chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2251861929251861930CT15GENIChomozygous110386673
2251861980251861981AG15GENIChomozygous110386675
2251862203251862204TG7GENIChomozygous110386679
2251864343251864344TC19GENIChomozygous125611498
2251864787251864788CT23GENIChomozygous110853306
2251865892251865893TC13GENIChomozygous110386697
2251866555251866556TC16GENIChomozygous110386699
2251867487251867488GT5GENIChomozygous110853308
2251868737251868738GA9GENIChomozygous110386701
2251868923251868924CT6GENIChomozygous110386703
2251870436251870437TA7GENICheterozygous110386709
2251874555251874556CA15GENIChomozygous110386715
2251875330251875331GA13GENIChomozygous110853310
2251878460251878461AG22GENIChomozygous110853312
2251879168251879169GT13GENIChomozygous110386719
2251879341251879342CT10GENIChomozygous110915137
2251879356251879357TC15GENICheterozygous110386721
2251880569251880570AG22GENIChomozygous110853316
2251880605251880606CT13GENIChomozygous110853318
2251880607251880608TC12GENIChomozygous110853320
2251882729251882730CA17GENIChomozygous110853324
2251884089251884090TG22GENIChomozygous110386743
2251884438251884439CG8GENIChomozygous110386746
2251884508251884509CT5GENIChomozygous110386748
2251884827251884828CT17GENIChomozygous110853328
2251884846251884847GT13GENIChomozygous110853330
2251885004251885005GT9GENIChomozygous110386754
2251885064251885065CA17GENIChomozygous110853332
2251885301251885302GA24GENIChomozygous110853334
2251886072251886073GT10GENICheterozygous110386762
2251886492251886493AG6GENIChomozygous110386766
2251887254251887255TC18GENIChomozygous110853336
2251887295251887296AG15GENIChomozygous110853338
2251887471251887472AG22GENIChomozygous110386770
2251889882251889883CT3GENICheterozygous110853340
2251890179251890180CT17GENIChomozygous110853344
2251892468251892469CT3GENICheterozygous110386800
2251894346251894347AG13GENIChomozygous110386806
2251866255251866256TG4GENICheterozygous125729296
2251890299251890300GT4GENICheterozygous125729297