chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115512383115512384CT27GENICheterozygous925281658
8115513030115513031CT6GENICheterozygous925281659
8115516330115516331CCG40GENICheterozygous925316046
8115518076115518077AG15GENICheterozygous925281660
8115519250115519251GA9GENICheterozygous925281661
8115523834115523835AG64GENICheterozygous925281662
8115527949115527950AC11GENICheterozygous925281663
8115527950115527951GA10GENICheterozygous925281664
8115541589115541590AAG6GENICheterozygous925316047
8115555931115555932CT22GENICheterozygous925281665
8115583690115583691CT7GENICheterozygous925281666
8115583713115583714C-7GENICheterozygous925316048
8115587025115587026CT20GENICheterozygous925281667
8115592854115592855AG15GENICheterozygous925281668
8115616477115616478AG10GENICheterozygous925281669
8115622529115622531CT--19GENICheterozygous925316049
8115626308115626309AT16GENICheterozygous925281670
8115632953115632954CT32GENICheterozygous925281671
8115639625115639626TA10GENICheterozygous925281672