140016
3114225996114225997AG59GENIChomozygous112010063
3114227036114227036GAG47GENICpossibly homozygous127920054
3114227148114227149TC49GENIChomozygous112140017
3114227271114227272GA66GENIChomozygous112140018
3114229070114229071CT66GENIChomozygous112140019
3114229100114229101TC64GENIChomozygous111678496
3114229101114229102GA65GENIChomozygous112140020
3114230221114230222CT65GENIChomozygous112140021
3114230233114230234CT61GENIChomozygous112140022
3114231605114231606TC45GENIChomozygous111678499
3114231870114231871AG40GENIChomozygous111678500
3114232230114232231CT4GENIChomozygous119855173
3114233647114233648TC58GENICpossibly homozygous112140023
3114233751114233752CG56GENIChomozygous111678502
3114233758114233759TA54GENICheterozygous111678503
3114234051114234052TC107GENICheterozygous111678504
3114234303114234304GA53GENICheterozygous125865559
3114234637114234638AG43GENIChomozygous112140024
3114235582114235583AG48GENIChomozygous112010077
3114236206114236207GA61GENICpossibly homozygous112140025
3114236701114236702AG62GENIChomozygous112140026
3114237306114237307CG62GENIChomozygous112140027