chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1123958722123958723CA6GENIChomozygous60838001
1123959364123959365CT16GENICheterozygous60838004
1123959376123959377CCTG2GENIChomozygous60838005
1123960173123960174AG4GENICheterozygous60838007
1123960419123960420CA19GENICpossibly homozygous60838008
1123960841123960842GT22GENICpossibly homozygous60838009
1123961179123961180AG5GENICheterozygous60838010
1123963073123963074TC17GENIChomozygous60838011
1123964072123964073TC21GENICpossibly homozygous60838012
1123964339123964340TA12GENIChomozygous60838013
1123964509123964510AT15GENICpossibly homozygous60838014
1123964887123964888AC25GENICheterozygous60838015
1123967306123967307CA15GENICpossibly homozygous60838019
1123981812123981813TC2GENIChomozygous60838024
1123982091123982092GA11GENICpossibly homozygous60838025
1123982423123982424TC15GENIChomozygous60838026
1123982704123982705TC4GENICheterozygous60838027
1123984851123984852TG23GENICpossibly homozygous60838041
1123984890123984893TCT---16GENICheterozygous60838043
1123984934123984935CCT15GENICheterozygous60838045
1123985018123985019GT21GENIChomozygous60838048
1123985628123985629CT23GENIChomozygous60838073
1123990928123990929T-8GENIChomozygous60838083