chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1123958470123958478ATATATAT--------14GENIChomozygous62155663
1123958722123958723CA17GENIChomozygous60838001
1123958966123958967AATGTCCCGAT31GENIChomozygous60838002
1123959376123959377CCTGTGTG17GENIChomozygous60838006
1123959599123959600A-31GENIChomozygous61513864
1123959084123959085T-21GENIChomozygous61513861
1123959538123959539TTA21GENIChomozygous61513863
1123959771123959772CT26GENIChomozygous61513865
1123960173123960174AG20GENIChomozygous60838007
1123961179123961180AG34GENIChomozygous60838010
1123962020123962021AG36GENIChomozygous61513866
1123962177123962178CCGT14GENICpossibly homozygous61513867
1123963073123963074TC24GENIChomozygous60838011
1123964072123964073TC20GENIChomozygous60838012
1123964339123964340TA29GENIChomozygous60838013
1123964509123964510AT38GENIChomozygous60838014
1123964887123964888AC21GENIChomozygous60838015
1123966654123966655AT20GENIChomozygous60838016
1123966719123966720A-14GENIChomozygous60838018
1123967306123967307CA33GENIChomozygous60838019
1123977181123977182GA28GENIChomozygous61513869
1123978376123978377TTAC7GENIChomozygous60838021
1123978402123978403AAACAC4GENICheterozygous60838022
1123978402123978403AAACACAC4GENICheterozygous62246175
1123981794123981795AT37GENIChomozygous61302794
1123981798123981799TA36GENIChomozygous61302795
1123981812123981813TC36GENIChomozygous60838024
1123982423123982424TC26GENIChomozygous60838026
1123982704123982705TC31GENIChomozygous60838027
1123984213123984214GT26GENIChomozygous60838028
1123984221123984222GT24GENIChomozygous60838029
1123984236123984237GT23GENIChomozygous60838030
1123984851123984852TG65GENICheterozygous60838041
1123984890123984893TCT---72GENICheterozygous60838043
1123984934123984935CCT58GENICheterozygous60838045
1123985018123985019GT39GENIChomozygous60838048
1123985628123985629CT28GENIChomozygous60838073
1123990563123990564CA34GENICpossibly homozygous61513873
1123990790123990791TC26GENIChomozygous61513874
1123990927123990928AAT32GENICpossibly homozygous61513875