chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31489543014895431GT6GENIChomozygous111453760
31493655214936552CATAGAGATGCTGGGATTACAGAACCTCGTGCTTGTATCACTGCACCCTGTTCACATGGCTTCTGGGGACCAGGACTCCGATTCTCGGTGAATTATATATGCGGAAGCACCCCATAGCACCAAGTCCCAGTCCCCGGTAGTCGATGTATTTAGATAGTTTTCTATAAAAAGGTCCTTAGG10GENICpossibly homozygous127852226
31497405714974059GG12GENIChomozygous130277571
31497401214974013C18GENIChomozygous130277567
31497401914974021TC17GENIChomozygous130277568
31497402814974028CC15GENIChomozygous130277569
31497404814974051CTT12GENIChomozygous130277570
31497401414974015CA18GENIChomozygous130285788
31497405214974053AC12GENIChomozygous130285789
31497406114974065TGGG12GENIChomozygous130277572
31499041014990411GT3GENIChomozygous119841014
31499041214990414CG3GENIChomozygous127852237
31499042614990426C1GENIChomozygous127852238
31499042914990429G1GENIChomozygous127852239
31499043214990433CG1GENIChomozygous119841015
31499043514990437GG1GENIChomozygous127852240
31499045014990450GT1GENIChomozygous127852241
31502066015020662GA5GENIChomozygous127852249
31502067015020671G4GENIChomozygous127852250
31502071415020715C10GENIChomozygous127852251
31502072015020720G13GENIChomozygous127852252
31502074415020748AGCC15GENIChomozygous127852253
31502075715020758A17GENIChomozygous127852254
31502077115020771GA18GENIChomozygous127852255
31502077615020777C18GENIChomozygous127852256
31502078015020785CTCGC19GENIChomozygous127852257
31502078915020789A20GENIChomozygous127852258
31499041914990420GT1GENIChomozygous119712242
31499044214990443GT1GENIChomozygous119647769
31502065015020651CG6GENIChomozygous127968610
31502066415020665GA4GENIChomozygous127968611
31502073915020740GT15GENIChomozygous127968612
31502074115020742GA15GENIChomozygous127968613
31502077815020779CT19GENIChomozygous127968614