chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6120816173120816174G-19GENICheterozygous55534388
6120819153120819154GC38GENIChomozygous54966131
6120819506120819507GA34GENIChomozygous54845153
6120819623120819624C-36GENICheterozygous54678372
6120820312120820313CA28GENICheterozygous54678423
6120820316120820317TC30GENICheterozygous54678425
6120820321120820322GT30GENICheterozygous54678427
6120820560120820562TC--25GENICheterozygous55534394
6120820562120820563AATG22GENICheterozygous55534396
6120821283120821284GGT74GENICheterozygous54966149
6120821499120821500GA46GENICheterozygous54966167
6120821506120821507CT45GENICheterozygous54966169
6120821619120821620TG49GENICheterozygous54966173
6120821680120821681CCA34GENICheterozygous54678485
6120821705120821706CA37GENICheterozygous54966179
6120821712120821713AC38GENICheterozygous54966181
6120821729120821730AC43GENICheterozygous54966183
6120822020120822021GGC23GENICheterozygous56075378
6120822030120822031TC29GENIChomozygous54678489
6120822854120822855C-29GENICheterozygous55534398
6120822915120822916CG32GENICpossibly homozygous54966195
6120822925120822926AT33GENICheterozygous54966197