chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115512383115512384CT18GENICheterozygous924921565
8115513030115513031CT14GENICheterozygous924921566
8115516330115516331CCG79GENICheterozygous924957294
8115518076115518077AG29GENICheterozygous924921567
8115519250115519251GA13GENICheterozygous924921568
8115523834115523835AG45GENICheterozygous924921569
8115527949115527950AC10GENICheterozygous924921570
8115527950115527951GA10GENICheterozygous924921571
8115539897115539898TTG14GENICheterozygous924957295
8115541589115541590AAG18GENICheterozygous924957296
8115555931115555932CT57GENICheterozygous924921572
8115583690115583691CT20GENICheterozygous924921573
8115583713115583714C-20GENICheterozygous924957297
8115587025115587026CT27GENICheterozygous924921574
8115592854115592855AG18GENICheterozygous924921575
8115616477115616478AG25GENICheterozygous924921576
8115622529115622531CT--15GENICheterozygous924957298
8115626308115626309AT13GENICheterozygous924921577
8115632953115632954CT40GENICheterozygous924921578
8115639625115639626TA14GENICheterozygous924921579