chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5137268621137268622TC34INTERGENIChomozygous55744611
5137268982137268983GC28INTERGENIChomozygous55744612
5137268991137268992CA27INTERGENIChomozygous55744613
5137270894137270895GA12INTERGENIChomozygous55744614
5137271318137271319AG31INTERGENIChomozygous55744615
5137271547137271548TC23INTERGENICpossibly homozygous55744616
5137271608137271609AG25INTERGENIChomozygous55744617
5137271957137271958CT22INTERGENIChomozygous55744618
5137274127137274128CT20INTERGENIChomozygous55744619
5137275320137275321TA18INTERGENIChomozygous55744620
5137275921137275925TGAG----19INTERGENIChomozygous55744621
5137277788137277789AAG19INTERGENIChomozygous55744622
5137279260137279261AG15INTERGENIChomozygous55744623
5137280709137280710CT20INTERGENIChomozygous55744624
5137281762137281763C-12INTERGENIChomozygous55744625
5137282131137282132AAAT13INTERGENICheterozygous55744626
5137282132137282134AT--13INTERGENICheterozygous55901244
5137283150137283151AG22INTERGENIChomozygous55744627
5137286112137286113AG15INTERGENIChomozygous55744628
5137286222137286223CCG6INTERGENIChomozygous55744629
5137286698137286699TC11GENIChomozygous55744630
5137288213137288214GGGTGTGTGT4GENIChomozygous55744631
5137288441137288442AG26GENIChomozygous55744632
5137289661137289662GGTGAA12GENICheterozygous55744633
5137289661137289662GGTGAATGAA12GENICpossibly homozygous55744634
5137289890137289891TC22GENIChomozygous55744635
5137290464137290465CA35GENIChomozygous55744636
5137290514137290515CT26GENIChomozygous55744637
5137290522137290523GA24GENIChomozygous55744638
5137290550137290551GA23GENIChomozygous55744639
5137290572137290573CT25GENIChomozygous55744640
5137290573137290574CG24GENIChomozygous55744641
5137290581137290582CT27GENIChomozygous55744642