chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101372412113724122AG5INTERGENIChomozygous51621980
101372521713725218AACAAT16INTERGENICpossibly homozygous51621982
101372576113725762AAG4INTERGENICheterozygous51621983
101372960113729602AACC1INTERGENIChomozygous51621987
101373105113731052CT18GENICheterozygous51621994
101373113113731132T-8GENIChomozygous51621995
101373143913731440TC14GENIChomozygous51621996
101373150113731502TG15GENIChomozygous51621997
101373311813733120TT--1GENIChomozygous51621998
101373438613734387GA24GENICpossibly homozygous51621999
101373616613736167AC5GENICheterozygous52313016
101373688613736887TTGG1GENIChomozygous51622006
101373690513736906G-9GENIChomozygous51622007
101373691513736916CT14GENIChomozygous51622008
101373707913737080AAG27GENIChomozygous51622009
101373711613737117CA19GENICpossibly homozygous51622010
101373735813737359TTA17GENICpossibly homozygous51622011
101373811513738116AAT5GENICheterozygous51622012
101373880113738802TC27GENICpossibly homozygous51622013
101373941713739418G-3GENIChomozygous51622014
101374088913740890TC20GENIChomozygous51622015
101374318413743185AT17GENICpossibly homozygous51622016
101374334113743342CT24GENIChomozygous51622017
101374505213745053TTTTTTTTTG2GENICheterozygous51622018
101374639613746397CT33GENICpossibly homozygous52992485
101374799413747995TC16GENIChomozygous51622022
101375176813751769AG18GENIChomozygous51622023
101375196813751969CCA5GENICheterozygous51622025
101375237413752375AG21GENIChomozygous51622026
101375255713752558GA19GENIChomozygous51622027
101375585413755855TC22GENICpossibly homozygous51622028
101375814513758146AG14GENICpossibly homozygous51622029
101376487513764876AG22GENICpossibly homozygous51809499
101376498513764986TC9GENICpossibly homozygous51622030
101376499213764993AC14GENICpossibly homozygous51622031
101376841113768412AG4GENICheterozygous51622033
101377398113773982TC9GENICpossibly homozygous51622034
101377485413774855GC25GENIChomozygous51622035
101377953613779537TC17GENICheterozygous51622036