chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123670346123670347AG3GENIChomozygous112447427
3123670811123670812GT6GENIChomozygous112447429
3123670969123670970GA5GENIChomozygous111692619
3123671415123671416TC2GENIChomozygous111692620
3123671489123671490TG3GENIChomozygous111692621
3123671700123671701GT7GENIChomozygous112447431
3123671761123671762GA4GENIChomozygous111692622
3123673686123673687TA4GENIChomozygous119869001
3123673702123673703AT8GENIChomozygous112027475
3123677173123677174TC4GENIChomozygous112447436
3123677206123677207TC5GENIChomozygous111692646
3123677390123677391TC7GENIChomozygous111692648
3123677579123677580TC6GENIChomozygous111692650
3123677792123677793AT3GENIChomozygous111692651
3123678427123678428TC7GENIChomozygous111692655
3123678614123678615AG6GENIChomozygous112447438
3123679915123679916TC6GENIChomozygous111692656
3123679974123679975GA9GENIChomozygous120084333
3123680687123680688TC2GENIChomozygous111692658
3123681627123681628AG8GENIChomozygous111692661
3123681869123681870TC8GENIChomozygous111692663
3123682104123682105TC4GENIChomozygous111692664
3123682320123682321TC9GENIChomozygous111692666
3123682934123682935GA5GENIChomozygous120084335
3123683337123683338AG4GENIChomozygous112447439
3123684451123684452GT8GENIChomozygous111692671
3123686097123686098TC2GENIChomozygous111692674
3123687334123687335GA4GENIChomozygous120084339