geneid | 389643 |
---|---|
ensemblid | ENSG00000189233.12 |
hgncid | 33550 |
symbol | NUGGC |
name | nuclear GTPase, germinal center associated |
refseq_nuc | NM_001010906.2 |
refseq_prot | NP_001010906.1 |
ensembl_nuc | ENST00000413272.7 |
ensembl_prot | ENSP00000408697.2 |
mane_status | MANE Select |
chr | chr8 |
start | 28021964 |
end | 28083936 |
strand | - |
ver | v1.2 |
region | chr8:28021964-28083936 |
region5000 | chr8:28016964-28088936 |
regionname0 | NUGGC_chr8_28021964_28083936 |
regionname5000 | NUGGC_chr8_28016964_28088936 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 796 | 151 | 23 | 35 | 68 | 9 | 15 | 52 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002 | 0/0 | 796 | 82 | 27 | 11 | 32 | 3 | 9 | 26 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003 | 0/0 | 796 | 64 | 3 | 11 | 43 | 3 | 4 | 35 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004 | 0/0 | 796 | 60 | 6 | 11 | 29 | 2 | 12 | 21 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005 | 0/0 | 796 | 8 | 6 | 1 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0006 | 0/0 | 796 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0007 | 0/0 | 796 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0008 | 1/0 | 796 | 4 | 3 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0009 | 0/0 | 796 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0010 | 0/0 | 796 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0011 | 0/0 | 796 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0012 | 0/0 | 796 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0013 | 0/0 | 796 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0014 | 0/0 | 796 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0015 | 0/0 | 796 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0016 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0017 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0018 | 0/0 | 796 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0019 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0020 | 0/0 | 796 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0021 | 0/0 | 796 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0022 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0023 | 0/0 | 796 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0024 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0025 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0026 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0027 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0028 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2391 | 59 | 8 | 11 | 34 | 2 | 3 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0002 | 0/0 | 2391 | 57 | 0 | 10 | 41 | 2 | 4 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0003 | 0/0 | 2391 | 49 | 3 | 13 | 19 | 6 | 8 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0004 | 0/0 | 2391 | 31 | 2 | 2 | 24 | 0 | 3 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0005 | 0/0 | 2391 | 30 | 5 | 4 | 17 | 1 | 3 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0006 | 0/0 | 2391 | 27 | 3 | 5 | 13 | 2 | 4 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0007 | 0/0 | 2391 | 19 | 3 | 4 | 4 | 2 | 6 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0008 | 0/0 | 2391 | 15 | 1 | 8 | 5 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0009 | 0/0 | 2391 | 8 | 0 | 1 | 5 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0010 | 0/0 | 2391 | 6 | 1 | 2 | 1 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0011 | 0/0 | 2391 | 5 | 4 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0012 | 0/0 | 2391 | 5 | 5 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0013 | 0/0 | 2391 | 4 | 4 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0014 | 0/0 | 2391 | 4 | 4 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0015 | 0/0 | 2391 | 4 | 0 | 0 | 4 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0016 | 0/0 | 2391 | 4 | 0 | 2 | 1 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0017 | 0/0 | 2391 | 3 | 0 | 0 | 3 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0018 | 0/0 | 2391 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0019 | 0/0 | 2391 | 3 | 1 | 1 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0020 | 0/0 | 2391 | 3 | 0 | 3 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0021 | 0/0 | 2391 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0022 | 0/0 | 2391 | 3 | 2 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0023 | 0/0 | 2391 | 2 | 1 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0024 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0025 | 0/0 | 2391 | 2 | 0 | 0 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0026 | 0/0 | 2391 | 2 | 1 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0027 | 0/0 | 2391 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0028 | 0/0 | 2391 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0029 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0030 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0031 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0032 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0033 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0034 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0035 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0036 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0037 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0038 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0039 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0040 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0041 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0042 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0043 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0044 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0045 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0046 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0047 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0048 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0049 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0050 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0051 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0052 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0053 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0054 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0055 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0056 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0057 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0058 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0059 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0060 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0061 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0062 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0063 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0064 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0065 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0066 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0067 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0068 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0069 | 1/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0070 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0071 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0072 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0073 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0074 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0075 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
c0076 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1562 | 124 | 17 | 17 | 80 | 3 | 6 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0002 | 0/1 | 1550 | 74 | 1 | 26 | 26 | 5 | 15 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0003 | 0/0 | 1562 | 65 | 9 | 8 | 37 | 6 | 5 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0004 | 0/0 | 1550 | 23 | 2 | 12 | 1 | 2 | 6 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0005 | 0/0 | 1551 | 13 | 11 | 0 | 1 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0006 | 0/0 | 1563 | 9 | 0 | 1 | 8 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0007 | 0/0 | 1562 | 8 | 0 | 0 | 8 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0008 | 0/0 | 1564 | 6 | 6 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0009 | 0/0 | 1563 | 6 | 0 | 0 | 2 | 0 | 4 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0010 | 0/0 | 1565 | 5 | 5 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0011 | 0/0 | 1551 | 4 | 4 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0012 | 0/0 | 1552 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0013 | 0/0 | 1551 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0014 | 0/0 | 1561 | 3 | 0 | 1 | 0 | 1 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0015 | 0/0 | 1552 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0016 | 0/0 | 1550 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0017 | 0/0 | 1551 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0018 | 0/0 | 1562 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0019 | 0/0 | 1561 | 2 | 1 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0020 | 0/0 | 1563 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0021 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0022 | 0/0 | 1562 | 2 | 0 | 1 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0023 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0024 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0025 | 0/0 | 1562 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0026 | 0/0 | 1277 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0027 | 0/0 | 1550 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0028 | 0/0 | 1550 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0029 | 0/0 | 1550 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0030 | 0/0 | 1552 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0031 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0032 | 0/0 | 1552 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0033 | 0/0 | 1562 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0034 | 0/0 | 1561 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0035 | 0/0 | 1562 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0036 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0037 | 0/0 | 1562 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0038 | 0/0 | 1552 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0039 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0040 | 0/0 | 1564 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0041 | 0/0 | 1562 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0042 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0043 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0044 | 0/0 | 1550 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0045 | 0/0 | 1552 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0046 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0047 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0048 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0049 | 0/0 | 1561 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0050 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0051 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0052 | 0/0 | 1550 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0053 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0054 | 0/0 | 1562 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0055 | 0/0 | 1564 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0056 | 0/0 | 1561 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0057 | 0/0 | 1561 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0058 | 0/0 | 1562 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0059 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0060 | 0/0 | 1562 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0061 | 0/0 | 1564 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0062 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0063 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
t0064 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0002 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2391 | 59 | 8 | 11 | 34 | 2 | 3 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003 | 0/0 | 2391 | 49 | 3 | 13 | 19 | 6 | 8 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0008 | 0/0 | 2391 | 15 | 1 | 8 | 5 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0009 | 0/0 | 2391 | 8 | 0 | 1 | 5 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0013 | 0/0 | 2391 | 4 | 4 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0017 | 0/0 | 2391 | 3 | 0 | 0 | 3 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0023 | 0/0 | 2391 | 2 | 1 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0025 | 0/0 | 2391 | 2 | 0 | 0 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0028 | 0/0 | 2391 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0034 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0035 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0036 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0040 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0057 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0063 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0064 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005 | 0/0 | 2391 | 30 | 5 | 4 | 17 | 1 | 3 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006 | 0/0 | 2391 | 27 | 3 | 5 | 13 | 2 | 4 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0010 | 0/0 | 2391 | 6 | 1 | 2 | 1 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0011 | 0/0 | 2391 | 5 | 4 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0012 | 0/0 | 2391 | 5 | 5 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0024 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0033 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0038 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0039 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0055 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0056 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0059 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0060 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002 | 0/0 | 2391 | 57 | 0 | 10 | 41 | 2 | 4 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0019 | 0/0 | 2391 | 3 | 1 | 1 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0044 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0045 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0049 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0067 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004 | 0/0 | 2391 | 31 | 2 | 2 | 24 | 0 | 3 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0007 | 0/0 | 2391 | 19 | 3 | 4 | 4 | 2 | 6 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0016 | 0/0 | 2391 | 4 | 0 | 2 | 1 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0020 | 0/0 | 2391 | 3 | 0 | 3 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0030 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0041 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0046 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0014 | 0/0 | 2391 | 4 | 4 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0042 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0052 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0053 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0054 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0006c0018 | 0/0 | 2391 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0006c0043 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0007c0015 | 0/0 | 2391 | 4 | 0 | 0 | 4 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0008c0021 | 0/0 | 2391 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0008c0069 | 1/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0009c0022 | 0/0 | 2391 | 3 | 2 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0010c0026 | 0/0 | 2391 | 2 | 1 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0010c0050 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0011c0074 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0011c0076 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0012c0027 | 0/0 | 2391 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0013c0047 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0013c0048 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0014c0029 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0015c0071 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0015c0072 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0016c0073 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0017c0075 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0018c0037 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0019c0058 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0020c0062 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0021c0061 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0022c0032 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0023c0065 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0024c0031 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0025c0066 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0026c0051 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0027c0068 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0028c0070 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3952 | 35 | 1 | 5 | 25 | 2 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0001t0002 | 0/1 | 3940 | 5 | 0 | 3 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0001t0003 | 0/0 | 3952 | 4 | 1 | 0 | 3 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0001t0004 | 0/0 | 3940 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0001t0005 | 0/0 | 3941 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0001t0006 | 0/0 | 3953 | 6 | 0 | 1 | 5 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0001t0007 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0001t0011 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0001t0046 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0001t0047 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0001 | 0/0 | 3952 | 4 | 0 | 1 | 3 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0002 | 0/0 | 3940 | 33 | 1 | 11 | 12 | 4 | 5 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0003 | 0/0 | 3952 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0005 | 0/0 | 3941 | 2 | 1 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0009 | 0/0 | 3953 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0013 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0014 | 0/0 | 3951 | 3 | 0 | 1 | 0 | 1 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0017 | 0/0 | 3941 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0019 | 0/0 | 3951 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0003t0056 | 0/0 | 3951 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0008t0001 | 0/0 | 3952 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0008t0002 | 0/0 | 3940 | 3 | 0 | 3 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0008t0003 | 0/0 | 3952 | 3 | 0 | 0 | 2 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0008t0004 | 0/0 | 3940 | 6 | 1 | 5 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0008t0005 | 0/0 | 3941 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0009t0001 | 0/0 | 3952 | 4 | 0 | 0 | 4 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0009t0002 | 0/0 | 3940 | 2 | 0 | 0 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0009t0003 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0009t0026 | 0/0 | 3667 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0013t0012 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0013t0013 | 0/0 | 3941 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0013t0029 | 0/0 | 3940 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0017t0003 | 0/0 | 3952 | 3 | 0 | 0 | 3 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0023t0001 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0023t0005 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0025t0002 | 0/0 | 3940 | 2 | 0 | 0 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0028t0002 | 0/0 | 3940 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0034t0015 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0035t0001 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0036t0012 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0040t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0057t0015 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0063t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0001c0064t0054 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005t0001 | 0/0 | 3952 | 17 | 1 | 1 | 13 | 1 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005t0002 | 0/0 | 3940 | 3 | 0 | 2 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005t0003 | 0/0 | 3952 | 2 | 1 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005t0007 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005t0009 | 0/0 | 3953 | 3 | 0 | 0 | 1 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005t0010 | 0/0 | 3955 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005t0033 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005t0037 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0005t0061 | 0/0 | 3954 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006t0001 | 0/0 | 3952 | 7 | 0 | 4 | 3 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006t0003 | 0/0 | 3952 | 12 | 0 | 1 | 6 | 2 | 3 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006t0004 | 0/0 | 3940 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006t0005 | 0/0 | 3941 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006t0009 | 0/0 | 3953 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006t0011 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006t0049 | 0/0 | 3951 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006t0053 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0006t0057 | 0/0 | 3951 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0010t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0010t0002 | 0/0 | 3940 | 3 | 0 | 0 | 1 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0010t0022 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0010t0063 | 0/0 | 3944 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0011t0001 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0011t0003 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0011t0011 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0011t0051 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0011t0052 | 0/0 | 3940 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0012t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0012t0010 | 0/0 | 3955 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0012t0034 | 0/0 | 3951 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0012t0036 | 0/0 | 3953 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0024t0003 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0024t0012 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0033t0023 | 0/0 | 3953 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0038t0010 | 0/0 | 3955 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0039t0008 | 0/0 | 3954 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0055t0039 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0056t0005 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0059t0025 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0002c0060t0028 | 0/0 | 3940 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0001 | 0/0 | 3952 | 19 | 0 | 3 | 15 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0002 | 0/0 | 3940 | 12 | 0 | 1 | 11 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0003 | 0/0 | 3952 | 15 | 0 | 6 | 6 | 2 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0007 | 0/0 | 3952 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0009 | 0/0 | 3953 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0016 | 0/0 | 3940 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0017 | 0/0 | 3941 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0018 | 0/0 | 3952 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0020 | 0/0 | 3953 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0035 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0002t0059 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0019t0003 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0019t0004 | 0/0 | 3940 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0019t0041 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0044t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0045t0006 | 0/0 | 3953 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0049t0021 | 0/0 | 3953 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0003c0067t0001 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004t0001 | 0/0 | 3952 | 8 | 0 | 2 | 6 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004t0003 | 0/0 | 3952 | 14 | 1 | 0 | 12 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004t0004 | 0/0 | 3940 | 2 | 0 | 0 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004t0006 | 0/0 | 3953 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004t0007 | 0/0 | 3952 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004t0024 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004t0050 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004t0060 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0004t0062 | 0/0 | 3953 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0007t0001 | 0/0 | 3952 | 3 | 2 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0007t0002 | 0/0 | 3940 | 4 | 0 | 1 | 1 | 1 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0007t0004 | 0/0 | 3940 | 8 | 0 | 3 | 1 | 1 | 3 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0007t0016 | 0/0 | 3940 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0007t0022 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0007t0030 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0007t0044 | 0/0 | 3940 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0016t0001 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0016t0003 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0016t0058 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0016t0064 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0020t0002 | 0/0 | 3940 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0020t0004 | 0/0 | 3940 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0030t0027 | 0/0 | 3940 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0041t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0004c0046t0002 | 0/0 | 3940 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0014t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0014t0003 | 0/0 | 3952 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0042t0003 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0052t0002 | 0/0 | 3940 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0053t0005 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0005c0054t0001 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0006c0018t0008 | 0/0 | 3954 | 3 | 3 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0006c0043t0005 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0007c0015t0001 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0007c0015t0003 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0007c0015t0007 | 0/0 | 3952 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0008c0021t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0008c0021t0008 | 0/0 | 3954 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0008c0021t0055 | 0/0 | 3954 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0008c0069t0001 | 1/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0009c0022t0001 | 0/0 | 3952 | 2 | 1 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0009c0022t0031 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0010c0026t0002 | 0/0 | 3940 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0010c0026t0010 | 0/0 | 3955 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0010c0050t0004 | 0/0 | 3940 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0011c0074t0021 | 0/0 | 3953 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0011c0076t0048 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0012c0027t0001 | 0/0 | 3952 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0013c0047t0008 | 0/0 | 3954 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0013c0048t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0014c0029t0011 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0014c0029t0038 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0015c0071t0015 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0015c0072t0032 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0016c0073t0040 | 0/0 | 3954 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0017c0075t0005 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0018c0037t0043 | 0/0 | 3944 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0019c0058t0045 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0020c0062t0001 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0021c0061t0006 | 0/0 | 3953 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0022c0032t0023 | 0/0 | 3953 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0023c0065t0002 | 0/0 | 3940 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0024c0031t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0025c0066t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0026c0051t0019 | 0/0 | 3951 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0027c0068t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
