chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25495165654951657TC16GENIChomozygous109762925
25495172454951725CT14GENIChomozygous109762927
25495429554954295A9GENICpossibly homozygous131601180
25495431954954320TC13GENIChomozygous109762933
25495499754954998AG18GENIChomozygous109762935
25495505354955054TC23GENIChomozygous109762937
25495560654955607TC17GENIChomozygous109762938
25495581154955812AG17GENIChomozygous109762942
25495600654956007CT20GENIChomozygous109762944
25495620854956209CT18GENIChomozygous109762946
25495750754957508AG27GENIChomozygous109762948
25495799254957993AG19GENIChomozygous109762950
25495811654958117GA15GENIChomozygous109762952
25495500554955005GATGATT17GENIChomozygous127624462
25495609454956094TT18GENIChomozygous127624463
25495722954957229A18GENIChomozygous127624464
25495820954958211TC24GENICpossibly homozygous127624466
25495837854958379GA23GENIChomozygous109762954
25495883554958836AG21GENIChomozygous109762956
25495889654958897AG17GENIChomozygous109762958
25495931954959320GA19GENIChomozygous109762960
25495986554959866TC27GENIChomozygous109762962
25496037454960375TG23GENIChomozygous109762964
25496039754960398CG23GENIChomozygous109762966
25496094454960945TC24GENIChomozygous109762968
25496148154961482TG9GENIChomozygous109762970
25496181754961818TC16GENIChomozygous109762972
25496185954961860GA13GENIChomozygous109762974
25496213054962131AT14GENIChomozygous109762976
25496237154962372AG6GENIChomozygous109762978
25496243554962436TA9GENIChomozygous109762980
25496287354962874AG24GENIChomozygous109762982
25496537154965372CA35GENIChomozygous109762984
25496607954966079TTTC11GENIChomozygous131601181
25495854454958545GA33GENIChomozygous120359096
25495917154959172CG28GENIChomozygous120359097
25496042254960423GA20GENIChomozygous120359098
25496196154961962AC9GENIChomozygous120359099