chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5169572826169572827GGTGTA20INTERGENICpossibly homozygous55838215
5169580561169580562TTCTTC22GENIChomozygous56085573
5169600987169600988GGC10GENIChomozygous55838218
5169603351169603352TTGGTTAAG6GENIChomozygous55838220
5169603524169603525GT30GENIChomozygous55838221
5169604179169604180T-25GENICheterozygous56085682
5169604195169604196AG35GENICpossibly homozygous55838222
5169609777169609778TTTC24INTERGENICheterozygous55838223
5169609801169609802AC43INTERGENICpossibly homozygous55838224
5169612310169612311CT17INTERGENICheterozygous55838225
5169618798169618800TA--17GENICheterozygous56085765
5169618867169618869GT--10GENICheterozygous56085768
5169618897169618899TG--13GENICheterozygous55838227
5169628539169628540TG36GENICheterozygous55838228
5169630329169630330GGA27GENICheterozygous55838230
5169632375169632376AAT6INTERGENICheterozygous55838231
5169635708169635709G-4INTERGENICheterozygous55838233
5169646348169646349AAT21GENICheterozygous55838234
5169653559169653560GGCTGGCCTC15GENIChomozygous55838235
5169654462169654463GGT5GENICheterozygous55838237
5169654463169654464T-5GENICheterozygous55838238