chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4212075588212075589AT34GENICheterozygous57615921
4212075641212075642GA20GENICheterozygous57615923
4212075708212075709TG32GENICheterozygous57073472
4212075713212075714AG34GENICheterozygous57073473
4212075721212075722CT38GENICheterozygous57073474
4212075734212075735TG42GENICheterozygous57073475
4212075735212075736TA42GENICheterozygous57073476
4212075747212075748GA44GENICheterozygous57073477
4212075755212075756CT45GENICheterozygous57615925
4212075815212075816CG54GENICheterozygous57073478
4212075957212075958TC24GENICheterozygous57073479
4212075982212075983CA21GENICheterozygous57073480
4212075988212075989AG21GENICheterozygous57073482
4212083529212083530GC85GENICheterozygous57616014
4212083616212083617CT56GENICheterozygous57616016
4212084178212084179TG36GENICheterozygous57616024
4212084182212084183TC34GENICheterozygous57616026
4212085245212085246GC18GENICheterozygous57616038
4212089389212089390CT30GENICheterozygous57616077
4212089432212089433CG37GENICheterozygous57616079
4212089442212089443GT35GENICheterozygous57616081
4212089447212089448TC32GENICheterozygous57616083