a0028c0070t0042 | 0/0 | 3955 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | copy fasta | chr8 | 28016964 | 28088936 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0002g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0011g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0046g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0001t0047g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0009g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0013g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0014g0002 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0017g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0019g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0003t0056g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0004g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0004g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0004g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0004g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0008t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0009t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0009t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0009t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0009t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0009t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0009t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0009t0026g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0013t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0013t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0013t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0013t0029g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0017t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0017t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0017t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0023t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0023t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0025t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0025t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0028t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0034t0015g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0035t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0036t0012g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0040t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0057t0015g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0063t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0001c0064t0054g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0009g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0009g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0009g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0033g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0037g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0005t0061g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0004g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0009g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0011g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0049g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0053g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0006t0057g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0010t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0010t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0010t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0010t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0010t0022g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0010t0063g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0011t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0011t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0011t0011g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0011t0051g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0011t0052g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0012t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0012t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0012t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0012t0034g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0012t0036g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0024t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0024t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0033t0023g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0038t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0039t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0055t0039g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0056t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0059t0025g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0002c0060t0028g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0003g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0009g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0016g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0017g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0018g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0018g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0020g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0020g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0035g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0002t0059g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0019t0003g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0019t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0019t0041g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0044t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0045t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0049t0021g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0003c0067t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0024g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0050g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0060g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0004t0062g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0004g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0004g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0004g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0016g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0022g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0030g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0007t0044g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0016t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0016t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0016t0058g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0016t0064g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0020t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0020t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0020t0004g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0030t0027g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0041t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0004c0046t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0005c0014t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0005c0014t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0005c0014t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0005c0014t0003g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0005c0042t0003g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0005c0052t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0005c0053t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0005c0054t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0006c0018t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0006c0018t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0006c0018t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0006c0043t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0007c0015t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0007c0015t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0007c0015t0007g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0008c0021t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0008c0021t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0008c0021t0055g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0008c0069t0001g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0009c0022t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0009c0022t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0009c0022t0031g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0010c0026t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0010c0026t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0010c0050t0004g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0011c0074t0021g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0011c0076t0048g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0012c0027t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0012c0027t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0013c0047t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0013c0048t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0014c0029t0011g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0014c0029t0038g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0015c0071t0015g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0015c0072t0032g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0016c0073t0040g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0017c0075t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0018c0037t0043g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0019c0058t0045g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0020c0062t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0021c0061t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0022c0032t0023g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0023c0065t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0024c0031t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0025c0066t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0026c0051t0019g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0027c0068t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
a0028c0070t0042g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0005 | t0001 | g0071 | EUR | GBR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00099 | hp2 | a0004 | c0007 | t0002 | g0227 | EUR | GBR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00140 | hp1 | a0001 | c0003 | t0002 | g0199 | EUR | GBR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00140 | hp2 | a0004 | c0007 | t0004 | g0345 | EUR | GBR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00280 | hp1 | a0001 | c0003 | t0002 | g0214 | EUR | FIN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00280 | hp2 | a0003 | c0019 | t0003 | g0342 | EUR | FIN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00323 | hp1 | a0001 | c0008 | t0003 | g0353 | EUR | FIN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00323 | hp2 | a0001 | c0003 | t0005 | g0215 | EUR | FIN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00408 | hp1 | a0004 | c0007 | t0004 | g0295 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00408 | hp2 | a0003 | c0002 | t0002 | g0088 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00423 | hp1 | a0002 | c0005 | t0001 | g0148 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00423 | hp2 | a0004 | c0004 | t0001 | g0013 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00438 | hp2 | a0004 | c0004 | t0003 | g0304 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00558 | hp2 | a0003 | c0002 | t0001 | g0111 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00597 | hp2 | a0002 | c0005 | t0001 | g0037 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00621 | hp2 | a0002 | c0005 | t0001 | g0053 | EAS | CHS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00639 | hp2 | a0004 | c0020 | t0004 | g0357 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00642 | hp2 | a0001 | c0003 | t0002 | g0205 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00733 | hp1 | a0001 | c0001 | t0006 | g0225 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00733 | hp2 | a0002 | c0010 | t0022 | g0371 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00735 | hp1 | a0001 | c0003 | t0002 | g0240 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00735 | hp2 | a0002 | c0005 | t0002 | g0271 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00738 | hp2 | a0009 | c0022 | t0001 | g0127 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00741 | hp1 | a0010 | c0026 | t0002 | g0113 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG00741 | hp2 | a0004 | c0004 | t0001 | g0210 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01069 | hp1 | a0001 | c0003 | t0002 | g0216 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01069 | hp2 | a0003 | c0002 | t0003 | g0356 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0312 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01070 | hp2 | a0004 | c0007 | t0002 | g0058 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0313 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01071 | hp2 | a0001 | c0003 | t0002 | g0211 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01074 | hp1 | a0005 | c0052 | t0002 | g0162 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01074 | hp2 | a0002 | c0005 | t0033 | g0270 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01081 | hp1 | a0003 | c0002 | t0003 | g0319 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01081 | hp2 | a0004 | c0020 | t0004 | g0284 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01099 | hp1 | a0001 | c0003 | t0002 | g0056 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01099 | hp2 | a0001 | c0009 | t0026 | g0202 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01106 | hp1 | a0002 | c0006 | t0001 | g0167 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01167 | hp1 | a0003 | c0002 | t0003 | g0287 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01167 | hp2 | a0001 | c0003 | t0002 | g0164 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01168 | hp1 | a0001 | c0028 | t0002 | g0017 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01168 | hp2 | a0001 | c0008 | t0002 | g0166 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01169 | hp1 | a0001 | c0028 | t0002 | g0017 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01169 | hp2 | a0003 | c0002 | t0003 | g0283 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01192 | hp1 | a0002 | c0005 | t0002 | g0158 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01243 | hp1 | a0018 | c0037 | t0043 | g0049 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01243 | hp2 | a0001 | c0003 | t0002 | g0197 | AMR | PUR | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01255 | hp1 | a0004 | c0016 | t0058 | g0274 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01255 | hp2 | a0003 | c0002 | t0002 | g0228 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01256 | hp1 | a0001 | c0003 | t0002 | g0163 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01256 | hp2 | a0001 | c0008 | t0002 | g0244 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01257 | hp1 | a0003 | c0002 | t0001 | g0257 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01257 | hp2 | a0004 | c0007 | t0004 | g0003 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01258 | hp1 | a0001 | c0008 | t0002 | g0243 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01258 | hp2 | a0004 | c0007 | t0004 | g0003 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01261 | hp1 | a0002 | c0010 | t0063 | g0310 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01261 | hp2 | a0003 | c0019 | t0041 | g0087 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01346 | hp1 | a0004 | c0020 | t0002 | g0057 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01346 | hp2 | a0003 | c0002 | t0003 | g0302 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01358 | hp2 | a0001 | c0008 | t0004 | g0005 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01361 | hp1 | a0004 | c0007 | t0004 | g0003 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01361 | hp2 | a0001 | c0008 | t0004 | g0005 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01433 | hp1 | a0003 | c0002 | t0001 | g0091 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01433 | hp2 | a0001 | c0003 | t0002 | g0223 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01496 | hp1 | a0002 | c0005 | t0001 | g0218 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01515 | hp1 | a0002 | c0006 | t0003 | g0347 | EUR | IBS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0217 | EUR | IBS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01516 | hp2 | a0010 | c0050 | t0004 | g0349 | EUR | IBS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01517 | hp1 | a0002 | c0006 | t0003 | g0338 | EUR | IBS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01884 | hp1 | a0001 | c0008 | t0004 | g0005 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01884 | hp2 | a0001 | c0013 | t0012 | g0189 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01891 | hp1 | a0006 | c0018 | t0008 | g0063 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01891 | hp2 | a0002 | c0006 | t0005 | g0014 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01928 | hp1 | a0001 | c0008 | t0004 | g0341 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01928 | hp2 | a0003 | c0002 | t0001 | g0086 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01934 | hp1 | a0002 | c0006 | t0001 | g0272 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01934 | hp2 | a0004 | c0004 | t0001 | g0209 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01943 | hp1 | a0001 | c0008 | t0004 | g0325 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01943 | hp2 | a0002 | c0006 | t0001 | g0258 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01975 | hp1 | a0001 | c0003 | t0014 | g0002 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01975 | hp2 | a0002 | c0006 | t0001 | g0168 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01981 | hp1 | a0004 | c0016 | t0003 | g0285 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02004 | hp1 | a0001 | c0003 | t0002 | g0204 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02004 | hp2 | a0003 | c0002 | t0003 | g0286 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02015 | hp1 | a0004 | c0004 | t0003 | g0021 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02015 | hp2 | a0003 | c0002 | t0001 | g0008 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02040 | hp1 | a0004 | c0004 | t0001 | g0112 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02040 | hp2 | a0002 | c0006 | t0003 | g0316 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02055 | hp1 | a0013 | c0048 | t0001 | g0207 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02055 | hp2 | a0014 | c0029 | t0038 | g0170 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02056 | hp2 | a0004 | c0004 | t0003 | g0297 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02071 | hp2 | a0003 | c0002 | t0001 | g0073 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02080 | hp1 | a0002 | c0006 | t0003 | g0327 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02080 | hp2 | a0001 | c0003 | t0002 | g0238 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02083 | hp2 | a0001 | c0035 | t0001 | g0116 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02129 | hp1 | a0004 | c0016 | t0064 | g0377 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02129 | hp2 | a0001 | c0008 | t0001 | g0134 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02132 | hp1 | a0001 | c0008 | t0001 | g0133 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02145 | hp1 | a0002 | c0055 | t0039 | g0161 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02145 | hp2 | a0003 | c0019 | t0004 | g0344 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02155 | hp1 | a0003 | c0002 | t0017 | g0118 | EAS | CDX | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02155 | hp2 | a0001 | c0023 | t0001 | g0241 | EAS | CDX | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02165 | hp1 | a0003 | c0002 | t0003 | g0354 | EAS | CDX | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02165 | hp2 | a0003 | c0002 | t0002 | g0009 | EAS | CDX | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02257 | hp1 | a0001 | c0003 | t0002 | g0046 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02257 | hp2 | a0002 | c0056 | t0005 | g0181 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02258 | hp1 | a0001 | c0013 | t0029 | g0179 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02258 | hp2 | a0009 | c0022 | t0031 | g0126 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02280 | hp1 | a0028 | c0070 | t0042 | g0137 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02280 | hp2 | a0002 | c0024 | t0012 | g0247 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02293 | hp1 | a0001 | c0003 | t0002 | g0221 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02293 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02300 | hp1 | a0001 | c0008 | t0004 | g0326 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02300 | hp2 | a0002 | c0006 | t0003 | g0301 | AMR | PEL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02451 | hp1 | a0002 | c0006 | t0011 | g0320 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02451 | hp2 | a0005 | c0014 | t0003 | g0280 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02523 | hp2 | a0003 | c0002 | t0002 | g0009 | EAS | KHV | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02572 | hp1 | a0002 | c0039 | t0008 | g0128 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02572 | hp2 | a0004 | c0007 | t0030 | g0195 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02602 | hp1 | a0004 | c0046 | t0002 | g0085 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02602 | hp2 | a0001 | c0003 | t0009 | g0268 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0360 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02615 | hp2 | a0001 | c0057 | t0015 | g0350 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02622 | hp1 | a0011 | c0076 | t0048 | g0365 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02622 | hp2 | a0005 | c0014 | t0003 | g0368 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02630 | hp1 | a0002 | c0012 | t0036 | g0185 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02630 | hp2 | a0025 | c0066 | t0001 | g0061 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02647 | hp1 | a0001 | c0003 | t0005 | g0212 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02647 | hp2 | a0015 | c0072 | t0032 | g0172 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02698 | hp1 | a0002 | c0006 | t0003 | g0317 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02698 | hp2 | a0004 | c0004 | t0004 | g0288 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02717 | hp1 | a0002 | c0005 | t0003 | g0318 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02717 | hp2 | a0013 | c0047 | t0008 | g0065 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02723 | hp1 | a0001 | c0034 | t0015 | g0376 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02723 | hp2 | a0001 | c0063 | t0001 | g0059 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02735 | hp1 | a0002 | c0010 | t0002 | g0267 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02735 | hp2 | a0023 | c0065 | t0002 | g0208 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02738 | hp1 | a0003 | c0002 | t0009 | g0120 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02738 | hp2 | a0002 | c0005 | t0009 | g0229 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02818 | hp1 | a0002 | c0005 | t0010 | g0042 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02818 | hp2 | a0005 | c0053 | t0005 | g0060 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02886 | hp1 | a0001 | c0036 | t0012 | g0193 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02886 | hp2 | a0001 | c0040 | t0001 | g0045 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02895 | hp1 | a0002 | c0012 | t0010 | g0192 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02895 | hp2 | a0002 | c0010 | t0001 | g0047 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02896 | hp1 | a0002 | c0011 | t0052 | g0375 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02896 | hp2 | a0002 | c0059 | t0025 | g0044 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02897 | hp1 | a0002 | c0012 | t0010 | g0191 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02897 | hp2 | a0002 | c0011 | t0051 | g0374 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02922 | hp1 | a0004 | c0007 | t0001 | g0194 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02922 | hp2 | a0001 | c0023 | t0005 | g0180 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02965 | hp1 | a0002 | c0012 | t0001 | g0051 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02965 | hp2 | a0004 | c0007 | t0001 | g0183 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02976 | hp1 | a0005 | c0014 | t0003 | g0279 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02976 | hp2 | a0002 | c0011 | t0003 | g0351 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03017 | hp1 | a0002 | c0006 | t0004 | g0333 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03017 | hp2 | a0001 | c0003 | t0002 | g0220 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03041 | hp1 | a0026 | c0051 | t0019 | g0187 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03041 | hp2 | a0006 | c0018 | t0008 | g0123 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03130 | hp1 | a0005 | c0042 | t0003 | g0367 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03130 | hp2 | a0002 | c0005 | t0061 | g0366 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03139 | hp1 | a0002 | c0005 | t0037 | g0263 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03139 | hp2 | a0001 | c0001 | t0046 | g0276 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03195 | hp1 | a0017 | c0075 | t0005 | g0036 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03195 | hp2 | a0003 | c0049 | t0021 | g0265 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03209 | hp1 | a0006 | c0018 | t0008 | g0062 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03209 | hp2 | a0027 | c0068 | t0001 | g0171 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03225 | hp2 | a0015 | c0071 | t0015 | g0369 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03239 | hp1 | a0002 | c0006 | t0003 | g0332 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03239 | hp2 | a0001 | c0003 | t0014 | g0002 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03453 | hp1 | a0002 | c0011 | t0011 | g0373 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03453 | hp2 | a0011 | c0074 | t0021 | g0125 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03486 | hp1 | a0001 | c0013 | t0013 | g0190 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03486 | hp2 | a0016 | c0073 | t0040 | g0160 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03490 | hp1 | a0003 | c0002 | t0001 | g0196 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03490 | hp2 | a0001 | c0009 | t0002 | g0020 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03491 | hp1 | a0004 | c0007 | t0004 | g0023 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03491 | hp2 | a0001 | c0003 | t0002 | g0246 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03492 | hp1 | a0004 | c0007 | t0004 | g0023 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03492 | hp2 | a0001 | c0009 | t0002 | g0020 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03516 | hp1 | a0004 | c0041 | t0001 | g0186 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03516 | hp2 | a0019 | c0058 | t0045 | g0281 | AFR | ESN | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03540 | hp1 | a0003 | c0044 | t0001 | g0224 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03540 | hp2 | a0006 | c0043 | t0005 | g0184 | AFR | GWD | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03579 | hp1 | a0002 | c0005 | t0001 | g0124 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03579 | hp2 | a0001 | c0013 | t0013 | g0200 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03654 | hp1 | a0003 | c0002 | t0035 | g0084 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03654 | hp2 | a0004 | c0004 | t0003 | g0358 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03669 | hp1 | a0005 | c0054 | t0001 | g0249 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03669 | hp2 | a0004 | c0004 | t0004 | g0290 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03688 | hp1 | a0004 | c0007 | t0004 | g0296 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03688 | hp2 | a0004 | c0007 | t0044 | g0273 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03704 | hp2 | a0003 | c0002 | t0003 | g0359 | SAS | PJL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03831 | hp1 | a0001 | c0025 | t0002 | g0114 | SAS | BEB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03834 | hp1 | a0001 | c0003 | t0056 | g0314 | SAS | BEB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03834 | hp2 | a0001 | c0003 | t0002 | g0203 | SAS | BEB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03942 | hp1 | a0004 | c0030 | t0027 | g0096 | SAS | BEB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03942 | hp2 | a0002 | c0006 | t0003 | g0330 | SAS | BEB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG04115 | hp1 | a0004 | c0007 | t0002 | g0072 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG04115 | hp2 | a0001 | c0025 | t0002 | g0115 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG04199 | hp1 | a0002 | c0005 | t0009 | g0232 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG04199 | hp2 | a0002 | c0010 | t0002 | g0248 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG04204 | hp1 | a0004 | c0016 | t0001 | g0076 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0222 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG04228 | hp2 | a0004 | c0007 | t0022 | g0298 | SAS | STU | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18522 | hp1 | a0008 | c0021 | t0001 | g0169 | AFR | YRI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18612 | hp1 | a0001 | c0008 | t0003 | g0339 | EAS | CHB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18612 | hp2 | a0002 | c0011 | t0001 | g0242 | EAS | CHB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | CHB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18747 | hp2 | a0004 | c0004 | t0003 | g0022 | EAS | CHB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18906 | hp1 | a0002 | c0060 | t0028 | g0206 | AFR | YRI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18906 | hp2 | a0024 | c0031 | t0001 | g0188 | AFR | YRI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18939 | hp1 | a0003 | c0002 | t0002 | g0010 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18939 | hp2 | a0001 | c0003 | t0002 | g0104 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18940 | hp1 | a0003 | c0002 | t0018 | g0082 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18940 | hp2 | a0004 | c0004 | t0050 | g0300 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18941 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18941 | hp2 | a0004 | c0004 | t0001 | g0080 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18942 | hp1 | a0002 | c0006 | t0049 | g0334 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18942 | hp2 | a0003 | c0002 | t0001 | g0007 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18943 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18943 | hp2 | a0002 | c0006 | t0003 | g0004 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18945 | hp1 | a0003 | c0002 | t0007 | g0027 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18945 | hp2 | a0002 | c0006 | t0003 | g0004 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18947 | hp1 | a0001 | c0003 | t0002 | g0105 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18947 | hp2 | a0002 | c0006 | t0003 | g0004 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18948 | hp1 | a0001 | c0003 | t0002 | g0155 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18948 | hp2 | a0003 | c0045 | t0006 | g0070 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18949 | hp1 | a0012 | c0027 | t0001 | g0173 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18949 | hp2 | a0003 | c0002 | t0001 | g0077 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18950 | hp1 | a0001 | c0017 | t0003 | g0329 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18950 | hp2 | a0002 | c0006 | t0001 | g0069 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18952 | hp1 | a0001 | c0003 | t0002 | g0152 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18952 | hp2 | a0003 | c0002 | t0001 | g0055 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18954 | hp1 | a0003 | c0002 | t0001 | g0078 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18956 | hp2 | a0003 | c0002 | t0003 | g0355 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18957 | hp1 | a0003 | c0002 | t0001 | g0090 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18959 | hp1 | a0001 | c0003 | t0002 | g0140 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18959 | hp2 | a0002 | c0005 | t0009 | g0151 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18960 | hp1 | a0002 | c0005 | t0001 | g0149 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18960 | hp2 | a0004 | c0004 | t0003 | g0294 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18962 | hp1 | a0002 | c0006 | t0053 | g0321 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18962 | hp2 | a0007 | c0015 | t0007 | g0006 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18963 | hp1 | a0001 | c0017 | t0003 | g0328 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18964 | hp1 | a0002 | c0005 | t0003 | g0282 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18964 | hp2 | a0004 | c0007 | t0001 | g0097 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18966 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18966 | hp2 | a0004 | c0007 | t0016 | g0029 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18968 | hp1 | a0004 | c0007 | t0002 | g0068 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18968 | hp2 | a0002 | c0005 | t0001 | g0041 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18969 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18971 | hp1 | a0002 | c0006 | t0003 | g0337 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18971 | hp2 | a0003 | c0002 | t0002 | g0010 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18972 | hp2 | a0004 | c0004 | t0001 | g0121 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18974 | hp1 | a0003 | c0067 | t0001 | g0095 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18974 | hp2 | a0001 | c0009 | t0001 | g0150 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18975 | hp1 | a0003 | c0002 | t0001 | g0008 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18975 | hp2 | a0001 | c0003 | t0002 | g0261 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0259 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18978 | hp1 | a0001 | c0008 | t0003 | g0331 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18978 | hp2 | a0003 | c0002 | t0001 | g0034 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18979 | hp1 | a0004 | c0004 | t0062 | g0303 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18979 | hp2 | a0002 | c0010 | t0002 | g0130 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18982 | hp1 | a0002 | c0006 | t0001 | g0132 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18982 | hp2 | a0001 | c0009 | t0003 | g0308 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18983 | hp2 | a0003 | c0002 | t0059 | g0305 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18984 | hp1 | a0004 | c0004 | t0003 | g0307 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18984 | hp2 | a0002 | c0006 | t0057 | g0335 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18985 | hp1 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18985 | hp2 | a0003 | c0002 | t0003 | g0322 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18986 | hp1 | a0004 | c0004 | t0003 | g0292 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18986 | hp2 | a0001 | c0003 | t0017 | g0146 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18987 | hp1 | a0002 | c0005 | t0002 | g0038 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18987 | hp2 | a0003 | c0002 | t0001 | g0089 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18991 | hp2 | a0003 | c0002 | t0020 | g0074 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18992 | hp1 | a0003 | c0002 | t0001 | g0067 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18992 | hp2 | a0002 | c0005 | t0001 | g0054 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18994 | hp1 | a0001 | c0008 | t0005 | g0117 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18994 | hp2 | a0020 | c0062 | t0001 | g0177 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18998 | hp1 | a0003 | c0002 | t0007 | g0030 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18998 | hp2 | a0003 | c0002 | t0001 | g0098 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18999 | hp1 | a0002 | c0005 | t0001 | g0239 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18999 | hp2 | a0003 | c0002 | t0002 | g0092 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19000 | hp1 | a0002 | c0005 | t0001 | g0040 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19000 | hp2 | a0001 | c0017 | t0003 | g0324 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19002 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19003 | hp1 | a0001 | c0001 | t0006 | g0110 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19003 | hp2 | a0002 | c0006 | t0009 | g0135 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19004 | hp1 | a0004 | c0004 | t0003 | g0022 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19004 | hp2 | a0001 | c0009 | t0001 | g0033 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19005 | hp1 | a0003 | c0002 | t0018 | g0083 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19009 | hp1 | a0001 | c0003 | t0002 | g0251 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19009 | hp2 | a0001 | c0009 | t0001 | g0143 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19011 | hp1 | a0004 | c0004 | t0003 | g0348 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19011 | hp2 | a0007 | c0015 | t0007 | g0006 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19012 | hp1 | a0001 | c0009 | t0001 | g0142 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19030 | hp1 | a0002 | c0038 | t0010 | g0048 | AFR | LWK | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19030 | hp2 | a0004 | c0004 | t0060 | g0346 | AFR | LWK | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19054 | hp1 | a0007 | c0015 | t0003 | g0299 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19054 | hp2 | a0004 | c0004 | t0007 | g0026 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19056 | hp1 | a0001 | c0003 | t0003 | g0363 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19056 | hp2 | a0002 | c0005 | t0001 | g0141 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19058 | hp1 | a0004 | c0004 | t0003 | g0362 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19058 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19060 | hp1 | a0002 | c0005 | t0001 | g0093 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19063 | hp1 | a0004 | c0004 | t0007 | g0028 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19065 | hp1 | a0004 | c0004 | t0003 | g0289 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19065 | hp2 | a0003 | c0002 | t0016 | g0031 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19066 | hp1 | a0004 | c0004 | t0003 | g0021 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19066 | hp2 | a0003 | c0002 | t0003 | g0306 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19067 | hp1 | a0004 | c0004 | t0006 | g0253 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19067 | hp2 | a0001 | c0003 | t0003 | g0364 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19070 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19070 | hp2 | a0003 | c0002 | t0003 | g0293 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19074 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19074 | hp2 | a0002 | c0005 | t0001 | g0255 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19076 | hp1 | a0003 | c0002 | t0001 | g0079 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19076 | hp2 | a0001 | c0003 | t0019 | g0138 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19080 | hp1 | a0002 | c0005 | t0007 | g0032 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19080 | hp2 | a0001 | c0003 | t0002 | g0153 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19082 | hp2 | a0003 | c0002 | t0003 | g0323 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19083 | hp1 | a0003 | c0002 | t0020 | g0119 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19083 | hp2 | a0007 | c0015 | t0001 | g0094 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19084 | hp2 | a0021 | c0061 | t0006 | g0154 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19085 | hp1 | a0004 | c0004 | t0001 | g0081 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19086 | hp1 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19086 | hp2 | a0003 | c0002 | t0001 | g0007 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19087 | hp1 | a0002 | c0005 | t0001 | g0262 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19087 | hp2 | a0012 | c0027 | t0001 | g0174 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19089 | hp1 | a0003 | c0002 | t0002 | g0075 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19091 | hp1 | a0002 | c0006 | t0001 | g0136 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19091 | hp2 | a0004 | c0004 | t0024 | g0024 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19240 | hp1 | a0002 | c0006 | t0005 | g0014 | AFR | YRI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA19240 | hp2 | a0001 | c0064 | t0054 | g0275 | AFR | YRI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20129 | hp1 | a0001 | c0001 | t0047 | g0361 | AFR | ASW | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20129 | hp2 | a0014 | c0029 | t0011 | g0372 | AFR | ASW | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20752 | hp1 | a0003 | c0002 | t0003 | g0311 | EUR | TSI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0213 | EUR | TSI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20805 | hp1 | a0003 | c0002 | t0003 | g0343 | EUR | TSI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20805 | hp2 | a0001 | c0003 | t0014 | g0002 | EUR | TSI | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20905 | hp1 | a0002 | c0005 | t0001 | g0236 | SAS | GIH | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20905 | hp2 | a0001 | c0003 | t0002 | g0219 | SAS | GIH | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02109 | hp1 | a0009 | c0022 | t0001 | g0035 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02109 | hp2 | a0008 | c0021 | t0055 | g0370 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0315 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG02559 | hp2 | a0005 | c0014 | t0001 | g0250 | AFR | ACB | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03471 | hp1 | a0008 | c0021 | t0008 | g0052 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG03471 | hp2 | a0022 | c0032 | t0023 | g0278 | AFR | MSL | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG06807 | hp1 | a0002 | c0024 | t0003 | g0336 | AFR | USA | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
HG06807 | hp2 | a0002 | c0033 | t0023 | g0277 | AFR | USA | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18955 | hp1 | a0001 | c0003 | t0002 | g0252 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA18955 | hp2 | a0002 | c0005 | t0001 | g0039 | EAS | JPT | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20300 | hp1 | a0002 | c0012 | t0034 | g0050 | AFR | USA | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA20300 | hp2 | a0001 | c0003 | t0013 | g0264 | AFR | USA | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA21309 | hp1 | a0010 | c0026 | t0010 | g0129 | AFR | LWK | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
NA21309 | hp2 | a0004 | c0004 | t0003 | g0340 | AFR | LWK | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0066 | REF | REF | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
homoSapiens_grch38 | hp1 | a0008 | c0069 | t0001 | g0182 | REF | REF | NUGGC_chr8_28016964_28088936 | NUGGC | chr8 | 28016964 | 28088936 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:28023334
|
G | T | 1 | a0021 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.2374C>A | p.Pro792Thr | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 2582/3952 | 2374/2391 | 792/796 | chr8 | 28023334 | ||
chr8:28023406
|
C | T | 2 | a0026a0027 | 2 | HG03041.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.2302G>A | p.Ala768Thr | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 2510/3952 | 2302/2391 | 768/796 | chr8 | 28023406 | ||
chr8:28029334
|
G | A | 1 | a0023 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.2086C>T | p.Arg696Trp | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/19 | 2294/3952 | 2086/2391 | 696/796 | chr8 | 28029334 | ||
chr8:28030408
|
A | T | 1 | a0022 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1919T>A | p.Ile640Asn | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/19 | 2127/3952 | 1919/2391 | 640/796 | chr8 | 28030408 | ||
chr8:28033666
|
G | A | 1 | a0020 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.1643C>T | p.Thr548Ile | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/19 | 1851/3952 | 1643/2391 | 548/796 | chr8 | 28033666 | ||
chr8:28041188
|
G | A | 1 | a0007 | 4 | NA18962.hp2 NA19011.hp2 NA19054.hp1 others(1): Show |
missense_variant | MODERATE | c.1474C>T | p.Arg492Trp | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/19 | 1682/3952 | 1474/2391 | 492/796 | chr8 | 28041188 | ||
chr8:28045528
|
G | A | 1 | a0017 | 1 | HG03195.hp1 | missense_variant&splice_region_variant | MODERATE | c.1445C>T | p.Pro482Leu | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/19 | 1653/3952 | 1445/2391 | 482/796 | chr8 | 28045528 | ||
chr8:28045552
|
C | T | 14 | a0002a0003a0007others(11): Show | 166 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(163): Show |
missense_variant | MODERATE | c.1421G>A | p.Ser474Asn | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/19 | 1629/3952 | 1421/2391 | 474/796 | chr8 | 28045552 | ||
chr8:28060533
|
G | T | 2 | a0024a0025 | 2 | HG02630.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.990C>A | p.His330Gln | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/19 | 1198/3952 | 990/2391 | 330/796 | chr8 | 28060533 | ||
chr8:28060540
|
T | C | 22 | a0001a0002a0003others(19): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
missense_variant | MODERATE | c.983A>G | p.Gln328Arg | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/19 | 1191/3952 | 983/2391 | 328/796 | chr8 | 28060540 | ||
chr8:28060562
|
T | C | 1 | a0013 | 2 | HG02055.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.961A>G | p.Ile321Val | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/19 | 1169/3952 | 961/2391 | 321/796 | chr8 | 28060562 | ||
chr8:28064652
|
C | T | 1 | a0012 | 2 | NA18949.hp1 NA19087.hp2 |
missense_variant | MODERATE | c.791G>A | p.Arg264His | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/19 | 999/3952 | 791/2391 | 264/796 | chr8 | 28064652 | ||
chr8:28067668
|
G | A | 3 | a0005a0010a0026 | 12 | HG00741.hp1 HG01074.hp1 HG01516.hp2 others(9): Show |
missense_variant | MODERATE | c.557C>T | p.Ala186Val | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/19 | 765/3952 | 557/2391 | 186/796 | chr8 | 28067668 | ||
chr8:28067687
|
T | C | 14 | a0001a0002a0009others(11): Show | 249 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(246): Show |
missense_variant | MODERATE | c.538A>G | p.Ser180Gly | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/19 | 746/3952 | 538/2391 | 180/796 | chr8 | 28067687 | ||
chr8:28070296
|
C | T | 1 | a0016 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.104G>A | p.Arg35Gln | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/19 | 312/3952 | 104/2391 | 35/796 | chr8 | 28070296 | ||
chr8:28070332
|
C | G | 23 | a0001a0002a0003others(20): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
missense_variant | MODERATE | c.68G>C | p.Arg23Pro | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/19 | 276/3952 | 68/2391 | 23/796 | chr8 | 28070332 | ||
chr8:28074376
|
G | A | 4 | a0009a0011a0016others(1): Show | 7 | HG00738.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
missense_variant | MODERATE | c.35C>T | p.Pro12Leu | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/19 | 243/3952 | 35/2391 | 12/796 | chr8 | 28074376 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:28023329
|
C | T | 1 | a0004c0046 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.2379G>A | p.Gly793Gly | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 2587/3952 | 2379/2391 | 793/796 | chr8 | 28023329 | ||
chr8:28026996
|
C | T | 1 | a0003c0045 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.2211G>A | p.Ser737Ser | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/19 | 2419/3952 | 2211/2391 | 737/796 | chr8 | 28026996 | ||
chr8:28029386
|
C | T | 33 | a0001c0003a0001c0013a0001c0025others(30): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
synonymous_variant | LOW | c.2034G>A | p.Thr678Thr | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/19 | 2242/3952 | 2034/2391 | 678/796 | chr8 | 28029386 | ||
chr8:28041063
|
T | C | 16 | a0001c0009a0001c0017a0001c0028others(13): Show | 34 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(31): Show |
synonymous_variant | LOW | c.1599A>G | p.Arg533Arg | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/19 | 1807/3952 | 1599/2391 | 533/796 | chr8 | 28041063 | ||
chr8:28041093
|
G | A | 3 | a0004c0041a0005c0014a0005c0042 | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.1569C>T | p.Thr523Thr | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/19 | 1777/3952 | 1569/2391 | 523/796 | chr8 | 28041093 | ||
chr8:28041177
|
C | T | 13 | a0001c0034a0001c0036a0001c0057others(10): Show | 16 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(13): Show |
synonymous_variant | LOW | c.1485G>A | p.Ala495Ala | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/19 | 1693/3952 | 1485/2391 | 495/796 | chr8 | 28041177 | ||
chr8:28041204
|
C | T | 2 | a0002c0059a0003c0044 | 2 | HG02896.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.1458G>A | p.Leu486Leu | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/19 | 1666/3952 | 1458/2391 | 486/796 | chr8 | 28041204 | ||
chr8:28045539
|
C | T | 1 | a0002c0038 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1434G>A | p.Thr478Thr | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/19 | 1642/3952 | 1434/2391 | 478/796 | chr8 | 28045539 | ||
chr8:28060527
|
G | A | 1 | a0006c0043 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.996C>T | p.Asp332Asp | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/19 | 1204/3952 | 996/2391 | 332/796 | chr8 | 28060527 | ||
chr8:28064606
|
G | A | 2 | a0003c0049a0011c0076 | 2 | HG02622.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.837C>T | p.Ser279Ser | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/19 | 1045/3952 | 837/2391 | 279/796 | chr8 | 28064606 | ||
chr8:28064678
|
A | G | 2 | a0001c0057a0002c0056 | 2 | HG02257.hp2 HG02615.hp2 |
synonymous_variant | LOW | c.765T>C | p.Asp255Asp | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/19 | 973/3952 | 765/2391 | 255/796 | chr8 | 28064678 | ||
chr8:28067604
|
C | T | 1 | a0002c0055 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.621G>A | p.Gly207Gly | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/19 | 829/3952 | 621/2391 | 207/796 | chr8 | 28067604 | ||
chr8:28067697
|
C | T | 3 | a0004c0041a0005c0014a0005c0042 | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.528G>A | p.Thr176Thr | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/19 | 736/3952 | 528/2391 | 176/796 | chr8 | 28067697 | ||
chr8:28067703
|
A | G | 5 | a0001c0040a0002c0012a0002c0038others(2): Show | 9 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
synonymous_variant | LOW | c.522T>C | p.His174His | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/19 | 730/3952 | 522/2391 | 174/796 | chr8 | 28067703 | ||
chr8:28068227
|
G | A | 1 | a0025c0066 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.469C>T | p.Leu157Leu | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 5/19 | 677/3952 | 469/2391 | 157/796 | chr8 | 28068227 | ||
chr8:28068279
|
A | T | 6 | a0001c0008a0001c0017a0001c0025others(3): Show | 50 | HG00323.hp1 HG01106.hp1 HG01168.hp2 others(47): Show |
synonymous_variant | LOW | c.417T>A | p.Ile139Ile | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 5/19 | 625/3952 | 417/2391 | 139/796 | chr8 | 28068279 | ||
chr8:28068306
|
A | G | 1 | a0001c0035 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.390T>C | p.Ser130Ser | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 5/19 | 598/3952 | 390/2391 | 130/796 | chr8 | 28068306 | ||
chr8:28069624
|
C | T | 7 | a0001c0013a0001c0023a0001c0034others(4): Show | 15 | HG01884.hp2 HG02155.hp2 HG02258.hp1 others(12): Show |
synonymous_variant | LOW | c.177G>A | p.Arg59Arg | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/19 | 385/3952 | 177/2391 | 59/796 | chr8 | 28069624 | ||
chr8:28070265
|
A | G | 1 | a0004c0030 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.135T>C | p.Ser45Ser | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/19 | 343/3952 | 135/2391 | 45/796 | chr8 | 28070265 | ||
chr8:28070310
|
T | C | 1 | a0003c0067 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.90A>G | p.Ser30Ser | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/19 | 298/3952 | 90/2391 | 30/796 | chr8 | 28070310 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:28022020
|
C | T | 57 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(54): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1297G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1297 | chr8 | 28022020 | |||||
chr8:28022030
|
T | C | 1 | a0001c0013t0029 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1287A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1287 | chr8 | 28022030 | |||||
chr8:28022078
|
G | T | 85 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(82): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1239C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1239 | chr8 | 28022078 | |||||
chr8:28022131
|
G | GTA | 5 | a0002c0039t0008a0006c0018t0008a0008c0021t0008others(2): Show | 7 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1184_*1185dupTA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1185 | chr8 | 28022131 | |||||
chr8:28022143
|
A | T | 3 | a0001c0013t0029a0001c0064t0054a0002c0060t0028 | 3 | HG02258.hp1 NA18906.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1174T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1174 | chr8 | 28022143 | |||||
chr8:28022143
|
AT | A | 5 | a0001c0003t0013a0001c0013t0013a0002c0011t0051others(2): Show | 6 | HG02896.hp1 HG02897.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1173delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1173 | chr8 | 28022143 | |||||
chr8:28022157
|
C | CT | 13 | a0001c0001t0006a0002c0005t0010a0002c0005t0061others(10): Show | 19 | HG00733.hp1 HG02071.hp1 HG02280.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1159dupA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1159 | chr8 | 28022157 | |||||
chr8:28022157
|
CT | C | 61 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(58): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1159delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1159 | chr8 | 28022157 | |||||
chr8:28022163
|
T | C | 1 | a0002c0005t0037 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1154A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1154 | chr8 | 28022163 | |||||
chr8:28022197
|
C | T | 1 | a0004c0030t0027 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1120G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1120 | chr8 | 28022197 | |||||
chr8:28022201
|
CAGGCTGG others(276): Show |
C | 1 | a0001c0009t0026 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833_*1115del | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 833 | chr8 | 28022201 | |||||
chr8:28022205
|
CTGGAGTG others(3): Show |
C | 65 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(62): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1102_*1111delCTGC others(6): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1102 | chr8 | 28022205 | |||||
chr8:28022219
|
C | T | 1 | a0002c0006t0053 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1098G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 1098 | chr8 | 28022219 | |||||
chr8:28022400
|
C | T | 1 | a0003c0002t0035 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*917G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 917 | chr8 | 28022400 | |||||
chr8:28022404
|
C | T | 5 | a0001c0003t0013a0001c0013t0013a0002c0011t0051others(2): Show | 6 | HG02896.hp1 HG02897.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*913G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 913 | chr8 | 28022404 | |||||
chr8:28022421
|
G | A | 1 | a0004c0016t0058 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 896 | chr8 | 28022421 | |||||
chr8:28022478
|
A | G | 2 | a0003c0002t0018a0003c0002t0020 | 4 | NA18940.hp1 NA18991.hp2 NA19005.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*839T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 839 | chr8 | 28022478 | |||||
chr8:28022509
|
A | C | 1 | a0028c0070t0042 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*808T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 808 | chr8 | 28022509 | |||||
chr8:28022528
|
A | G | 2 | a0009c0022t0031a0011c0076t0048 | 2 | HG02258.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*789T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 789 | chr8 | 28022528 | |||||
chr8:28022638
|
G | A | 61 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(58): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*679C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 679 | chr8 | 28022638 | |||||
chr8:28022649
|
C | T | 2 | a0001c0001t0047a0004c0007t0030 | 2 | HG02572.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*668G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 668 | chr8 | 28022649 | |||||
chr8:28022772
|
A | T | 1 | a0004c0004t0050 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*545T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 545 | chr8 | 28022772 | |||||
chr8:28022900
|
G | A | 1 | a0003c0002t0059 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*417C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 417 | chr8 | 28022900 | |||||
chr8:28022944
|
G | A | 1 | a0004c0004t0060 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 373 | chr8 | 28022944 | |||||
chr8:28023069
|
C | CA | 19 | a0001c0003t0009a0001c0013t0012a0001c0034t0015others(16): Show | 22 | HG01261.hp2 HG01884.hp2 HG02280.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*247dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 247 | chr8 | 28023069 | |||||
chr8:28023069
|
C | CAA | 7 | a0002c0005t0010a0002c0010t0063a0002c0012t0010others(4): Show | 8 | HG01243.hp1 HG01261.hp1 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*246_*247dupTT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 247 | chr8 | 28023069 | |||||
chr8:28023069
|
CA | C | 34 | a0001c0001t0002a0001c0001t0004a0001c0003t0002others(31): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*247delT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 247 | chr8 | 28023069 | |||||
chr8:28023190
|
A | T | 1 | a0002c0005t0033 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*127T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 127 | chr8 | 28023190 | |||||
chr8:28023309
|
C | T | 56 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(53): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*8G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 19/19 | 8 | chr8 | 28023309 | |||||
chr8:28074412
|
C | T | 3 | a0001c0001t0046a0002c0059t0025a0019c0058t0045 | 3 | HG02896.hp2 HG03139.hp2 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-2G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/19 | 2 | chr8 | 28074412 | |||||
chr8:28083785
|
T | C | 1 | a0004c0007t0044 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-57A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/19 | 9375 | chr8 | 28083785 | |||||
chr8:28083827
|
G | A | 63 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(60): Show | 130 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
5_prime_UTR_variant | MODIFIER | c.-99C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/19 | 9417 | chr8 | 28083827 | |||||
chr8:28083858
|
T | C | 1 | a0004c0016t0064 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-130A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/19 | 9448 | chr8 | 28083858 | |||||
chr8:28083863
|
C | G | 7 | a0001c0001t0007a0002c0005t0007a0003c0002t0007others(4): Show | 10 | NA18945.hp1 NA18962.hp2 NA18966.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-135G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/19 | 9453 | chr8 | 28083863 | |||||
chr8:28083888
|
C | T | 1 | a0004c0004t0024 | 1 | NA19091.hp2 | 5_prime_UTR_variant | MODIFIER | c.-160G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/19 | 9478 | chr8 | 28083888 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:28023480
|
G | T | 1 | a0004c0004t0006g0253 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2246-18C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023480 | ||||||
chr8:28023513
|
C | T | 4 | a0002c0033t0023g0277a0003c0049t0021g0265a0011c0074t0021g0125others(1): Show | 4 | HG03195.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2246-51G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023513 | ||||||
chr8:28023549
|
C | T | 1 | a0002c0010t0022g0371 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2246-87G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023549 | ||||||
chr8:28023574
|
G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0140a0001c0003t0002g0152others(3): Show | 7 | NA18941.hp1 NA18948.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2246-112C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023574 | ||||||
chr8:28023705
|
A | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0230a0001c0001t0001g0231 | 4 | HG02056.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2246-243T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023705 | ||||||
chr8:28023724
|
G | A | 2 | a0002c0005t0033g0270a0004c0004t0001g0210 | 2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2246-262C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023724 | ||||||
chr8:28023776
|
C | T | 1 | a0003c0002t0003g0354 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2246-314G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023776 | ||||||
chr8:28023783
|
C | T | 3 | a0002c0010t0063g0310a0014c0029t0038g0170a0018c0037t0043g0049 | 3 | HG01243.hp1 HG01261.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.2246-321G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023783 | ||||||
chr8:28023788
|
T | A | 5 | a0001c0001t0003g0352a0003c0002t0001g0055a0003c0002t0007g0027others(2): Show | 5 | NA18941.hp2 NA18945.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2246-326A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023788 | ||||||
chr8:28023867
|
T | A | 96 | a0001c0001t0002g0066a0001c0001t0002g0198a0001c0001t0002g0226others(93): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.2246-405A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023867 | ||||||
chr8:28023971
|
C | T | 8 | a0001c0001t0047g0361a0001c0013t0012g0189a0001c0034t0015g0376others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2246-509G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28023971 | ||||||
chr8:28024188
|
A | T | 150 | a0001c0001t0002g0066a0001c0001t0002g0198a0001c0001t0002g0226others(147): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.2246-726T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024188 | ||||||
chr8:28024195
|
C | CT | 65 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0165others(62): Show | 70 | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.2246-734dupA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024195 | ||||||
chr8:28024195
|
CT | C | 14 | a0001c0001t0002g0237a0001c0003t0002g0238a0001c0003t0005g0215others(11): Show | 16 | HG00323.hp2 HG00733.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2246-734delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024195 | ||||||
chr8:28024199
|
T | C | 2 | a0004c0007t0004g0003a0004c0007t0044g0273 | 4 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2246-737A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024199 | ||||||
chr8:28024247
|
G | A | 2 | a0001c0063t0001g0059a0004c0007t0001g0183 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2246-785C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024247 | ||||||
chr8:28024286
|
A | G | 8 | a0001c0003t0013g0264a0001c0013t0013g0190a0001c0013t0013g0200others(5): Show | 8 | HG02145.hp1 HG02818.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2246-824T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024286 | ||||||
chr8:28024413
|
G | A | 1 | a0002c0005t0009g0151 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2246-951C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024413 | ||||||
chr8:28024433
|
G | A | 1 | a0016c0073t0040g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2246-971C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024433 | ||||||
chr8:28024532
|
T | G | 14 | a0001c0001t0005g0043a0001c0001t0005g0201a0001c0001t0005g0266others(11): Show | 15 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2246-1070A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024532 | ||||||
chr8:28024586
|
C | T | 114 | a0001c0001t0002g0066a0001c0001t0002g0198a0001c0001t0002g0226others(111): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.2246-1124G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024586 | ||||||
chr8:28024703
|
G | A | 92 | a0001c0001t0002g0066a0001c0001t0002g0198a0001c0001t0002g0226others(89): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2246-1241C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024703 | ||||||
chr8:28024792
|
A | T | 1 | a0003c0002t0003g0323 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1330T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024792 | ||||||
chr8:28024882
|
