chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184024106740241068AAG13GENIChomozygous46426595
184024177140241772TG18GENIChomozygous46426596
184024184540241846CT23GENIChomozygous46426597
184024242140242425TATA----16GENIChomozygous46426598
184024244540242447TA--13GENIChomozygous46426599
184024255440242555GA33GENIChomozygous46426600
184024329440243295CA28GENIChomozygous46426601
184024467140244674AAA---24GENIChomozygous46426602
184024487640244877GA31GENIChomozygous46426603
184024548540245486AAT20GENICheterozygous46828006
184024554240245544GA--25GENIChomozygous46426604
184024637140246372GC24GENIChomozygous46426605
184024696040246961TTGGG3GENIChomozygous46426606
184024705040247051CCAA7GENICheterozygous46814598
184024789740248003AAAAATAGTGGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAGGGCCCTGGGTTCGATCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAA----------------------------------------------------------------------------------------------------------19GENIChomozygous46814600
184024810440248105A-25GENICpossibly homozygous46426619
184024846340248465CC--14GENICpossibly homozygous46814601
184024846440248465C-14GENICheterozygous46911611
184024860540248606A-37GENIChomozygous46426622
184024888340248884CT23GENIChomozygous46426623
184024889740248898CG23GENIChomozygous46426624
184024954640249553TGTGGTA-------7GENICheterozygous46845691
184024954840249553TGGTA-----7GENICpossibly homozygous46897135
184024961540249616G-15GENIChomozygous46426630
184024977340249774TTA19GENIChomozygous46426631
184025013240250133GA26GENIChomozygous46426633
184025040740250408AG29GENIChomozygous46426634
184025068640250687AG26GENIChomozygous46426636
184025214340252144TG35GENIChomozygous46426637
184025244740252448T-29GENICpossibly homozygous46591485
184025251840252519AG28GENIChomozygous46426639
184025298440252985AAT30GENIChomozygous46426640