chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119054689119054690CCGTGT4INTERGENICheterozygous54232158
7119054809119054817TATTTATT--------4INTERGENIChomozygous55361603
7119055128119055129GGTTC37INTERGENIChomozygous54080364
7119056013119056014AC32INTERGENIChomozygous54080365
7119058214119058216GT--9INTERGENICpossibly homozygous55030374
7119058660119058661CT30INTERGENIChomozygous55878312
7119060332119060333CCT32INTERGENICpossibly homozygous54232169
7119060638119060639TG28INTERGENIChomozygous54080372
7119060676119060680CCCT----25INTERGENIChomozygous54080373
7119060988119060989CT26INTERGENIChomozygous54080374
7119061805119061806CT23INTERGENIChomozygous54750688
7119062366119062367AG34INTERGENIChomozygous54750690
7119062556119062557AG34INTERGENIChomozygous54750692
7119063659119063660TG32INTERGENIChomozygous54080378
7119063979119064004TTTTTTTTTTTTTTTTTTTTTTTTT-------------------------15INTERGENICheterozygous55878314
7119065285119065286CT15INTERGENIChomozygous54750696
7119066563119066564AG10INTERGENIChomozygous54750698
7119066575119066576CCGGG7INTERGENIChomozygous54586959
7119067033119067034CA10INTERGENIChomozygous54750702