T | A | 5 | a0001c0001t0001g0015a0004c0004t0003g0297a0004c0016t0003g0285others(2): Show | 6 | HG01255.hp1 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.2246-1420A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024882 | ||||||
chr8:28024975
|
A | G | 11 | a0001c0001t0046g0276a0001c0001t0047g0361a0001c0013t0012g0189others(8): Show | 11 | HG00733.hp2 HG01261.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2246-1513T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024975 | ||||||
chr8:28024999
|
CT | C | 3 | a0002c0011t0003g0351a0002c0011t0051g0374a0002c0011t0052g0375 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2246-1538delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28024999 | ||||||
chr8:28025151
|
G | T | 1 | a0002c0010t0022g0371 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2246-1689C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025151 | ||||||
chr8:28025323
|
C | T | 9 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2245+1639G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025323 | ||||||
chr8:28025584
|
A | G | 85 | a0001c0001t0001g0122a0001c0001t0002g0066a0001c0001t0002g0198others(82): Show | 92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.2245+1378T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025584 | ||||||
chr8:28025585
|
T | C | 2 | a0001c0001t0046g0276a0011c0076t0048g0365 | 2 | HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2245+1377A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025585 | ||||||
chr8:28025603
|
T | C | 1 | a0001c0025t0002g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2245+1359A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025603 | ||||||
chr8:28025642
|
A | AG | 277 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0064others(274): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.2245+1319dupC | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025642 | ||||||
chr8:28025700
|
G | C | 4 | a0002c0033t0023g0277a0002c0055t0039g0161a0011c0074t0021g0125others(1): Show | 4 | HG02145.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245+1262C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025700 | ||||||
chr8:28025718
|
G | A | 1 | a0001c0001t0046g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2245+1244C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025718 | ||||||
chr8:28025775
|
A | G | 84 | a0001c0001t0002g0066a0001c0001t0002g0198a0001c0001t0004g0312others(81): Show | 91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.2245+1187T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025775 | ||||||
chr8:28025882
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0230a0001c0001t0001g0231 | 4 | HG02056.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245+1080G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28025882 | ||||||
chr8:28026039
|
AT | A | 3 | a0002c0011t0003g0351a0002c0011t0051g0374a0002c0011t0052g0375 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2245+922delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026039 | ||||||
chr8:28026291
|
C | A | 3 | a0002c0059t0025g0044a0009c0022t0001g0127a0009c0022t0031g0126 | 3 | HG00738.hp2 HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2245+671G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026291 | ||||||
chr8:28026339
|
G | A | 3 | a0002c0011t0003g0351a0002c0011t0051g0374a0002c0011t0052g0375 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2245+623C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026339 | ||||||
chr8:28026350
|
G | C | 9 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2245+612C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026350 | ||||||
chr8:28026556
|
G | A | 79 | a0001c0001t0002g0066a0001c0001t0002g0198a0001c0001t0004g0312others(76): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.2245+406C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026556 | ||||||
chr8:28026617
|
A | G | 257 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0064others(254): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.2245+345T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026617 | ||||||
chr8:28026655
|
A | G | 1 | a0002c0006t0003g0317 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2245+307T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026655 | ||||||
chr8:28026718
|
G | C | 12 | a0001c0063t0001g0059a0002c0024t0003g0336a0002c0039t0008g0128others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2245+244C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026718 | ||||||
chr8:28026736
|
G | T | 6 | a0001c0003t0002g0211a0001c0003t0002g0216a0001c0003t0002g0217others(3): Show | 6 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2245+226C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026736 | ||||||
chr8:28026762
|
T | TTCA | 7 | a0002c0005t0001g0218a0003c0002t0001g0091a0004c0004t0001g0080others(4): Show | 8 | HG01433.hp1 HG01496.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2245+197_2245+199d others(5): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026762 | ||||||
chr8:28026762
|
TTCA | T | 122 | a0001c0001t0001g0015a0001c0001t0002g0066a0001c0001t0002g0226others(119): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2245+197_2245+199d others(5): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026762 | ||||||
chr8:28026769
|
T | C | 1 | a0004c0007t0002g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2245+193A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026769 | ||||||
chr8:28026793
|
T | C | 4 | a0002c0033t0023g0277a0002c0055t0039g0161a0011c0074t0021g0125others(1): Show | 4 | HG02145.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245+169A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026793 | ||||||
chr8:28026833
|
T | G | 7 | a0001c0013t0012g0189a0001c0034t0015g0376a0001c0036t0012g0193others(4): Show | 7 | HG01261.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2245+129A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026833 | ||||||
chr8:28026900
|
G | C | 7 | a0001c0013t0012g0189a0001c0034t0015g0376a0001c0036t0012g0193others(4): Show | 7 | HG01261.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2245+62C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 18/18 | chr8 | 28026900 | ||||||
chr8:28027089
|
C | T | 3 | a0002c0011t0003g0351a0002c0011t0051g0374a0002c0011t0052g0375 | 3 | HG02896.hp1 HG02897.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2155-37G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027089 | ||||||
chr8:28027232
|
G | A | 2 | a0001c0013t0029g0179a0002c0060t0028g0206 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2155-180C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027232 | ||||||
chr8:28027287
|
A | G | 125 | a0001c0001t0002g0066a0001c0001t0046g0276a0001c0001t0047g0361others(122): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2155-235T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027287 | ||||||
chr8:28027595
|
G | A | 4 | a0001c0001t0047g0361a0002c0011t0003g0351a0002c0011t0051g0374others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2155-543C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027595 | ||||||
chr8:28027623
|
C | T | 120 | a0001c0001t0002g0066a0001c0001t0046g0276a0001c0003t0002g0011others(117): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.2155-571G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027623 | ||||||
chr8:28027683
|
G | A | 1 | a0001c0003t0001g0157 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2155-631C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027683 | ||||||
chr8:28027797
|
C | T | 1 | a0002c0005t0037g0263 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2155-745G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027797 | ||||||
chr8:28027889
|
G | A | 1 | a0004c0007t0001g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2155-837C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027889 | ||||||
chr8:28027916
|
A | G | 1 | a0004c0004t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2155-864T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027916 | ||||||
chr8:28027969
|
G | A | 3 | a0001c0040t0001g0045a0004c0041t0001g0186a0024c0031t0001g0188 | 3 | HG02886.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2155-917C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28027969 | ||||||
chr8:28028029
|
T | C | 2 | a0011c0076t0048g0365a0013c0048t0001g0207 | 2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2155-977A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028029 | ||||||
chr8:28028060
|
T | TA | 8 | a0001c0008t0003g0339a0001c0017t0003g0324a0001c0064t0054g0275others(5): Show | 8 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2155-1009dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028060 | ||||||
chr8:28028060
|
TA | T | 56 | a0001c0001t0001g0015a0001c0001t0001g0106a0001c0001t0002g0237others(53): Show | 57 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2155-1009delT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028060 | ||||||
chr8:28028122
|
C | G | 1 | a0004c0004t0003g0292 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2155-1070G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028122 | ||||||
chr8:28028254
|
T | C | 8 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1012A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028254 | ||||||
chr8:28028290
|
G | A | 2 | a0011c0076t0048g0365a0013c0048t0001g0207 | 2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2154+976C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028290 | ||||||
chr8:28028326
|
A | G | 273 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0099others(270): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.2154+940T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028326 | ||||||
chr8:28028504
|
C | T | 115 | a0001c0001t0002g0066a0001c0003t0001g0012a0001c0003t0001g0156others(112): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.2154+762G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028504 | ||||||
chr8:28028528
|
G | A | 1 | a0004c0004t0007g0026 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2154+738C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028528 | ||||||
chr8:28028625
|
A | AG | 6 | a0001c0017t0003g0324a0002c0005t0009g0232a0003c0002t0001g0079others(3): Show | 6 | HG01928.hp2 HG03669.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+640dupC | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028625 | ||||||
chr8:28028718
|
G | A | 123 | a0001c0001t0002g0066a0001c0003t0001g0012a0001c0003t0001g0156others(120): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2154+548C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028718 | ||||||
chr8:28028780
|
G | C | 16 | a0001c0063t0001g0059a0002c0024t0003g0336a0002c0039t0008g0128others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2154+486C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028780 | ||||||
chr8:28028945
|
T | C | 4 | a0001c0001t0047g0361a0002c0011t0003g0351a0002c0011t0051g0374others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154+321A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28028945 | ||||||
chr8:28029138
|
G | C | 1 | a0003c0049t0021g0265 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2154+128C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28029138 | ||||||
chr8:28029183
|
A | G | 81 | a0001c0001t0001g0122a0001c0001t0002g0066a0001c0003t0001g0012others(78): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2154+83T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28029183 | ||||||
chr8:28029202
|
C | T | 8 | a0002c0039t0008g0128a0006c0018t0008g0062a0006c0018t0008g0063others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+64G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28029202 | ||||||
chr8:28029205
|
G | A | 1 | a0003c0002t0001g0098 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2154+61C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28029205 | ||||||
chr8:28029206
|
C | A | 1 | a0001c0001t0047g0361 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2154+60G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28029206 | ||||||
chr8:28029213
|
T | C | 7 | a0002c0012t0001g0051a0002c0012t0034g0050a0002c0033t0023g0277others(4): Show | 7 | HG02145.hp1 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154+53A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 17/18 | chr8 | 28029213 | ||||||
chr8:28029467
|
G | A | 4 | a0005c0014t0001g0250a0005c0014t0003g0279a0005c0014t0003g0280others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-65C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28029467 | ||||||
chr8:28029468
|
G | A | 4 | a0005c0014t0001g0250a0005c0014t0003g0279a0005c0014t0003g0280others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-66C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28029468 | ||||||
chr8:28029530
|
G | C | 109 | a0001c0001t0001g0122a0001c0001t0002g0066a0001c0003t0001g0012others(106): Show | 117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.2018-128C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28029530 | ||||||
chr8:28029614
|
G | A | 4 | a0003c0002t0001g0055a0003c0002t0007g0027a0003c0002t0007g0030others(1): Show | 4 | NA18945.hp1 NA18952.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018-212C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28029614 | ||||||
chr8:28029951
|
G | T | 19 | a0001c0001t0002g0066a0001c0003t0002g0056a0001c0003t0002g0213others(16): Show | 19 | HG01099.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.2017+359C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28029951 | ||||||
chr8:28029952
|
C | T | 19 | a0001c0001t0002g0066a0001c0003t0002g0056a0001c0003t0002g0213others(16): Show | 19 | HG01099.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.2017+358G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28029952 | ||||||
chr8:28029958
|
A | C | 7 | a0003c0049t0021g0265a0004c0041t0001g0186a0005c0014t0001g0250others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+352T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28029958 | ||||||
chr8:28029961
|
C | G | 1 | a0003c0019t0003g0342 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2017+349G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28029961 | ||||||
chr8:28030035
|
A | G | 1 | a0001c0003t0017g0146 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2017+275T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28030035 | ||||||
chr8:28030045
|
C | A | 9 | a0001c0003t0002g0211a0001c0003t0002g0216a0001c0003t0002g0217others(6): Show | 9 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2017+265G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28030045 | ||||||
chr8:28030058
|
C | T | 101 | a0001c0001t0001g0019a0001c0001t0001g0122a0001c0001t0001g0131others(98): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2017+252G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28030058 | ||||||
chr8:28030089
|
G | T | 5 | a0002c0033t0023g0277a0002c0055t0039g0161a0003c0049t0021g0265others(2): Show | 5 | HG02145.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017+221C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28030089 | ||||||
chr8:28030112
|
G | A | 1 | a0004c0007t0044g0273 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2017+198C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28030112 | ||||||
chr8:28030205
|
G | C | 308 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(305): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2017+105C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28030205 | ||||||
chr8:28030206
|
G | A | 1 | a0001c0001t0003g0360 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2017+104C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28030206 | ||||||
chr8:28030296
|
T | C | 61 | a0001c0001t0001g0122a0001c0001t0003g0360a0001c0001t0005g0043others(58): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.2017+14A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28030296 | ||||||
chr8:28030299
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2017+11C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 16/18 | chr8 | 28030299 | ||||||
chr8:28030517
|
T | C | 1 | a0001c0013t0029g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1909-99A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28030517 | ||||||
chr8:28030543
|
T | G | 4 | a0002c0024t0003g0336a0010c0026t0010g0129a0011c0076t0048g0365others(1): Show | 4 | HG02055.hp1 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909-125A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28030543 | ||||||
chr8:28030591
|
C | T | 1 | a0004c0016t0064g0377 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1909-173G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28030591 | ||||||
chr8:28030686
|
G | A | 1 | a0003c0002t0001g0073 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1909-268C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28030686 | ||||||
chr8:28030836
|
A | G | 3 | a0002c0012t0010g0191a0002c0012t0010g0192a0002c0012t0036g0185 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1908+407T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28030836 | ||||||
chr8:28031081
|
C | T | 8 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1908+162G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28031081 | ||||||
chr8:28031109
|
A | C | 64 | a0001c0001t0001g0019a0001c0001t0001g0131a0001c0001t0001g0144others(61): Show | 72 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1908+134T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28031109 | ||||||
chr8:28031112
|
G | A | 78 | a0001c0001t0001g0019a0001c0001t0001g0131a0001c0001t0001g0144others(75): Show | 86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1908+131C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28031112 | ||||||
chr8:28031174
|
C | T | 3 | a0001c0034t0015g0376a0001c0057t0015g0350a0015c0071t0015g0369 | 3 | HG02615.hp2 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1908+69G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28031174 | ||||||
chr8:28031177
|
C | A | 1 | a0015c0071t0015g0369 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1908+66G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 15/18 | chr8 | 28031177 | ||||||
chr8:28031477
|
G | A | 1 | a0001c0003t0002g0240 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1770-96C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28031477 | ||||||
chr8:28031544
|
C | A | 3 | a0001c0001t0005g0043a0001c0023t0005g0180a0002c0006t0011g0320 | 3 | HG02451.hp1 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1770-163G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28031544 | ||||||
chr8:28031571
|
G | A | 1 | a0002c0005t0033g0270 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1770-190C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28031571 | ||||||
chr8:28031571
|
G | T | 1 | a0001c0017t0003g0328 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1770-190C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28031571 | ||||||
chr8:28031976
|
G | A | 1 | a0002c0005t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1770-595C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28031976 | ||||||
chr8:28032034
|
A | G | 7 | a0001c0001t0001g0175a0001c0001t0003g0352a0001c0001t0007g0025others(4): Show | 7 | NA18941.hp2 NA18949.hp1 NA19002.hp1 others(4): Show |
intron_variant | MODIFIER | c.1770-653T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032034 | ||||||
chr8:28032248
|
G | A | 1 | a0002c0005t0003g0282 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1770-867C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032248 | ||||||
chr8:28032385
|
T | C | 6 | a0004c0041t0001g0186a0005c0014t0001g0250a0005c0014t0003g0279others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1770-1004A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032385 | ||||||
chr8:28032449
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0006g0225a0004c0004t0003g0358 | 3 | HG00639.hp1 HG00733.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1770-1068C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032449 | ||||||
chr8:28032455
|
T | C | 247 | a0001c0001t0001g0019a0001c0001t0001g0101a0001c0001t0001g0131others(244): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1770-1074A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032455 | ||||||
chr8:28032489
|
G | A | 1 | a0004c0004t0007g0026 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1769+1051C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032489 | ||||||
chr8:28032545
|
A | G | 1 | a0004c0004t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1769+995T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032545 | ||||||
chr8:28032550
|
T | C | 1 | a0004c0004t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1769+990A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032550 | ||||||
chr8:28032684
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1769+856G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032684 | ||||||
chr8:28032699
|
C | T | 144 | a0001c0001t0001g0101a0001c0001t0001g0175a0001c0001t0001g0178others(141): Show | 153 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1769+841G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032699 | ||||||
chr8:28032707
|
C | T | 144 | a0001c0001t0001g0101a0001c0001t0001g0175a0001c0001t0001g0178others(141): Show | 153 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1769+833G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032707 | ||||||
chr8:28032723
|
G | GA | 11 | a0001c0001t0005g0201a0001c0001t0006g0110a0001c0001t0046g0276others(8): Show | 11 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1769+816dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032723 | ||||||
chr8:28032723
|
GA | G | 78 | a0001c0001t0001g0019a0001c0001t0001g0131a0001c0001t0001g0144others(75): Show | 86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1769+816delT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032723 | ||||||
chr8:28032811
|
T | C | 1 | a0025c0066t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1769+729A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032811 | ||||||
chr8:28032926
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1769+614C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28032926 | ||||||
chr8:28033166
|
T | A | 8 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1769+374A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28033166 | ||||||
chr8:28033320
|
T | G | 1 | a0001c0036t0012g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1769+220A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28033320 | ||||||
chr8:28033341
|
G | A | 81 | a0001c0001t0001g0019a0001c0001t0001g0131a0001c0001t0001g0144others(78): Show | 89 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1769+199C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28033341 | ||||||
chr8:28033410
|
GGACTA | G | 66 | a0001c0001t0001g0019a0001c0001t0001g0131a0001c0001t0001g0144others(63): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1769+125_1769+129d others(7): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28033410 | ||||||
chr8:28033435
|
C | T | 1 | a0002c0006t0003g0316 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1769+105G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28033435 | ||||||
chr8:28033481
|
A | C | 1 | a0004c0030t0027g0096 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1769+59T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 14/18 | chr8 | 28033481 | ||||||
chr8:28033723
|
G | A | 2 | a0002c0024t0003g0336a0010c0026t0010g0129 | 2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1612-26C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28033723 | ||||||
chr8:28033761
|
G | A | 4 | a0002c0024t0003g0336a0010c0026t0010g0129a0011c0076t0048g0365others(1): Show | 4 | HG02055.hp1 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1612-64C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28033761 | ||||||
chr8:28033818
|
G | A | 1 | a0001c0001t0006g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1612-121C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28033818 | ||||||
chr8:28033864
|
C | T | 168 | a0001c0001t0001g0101a0001c0001t0001g0175a0001c0001t0001g0178others(165): Show | 178 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.1612-167G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28033864 | ||||||
chr8:28033972
|
G | A | 4 | a0002c0024t0003g0336a0010c0026t0010g0129a0011c0076t0048g0365others(1): Show | 4 | HG02055.hp1 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1612-275C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28033972 | ||||||
chr8:28034047
|
G | C | 250 | a0001c0001t0001g0019a0001c0001t0001g0101a0001c0001t0001g0131others(247): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1612-350C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034047 | ||||||
chr8:28034088
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0004c0004t0062g0303 | 3 | NA18979.hp1 NA19005.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1612-391G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034088 | ||||||
chr8:28034108
|
A | G | 140 | a0001c0001t0001g0101a0001c0001t0001g0175a0001c0001t0001g0178others(137): Show | 149 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1612-411T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034108 | ||||||
chr8:28034220
|
T | G | 66 | a0001c0001t0001g0019a0001c0001t0001g0131a0001c0001t0001g0144others(63): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1612-523A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034220 | ||||||
chr8:28034324
|
C | T | 1 | a0004c0016t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1612-627G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034324 | ||||||
chr8:28034359
|
A | C | 6 | a0001c0001t0002g0066a0001c0001t0002g0198a0001c0001t0004g0312others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1612-662T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034359 | ||||||
chr8:28034461
|
C | T | 1 | a0001c0008t0003g0331 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1612-764G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034461 | ||||||
chr8:28034574
|
G | A | 2 | a0002c0012t0001g0051a0002c0012t0034g0050 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1612-877C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034574 | ||||||
chr8:28034766
|
G | A | 1 | a0003c0002t0001g0090 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1612-1069C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034766 | ||||||
chr8:28034804
|
C | T | 1 | a0025c0066t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1612-1107G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034804 | ||||||
chr8:28034864
|
T | A | 2 | a0002c0012t0001g0051a0002c0012t0034g0050 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1612-1167A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034864 | ||||||
chr8:28034893
|
C | T | 1 | a0025c0066t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1612-1196G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034893 | ||||||
chr8:28034895
|
C | T | 1 | a0004c0004t0003g0340 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1612-1198G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034895 | ||||||
chr8:28034956
|
T | C | 22 | a0001c0001t0005g0043a0001c0001t0005g0201a0001c0001t0046g0276others(19): Show | 23 | HG01261.hp1 HG01891.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1612-1259A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034956 | ||||||
chr8:28034997
|
T | C | 21 | a0001c0001t0005g0043a0001c0001t0005g0201a0001c0001t0046g0276others(18): Show | 22 | HG01261.hp1 HG01891.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1612-1300A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28034997 | ||||||
chr8:28035098
|
C | T | 1 | a0004c0004t0060g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1612-1401G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035098 | ||||||
chr8:28035100
|
C | T | 1 | a0004c0030t0027g0096 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1612-1403G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035100 | ||||||
chr8:28035137
|
A | T | 1 | a0009c0022t0031g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1612-1440T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035137 | ||||||
chr8:28035141
|
T | A | 3 | a0002c0033t0023g0277a0011c0074t0021g0125a0022c0032t0023g0278 | 3 | HG03453.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1612-1444A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035141 | ||||||
chr8:28035298
|
G | C | 160 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(157): Show | 170 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.1612-1601C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035298 | ||||||
chr8:28035303
|
G | A | 1 | a0025c0066t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1612-1606C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035303 | ||||||
chr8:28035397
|
T | G | 1 | a0004c0030t0027g0096 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1612-1700A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035397 | ||||||
chr8:28035689
|
C | A | 1 | a0001c0009t0001g0142 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1612-1992G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035689 | ||||||
chr8:28035781
|
C | T | 1 | a0001c0034t0015g0376 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1612-2084G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035781 | ||||||
chr8:28035784
|
A | G | 2 | a0001c0001t0005g0266a0004c0007t0030g0195 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1612-2087T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035784 | ||||||
chr8:28035805
|
T | C | 10 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1612-2108A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035805 | ||||||
chr8:28035871
|
G | A | 21 | a0001c0001t0005g0043a0001c0001t0005g0201a0001c0001t0046g0276others(18): Show | 22 | HG01261.hp1 HG01891.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1612-2174C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035871 | ||||||
chr8:28035895
|
T | C | 14 | a0001c0001t0047g0361a0001c0036t0012g0193a0001c0063t0001g0059others(11): Show | 14 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1612-2198A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035895 | ||||||
chr8:28035919
|
G | C | 14 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(11): Show | 14 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1612-2222C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035919 | ||||||
chr8:28035948
|
C | T | 14 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(11): Show | 14 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1612-2251G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035948 | ||||||
chr8:28035974
|
C | T | 1 | a0004c0004t0060g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1612-2277G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035974 | ||||||
chr8:28035979
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1612-2282G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28035979 | ||||||
chr8:28036046
|
CT | C | 69 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0099others(66): Show | 73 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1612-2350delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036046 | ||||||
chr8:28036075
|
A | G | 3 | a0001c0001t0005g0266a0004c0007t0001g0194a0004c0007t0030g0195 | 3 | HG02572.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1612-2378T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036075 | ||||||
chr8:28036165
|
C | T | 1 | a0004c0004t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1612-2468G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036165 | ||||||
chr8:28036270
|
G | A | 173 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(170): Show | 183 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1612-2573C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036270 | ||||||
chr8:28036393
|
C | T | 2 | a0001c0001t0001g0178a0001c0035t0001g0116 | 2 | HG02083.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1612-2696G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036393 | ||||||
chr8:28036418
|
