chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173256579173256580CG66GENIChomozygous114293426
5173258056173258057AT61GENIChomozygous114293428
5173258235173258235A65GENIChomozygous130965212
5173258642173258642CGCA52GENIChomozygous130965213
5173258664173258666CG52GENIChomozygous130965214
5173259112173259112GT28GENICheterozygous130965215
5173259717173259718T63GENICpossibly homozygous130965216
5173260082173260082AT78GENIChomozygous130965217
5173260135173260136CA82GENIChomozygous114293430
5173260146173260147CT79GENIChomozygous114293432
5173260590173260591TC60GENIChomozygous114293434
5173261473173261473GT61GENIChomozygous130965218
5173261508173261509GA66GENIChomozygous114293436
5173261766173261767CG66GENIChomozygous114293438
5173261809173261810CT62GENIChomozygous114293440
5173263753173263754AG59GENIChomozygous114293442
5173264156173264156C74GENIChomozygous130965219
5173264932173264935GTG57GENIChomozygous130965220
5173265096173265099ATG68GENICpossibly homozygous130965221
5173265237173265238T66GENIChomozygous130965222
5173265416173265417GA70GENIChomozygous114293444
5173265745173265746AG63GENIChomozygous114293446
5173265749173265750CT66GENIChomozygous114293448
5173266182173266183AG57GENIChomozygous114293450
5173266544173266545GA56GENIChomozygous114293452
5173266632173266632T33GENICheterozygous130965223
5173260997173260998TG69GENIChomozygous114094562
5173265805173265806GA68GENIChomozygous114094566
5173261473173261474CT61GENIChomozygous118859209