chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2209990830209990831CT18INTERGENIChomozygous59364006
2209990861209990862AG21INTERGENIChomozygous60342832
2209991010209991011CCCACA14INTERGENIChomozygous60342834
2209991133209991134TG28INTERGENICheterozygous60232495
2209991154209991155CT51INTERGENICheterozygous59364007
2209991188209991189GA73INTERGENICheterozygous59364008
2209991231209991232AG102INTERGENICheterozygous59364009
2209991264209991265TC144INTERGENICheterozygous59772144
2209991267209991268GT97INTERGENICheterozygous59933327
2209991267209991268GA136INTERGENICheterozygous60159388
2209991437209991438TA184INTERGENICheterozygous59364011
2209991468209991469TC157INTERGENICheterozygous60342836
2209991567209991568CG28INTERGENIChomozygous59364012
2209991652209991653GT55INTERGENICheterozygous60342838
2209991926209991927CT50INTERGENIChomozygous59772145
2209991927209991928AG51INTERGENIChomozygous59772146
2209992106209992107CT40INTERGENICpossibly homozygous60342840
2209992124209992125C-20INTERGENICheterozygous60342842
2209992215209992216A-2INTERGENIChomozygous59364020
2209992350209992351AG4INTERGENIChomozygous60342844
2209992541209992542GC17INTERGENIChomozygous60342846
2209992736209992737GA72INTERGENICheterozygous60342848
2209992750209992751GA61INTERGENICpossibly homozygous60342850