chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141702831017028311CA10GENIChomozygous142431501
141702861017028611TC22GENIChomozygous139462033
141702885317028854CT20GENIChomozygous142431502
141702897917028980GA19GENIChomozygous403353399
141702897917028980G19GENICheterozygous403353400
141702898317028984GA19GENIChomozygous403353401
141702898317028984G19GENICheterozygous403353402
141702915917029160TC23GENIChomozygous142431503
141703025417030255CG8GENIChomozygous154827179
141703025417030255C8GENICheterozygous403353403
141703312917033130AC21GENICheterozygous154827180
141703312917033130A21GENIChomozygous403353405
141703442417034425GA17GENIChomozygous146552747
141703004217030043GA12GENIChomozygous146552744
141703025817030259CG8GENIChomozygous146552745
141703274417032745CA11GENIChomozygous146552746
141703561517035616GA26GENICheterozygous144117308
141703599517035996CA14GENIChomozygous142431509
141703630917036310AG22GENIChomozygous146552748
141703687917036880GA22GENIChomozygous146552749
141703751417037515TA25GENIChomozygous142431512
141703813917038140TC25GENIChomozygous139462041
141703830217038303CT19GENIChomozygous142431513
141703835017038351TC26GENIChomozygous142431514
141703868817038689CG19GENIChomozygous142431515
141703872017038721CT14GENIChomozygous142431516
141703873717038738TC10GENIChomozygous142431517
141703880617038807CA11GENIChomozygous142431518
141703890017038901TC30GENIChomozygous139462042
141703561817035619AG27GENICheterozygous144960040
141703499117034991CT17GENIChomozygous139381808
141703562017035620TGTAGTCATGG27GENICheterozygous146546793
141703902917039030CT19GENIChomozygous142431519
141703962517039626AG23GENIChomozygous142431520
141704017517040176GA25GENIChomozygous142431521
141704051717040518CA19GENIChomozygous142431522
141704061317040614CA14GENIChomozygous142431523