G | T | 47 | a0001c0001t0005g0043a0001c0001t0005g0201a0001c0001t0046g0276others(44): Show | 48 | HG00733.hp2 HG01243.hp1 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.1612-2721C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036418 | ||||||
chr8:28036421
|
T | C | 1 | a0001c0003t0002g0056 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1612-2724A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036421 | ||||||
chr8:28036593
|
C | T | 7 | a0002c0060t0028g0206a0004c0041t0001g0186a0005c0014t0001g0250others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612-2896G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036593 | ||||||
chr8:28036673
|
A | G | 1 | a0004c0004t0003g0340 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1612-2976T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036673 | ||||||
chr8:28036802
|
A | T | 1 | a0004c0007t0002g0068 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1612-3105T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036802 | ||||||
chr8:28036870
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0230a0001c0001t0001g0231 | 4 | HG02056.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1612-3173G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036870 | ||||||
chr8:28036904
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1612-3207C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28036904 | ||||||
chr8:28037028
|
C | T | 3 | a0007c0015t0001g0094a0007c0015t0003g0299a0007c0015t0007g0006 | 4 | NA18962.hp2 NA19011.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1612-3331G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037028 | ||||||
chr8:28037043
|
C | A | 171 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(168): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1612-3346G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037043 | ||||||
chr8:28037117
|
G | C | 1 | a0001c0003t0002g0240 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1612-3420C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037117 | ||||||
chr8:28037224
|
G | A | 171 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(168): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1612-3527C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037224 | ||||||
chr8:28037272
|
C | A | 1 | a0004c0007t0002g0068 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1612-3575G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037272 | ||||||
chr8:28037291
|
C | A | 1 | a0004c0007t0002g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1612-3594G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037291 | ||||||
chr8:28037292
|
A | T | 1 | a0004c0007t0002g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1612-3595T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037292 | ||||||
chr8:28037365
|
T | C | 8 | a0002c0010t0022g0371a0002c0024t0003g0336a0002c0059t0025g0044others(5): Show | 8 | HG00733.hp2 HG02055.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1612-3668A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037365 | ||||||
chr8:28037468
|
C | A | 13 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(10): Show | 13 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1611+3583G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037468 | ||||||
chr8:28037516
|
C | T | 3 | a0001c0063t0001g0059a0016c0073t0040g0160a0026c0051t0019g0187 | 3 | HG02723.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1611+3535G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037516 | ||||||
chr8:28037581
|
G | A | 3 | a0002c0010t0022g0371a0002c0059t0025g0044a0003c0044t0001g0224 | 3 | HG00733.hp2 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1611+3470C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037581 | ||||||
chr8:28037624
|
A | T | 171 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(168): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1611+3427T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037624 | ||||||
chr8:28037755
|
G | A | 9 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1611+3296C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037755 | ||||||
chr8:28037861
|
AG | A | 5 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1611+3189delC | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037861 | ||||||
chr8:28037863
|
G | C | 170 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(167): Show | 181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1611+3188C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037863 | ||||||
chr8:28037863
|
G | T | 1 | a0003c0002t0017g0118 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1611+3188C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037863 | ||||||
chr8:28037869
|
G | A | 8 | a0001c0003t0002g0163a0001c0003t0002g0164a0001c0003t0002g0214others(5): Show | 10 | HG00280.hp1 HG00323.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1611+3182C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037869 | ||||||
chr8:28037954
|
G | C | 5 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1611+3097C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28037954 | ||||||
chr8:28038010
|
T | G | 1 | a0001c0001t0006g0259 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1611+3041A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038010 | ||||||
chr8:28038116
|
G | A | 1 | a0002c0005t0001g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1611+2935C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038116 | ||||||
chr8:28038118
|
G | A | 2 | a0002c0012t0001g0051a0002c0012t0034g0050 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1611+2933C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038118 | ||||||
chr8:28038241
|
C | G | 1 | a0002c0060t0028g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1611+2810G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038241 | ||||||
chr8:28038311
|
T | A | 171 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(168): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1611+2740A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038311 | ||||||
chr8:28038324
|
G | C | 2 | a0009c0022t0001g0127a0009c0022t0031g0126 | 2 | HG00738.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1611+2727C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038324 | ||||||
chr8:28038450
|
C | T | 1 | a0002c0005t0003g0318 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1611+2601G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038450 | ||||||
chr8:28038451
|
G | A | 13 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(10): Show | 13 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1611+2600C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038451 | ||||||
chr8:28038497
|
A | G | 1 | a0002c0005t0002g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1611+2554T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038497 | ||||||
chr8:28038538
|
A | G | 3 | a0002c0006t0003g0327a0002c0006t0009g0135a0003c0002t0001g0073 | 3 | HG02071.hp2 HG02080.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1611+2513T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038538 | ||||||
chr8:28038539
|
T | C | 3 | a0001c0001t0005g0201a0001c0001t0046g0276a0005c0053t0005g0060 | 3 | HG02809.hp1 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1611+2512A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038539 | ||||||
chr8:28038600
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1611+2451C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038600 | ||||||
chr8:28038735
|
A | G | 5 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1611+2316T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038735 | ||||||
chr8:28038773
|
T | G | 3 | a0002c0010t0022g0371a0002c0059t0025g0044a0003c0044t0001g0224 | 3 | HG00733.hp2 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1611+2278A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038773 | ||||||
chr8:28038925
|
A | T | 10 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1611+2126T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28038925 | ||||||
chr8:28039002
|
G | A | 8 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1611+2049C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039002 | ||||||
chr8:28039082
|
A | G | 4 | a0003c0002t0001g0055a0003c0002t0007g0027a0003c0002t0007g0030others(1): Show | 4 | NA18945.hp1 NA18952.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1611+1969T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039082 | ||||||
chr8:28039201
|
T | A | 1 | a0002c0006t0003g0316 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1611+1850A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039201 | ||||||
chr8:28039202
|
C | T | 1 | a0002c0006t0003g0316 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1611+1849G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039202 | ||||||
chr8:28039210
|
C | T | 2 | a0001c0003t0002g0211a0001c0003t0002g0216 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1611+1841G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039210 | ||||||
chr8:28039234
|
AT | A | 9 | a0001c0003t0017g0146a0001c0013t0012g0189a0001c0013t0013g0190others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1611+1816delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039234 | ||||||
chr8:28039234
|
ATT | A | 170 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(167): Show | 181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1611+1815_1611+181 others(6): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039234 | ||||||
chr8:28039234
|
ATTT | A | 14 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(11): Show | 14 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1611+1814_1611+181 others(7): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039234 | ||||||
chr8:28039272
|
A | ACCTCAGC others(16): Show |
1 | a0004c0007t0002g0068 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1611+1756_1611+177 others(27): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039272 | ||||||
chr8:28039368
|
G | A | 1 | a0002c0010t0001g0047 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1611+1683C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039368 | ||||||
chr8:28039382
|
C | T | 5 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1611+1669G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039382 | ||||||
chr8:28039610
|
G | A | 1 | a0001c0001t0003g0360 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1611+1441C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039610 | ||||||
chr8:28039644
|
A | G | 1 | a0001c0009t0001g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1611+1407T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039644 | ||||||
chr8:28039759
|
G | A | 13 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(10): Show | 13 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1611+1292C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039759 | ||||||
chr8:28039764
|
G | C | 8 | a0002c0060t0028g0206a0004c0041t0001g0186a0005c0014t0001g0250others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1611+1287C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039764 | ||||||
chr8:28039919
|
G | A | 1 | a0004c0030t0027g0096 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1611+1132C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039919 | ||||||
chr8:28039935
|
C | T | 171 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(168): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1611+1116G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28039935 | ||||||
chr8:28040016
|
G | A | 1 | a0001c0003t0002g0164 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1611+1035C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040016 | ||||||
chr8:28040056
|
GGA | G | 5 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1611+993_1611+994d others(4): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040056 | ||||||
chr8:28040129
|
C | T | 1 | a0001c0003t0003g0363 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1611+922G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040129 | ||||||
chr8:28040190
|
A | G | 2 | a0003c0002t0002g0092a0003c0002t0017g0118 | 2 | HG02155.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1611+861T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040190 | ||||||
chr8:28040300
|
C | T | 13 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(10): Show | 13 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1611+751G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040300 | ||||||
chr8:28040342
|
G | A | 3 | a0001c0001t0007g0025a0012c0027t0001g0173a0012c0027t0001g0174 | 3 | NA18949.hp1 NA19074.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1611+709C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040342 | ||||||
chr8:28040441
|
G | A | 13 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(10): Show | 13 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1611+610C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040441 | ||||||
chr8:28040465
|
C | T | 5 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1611+586G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040465 | ||||||
chr8:28040524
|
A | T | 3 | a0002c0010t0022g0371a0002c0059t0025g0044a0003c0044t0001g0224 | 3 | HG00733.hp2 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1611+527T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040524 | ||||||
chr8:28040622
|
C | T | 3 | a0002c0010t0022g0371a0002c0059t0025g0044a0003c0044t0001g0224 | 3 | HG00733.hp2 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1611+429G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040622 | ||||||
chr8:28040624
|
C | CT | 23 | a0001c0001t0005g0043a0001c0001t0005g0201a0001c0001t0046g0276others(20): Show | 24 | HG01261.hp1 HG01891.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1611+426dupA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040624 | ||||||
chr8:28040624
|
CT | C | 7 | a0001c0001t0047g0361a0001c0003t0002g0240a0001c0036t0012g0193others(4): Show | 7 | HG00735.hp1 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1611+426delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040624 | ||||||
chr8:28040651
|
C | T | 184 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(181): Show | 195 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.1611+400G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040651 | ||||||
chr8:28040686
|
C | T | 1 | a0004c0004t0060g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1611+365G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040686 | ||||||
chr8:28040733
|
G | A | 1 | a0005c0053t0005g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1611+318C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040733 | ||||||
chr8:28040785
|
G | C | 1 | a0003c0002t0002g0010 | 2 | NA18939.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1611+266C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040785 | ||||||
chr8:28040887
|
C | A | 10 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1611+164G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040887 | ||||||
chr8:28040888
|
G | A | 2 | a0001c0001t0047g0361a0001c0003t0002g0240 | 2 | HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1611+163C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040888 | ||||||
chr8:28040935
|
A | G | 188 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0235others(185): Show | 200 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1611+116T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040935 | ||||||
chr8:28040956
|
T | C | 1 | a0003c0002t0003g0302 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1611+95A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040956 | ||||||
chr8:28040978
|
A | T | 1 | a0025c0066t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1611+73T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 13/18 | chr8 | 28040978 | ||||||
chr8:28041250
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1447-35G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041250 | ||||||
chr8:28041270
|
T | C | 2 | a0002c0059t0025g0044a0003c0044t0001g0224 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1447-55A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041270 | ||||||
chr8:28041589
|
G | A | 2 | a0009c0022t0001g0127a0009c0022t0031g0126 | 2 | HG00738.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1447-374C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041589 | ||||||
chr8:28041590
|
G | A | 376 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(373): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1447-375C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041590 | ||||||
chr8:28041595
|
G | T | 376 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(373): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1447-380C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041595 | ||||||
chr8:28041606
|
G | A | 229 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(226): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1447-391C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041606 | ||||||
chr8:28041627
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1447-412C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041627 | ||||||
chr8:28041645
|
T | C | 2 | a0009c0022t0001g0127a0009c0022t0031g0126 | 2 | HG00738.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1447-430A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041645 | ||||||
chr8:28041736
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1447-521G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041736 | ||||||
chr8:28041961
|
G | T | 2 | a0004c0007t0004g0295a0004c0007t0016g0029 | 2 | HG00408.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1447-746C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041961 | ||||||
chr8:28041984
|
T | C | 1 | a0002c0060t0028g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1447-769A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28041984 | ||||||
chr8:28042064
|
G | GAAACCTT others(3): Show |
1 | a0002c0005t0007g0032 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1447-859_1447-850d others(12): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042064 | ||||||
chr8:28042079
|
C | A | 5 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447-864G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042079 | ||||||
chr8:28042098
|
T | C | 1 | a0002c0006t0003g0316 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1447-883A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042098 | ||||||
chr8:28042109
|
C | T | 1 | a0002c0024t0012g0247 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1447-894G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042109 | ||||||
chr8:28042121
|
A | C | 16 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(13): Show | 16 | HG00738.hp2 HG02258.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1447-906T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042121 | ||||||
chr8:28042198
|
C | T | 1 | a0001c0003t0002g0240 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1447-983G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042198 | ||||||
chr8:28042203
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0006g0259 | 2 | NA18961.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1447-988T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042203 | ||||||
chr8:28042350
|
A | G | 1 | a0004c0030t0027g0096 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1447-1135T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042350 | ||||||
chr8:28042424
|
C | T | 4 | a0001c0034t0015g0376a0001c0057t0015g0350a0004c0004t0060g0346others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-1209G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042424 | ||||||
chr8:28042618
|
T | TCTCCTGC | 3 | a0001c0003t0002g0140a0001c0003t0002g0152a0001c0003t0002g0155 | 3 | NA18948.hp1 NA18952.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1447-1410_1447-140 others(11): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042618 | ||||||
chr8:28042768
|
G | A | 21 | a0001c0001t0005g0043a0001c0023t0005g0180a0002c0005t0037g0263others(18): Show | 22 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1447-1553C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042768 | ||||||
chr8:28042896
|
T | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0230a0001c0001t0001g0231 | 4 | HG02056.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-1681A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042896 | ||||||
chr8:28042953
|
T | A | 1 | a0003c0002t0009g0120 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1447-1738A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28042953 | ||||||
chr8:28043003
|
C | T | 6 | a0004c0041t0001g0186a0005c0014t0001g0250a0005c0014t0003g0279others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1447-1788G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043003 | ||||||
chr8:28043004
|
G | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0235a0001c0035t0001g0116 | 3 | HG02083.hp2 NA18957.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1447-1789C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043004 | ||||||
chr8:28043081
|
C | A | 4 | a0002c0024t0003g0336a0010c0026t0010g0129a0011c0076t0048g0365others(1): Show | 4 | HG02055.hp1 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-1866G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043081 | ||||||
chr8:28043126
|
G | T | 1 | a0002c0005t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1447-1911C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043126 | ||||||
chr8:28043193
|
G | A | 232 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(229): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1447-1978C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043193 | ||||||
chr8:28043201
|
A | C | 5 | a0001c0001t0002g0066a0001c0001t0002g0198a0001c0001t0004g0312others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447-1986T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043201 | ||||||
chr8:28043257
|
G | C | 1 | a0001c0001t0006g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1447-2042C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043257 | ||||||
chr8:28043286
|
T | C | 214 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(211): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1447-2071A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043286 | ||||||
chr8:28043310
|
C | A | 243 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1447-2095G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043310 | ||||||
chr8:28043679
|
C | T | 5 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1446+1848G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043679 | ||||||
chr8:28043715
|
C | T | 6 | a0004c0041t0001g0186a0005c0014t0001g0250a0005c0014t0003g0279others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1446+1812G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043715 | ||||||
chr8:28043763
|
G | A | 1 | a0004c0007t0001g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1446+1764C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043763 | ||||||
chr8:28043826
|
C | G | 2 | a0001c0001t0047g0361a0001c0003t0002g0240 | 2 | HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1446+1701G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043826 | ||||||
chr8:28043882
|
G | A | 1 | a0002c0005t0001g0218 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1446+1645C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043882 | ||||||
chr8:28043977
|
A | T | 1 | a0002c0010t0022g0371 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1446+1550T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28043977 | ||||||
chr8:28044072
|
G | A | 2 | a0011c0076t0048g0365a0013c0048t0001g0207 | 2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1446+1455C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044072 | ||||||
chr8:28044076
|
C | T | 1 | a0001c0036t0012g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1446+1451G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044076 | ||||||
chr8:28044139
|
C | T | 1 | a0019c0058t0045g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1446+1388G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044139 | ||||||
chr8:28044173
|
G | C | 232 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(229): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1446+1354C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044173 | ||||||
chr8:28044282
|
C | T | 214 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(211): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1446+1245G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044282 | ||||||
chr8:28044314
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1446+1213G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044314 | ||||||
chr8:28044342
|
T | C | 6 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1446+1185A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044342 | ||||||
chr8:28044463
|
C | T | 1 | a0004c0004t0003g0340 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1446+1064G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044463 | ||||||
chr8:28044571
|
A | G | 1 | a0001c0001t0003g0360 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1446+956T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044571 | ||||||
chr8:28044803
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0230a0001c0001t0001g0231 | 4 | HG02056.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+724C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044803 | ||||||
chr8:28044866
|
G | A | 1 | a0002c0006t0003g0330 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1446+661C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044866 | ||||||
chr8:28044965
|
A | C | 1 | a0001c0001t0002g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1446+562T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044965 | ||||||
chr8:28044976
|
T | C | 1 | a0001c0003t0002g0238 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1446+551A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28044976 | ||||||
chr8:28045090
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1446+437A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28045090 | ||||||
chr8:28045098
|
T | A | 2 | a0001c0001t0003g0360a0001c0003t0056g0314 | 2 | HG02615.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1446+429A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28045098 | ||||||
chr8:28045171
|
C | T | 2 | a0002c0005t0001g0037a0002c0005t0001g0041 | 2 | HG00597.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1446+356G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28045171 | ||||||
chr8:28045226
|
G | A | 1 | a0001c0001t0002g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1446+301C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28045226 | ||||||
chr8:28045399
|
A | T | 3 | a0002c0005t0001g0236a0002c0005t0009g0229a0002c0005t0009g0232 | 3 | HG02738.hp2 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1446+128T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28045399 | ||||||
chr8:28045511
|
C | T | 1 | a0004c0004t0001g0081 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1446+16G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 12/18 | chr8 | 28045511 | ||||||
chr8:28045773
|
C | A | 1 | a0028c0070t0042g0137 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1313-113G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28045773 | ||||||
chr8:28045894
|
A | C | 19 | a0001c0003t0002g0240a0001c0034t0015g0376a0001c0036t0012g0193others(16): Show | 19 | HG00735.hp1 HG00738.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1313-234T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28045894 | ||||||
chr8:28045945
|
T | G | 1 | a0002c0006t0003g0317 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1313-285A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28045945 | ||||||
chr8:28045988
|
G | A | 234 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(231): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1313-328C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28045988 | ||||||
chr8:28046060
|
A | G | 121 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0040others(118): Show | 131 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1313-400T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046060 | ||||||
chr8:28046068
|
T | C | 121 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0040others(118): Show | 131 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1313-408A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046068 | ||||||
chr8:28046427
|
T | A | 1 | a0004c0046t0002g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1313-767A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046427 | ||||||
chr8:28046434
|
C | T | 3 | a0002c0005t0001g0071a0002c0006t0003g0338a0002c0006t0003g0347 | 3 | HG00099.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1313-774G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046434 | ||||||
chr8:28046458
|
G | A | 3 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0041 | 3 | HG00597.hp2 NA18955.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1313-798C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046458 | ||||||
chr8:28046680
|
A | ATT | 7 | a0002c0005t0001g0149a0002c0006t0001g0258a0002c0006t0009g0135others(4): Show | 7 | HG01943.hp2 HG02451.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312+825_1312+826d others(4): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046680 | ||||||
chr8:28046680
|
A | ATTT | 131 | a0001c0003t0002g0240a0001c0034t0015g0376a0001c0036t0012g0193others(128): Show | 141 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1312+824_1312+826d others(5): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046680 | ||||||
chr8:28046680
|
AT | A | 78 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(75): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1312+826delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046680 | ||||||
chr8:28046750
|
G | A | 1 | a0010c0026t0010g0129 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1312+757C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046750 | ||||||
chr8:28046805
|
C | T | 1 | a0004c0004t0004g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1312+702G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046805 | ||||||
chr8:28046826
|
T | C | 218 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(215): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1312+681A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046826 | ||||||
chr8:28046907
|
G | T | 3 | a0002c0010t0022g0371a0002c0059t0025g0044a0003c0044t0001g0224 | 3 | HG00733.hp2 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1312+600C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046907 | ||||||
chr8:28046952
|
A | G | 1 | a0004c0004t0003g0340 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1312+555T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046952 | ||||||
chr8:28046981
|
G | T | 2 | a0002c0024t0003g0336a0010c0026t0010g0129 | 2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1312+526C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046981 | ||||||
chr8:28046982
|
T | G | 2 | a0002c0024t0003g0336a0010c0026t0010g0129 | 2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1312+525A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046982 | ||||||
chr8:28046983
|
G | T | 218 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(215): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1312+524C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28046983 | ||||||
chr8:28047039
|
T | C | 140 | a0001c0003t0002g0240a0001c0034t0015g0376a0001c0036t0012g0193others(137): Show | 150 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1312+468A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28047039 | ||||||
chr8:28047058
|
C | T | 1 | a0004c0007t0004g0295 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1312+449G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28047058 | ||||||
chr8:28047185
|
T | G | 225 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(222): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1312+322A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28047185 | ||||||
