chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25495165654951657TC17GENIChomozygous109762925
25495172454951725CT16GENIChomozygous109762927
25495211454952115GA24GENIChomozygous109762929
25495405054954051CT18GENIChomozygous109762931
25495431954954320TC18GENIChomozygous109762933
25495499754954998AG20GENIChomozygous109762935
25495500554955005GATGATT19GENIChomozygous127624462
25495505354955054TC22GENIChomozygous109762937
25495560654955607TC19GENIChomozygous109762938
25495573854955739GA22GENIChomozygous109762940
25495581154955812AG24GENIChomozygous109762942
25495600654956007CT26GENIChomozygous109762944
25495609454956094TT24GENIChomozygous127624463
25495620854956209CT26GENIChomozygous109762946
25495722954957229A19GENIChomozygous127624464
25495750754957508AG26GENIChomozygous109762948
25495799254957993AG21GENIChomozygous109762950
25495811654958117GA21GENIChomozygous109762952
25495820954958211TC18GENICheterozygous127624466
25495837854958379GA13GENIChomozygous109762954
25495883554958836AG24GENIChomozygous109762956
25495889654958897AG24GENIChomozygous109762958
25495931954959320GA18GENIChomozygous109762960
25495986554959866TC17GENIChomozygous109762962
25496037454960375TG21GENIChomozygous109762964
25496039754960398CG19GENIChomozygous109762966
25496094454960945TC23GENIChomozygous109762968
25496148154961482TG6GENIChomozygous109762970
25496181754961818TC10GENIChomozygous109762972
25496185954961860GA7GENIChomozygous109762974
25496213054962131AT15GENIChomozygous109762976
25496237154962372AG11GENIChomozygous109762978
25496243554962436TA19GENIChomozygous109762980
25496287354962874AG20GENIChomozygous109762982
25496537154965372CA18GENICpossibly homozygous109762984
25496606054966068TTTCTTTT10GENIChomozygous127624467