chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226692101226692102TC21GENIChomozygous110276932
2226693524226693525AG13GENIChomozygous110276941
2226693556226693557TC13GENIChomozygous110276943
2226693810226693811GA19GENIChomozygous110276945
2226702528226702529AG24GENIChomozygous110276962
2226706532226706533TA18GENIChomozygous120246021
2226706729226706730A19GENIChomozygous127743644
2226706852226706852TATTAAC18GENIChomozygous127743645
2226706854226706854TATTA17GENIChomozygous127743646
2226716280226716281AT20GENIChomozygous110828990
2226696654226696655CG19GENIChomozygous110828977
2226699696226699697CT15GENIChomozygous110828978
2226703554226703555CG21GENIChomozygous110828982
2226704195226704196CT22GENIChomozygous110828984
2226712216226712217AG20GENIChomozygous110828988
2226699208226699208A15GENIChomozygous131302329
2226713939226713939TTGG21GENIChomozygous131302330
2226702416226702417T20GENIChomozygous132809553
2226706734226706735GT20GENIChomozygous120131065
2226706854226706855GT17GENIChomozygous120131066
2226706849226706850CT17GENIChomozygous110627195
2226720375226720376TA8GENIChomozygous110828992
2226723234226723235GA18GENIChomozygous110828994
2226728906226728907AT6GENICheterozygous130275888
2226728948226728952AATA5GENICheterozygous130255137
2226730775226730776AG11GENIChomozygous110277031
2226731327226731328CA10GENIChomozygous110277035
2226732381226732382CT17GENIChomozygous110829000
2226734052226734053CT15GENIChomozygous120246022
2226734250226734251GA26GENIChomozygous110277037
2226734792226734793GT6GENIChomozygous110829002
2226734910226734911G9GENIChomozygous131302331
2226735847226735848CT11GENIChomozygous110829004
2226741628226741629GA23GENIChomozygous110829006