chr8:28047320
|
G | A | 1 | a0017c0075t0005g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1312+187C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28047320 | ||||||
chr8:28047412
|
T | A | 1 | a0001c0001t0006g0100 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1312+95A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28047412 | ||||||
chr8:28047429
|
G | C | 1 | a0003c0067t0001g0095 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1312+78C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 11/18 | chr8 | 28047429 | ||||||
chr8:28047848
|
A | G | 1 | a0001c0040t0001g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1207-236T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28047848 | ||||||
chr8:28047957
|
A | G | 1 | a0003c0002t0001g0196 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1207-345T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28047957 | ||||||
chr8:28048025
|
A | G | 2 | a0002c0024t0003g0336a0010c0026t0010g0129 | 2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1207-413T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048025 | ||||||
chr8:28048082
|
T | C | 78 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(75): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1207-470A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048082 | ||||||
chr8:28048175
|
G | A | 19 | a0002c0005t0061g0366a0002c0010t0022g0371a0002c0012t0010g0191others(16): Show | 19 | HG00733.hp2 HG01243.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1207-563C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048175 | ||||||
chr8:28048326
|
A | C | 139 | a0001c0003t0002g0240a0001c0013t0012g0189a0001c0013t0013g0190others(136): Show | 149 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1207-714T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048326 | ||||||
chr8:28048344
|
C | T | 217 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(214): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1207-732G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048344 | ||||||
chr8:28048369
|
G | A | 1 | a0001c0001t0007g0025 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1207-757C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048369 | ||||||
chr8:28048371
|
A | T | 139 | a0001c0003t0002g0240a0001c0013t0012g0189a0001c0013t0013g0190others(136): Show | 149 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1207-759T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048371 | ||||||
chr8:28048405
|
T | TTTTG | 11 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207-797_1207-794d others(6): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048405 | ||||||
chr8:28048448
|
CAA | C | 139 | a0001c0003t0002g0240a0001c0013t0012g0189a0001c0013t0013g0190others(136): Show | 149 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1207-838_1207-837d others(4): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048448 | ||||||
chr8:28048461
|
G | T | 1 | a0002c0005t0003g0318 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1207-849C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048461 | ||||||
chr8:28048639
|
G | A | 6 | a0001c0034t0015g0376a0001c0057t0015g0350a0004c0004t0060g0346others(3): Show | 6 | HG00738.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-1027C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048639 | ||||||
chr8:28048682
|
T | G | 1 | a0002c0060t0028g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1207-1070A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048682 | ||||||
chr8:28048756
|
G | A | 5 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-1144C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048756 | ||||||
chr8:28048769
|
A | G | 3 | a0008c0021t0001g0169a0008c0021t0008g0052a0008c0021t0055g0370 | 3 | HG02109.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1207-1157T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048769 | ||||||
chr8:28048803
|
C | T | 6 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-1191G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048803 | ||||||
chr8:28048860
|
C | CA | 15 | a0001c0001t0001g0178a0001c0001t0001g0235a0001c0001t0001g0245others(12): Show | 15 | HG02083.hp2 HG02630.hp2 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.1207-1249dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048860 | ||||||
chr8:28048860
|
CA | C | 19 | a0001c0001t0001g0015a0001c0001t0002g0066a0001c0001t0003g0360others(16): Show | 20 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1207-1249delT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048860 | ||||||
chr8:28048860
|
CAA | C | 67 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(64): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1207-1250_1207-124 others(6): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048860 | ||||||
chr8:28048860
|
CAAA | C | 8 | a0001c0008t0002g0166a0002c0012t0010g0191a0002c0012t0036g0185others(5): Show | 8 | HG01168.hp2 HG02055.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207-1251_1207-124 others(7): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048860 | ||||||
chr8:28048860
|
CAAAAAA | C | 138 | a0001c0003t0002g0240a0001c0013t0012g0189a0001c0013t0013g0190others(135): Show | 148 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1207-1254_1207-124 others(10): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048860 | ||||||
chr8:28048882
|
T | A | 2 | a0001c0001t0047g0361a0025c0066t0001g0061 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1207-1270A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048882 | ||||||
chr8:28048994
|
TCTTA | T | 5 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207-1386_1207-138 others(8): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28048994 | ||||||
chr8:28049080
|
A | G | 1 | a0003c0002t0018g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1207-1468T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049080 | ||||||
chr8:28049189
|
G | A | 1 | a0001c0003t0002g0203 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1207-1577C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049189 | ||||||
chr8:28049307
|
G | A | 1 | a0002c0060t0028g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1207-1695C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049307 | ||||||
chr8:28049407
|
A | G | 79 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(76): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1207-1795T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049407 | ||||||
chr8:28049584
|
G | C | 5 | a0001c0036t0012g0193a0001c0063t0001g0059a0001c0064t0054g0275others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207-1972C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049584 | ||||||
chr8:28049591
|
A | G | 1 | a0002c0060t0028g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1207-1979T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049591 | ||||||
chr8:28049621
|
C | T | 235 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(232): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1207-2009G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049621 | ||||||
chr8:28049810
|
G | A | 1 | a0002c0006t0001g0069 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1207-2198C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049810 | ||||||
chr8:28049915
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1207-2303C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049915 | ||||||
chr8:28049962
|
C | G | 1 | a0001c0003t0002g0240 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1207-2350G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049962 | ||||||
chr8:28049980
|
G | A | 5 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-2368C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28049980 | ||||||
chr8:28050043
|
C | T | 1 | a0002c0010t0001g0047 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1207-2431G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050043 | ||||||
chr8:28050107
|
C | T | 1 | a0002c0060t0028g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1207-2495G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050107 | ||||||
chr8:28050143
|
C | T | 153 | a0001c0001t0047g0361a0001c0003t0002g0240a0001c0013t0012g0189others(150): Show | 164 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1207-2531G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050143 | ||||||
chr8:28050156
|
C | T | 11 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1207-2544G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050156 | ||||||
chr8:28050157
|
G | A | 121 | a0001c0003t0002g0240a0001c0036t0012g0193a0001c0063t0001g0059others(118): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1207-2545C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050157 | ||||||
chr8:28050169
|
G | A | 1 | a0002c0010t0022g0371 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1207-2557C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050169 | ||||||
chr8:28050268
|
C | G | 1 | a0001c0003t0002g0240 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1207-2656G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050268 | ||||||
chr8:28050271
|
G | A | 4 | a0001c0034t0015g0376a0001c0057t0015g0350a0004c0004t0060g0346others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-2659C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050271 | ||||||
chr8:28050283
|
G | C | 1 | a0001c0008t0001g0134 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1207-2671C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050283 | ||||||
chr8:28050325
|
T | C | 93 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1207-2713A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050325 | ||||||
chr8:28050383
|
T | TA | 136 | a0001c0003t0002g0240a0001c0036t0012g0193a0001c0063t0001g0059others(133): Show | 146 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1207-2772dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050383 | ||||||
chr8:28050650
|
A | C | 2 | a0001c0001t0005g0043a0001c0023t0005g0180 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1207-3038T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050650 | ||||||
chr8:28050762
|
C | G | 370 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(367): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1207-3150G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050762 | ||||||
chr8:28050805
|
C | T | 1 | a0003c0002t0009g0120 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1207-3193G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050805 | ||||||
chr8:28050806
|
G | A | 3 | a0003c0002t0002g0088a0003c0002t0002g0092a0003c0002t0017g0118 | 3 | HG00408.hp2 HG02155.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1207-3194C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050806 | ||||||
chr8:28050810
|
C | CA | 82 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0165others(79): Show | 87 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1207-3199dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050810 | ||||||
chr8:28050825
|
A | T | 5 | a0001c0003t0002g0211a0001c0003t0002g0216a0001c0003t0002g0217others(2): Show | 5 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-3213T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050825 | ||||||
chr8:28050873
|
A | G | 16 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(13): Show | 16 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1207-3261T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050873 | ||||||
chr8:28050959
|
T | C | 1 | a0003c0002t0020g0119 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1207-3347A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050959 | ||||||
chr8:28050989
|
C | CA | 59 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(56): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1207-3378_1207-337 others(5): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28050989 | ||||||
chr8:28051075
|
C | T | 2 | a0002c0059t0025g0044a0003c0044t0001g0224 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1207-3463G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051075 | ||||||
chr8:28051077
|
G | A | 1 | a0002c0060t0028g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1207-3465C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051077 | ||||||
chr8:28051158
|
A | C | 1 | a0004c0016t0064g0377 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1207-3546T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051158 | ||||||
chr8:28051280
|
C | T | 5 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-3668G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051280 | ||||||
chr8:28051301
|
G | T | 3 | a0001c0034t0015g0376a0001c0057t0015g0350a0015c0071t0015g0369 | 3 | HG02615.hp2 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1207-3689C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051301 | ||||||
chr8:28051378
|
A | G | 11 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207-3766T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051378 | ||||||
chr8:28051569
|
C | T | 6 | a0001c0001t0011g0315a0002c0024t0003g0336a0010c0026t0010g0129others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-3957G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051569 | ||||||
chr8:28051595
|
T | C | 1 | a0002c0005t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1207-3983A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051595 | ||||||
chr8:28051713
|
G | A | 1 | a0002c0039t0008g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1207-4101C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051713 | ||||||
chr8:28051768
|
C | T | 1 | a0004c0016t0003g0285 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1207-4156G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051768 | ||||||
chr8:28051934
|
C | A | 168 | a0001c0001t0011g0315a0001c0003t0002g0240a0001c0013t0012g0189others(165): Show | 179 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1206+4031G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051934 | ||||||
chr8:28051959
|
C | A | 198 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(195): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1206+4006G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28051959 | ||||||
chr8:28052269
|
C | T | 1 | a0005c0052t0002g0162 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1206+3696G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28052269 | ||||||
chr8:28052275
|
G | A | 60 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(57): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1206+3690C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28052275 | ||||||
chr8:28052305
|
T | C | 1 | a0007c0015t0001g0094 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1206+3660A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28052305 | ||||||
chr8:28052366
|
C | T | 1 | a0004c0004t0060g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1206+3599G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28052366 | ||||||
chr8:28052486
|
A | T | 2 | a0013c0047t0008g0065a0013c0048t0001g0207 | 2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1206+3479T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28052486 | ||||||
chr8:28052629
|
C | T | 6 | a0004c0041t0001g0186a0005c0014t0001g0250a0005c0014t0003g0279others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1206+3336G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28052629 | ||||||
chr8:28052651
|
G | A | 112 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0040others(109): Show | 122 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1206+3314C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28052651 | ||||||
chr8:28052692
|
G | A | 6 | a0002c0005t0001g0236a0002c0005t0009g0229a0002c0005t0009g0232others(3): Show | 6 | HG00733.hp2 HG02738.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1206+3273C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28052692 | ||||||
chr8:28052883
|
G | A | 109 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0040others(106): Show | 119 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1206+3082C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28052883 | ||||||
chr8:28053050
|
T | C | 1 | a0001c0008t0003g0353 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1206+2915A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053050 | ||||||
chr8:28053084
|
C | CCAGCCAA others(6): Show |
1 | a0001c0003t0002g0153 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1206+2868_1206+288 others(17): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053084 | ||||||
chr8:28053089
|
CA | C | 7 | a0001c0001t0001g0131a0001c0001t0011g0315a0002c0024t0003g0336others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1206+2875delT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053089 | ||||||
chr8:28053139
|
T | C | 8 | a0004c0041t0001g0186a0005c0014t0001g0250a0005c0014t0003g0279others(5): Show | 8 | HG00738.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1206+2826A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053139 | ||||||
chr8:28053257
|
G | C | 1 | a0001c0001t0011g0315 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1206+2708C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053257 | ||||||
chr8:28053259
|
G | C | 2 | a0002c0006t0011g0320a0002c0056t0005g0181 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1206+2706C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053259 | ||||||
chr8:28053329
|
G | A | 3 | a0001c0034t0015g0376a0001c0057t0015g0350a0015c0071t0015g0369 | 3 | HG02615.hp2 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1206+2636C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053329 | ||||||
chr8:28053457
|
G | A | 1 | a0002c0006t0003g0316 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1206+2508C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053457 | ||||||
chr8:28053486
|
GA | G | 68 | a0001c0001t0001g0064a0001c0001t0001g0131a0001c0001t0001g0144others(65): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1206+2478delT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053486 | ||||||
chr8:28053509
|
C | T | 7 | a0001c0001t0001g0015a0001c0003t0002g0211a0001c0003t0002g0216others(4): Show | 8 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1206+2456G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053509 | ||||||
chr8:28053510
|
G | A | 113 | a0001c0001t0047g0361a0002c0005t0001g0037a0002c0005t0001g0039others(110): Show | 123 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1206+2455C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053510 | ||||||
chr8:28053548
|
C | T | 6 | a0001c0001t0011g0315a0002c0024t0003g0336a0010c0026t0010g0129others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+2417G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053548 | ||||||
chr8:28053681
|
C | T | 1 | a0007c0015t0001g0094 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1206+2284G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053681 | ||||||
chr8:28053788
|
A | G | 18 | a0001c0063t0001g0059a0002c0005t0037g0263a0002c0006t0005g0014others(15): Show | 19 | HG01261.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1206+2177T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053788 | ||||||
chr8:28053992
|
T | C | 6 | a0001c0001t0011g0315a0002c0024t0003g0336a0010c0026t0010g0129others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+1973A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28053992 | ||||||
chr8:28054188
|
A | G | 6 | a0001c0001t0011g0315a0002c0024t0003g0336a0010c0026t0010g0129others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+1777T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28054188 | ||||||
chr8:28054208
|
G | A | 104 | a0001c0001t0047g0361a0002c0005t0001g0037a0002c0005t0001g0039others(101): Show | 114 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.1206+1757C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28054208 | ||||||
chr8:28054289
|
C | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0256 | 2 | HG00558.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1206+1676G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28054289 | ||||||
chr8:28054351
|
A | G | 10 | a0001c0034t0015g0376a0001c0057t0015g0350a0002c0011t0003g0351others(7): Show | 10 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1206+1614T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28054351 | ||||||
chr8:28054475
|
C | G | 5 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1206+1490G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28054475 | ||||||
chr8:28054768
|
GCACTGTG others(6): Show |
G | 1 | a0003c0002t0059g0305 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1206+1184_1206+119 others(17): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28054768 | ||||||
chr8:28054783
|
C | T | 7 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(4): Show | 7 | HG02280.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1206+1182G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28054783 | ||||||
chr8:28054785
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0002g0269 | 3 | HG00642.hp1 HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1206+1180C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28054785 | ||||||
chr8:28054904
|
T | C | 2 | a0001c0001t0006g0139a0004c0004t0003g0362 | 2 | NA19058.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1206+1061A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28054904 | ||||||
chr8:28055016
|
G | GTCTCTAC others(59): Show |
4 | a0001c0001t0005g0201a0001c0001t0046g0276a0003c0049t0021g0265others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+883_1206+948d others(68): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28055016 | ||||||
chr8:28055023
|
C | T | 1 | a0009c0022t0001g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1206+942G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28055023 | ||||||
chr8:28055109
|
C | T | 3 | a0001c0063t0001g0059a0016c0073t0040g0160a0026c0051t0019g0187 | 3 | HG02723.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1206+856G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28055109 | ||||||
chr8:28055455
|
T | C | 370 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(367): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1206+510A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28055455 | ||||||
chr8:28055567
|
A | G | 1 | a0004c0004t0060g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1206+398T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28055567 | ||||||
chr8:28055661
|
C | T | 3 | a0003c0002t0002g0009a0003c0002t0002g0010a0003c0002t0002g0075 | 5 | HG02165.hp2 HG02523.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1206+304G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28055661 | ||||||
chr8:28055792
|
C | T | 15 | a0001c0034t0015g0376a0001c0057t0015g0350a0002c0005t0061g0366others(12): Show | 15 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1206+173G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28055792 | ||||||
chr8:28055848
|
T | A | 123 | a0001c0001t0011g0315a0001c0001t0047g0361a0001c0034t0015g0376others(120): Show | 133 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.1206+117A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28055848 | ||||||
chr8:28055916
|
T | C | 1 | a0001c0003t0013g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1206+49A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 10/18 | chr8 | 28055916 | ||||||
chr8:28056201
|
G | A | 1 | a0004c0004t0060g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1117-147C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056201 | ||||||
chr8:28056243
|
C | A | 4 | a0004c0007t0002g0058a0004c0007t0002g0227a0004c0007t0004g0023others(1): Show | 5 | HG00099.hp2 HG01070.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-189G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056243 | ||||||
chr8:28056280
|
C | A | 1 | a0002c0010t0001g0047 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1117-226G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056280 | ||||||
chr8:28056314
|
T | TAAGAATA others(313): Show |
1 | a0002c0039t0008g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1117-261_1117-260i others(322): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056314 | ||||||
chr8:28056417
|
G | T | 1 | a0001c0001t0001g0175 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1117-363C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056417 | ||||||
chr8:28056457
|
G | A | 2 | a0004c0004t0003g0289a0004c0004t0050g0300 | 2 | NA18940.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1117-403C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056457 | ||||||
chr8:28056472
|
T | C | 163 | a0001c0001t0011g0315a0001c0001t0047g0361a0001c0003t0002g0240others(160): Show | 174 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(171): Show |
intron_variant | MODIFIER | c.1117-418A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056472 | ||||||
chr8:28056477
|
C | CA | 9 | a0001c0003t0017g0146a0001c0034t0015g0376a0001c0057t0015g0350others(6): Show | 9 | HG01261.hp1 HG02615.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1117-424dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056477 | ||||||
chr8:28056477
|
CA | C | 10 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-424delT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056477 | ||||||
chr8:28056677
|
T | C | 1 | a0001c0003t0002g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1117-623A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056677 | ||||||
chr8:28056960
|
A | G | 108 | a0001c0001t0047g0361a0002c0005t0001g0037a0002c0005t0001g0039others(105): Show | 118 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1117-906T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28056960 | ||||||
chr8:28057072
|
C | T | 2 | a0001c0003t0002g0222a0001c0003t0014g0002 | 4 | HG01975.hp1 HG03239.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-1018G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057072 | ||||||
chr8:28057330
|
C | CT | 186 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0145others(183): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1116+927dupA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057330 | ||||||
chr8:28057330
|
C | CTT | 13 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(10): Show | 13 | HG00733.hp2 HG00738.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116+926_1116+927d others(4): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057330 | ||||||
chr8:28057330
|
CT | C | 7 | a0001c0001t0001g0245a0001c0001t0011g0315a0002c0024t0003g0336others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116+927delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057330 | ||||||
chr8:28057330
|
CTT | C | 6 | a0002c0005t0061g0366a0002c0012t0010g0191a0002c0012t0010g0192others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+926_1116+927d others(4): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057330 | ||||||
chr8:28057346
|
T | TG | 4 | a0002c0006t0001g0069a0002c0006t0003g0301a0003c0002t0001g0257others(1): Show | 4 | HG01257.hp1 HG01346.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+911_1116+912i others(3): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057346 | ||||||
chr8:28057349
|
G | T | 4 | a0003c0002t0018g0082a0003c0002t0018g0083a0003c0002t0020g0074others(1): Show | 4 | NA18940.hp1 NA18991.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116+909C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057349 | ||||||
chr8:28057416
|
A | G | 1 | a0001c0003t0056g0314 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1116+842T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057416 | ||||||
chr8:28057516
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1116+742C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057516 | ||||||
chr8:28057531
|
G | A | 5 | a0001c0001t0011g0315a0002c0024t0003g0336a0010c0026t0010g0129others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+727C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057531 | ||||||
chr8:28057675
|
A | G | 2 | a0002c0055t0039g0161a0003c0049t0021g0265 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1116+583T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057675 | ||||||
chr8:28057963
|
C | T | 2 | a0003c0002t0003g0293a0004c0004t0060g0346 | 2 | NA19030.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1116+295G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28057963 | ||||||
chr8:28058010
|
G | A | 6 | a0001c0001t0011g0315a0002c0024t0003g0336a0010c0026t0010g0129others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+248C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28058010 | ||||||
chr8:28058134
|
G | A | 9 | a0002c0005t0002g0038a0003c0002t0001g0089a0003c0002t0002g0001others(6): Show | 14 | HG00408.hp2 HG02155.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116+124C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28058134 | ||||||
chr8:28058147
|
G | A | 2 | a0024c0031t0001g0188a0025c0066t0001g0061 | 2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1116+111C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 9/18 | chr8 | 28058147 | ||||||
chr8:28058313
|
T | C | 370 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(367): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1098-37A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28058313 | ||||||
chr8:28058409
|
T | C | 1 | a0001c0008t0004g0326 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1098-133A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28058409 | ||||||
chr8:28058514
|
C | T | 6 | a0001c0001t0011g0315a0002c0024t0003g0336a0010c0026t0010g0129others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098-238G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28058514 | ||||||
chr8:28058563
|
C | T | 8 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098-287G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28058563 | ||||||
chr8:28058706
|
A | AT | 33 | a0002c0005t0001g0040a0002c0005t0001g0218a0002c0005t0002g0038others(30): Show | 38 | HG00408.hp2 HG01069.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1098-431dupA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28058706 | ||||||
chr8:28058880
|
AT | A | 3 | a0002c0010t0022g0371a0002c0059t0025g0044a0003c0044t0001g0224 | 3 | HG00733.hp2 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1098-605delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28058880 | ||||||
chr8:28058906
|
A | AT | 6 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098-631dupA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28058906 | ||||||
chr8:28058937
|
C | T | 1 | a0002c0010t0063g0310 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1098-661G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28058937 | ||||||
chr8:28058950
|
C | A | 1 | a0002c0010t0022g0371 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1098-674G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28058950 | ||||||
chr8:28059113
|
A | C | 4 | a0002c0010t0063g0310a0002c0012t0001g0051a0002c0012t0034g0050others(1): Show | 4 | HG01261.hp1 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098-837T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059113 | ||||||
chr8:28059115
|
C | G | 2 | a0001c0003t0002g0222a0001c0003t0014g0002 | 4 | HG01975.hp1 HG03239.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098-839G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059115 | ||||||
chr8:28059229
|
T | A | 1 | a0004c0007t0022g0298 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1098-953A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059229 | ||||||
chr8:28059297
|
C | G | 1 | a0001c0001t0047g0361 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1098-1021G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059297 | ||||||
chr8:28059300
|
C | A | 1 | a0001c0040t0001g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1098-1024G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059300 | ||||||
chr8:28059322
|
C | G | 1 | a0002c0060t0028g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1098-1046G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059322 | ||||||
chr8:28059413
|
