chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261291743261291744CG34GENIChomozygous108629262
1261292391261292392CT52GENIChomozygous108629263
1261294747261294747TATCTTCATTTTTAAATTTTTTTTTTCTTTTTTTTTCTTTTTTTTCTGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTCGCTAGGCAAGCGCTCTACCGCTGAGCTAAATCCCCAACCCC33GENICheterozygous127507096
1261295212261295213GA39GENIChomozygous108629264
1261296768261296769GC47GENIChomozygous108629265
1261297145261297145G44GENIChomozygous127507097
1261298479261298480GA58GENIChomozygous108629266
1261299342261299343GA53GENIChomozygous108629267
1261301176261301177GA53GENIChomozygous108629268
1261301336261301337GA6GENIChomozygous108629269
1261301357261301363TGTGTT11GENIChomozygous127507098
1261301411261301412TA26GENIChomozygous108629270
1261302568261302569GA56GENIChomozygous108629271
1261302633261302634GA55GENIChomozygous108629272
1261302838261302839GA51GENIChomozygous108629273
1261303088261303089CT45GENIChomozygous108629274
1261303306261303307AG57GENIChomozygous108629275
1261303479261303480GA46GENIChomozygous108629276
1261303595261303596AG46GENIChomozygous108629277
1261303884261303885TC47GENICpossibly homozygous108629278
1261304135261304136GA49GENIChomozygous108629279
1261304255261304256TA45GENICpossibly homozygous108629280
1261304278261304279TG45GENICpossibly homozygous108629281
1261304622261304623GA44GENIChomozygous108629282
1261304858261304859AT33GENIChomozygous108629283
1261304978261304979GA21GENIChomozygous108629284
1261305061261305061A37GENIChomozygous127507099
1261305165261305171TTTTTG36GENIChomozygous127507100
1261305755261305755C37GENIChomozygous127507101
1261305864261305865AT43GENIChomozygous108629286
1261306633261306634GA33GENIChomozygous108629287
1261306652261306653TC29GENIChomozygous108629288
1261306760261306761CT21GENIChomozygous108629289
1261307072261307078AAATTA5GENIChomozygous127507102
1261307485261307486GT25GENIChomozygous108629291
1261308180261308181CT61GENIChomozygous108629292
1261309744261309744TCTT32GENIChomozygous127507104
1261309785261309786TC37GENICheterozygous109377023
1261310119261310120AG44GENICpossibly homozygous108629296
1261310633261310634GA47GENIChomozygous108629297
1261311281261311282AC45GENIChomozygous108629298
1261312340261312341GT42GENIChomozygous108629299
1261312557261312558TC54GENIChomozygous108629300
1261312846261312847CT60GENIChomozygous108629301
1261312949261312950GA60GENIChomozygous108629302
1261313962261313962T49GENICheterozygous132542968
1261314892261314893TA21GENIChomozygous108629303
1261314920261314921TA23GENIChomozygous108629304
1261303418261303422TGTA38GENICheterozygous131784719
1261315528261315528TC24GENIChomozygous127507105
1261316958261316959GT50GENIChomozygous108629305
1261317226261317227AG37GENIChomozygous108629306
1261318002261318002AGCTACCTTCAGATACACC47GENIChomozygous127507106
1261318007261318008A48GENIChomozygous127507107
1261318264261318265CT47GENIChomozygous108629307
1261319273261319277AATA49GENIChomozygous127507108