A | G | 6 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1097+1013T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059413 | ||||||
chr8:28059460
|
A | G | 3 | a0002c0010t0022g0371a0002c0059t0025g0044a0003c0044t0001g0224 | 3 | HG00733.hp2 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1097+966T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059460 | ||||||
chr8:28059567
|
A | G | 1 | a0010c0026t0010g0129 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1097+859T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059567 | ||||||
chr8:28059597
|
T | A | 155 | a0001c0001t0001g0064a0001c0001t0001g0131a0001c0001t0001g0144others(152): Show | 167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1097+829A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059597 | ||||||
chr8:28059813
|
G | A | 7 | a0001c0003t0013g0264a0006c0043t0005g0184a0014c0029t0011g0372others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1097+613C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059813 | ||||||
chr8:28059872
|
T | G | 2 | a0002c0005t0061g0366a0002c0038t0010g0048 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1097+554A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059872 | ||||||
chr8:28059890
|
C | T | 1 | a0003c0002t0002g0092 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1097+536G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059890 | ||||||
chr8:28059891
|
G | A | 26 | a0001c0001t0001g0015a0001c0001t0003g0360a0001c0001t0004g0312others(23): Show | 27 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097+535C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28059891 | ||||||
chr8:28060013
|
T | A | 223 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(220): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1097+413A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28060013 | ||||||
chr8:28060020
|
C | CA | 63 | a0001c0001t0001g0064a0001c0001t0001g0131a0001c0001t0001g0144others(60): Show | 69 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1097+405dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 8/18 | chr8 | 28060020 | ||||||
chr8:28060753
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0003g0309 | 3 | HG01358.hp1 HG01981.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.922-152T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28060753 | ||||||
chr8:28060845
|
C | T | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.922-244G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28060845 | ||||||
chr8:28060851
|
T | C | 79 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0099others(76): Show | 86 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.922-250A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28060851 | ||||||
chr8:28060863
|
C | T | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.922-262G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28060863 | ||||||
chr8:28060953
|
C | T | 5 | a0001c0003t0002g0240a0002c0010t0002g0248a0002c0059t0025g0044others(2): Show | 5 | HG00735.hp1 HG01516.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.922-352G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28060953 | ||||||
chr8:28060970
|
C | T | 3 | a0004c0007t0002g0058a0004c0007t0002g0227a0004c0020t0002g0057 | 3 | HG00099.hp2 HG01070.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.922-369G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28060970 | ||||||
chr8:28060998
|
C | T | 19 | a0002c0005t0001g0093a0002c0005t0001g0255a0002c0005t0001g0262others(16): Show | 21 | HG00558.hp2 HG02015.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.922-397G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28060998 | ||||||
chr8:28061136
|
C | T | 1 | a0004c0007t0002g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.922-535G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061136 | ||||||
chr8:28061223
|
C | A | 1 | a0001c0003t0056g0314 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.922-622G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061223 | ||||||
chr8:28061224
|
G | A | 1 | a0003c0049t0021g0265 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.922-623C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061224 | ||||||
chr8:28061234
|
A | T | 1 | a0001c0001t0001g0260 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.922-633T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061234 | ||||||
chr8:28061318
|
T | C | 1 | a0002c0006t0003g0332 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.922-717A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061318 | ||||||
chr8:28061351
|
C | T | 6 | a0002c0024t0003g0336a0002c0059t0025g0044a0003c0044t0001g0224others(3): Show | 6 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.922-750G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061351 | ||||||
chr8:28061605
|
C | T | 5 | a0002c0005t0001g0053a0002c0005t0001g0054a0002c0005t0001g0148others(2): Show | 5 | HG00423.hp1 HG00621.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.922-1004G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061605 | ||||||
chr8:28061639
|
G | C | 4 | a0002c0024t0003g0336a0011c0076t0048g0365a0013c0047t0008g0065others(1): Show | 4 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.922-1038C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061639 | ||||||
chr8:28061642
|
C | T | 1 | a0001c0001t0005g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.922-1041G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061642 | ||||||
chr8:28061661
|
A | G | 1 | a0002c0006t0005g0014 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.922-1060T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061661 | ||||||
chr8:28061679
|
T | C | 1 | a0017c0075t0005g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.922-1078A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061679 | ||||||
chr8:28061740
|
C | A | 2 | a0013c0047t0008g0065a0013c0048t0001g0207 | 2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.922-1139G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061740 | ||||||
chr8:28061790
|
G | T | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.922-1189C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061790 | ||||||
chr8:28061795
|
G | C | 1 | a0002c0006t0001g0136 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.922-1194C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061795 | ||||||
chr8:28061863
|
T | C | 1 | a0001c0017t0003g0329 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.922-1262A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061863 | ||||||
chr8:28061865
|
C | T | 2 | a0004c0004t0003g0294a0004c0004t0007g0026 | 2 | NA18960.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.922-1264G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061865 | ||||||
chr8:28061898
|
T | C | 5 | a0001c0003t0002g0240a0002c0010t0002g0248a0002c0059t0025g0044others(2): Show | 5 | HG00735.hp1 HG01516.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.922-1297A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061898 | ||||||
chr8:28061935
|
GT | G | 5 | a0001c0063t0001g0059a0002c0005t0037g0263a0002c0010t0063g0310others(2): Show | 5 | HG01261.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.922-1335delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28061935 | ||||||
chr8:28062077
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.922-1476G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28062077 | ||||||
chr8:28062291
|
T | C | 1 | a0001c0003t0002g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.922-1690A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28062291 | ||||||
chr8:28062302
|
A | G | 3 | a0002c0033t0023g0277a0011c0074t0021g0125a0022c0032t0023g0278 | 3 | HG03453.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.922-1701T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28062302 | ||||||
chr8:28062332
|
C | T | 1 | a0004c0007t0001g0097 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.922-1731G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28062332 | ||||||
chr8:28062425
|
G | C | 6 | a0001c0001t0001g0015a0001c0001t0005g0201a0004c0004t0060g0346others(3): Show | 7 | HG00738.hp2 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.922-1824C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28062425 | ||||||
chr8:28062426
|
G | T | 1 | a0022c0032t0023g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.922-1825C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28062426 | ||||||
chr8:28062452
|
C | CA | 125 | a0001c0001t0001g0016a0001c0001t0001g0103a0001c0001t0001g0108others(122): Show | 137 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.922-1852dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28062452 | ||||||
chr8:28062648
|
C | T | 1 | a0002c0005t0001g0236 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.921+1874G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28062648 | ||||||
chr8:28062896
|
C | T | 2 | a0001c0009t0003g0308a0001c0017t0003g0329 | 2 | NA18950.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.921+1626G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28062896 | ||||||
chr8:28063232
|
G | A | 1 | a0002c0005t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.921+1290C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063232 | ||||||
chr8:28063247
|
G | A | 1 | a0002c0024t0012g0247 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.921+1275C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063247 | ||||||
chr8:28063286
|
G | A | 1 | a0001c0001t0047g0361 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.921+1236C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063286 | ||||||
chr8:28063650
|
C | T | 1 | a0002c0006t0003g0330 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.921+872G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063650 | ||||||
chr8:28063669
|
T | C | 1 | a0002c0024t0003g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.921+853A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063669 | ||||||
chr8:28063775
|
T | C | 1 | a0002c0006t0001g0069 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.921+747A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063775 | ||||||
chr8:28063838
|
C | G | 1 | a0002c0005t0001g0236 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.921+684G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063838 | ||||||
chr8:28063896
|
C | G | 12 | a0001c0001t0001g0159a0001c0001t0001g0254a0001c0001t0006g0100others(9): Show | 12 | HG00438.hp1 HG02071.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.921+626G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063896 | ||||||
chr8:28063902
|
C | T | 3 | a0003c0044t0001g0224a0013c0047t0008g0065a0013c0048t0001g0207 | 3 | HG02055.hp1 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.921+620G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063902 | ||||||
chr8:28063904
|
C | T | 2 | a0001c0001t0011g0315a0002c0005t0010g0042 | 2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.921+618G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063904 | ||||||
chr8:28063917
|
C | T | 3 | a0003c0044t0001g0224a0013c0047t0008g0065a0013c0048t0001g0207 | 3 | HG02055.hp1 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.921+605G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063917 | ||||||
chr8:28063919
|
C | T | 1 | a0001c0028t0002g0017 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.921+603G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28063919 | ||||||
chr8:28064182
|
T | C | 1 | a0002c0010t0001g0047 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.921+340A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28064182 | ||||||
chr8:28064343
|
C | T | 2 | a0001c0001t0005g0201a0002c0039t0008g0128 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.921+179G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28064343 | ||||||
chr8:28064349
|
T | C | 4 | a0001c0009t0001g0033a0001c0009t0003g0308a0001c0017t0003g0324others(1): Show | 4 | NA18963.hp1 NA18982.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.921+173A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28064349 | ||||||
chr8:28064363
|
C | T | 50 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0101others(47): Show | 53 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.921+159G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28064363 | ||||||
chr8:28064415
|
C | T | 1 | a0002c0010t0002g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.921+107G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28064415 | ||||||
chr8:28064419
|
T | G | 6 | a0001c0001t0005g0043a0001c0023t0005g0180a0009c0022t0001g0035others(3): Show | 6 | HG00738.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.921+103A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 7/18 | chr8 | 28064419 | ||||||
chr8:28064765
|
C | T | 1 | a0002c0006t0011g0320 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.712-34G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28064765 | ||||||
chr8:28064810
|
A | T | 1 | a0006c0018t0008g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.712-79T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28064810 | ||||||
chr8:28065026
|
C | T | 1 | a0004c0007t0004g0003 | 3 | HG01257.hp2 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.712-295G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065026 | ||||||
chr8:28065057
|
T | C | 275 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(272): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.712-326A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065057 | ||||||
chr8:28065152
|
C | CT | 39 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.712-422dupA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065152 | ||||||
chr8:28065152
|
CT | C | 101 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(98): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.712-422delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065152 | ||||||
chr8:28065152
|
CTT | C | 6 | a0001c0001t0003g0291a0001c0003t0002g0155a0001c0003t0002g0216others(3): Show | 6 | HG01069.hp1 HG01515.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.712-423_712-422del others(2): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065152 | ||||||
chr8:28065180
|
A | T | 18 | a0004c0041t0001g0186a0005c0014t0001g0250a0005c0014t0003g0279others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.712-449T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065180 | ||||||
chr8:28065198
|
T | C | 1 | a0003c0002t0002g0092 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.712-467A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065198 | ||||||
chr8:28065204
|
A | G | 1 | a0016c0073t0040g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.712-473T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065204 | ||||||
chr8:28065205
|
G | T | 46 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0002g0166others(43): Show | 51 | HG00323.hp1 HG00733.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.712-474C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065205 | ||||||
chr8:28065206
|
A | G | 143 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(140): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.712-475T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065206 | ||||||
chr8:28065261
|
C | T | 2 | a0001c0025t0002g0114a0001c0025t0002g0115 | 2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.712-530G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065261 | ||||||
chr8:28065350
|
C | A | 132 | a0001c0003t0013g0264a0001c0013t0012g0189a0001c0013t0013g0190others(129): Show | 143 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.712-619G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065350 | ||||||
chr8:28065385
|
C | G | 9 | a0001c0040t0001g0045a0008c0021t0001g0169a0008c0021t0008g0052others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.712-654G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065385 | ||||||
chr8:28065392
|
C | G | 2 | a0001c0001t0005g0201a0002c0005t0037g0263 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.712-661G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065392 | ||||||
chr8:28065393
|
G | T | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.712-662C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065393 | ||||||
chr8:28065412
|
A | G | 376 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(373): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.712-681T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065412 | ||||||
chr8:28065569
|
T | C | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.712-838A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065569 | ||||||
chr8:28065843
|
C | T | 1 | a0001c0063t0001g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.712-1112G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065843 | ||||||
chr8:28065871
|
C | T | 71 | a0001c0001t0001g0015a0001c0001t0002g0066a0001c0001t0002g0198others(68): Show | 75 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.712-1140G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065871 | ||||||
chr8:28065990
|
G | A | 2 | a0001c0003t0009g0268a0002c0005t0001g0218 | 2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.712-1259C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28065990 | ||||||
chr8:28066002
|
C | CAACT | 286 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(283): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.712-1272_712-1271i others(6): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066002 | ||||||
chr8:28066003
|
T | C | 286 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(283): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.712-1272A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066003 | ||||||
chr8:28066004
|
T | A | 286 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(283): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.712-1273A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066004 | ||||||
chr8:28066022
|
T | C | 33 | a0001c0001t0001g0015a0001c0001t0002g0066a0001c0001t0002g0198others(30): Show | 34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.712-1291A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066022 | ||||||
chr8:28066034
|
A | G | 108 | a0001c0008t0002g0243a0001c0008t0002g0244a0001c0008t0003g0339others(105): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.712-1303T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066034 | ||||||
chr8:28066082
|
G | A | 1 | a0002c0006t0003g0337 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.712-1351C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066082 | ||||||
chr8:28066106
|
A | T | 15 | a0001c0013t0012g0189a0001c0013t0013g0190a0001c0013t0013g0200others(12): Show | 15 | HG01884.hp2 HG02155.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.712-1375T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066106 | ||||||
chr8:28066121
|
T | C | 1 | a0001c0001t0005g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.712-1390A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066121 | ||||||
chr8:28066384
|
T | G | 1 | a0001c0001t0006g0259 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.711+1130A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066384 | ||||||
chr8:28066404
|
C | T | 2 | a0001c0001t0003g0291a0001c0009t0001g0033 | 2 | NA18747.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.711+1110G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066404 | ||||||
chr8:28066612
|
A | T | 1 | a0001c0001t0011g0315 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.711+902T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066612 | ||||||
chr8:28066796
|
G | A | 3 | a0004c0004t0060g0346a0004c0007t0002g0058a0004c0020t0002g0057 | 3 | HG01070.hp2 HG01346.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.711+718C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066796 | ||||||
chr8:28066934
|
T | G | 39 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0101others(36): Show | 43 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.711+580A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28066934 | ||||||
chr8:28067070
|
G | A | 10 | a0001c0040t0001g0045a0002c0012t0001g0051a0002c0012t0010g0191others(7): Show | 10 | HG01243.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+444C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28067070 | ||||||
chr8:28067091
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.711+423C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28067091 | ||||||
chr8:28067377
|
G | A | 1 | a0022c0032t0023g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.711+137C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28067377 | ||||||
chr8:28067407
|
T | C | 45 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(42): Show | 49 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.711+107A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28067407 | ||||||
chr8:28067506
|
G | A | 4 | a0001c0003t0001g0012a0001c0003t0001g0156a0001c0003t0001g0157others(1): Show | 5 | HG02293.hp2 NA18943.hp1 NA18977.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.711+8C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 6/18 | chr8 | 28067506 | ||||||
chr8:28067880
|
C | T | 9 | a0001c0040t0001g0045a0002c0012t0001g0051a0002c0012t0010g0191others(6): Show | 9 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.481-136G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 5/18 | chr8 | 28067880 | ||||||
chr8:28067939
|
C | T | 1 | a0001c0003t0002g0261 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.481-195G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 5/18 | chr8 | 28067939 | ||||||
chr8:28068156
|
A | C | 1 | a0004c0004t0003g0348 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.480+60T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 5/18 | chr8 | 28068156 | ||||||
chr8:28068157
|
G | T | 2 | a0001c0001t0001g0099a0002c0005t0001g0262 | 2 | NA18961.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.480+59C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 5/18 | chr8 | 28068157 | ||||||
chr8:28068471
|
T | C | 2 | a0001c0001t0005g0201a0002c0005t0037g0263 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.258-33A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28068471 | ||||||
chr8:28068551
|
G | A | 1 | a0002c0006t0011g0320 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.258-113C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28068551 | ||||||
chr8:28068600
|
C | T | 192 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(189): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.258-162G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28068600 | ||||||
chr8:28068635
|
G | C | 1 | a0002c0005t0002g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.258-197C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28068635 | ||||||
chr8:28068725
|
A | G | 6 | a0001c0001t0001g0165a0002c0005t0001g0037a0002c0005t0001g0039others(3): Show | 6 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-287T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28068725 | ||||||
chr8:28068839
|
C | A | 2 | a0001c0001t0005g0201a0002c0005t0037g0263 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.258-401G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28068839 | ||||||
chr8:28068972
|
G | A | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.258-534C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28068972 | ||||||
chr8:28069058
|
T | C | 2 | a0003c0002t0001g0257a0003c0002t0003g0302 | 2 | HG01257.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.257+486A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28069058 | ||||||
chr8:28069069
|
A | C | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.257+475T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28069069 | ||||||
chr8:28069142
|
G | A | 1 | a0004c0004t0003g0340 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.257+402C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28069142 | ||||||
chr8:28069443
|
T | A | 2 | a0003c0002t0020g0119a0007c0015t0001g0094 | 2 | NA19083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.257+101A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 4/18 | chr8 | 28069443 | ||||||
chr8:28069726
|
T | G | 9 | a0001c0040t0001g0045a0002c0012t0001g0051a0002c0012t0010g0191others(6): Show | 9 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-74A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28069726 | ||||||
chr8:28069737
|
G | T | 1 | a0001c0001t0011g0315 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.149-85C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28069737 | ||||||
chr8:28069799
|
C | T | 2 | a0001c0001t0005g0201a0002c0005t0037g0263 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.149-147G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28069799 | ||||||
chr8:28069802
|
G | A | 6 | a0001c0063t0001g0059a0009c0022t0001g0035a0009c0022t0001g0127others(3): Show | 6 | HG00738.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-150C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28069802 | ||||||
chr8:28069863
|
C | T | 5 | a0001c0001t0003g0360a0001c0001t0011g0315a0001c0001t0047g0361others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-211G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28069863 | ||||||
chr8:28069907
|
C | T | 2 | a0002c0005t0009g0229a0002c0005t0009g0232 | 2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.149-255G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28069907 | ||||||
chr8:28069949
|
A | T | 7 | a0001c0001t0001g0165a0001c0009t0001g0033a0002c0005t0001g0037others(4): Show | 7 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-297T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28069949 | ||||||
chr8:28069990
|
G | A | 7 | a0001c0001t0001g0165a0001c0009t0001g0033a0002c0005t0001g0037others(4): Show | 7 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+262C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28069990 | ||||||
chr8:28069997
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.148+255G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28069997 | ||||||
chr8:28070191
|
C | T | 13 | a0004c0041t0001g0186a0005c0014t0001g0250a0005c0014t0003g0279others(10): Show | 13 | HG00741.hp1 HG01074.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.148+61G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 3/18 | chr8 | 28070191 | ||||||
chr8:28070471
|
T | G | 2 | a0001c0001t0005g0201a0002c0005t0037g0263 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.44-115A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070471 | ||||||
chr8:28070557
|
C | T | 1 | a0001c0003t0013g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.44-201G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070557 | ||||||
chr8:28070593
|
A | T | 6 | a0001c0001t0001g0165a0002c0005t0001g0037a0002c0005t0001g0039others(3): Show | 6 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-237T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070593 | ||||||
chr8:28070594
|
A | T | 1 | a0001c0009t0001g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.44-238T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070594 | ||||||
chr8:28070595
|
T | A | 1 | a0025c0066t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.44-239A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070595 | ||||||
chr8:28070664
|
C | T | 49 | a0001c0001t0005g0266a0001c0003t0002g0046a0001c0008t0001g0133others(46): Show | 54 | HG00323.hp1 HG00733.hp2 HG01256.hp2 others(51): Show |
intron_variant | MODIFIER | c.44-308G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070664 | ||||||
chr8:28070750
|
C | T | 2 | a0001c0001t0005g0201a0002c0005t0037g0263 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.44-394G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070750 | ||||||
chr8:28070785
|
G | A | 35 | a0001c0001t0003g0291a0003c0002t0001g0055a0003c0002t0001g0257others(32): Show | 39 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.44-429C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070785 | ||||||
chr8:28070834
|
A | T | 2 | a0003c0002t0001g0257a0003c0002t0003g0302 | 2 | HG01257.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.44-478T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070834 | ||||||
chr8:28070836
|
T | A | 2 | a0001c0003t0002g0219a0002c0005t0061g0366 | 2 | HG03130.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.44-480A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070836 | ||||||
chr8:28070969
|
G | A | 6 | a0001c0001t0001g0165a0002c0005t0001g0037a0002c0005t0001g0039others(3): Show | 6 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-613C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28070969 | ||||||
chr8:28071004
|
A | G | 1 | a0004c0007t0002g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.44-648T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071004 | ||||||
chr8:28071027
|
C | T | 1 | a0002c0006t0003g0327 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.44-671G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071027 | ||||||
chr8:28071160
|
T | A | 265 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0131others(262): Show | 286 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.44-804A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071160 | ||||||
chr8:28071320
|
A | T | 1 | a0002c0005t0001g0141 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.44-964T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071320 | ||||||
chr8:28071324
|
G | A | 1 | a0001c0003t0013g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.44-968C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071324 | ||||||
chr8:28071341
|
A | G | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.44-985T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071341 | ||||||
chr8:28071442
|
A | C | 2 | a0004c0004t0001g0209a0004c0004t0001g0210 | 2 | HG00741.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.44-1086T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071442 | ||||||
chr8:28071462
|
T | C | 1 | a0002c0006t0001g0136 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.44-1106A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071462 | ||||||
chr8:28071590
|
G | A | 1 | a0004c0007t0001g0097 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.44-1234C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071590 | ||||||
chr8:28071601
|
C | G | 1 | a0004c0004t0003g0289 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.44-1245G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071601 | ||||||
chr8:28071825
|
C | G | 10 | a0003c0002t0001g0257a0003c0002t0003g0302a0003c0002t0003g0306others(7): Show | 12 | HG00438.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-1469G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071825 | ||||||
chr8:28071834
|
G | A | 1 | a0001c0003t0002g0220 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.44-1478C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071834 | ||||||
chr8:28071852
|
C | A | 5 | a0001c0034t0015g0376a0002c0011t0003g0351a0002c0011t0011g0373others(2): Show | 5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-1496G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28071852 | ||||||
chr8:28072045
|
A | G | 1 | a0001c0003t0002g0140 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.44-1689T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072045 | ||||||
chr8:28072158
|
A | T | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.44-1802T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072158 | ||||||
chr8:28072195
|
C | T | 1 | a0023c0065t0002g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.44-1839G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072195 | ||||||
chr8:28072245
|
C | T | 1 | a0001c0003t0013g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.44-1889G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072245 | ||||||
chr8:28072255
|
C | T | 3 | a0001c0001t0046g0276a0002c0059t0025g0044a0019c0058t0045g0281 | 3 | HG02896.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.44-1899G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072255 | ||||||
chr8:28072410
|
A | G | 46 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(43): Show | 50 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.43+1958T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072410 | ||||||
chr8:28072462
|
T | C | 264 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0131others(261): Show | 285 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.43+1906A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072462 | ||||||
chr8:28072737
|
C | T | 17 | a0001c0001t0001g0165a0001c0001t0005g0043a0001c0009t0001g0033others(14): Show | 17 | HG00597.hp2 HG01243.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.43+1631G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072737 | ||||||
chr8:28072742
|
G | C | 1 | a0004c0016t0064g0377 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43+1626C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072742 | ||||||
chr8:28072751
|
T | C | 7 | a0001c0001t0001g0165a0001c0009t0001g0033a0002c0005t0001g0037others(4): Show | 7 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+1617A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072751 | ||||||
chr8:28072839
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.43+1529G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072839 | ||||||
chr8:28072845
|
A | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(38): Show | 45 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.43+1523T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072845 | ||||||
chr8:28072900
|
G | C | 149 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0101others(146): Show | 164 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.43+1468C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072900 | ||||||
chr8:28072993
|
T | C | 54 | a0001c0001t0005g0201a0001c0001t0005g0266a0001c0003t0002g0046others(51): Show | 59 | HG00323.hp1 HG00733.hp2 HG01256.hp2 others(56): Show |
intron_variant | MODIFIER | c.43+1375A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28072993 | ||||||
chr8:28073005
|
AT | A | 227 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0102others(224): Show | 246 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.43+1362delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073005 | ||||||
chr8:28073102
|
A | G | 40 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0101others(37): Show | 44 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.43+1266T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073102 | ||||||
chr8:28073163
|
G | A | 3 | a0001c0001t0046g0276a0002c0059t0025g0044a0019c0058t0045g0281 | 3 | HG02896.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.43+1205C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073163 | ||||||
chr8:28073178
|
C | CT | 263 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0165others(260): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.43+1189dupA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073178 | ||||||
chr8:28073220
|
T | C | 112 | a0001c0001t0003g0291a0001c0001t0003g0309a0001c0001t0011g0315others(109): Show | 122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.43+1148A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073220 | ||||||
chr8:28073333
|
A | G | 1 | a0001c0036t0012g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.43+1035T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073333 | ||||||
chr8:28073360
|
A | G | 55 | a0001c0001t0005g0201a0001c0001t0005g0266a0001c0003t0002g0046others(52): Show | 60 | HG00323.hp1 HG00733.hp2 HG01256.hp2 others(57): Show |
intron_variant | MODIFIER | c.43+1008T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073360 | ||||||
chr8:28073413
|
G | C | 1 | a0025c0066t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.43+955C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073413 | ||||||
chr8:28073544
|
G | A | 1 | a0001c0001t0011g0315 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.43+824C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073544 | ||||||
chr8:28073666
|
A | C | 1 | a0025c0066t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.43+702T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073666 | ||||||
chr8:28073721
|
G | A | 73 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(70): Show | 77 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.43+647C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073721 | ||||||
chr8:28073736
|
G | A | 1 | a0002c0005t0007g0032 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.43+632C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073736 | ||||||
chr8:28073766
|
C | T | 12 | a0004c0041t0001g0186a0005c0014t0001g0250a0005c0014t0003g0279others(9): Show | 12 | HG00741.hp1 HG01074.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.43+602G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073766 | ||||||
chr8:28073853
|
C | T | 3 | a0001c0003t0002g0056a0001c0003t0002g0204a0001c0003t0002g0205 | 3 | HG00642.hp2 HG01099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.43+515G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28073853 | ||||||
chr8:28074060
|
A | G | 4 | a0001c0003t0013g0264a0004c0004t0060g0346a0004c0007t0002g0058others(1): Show | 4 | HG01070.hp2 HG01346.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+308T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28074060 | ||||||
chr8:28074104
|
CT | C | 20 | a0001c0001t0046g0276a0001c0008t0002g0244a0002c0006t0003g0347others(17): Show | 20 | HG00741.hp1 HG01070.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.43+263delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28074104 | ||||||
chr8:28074115
|
T | C | 1 | a0002c0010t0022g0371 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.43+253A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28074115 | ||||||
chr8:28074160
|
T | C | 1 | a0003c0002t0001g0034 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.43+208A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28074160 | ||||||
chr8:28074234
|
C | T | 72 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(69): Show | 76 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.43+134G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28074234 | ||||||
chr8:28074235
|
G | A | 2 | a0004c0007t0001g0194a0004c0007t0030g0195 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.43+133C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28074235 | ||||||
chr8:28074358
|
A | G | 72 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(69): Show | 76 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.43+10T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 2/18 | chr8 | 28074358 | ||||||
chr8:28074496
|
T | C | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-46-40A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074496 | ||||||
chr8:28074506
|
C | A | 2 | a0001c0001t0001g0109a0001c0001t0006g0110 | 2 | NA18969.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-46-50G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074506 | ||||||
chr8:28074512
|
G | A | 1 | a0014c0029t0011g0372 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-46-56C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074512 | ||||||
chr8:28074517
|
C | A | 72 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(69): Show | 76 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.-46-61G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074517 | ||||||
chr8:28074534
|
T | C | 1 | a0001c0003t0002g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-46-78A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074534 | ||||||
chr8:28074566
|
G | A | 3 | a0001c0001t0046g0276a0002c0059t0025g0044a0019c0058t0045g0281 | 3 | HG02896.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-46-110C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074566 | ||||||
chr8:28074834
|
G | A | 72 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(69): Show | 76 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.-46-378C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074834 | ||||||
chr8:28074862
|
C | G | 1 | a0001c0009t0001g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-46-406G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074862 | ||||||
chr8:28074924
|
G | A | 1 | a0005c0053t0005g0060 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-46-468C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074924 | ||||||
chr8:28074949
|
A | C | 1 | a0004c0004t0004g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-493T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074949 | ||||||
chr8:28074991
|
A | T | 1 | a0001c0017t0003g0324 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-46-535T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28074991 | ||||||
chr8:28075149
|
G | A | 1 | a0003c0002t0003g0319 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-46-693C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075149 | ||||||
chr8:28075154
|
A | C | 1 | a0001c0003t0019g0138 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-46-698T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075154 | ||||||
chr8:28075197
|
C | T | 2 | a0001c0001t0046g0276a0019c0058t0045g0281 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-46-741G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075197 | ||||||
chr8:28075271
|
A | T | 4 | a0009c0022t0001g0035a0009c0022t0001g0127a0009c0022t0031g0126others(1): Show | 4 | HG00738.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-815T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075271 | ||||||
chr8:28075346
|
A | G | 3 | a0002c0006t0053g0321a0003c0002t0003g0322a0003c0002t0003g0323 | 3 | NA18962.hp1 NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-46-890T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075346 | ||||||
chr8:28075349
|
AG | A | 113 | a0001c0001t0003g0291a0001c0001t0003g0309a0001c0001t0011g0315others(110): Show | 123 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-46-894delC | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075349 | ||||||
chr8:28075514
|
C | A | 3 | a0001c0001t0046g0276a0002c0059t0025g0044a0019c0058t0045g0281 | 3 | HG02896.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-46-1058G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075514 | ||||||
chr8:28075579
|
G | A | 54 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0131others(51): Show | 58 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-46-1123C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075579 | ||||||
chr8:28075580
|
T | C | 75 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(72): Show | 79 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-46-1124A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075580 | ||||||
chr8:28075761
|
G | A | 1 | a0003c0049t0021g0265 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-46-1305C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075761 | ||||||
chr8:28075934
|
G | A | 1 | a0002c0059t0025g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-46-1478C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075934 | ||||||
chr8:28075999
|
A | G | 1 | a0025c0066t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-46-1543T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28075999 | ||||||
chr8:28076057
|
C | T | 6 | a0001c0001t0001g0165a0002c0005t0001g0037a0002c0005t0001g0039others(3): Show | 6 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-1601G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076057 | ||||||
chr8:28076068
|
G | A | 28 | a0001c0001t0001g0064a0001c0013t0012g0189a0001c0013t0013g0190others(25): Show | 28 | HG01243.hp1 HG01884.hp2 HG02155.hp2 others(25): Show |
intron_variant | MODIFIER | c.-46-1612C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076068 | ||||||
chr8:28076389
|
C | T | 1 | a0002c0055t0039g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-46-1933G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076389 | ||||||
chr8:28076538
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-46-2082G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076538 | ||||||
chr8:28076596
|
C | T | 1 | a0002c0006t0011g0320 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-46-2140G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076596 | ||||||
chr8:28076682
|
G | A | 186 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(183): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-46-2226C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076682 | ||||||
chr8:28076734
|
T | A | 201 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(198): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-46-2278A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076734 | ||||||
chr8:28076881
|
G | A | 76 | a0001c0001t0001g0064a0001c0001t0003g0352a0001c0001t0005g0043others(73): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-46-2425C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076881 | ||||||
chr8:28076898
|
T | C | 10 | a0001c0001t0001g0064a0001c0003t0002g0046a0002c0010t0001g0047others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46-2442A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076898 | ||||||
chr8:28076959
|
G | A | 1 | a0003c0002t0003g0354 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-46-2503C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28076959 | ||||||
chr8:28077015
|
C | T | 6 | a0001c0003t0013g0264a0002c0005t0037g0263a0002c0012t0010g0191others(3): Show | 6 | HG02559.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46-2559G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077015 | ||||||
chr8:28077128
|
T | C | 4 | a0001c0001t0005g0043a0001c0001t0005g0266a0001c0036t0012g0193others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-2672A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077128 | ||||||
chr8:28077156
|
T | C | 56 | a0001c0001t0003g0352a0001c0001t0004g0312a0001c0001t0004g0313others(53): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-46-2700A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077156 | ||||||
chr8:28077234
|
T | C | 1 | a0001c0063t0001g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-46-2778A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077234 | ||||||
chr8:28077370
|
A | G | 1 | a0008c0021t0008g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-46-2914T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077370 | ||||||
chr8:28077394
|
CA | C | 102 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(99): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-46-2939delT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077394 | ||||||
chr8:28077561
|
T | G | 1 | a0001c0001t0047g0361 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-46-3105A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077561 | ||||||
chr8:28077585
|
T | A | 1 | a0001c0035t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-46-3129A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077585 | ||||||
chr8:28077800
|
G | A | 5 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0040others(2): Show | 5 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-3344C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077800 | ||||||
chr8:28077971
|
A | G | 374 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(371): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.-46-3515T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28077971 | ||||||
chr8:28078012
|
T | C | 5 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0040others(2): Show | 5 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-3556A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078012 | ||||||
chr8:28078018
|
C | T | 100 | a0001c0001t0003g0291a0001c0001t0003g0309a0001c0001t0003g0352others(97): Show | 110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-46-3562G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078018 | ||||||
chr8:28078019
|
A | T | 1 | a0001c0001t0046g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-46-3563T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078019 | ||||||
chr8:28078233
|
T | C | 2 | a0001c0001t0003g0352a0002c0005t0003g0282 | 2 | NA18964.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-46-3777A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078233 | ||||||
chr8:28078714
|
G | A | 1 | a0001c0008t0003g0353 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-46-4258C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078714 | ||||||
chr8:28078716
|
C | G | 5 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0040others(2): Show | 5 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-4260G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078716 | ||||||
chr8:28078731
|
A | G | 164 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0101others(161): Show | 174 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.-46-4275T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078731 | ||||||
chr8:28078877
|
G | A | 7 | a0001c0001t0001g0064a0001c0063t0001g0059a0005c0053t0005g0060others(4): Show | 7 | HG01891.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-4421C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078877 | ||||||
chr8:28078881
|
T | C | 2 | a0001c0009t0001g0033a0003c0002t0001g0034 | 2 | NA18978.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-46-4425A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078881 | ||||||
chr8:28078927
|
G | A | 2 | a0002c0010t0002g0248a0005c0054t0001g0249 | 2 | HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-46-4471C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28078927 | ||||||
chr8:28079258
|
C | T | 1 | a0001c0001t0003g0360 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-47+4517G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079258 | ||||||
chr8:28079265
|
G | A | 1 | a0003c0002t0003g0354 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47+4510C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079265 | ||||||
chr8:28079412
|
C | T | 1 | a0001c0064t0054g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+4363G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079412 | ||||||
chr8:28079413
|
G | T | 69 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(66): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-47+4362C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079413 | ||||||
chr8:28079554
|
G | A | 2 | a0001c0001t0005g0266a0002c0005t0010g0042 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-47+4221C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079554 | ||||||
chr8:28079618
|
A | C | 1 | a0008c0021t0008g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-47+4157T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079618 | ||||||
chr8:28079626
|
A | G | 21 | a0001c0001t0046g0276a0001c0003t0002g0046a0001c0040t0001g0045others(18): Show | 21 | HG00597.hp2 HG01243.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-47+4149T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079626 | ||||||
chr8:28079720
|
C | G | 1 | a0002c0005t0003g0282 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-47+4055G>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079720 | ||||||
chr8:28079732
|
A | T | 152 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0101others(149): Show | 162 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-47+4043T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079732 | ||||||
chr8:28079742
|
T | C | 1 | a0003c0002t0003g0355 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-47+4033A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079742 | ||||||
chr8:28079763
|
G | A | 2 | a0001c0001t0005g0266a0002c0005t0010g0042 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-47+4012C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079763 | ||||||
chr8:28079794
|
G | A | 1 | a0019c0058t0045g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-47+3981C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079794 | ||||||
chr8:28079840
|
G | A | 1 | a0013c0047t0008g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-47+3935C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079840 | ||||||
chr8:28079902
|
T | A | 3 | a0001c0003t0002g0056a0004c0007t0002g0058a0004c0020t0002g0057 | 3 | HG01070.hp2 HG01099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-47+3873A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079902 | ||||||
chr8:28079932
|
T | TTTTG | 237 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(234): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.-47+3839_-47+3842d others(6): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079932 | ||||||
chr8:28079977
|
T | C | 5 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0040others(2): Show | 5 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+3798A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28079977 | ||||||
chr8:28080029
|
C | T | 1 | a0001c0003t0002g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-47+3746G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28080029 | ||||||
chr8:28080044
|
C | T | 72 | a0001c0001t0001g0019a0001c0001t0001g0122a0001c0001t0001g0131others(69): Show | 75 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-47+3731G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28080044 | ||||||
chr8:28080220
|
G | A | 8 | a0001c0001t0046g0276a0001c0064t0054g0275a0002c0033t0023g0277others(5): Show | 8 | HG02451.hp2 HG02976.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47+3555C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28080220 | ||||||
chr8:28080400
|
A | G | 4 | a0001c0001t0002g0066a0001c0001t0002g0198a0001c0003t0002g0197others(1): Show | 4 | HG01192.hp2 HG01243.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+3375T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28080400 | ||||||
chr8:28080657
|
T | C | 72 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(69): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.-47+3118A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28080657 | ||||||
chr8:28080664
|
C | A | 1 | a0002c0005t0001g0039 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-47+3111G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28080664 | ||||||
chr8:28080682
|
C | A | 5 | a0001c0001t0003g0360a0001c0001t0047g0361a0001c0003t0002g0056others(2): Show | 5 | HG01070.hp2 HG01099.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+3093G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28080682 | ||||||
chr8:28081007
|
T | TA | 17 | a0001c0001t0046g0276a0001c0003t0002g0046a0001c0040t0001g0045others(14): Show | 17 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+2767dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081007 | ||||||
chr8:28081088
|
G | A | 6 | a0001c0001t0001g0064a0005c0053t0005g0060a0006c0018t0008g0062others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+2687C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081088 | ||||||
chr8:28081105
|
G | A | 3 | a0001c0003t0002g0251a0001c0003t0002g0252a0001c0003t0002g0261 | 3 | NA18955.hp1 NA18975.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-47+2670C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081105 | ||||||
chr8:28081200
|
T | G | 1 | a0003c0002t0003g0356 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-47+2575A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081200 | ||||||
chr8:28081220
|
G | A | 8 | a0001c0001t0046g0276a0001c0064t0054g0275a0002c0033t0023g0277others(5): Show | 8 | HG02451.hp2 HG02976.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47+2555C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081220 | ||||||
chr8:28081273
|
C | T | 68 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0102others(65): Show | 75 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-47+2502G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081273 | ||||||
chr8:28081346
|
GT | G | 99 | a0001c0001t0003g0291a0001c0001t0003g0309a0001c0001t0003g0352others(96): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-47+2428delA | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081346 | ||||||
chr8:28081479
|
G | A | 1 | a0002c0005t0001g0262 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-47+2296C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081479 | ||||||
chr8:28081518
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-47+2257C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081518 | ||||||
chr8:28081637
|
G | C | 3 | a0003c0002t0003g0359a0004c0004t0003g0358a0004c0020t0004g0357 | 3 | HG00639.hp2 HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-47+2138C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081637 | ||||||
chr8:28081647
|
G | C | 16 | a0001c0001t0046g0276a0001c0003t0002g0046a0001c0040t0001g0045others(13): Show | 16 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+2128C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081647 | ||||||
chr8:28081669
|
G | A | 2 | a0003c0002t0017g0118a0003c0002t0020g0119 | 2 | HG02155.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-47+2106C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081669 | ||||||
chr8:28081682
|
T | A | 12 | a0001c0034t0015g0376a0002c0005t0061g0366a0002c0010t0022g0371others(9): Show | 12 | HG00733.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+2093A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081682 | ||||||
chr8:28081810
|
G | A | 8 | a0001c0003t0002g0046a0001c0040t0001g0045a0002c0010t0001g0047others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47+1965C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081810 | ||||||
chr8:28081877
|
C | CA | 21 | a0001c0001t0001g0019a0001c0001t0001g0254a0001c0001t0001g0256others(18): Show | 22 | HG00438.hp1 HG01070.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47+1897dupT | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081877 | ||||||
chr8:28081923
|
CAAG | C | 16 | a0001c0001t0046g0276a0001c0003t0002g0046a0001c0040t0001g0045others(13): Show | 16 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+1849_-47+1851d others(5): Show |
NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081923 | ||||||
chr8:28081954
|
A | C | 6 | a0001c0001t0001g0064a0005c0053t0005g0060a0006c0018t0008g0062others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+1821T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081954 | ||||||
chr8:28081994
|
A | C | 3 | a0001c0003t0013g0264a0002c0005t0037g0263a0003c0049t0021g0265 | 3 | HG03139.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-47+1781T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28081994 | ||||||
chr8:28082015
|
C | A | 2 | a0001c0009t0001g0033a0003c0002t0001g0034 | 2 | NA18978.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-47+1760G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082015 | ||||||
chr8:28082164
|
G | T | 61 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0102others(58): Show | 68 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-47+1611C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082164 | ||||||
chr8:28082197
|
T | A | 5 | a0002c0005t0001g0037a0002c0005t0001g0039a0002c0005t0001g0040others(2): Show | 5 | HG00597.hp2 NA18955.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+1578A>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082197 | ||||||
chr8:28082214
|
G | A | 16 | a0001c0001t0046g0276a0001c0003t0002g0046a0001c0040t0001g0045others(13): Show | 16 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+1561C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082214 | ||||||
chr8:28082217
|
T | G | 3 | a0001c0003t0013g0264a0002c0005t0037g0263a0003c0049t0021g0265 | 3 | HG03139.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-47+1558A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082217 | ||||||
chr8:28082409
|
T | C | 8 | a0001c0001t0046g0276a0001c0064t0054g0275a0002c0033t0023g0277others(5): Show | 8 | HG02451.hp2 HG02976.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47+1366A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082409 | ||||||
chr8:28082420
|
A | G | 1 | a0001c0001t0002g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-47+1355T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082420 | ||||||
chr8:28082562
|
G | C | 2 | a0001c0001t0005g0266a0002c0005t0010g0042 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-47+1213C>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082562 | ||||||
chr8:28082650
|
C | T | 115 | a0001c0001t0003g0291a0001c0001t0003g0309a0001c0001t0003g0352others(112): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-47+1125G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082650 | ||||||
chr8:28082697
|
G | T | 17 | a0001c0001t0005g0043a0001c0001t0046g0276a0001c0003t0002g0046others(14): Show | 17 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+1078C>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082697 | ||||||
chr8:28082772
|
A | G | 6 | a0001c0001t0001g0064a0005c0053t0005g0060a0006c0018t0008g0062others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+1003T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082772 | ||||||
chr8:28082892
|
C | T | 12 | a0001c0034t0015g0376a0002c0005t0061g0366a0002c0010t0022g0371others(9): Show | 12 | HG00733.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+883G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082892 | ||||||
chr8:28082911
|
A | C | 2 | a0001c0009t0001g0033a0003c0002t0001g0034 | 2 | NA18978.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-47+864T>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28082911 | ||||||
chr8:28083174
|
C | A | 1 | a0004c0007t0004g0023 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47+601G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083174 | ||||||
chr8:28083187
|
C | A | 4 | a0001c0001t0002g0269a0001c0003t0009g0268a0002c0005t0033g0270others(1): Show | 4 | HG01074.hp2 HG01106.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+588G>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083187 | ||||||
chr8:28083241
|
T | C | 9 | a0001c0009t0001g0033a0002c0005t0001g0037a0002c0005t0001g0039others(6): Show | 9 | HG00597.hp2 HG02109.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+534A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083241 | ||||||
chr8:28083313
|
A | G | 135 | a0001c0001t0003g0291a0001c0001t0003g0309a0001c0001t0003g0352others(132): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-47+462T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083313 | ||||||
chr8:28083438
|
C | T | 2 | a0002c0005t0001g0053a0002c0005t0001g0054 | 2 | HG00621.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-47+337G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083438 | ||||||
chr8:28083439
|
G | A | 1 | a0002c0005t0002g0271 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-47+336C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083439 | ||||||
chr8:28083457
|
C | T | 1 | a0001c0001t0007g0025 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-47+318G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083457 | ||||||
chr8:28083468
|
T | C | 1 | a0001c0009t0002g0020 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-47+307A>G | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083468 | ||||||
chr8:28083582
|
T | G | 12 | a0001c0034t0015g0376a0002c0005t0061g0366a0002c0010t0022g0371others(9): Show | 12 | HG00733.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+193A>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083582 | ||||||
chr8:28083612
|
A | G | 10 | a0001c0001t0005g0043a0001c0003t0002g0046a0001c0040t0001g0045others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+163T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083612 | ||||||
chr8:28083652
|
G | A | 1 | a0002c0006t0001g0272 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-47+123C>T | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083652 | ||||||
chr8:28083675
|
C | T | 1 | a0004c0016t0058g0274 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-47+100G>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083675 | ||||||
chr8:28083724
|
A | T | 1 | a0002c0005t0010g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-47+51T>A | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083724 | ||||||
chr8:28083757
|
A | G | 9 | a0001c0009t0001g0033a0002c0005t0001g0037a0002c0005t0001g0039others(6): Show | 9 | HG00597.hp2 HG02109.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+18T>C | NUGGC | ENSG00000189233.12 | transcript | ENST00000413272.7 | protein_coding | 1/18 | chr8 | 28083757 |