geneid | 729 |
---|---|
ensemblid | ENSG00000039537.16 |
hgncid | 1339 |
symbol | C6 |
name | complement C6 |
refseq_nuc | NM_000065.5 |
refseq_prot | NP_000056.2 |
ensembl_nuc | ENST00000337836.10 |
ensembl_prot | ENSP00000338861.5 |
mane_status | MANE Select |
chr | chr5 |
start | 41142116 |
end | 41213532 |
strand | - |
ver | v1.2 |
region | chr5:41142116-41213532 |
region5000 | chr5:41137116-41218532 |
regionname0 | C6_chr5_41142116_41213532 |
regionname5000 | C6_chr5_41137116_41218532 |
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 | 0/0 | 934 | 187 | 38 | 37 | 80 | 6 | 26 | 55 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002 | 1/1 | 934 | 177 | 37 | 25 | 91 | 10 | 12 | 72 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0003 | 0/0 | 934 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0004 | 0/0 | 934 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0005 | 0/0 | 934 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0006 | 0/0 | 934 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0007 | 0/0 | 934 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0008 | 0/0 | 934 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0009 | 0/0 | 934 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0010 | 0/0 | 934 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0011 | 0/0 | 934 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0012 | 0/0 | 934 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0013 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0014 | 0/0 | 934 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0015 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0016 | 0/0 | 934 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0017 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0018 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0019 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0020 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0021 | 0/0 | 934 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
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 | 0/0 | 2805 | 170 | 31 | 31 | 80 | 5 | 23 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0002 | 0/1 | 2805 | 170 | 34 | 25 | 89 | 10 | 11 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0003 | 0/0 | 2805 | 11 | 7 | 2 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0004 | 0/0 | 2805 | 8 | 0 | 0 | 8 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0005 | 0/0 | 2805 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0006 | 0/0 | 2805 | 3 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0007 | 0/0 | 2805 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0008 | 0/0 | 2805 | 3 | 2 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0009 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0010 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0011 | 0/0 | 2805 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0012 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0013 | 0/0 | 2805 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0014 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0015 | 1/0 | 2805 | 2 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0016 | 0/0 | 2805 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0017 | 0/0 | 2805 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0018 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0019 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0020 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0021 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0022 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0023 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0024 | 0/0 | 2805 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0025 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0026 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0027 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0028 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0029 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
c0030 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
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 | 0/1 | 887 | 224 | 52 | 35 | 107 | 7 | 22 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0002 | 1/0 | 887 | 101 | 10 | 18 | 51 | 6 | 15 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0003 | 0/0 | 887 | 44 | 10 | 7 | 23 | 2 | 2 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0004 | 0/0 | 887 | 11 | 9 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0005 | 0/0 | 887 | 7 | 1 | 1 | 5 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0006 | 0/0 | 887 | 4 | 4 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0007 | 0/0 | 887 | 3 | 2 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0008 | 0/0 | 887 | 3 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0009 | 0/0 | 887 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0010 | 0/0 | 887 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0011 | 0/0 | 887 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0012 | 0/0 | 887 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
t0013 | 0/0 | 887 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
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 | 8 | 0 | 0 | 8 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0013 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
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 | 0/0 | 2805 | 170 | 31 | 31 | 80 | 5 | 23 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0003 | 0/0 | 2805 | 11 | 7 | 2 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0006 | 0/0 | 2805 | 3 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0011 | 0/0 | 2805 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0022 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0002 | 0/1 | 2805 | 170 | 34 | 25 | 89 | 10 | 11 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0014 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0015 | 1/0 | 2805 | 2 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0027 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0028 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0029 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0003c0004 | 0/0 | 2805 | 8 | 0 | 0 | 8 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0004c0008 | 0/0 | 2805 | 3 | 2 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0005c0007 | 0/0 | 2805 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0006c0005 | 0/0 | 2805 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0007c0017 | 0/0 | 2805 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0008c0016 | 0/0 | 2805 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0009c0013 | 0/0 | 2805 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0010c0012 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0011c0010 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0012c0009 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0013c0025 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0014c0026 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0015c0030 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0016c0024 | 0/0 | 2805 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0017c0021 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0018c0019 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0019c0020 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0020c0018 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0021c0023 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3691 | 106 | 17 | 20 | 57 | 0 | 12 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0001t0002 | 0/0 | 3691 | 52 | 4 | 10 | 23 | 4 | 11 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0001t0004 | 0/0 | 3691 | 7 | 7 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0001t0007 | 0/0 | 3691 | 3 | 2 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0001t0012 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0001t0013 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0003t0001 | 0/0 | 3691 | 11 | 7 | 2 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0006t0002 | 0/0 | 3691 | 3 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0011t0002 | 0/0 | 3691 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0001c0022t0001 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0002t0001 | 0/1 | 3691 | 82 | 22 | 11 | 36 | 6 | 6 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0002t0002 | 0/0 | 3691 | 39 | 4 | 4 | 27 | 2 | 2 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0002t0003 | 0/0 | 3691 | 39 | 7 | 7 | 21 | 2 | 2 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0002t0005 | 0/0 | 3691 | 6 | 0 | 1 | 5 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0002t0008 | 0/0 | 3691 | 3 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0002t0010 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0014t0009 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0014t0011 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0015t0002 | 1/0 | 3691 | 2 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0027t0002 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0028t0001 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0002c0029t0005 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0003c0004t0001 | 0/0 | 3691 | 8 | 0 | 0 | 8 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0004c0008t0001 | 0/0 | 3691 | 3 | 2 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0005c0007t0003 | 0/0 | 3691 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0006c0005t0006 | 0/0 | 3691 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0007c0017t0004 | 0/0 | 3691 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0008c0016t0003 | 0/0 | 3691 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0009c0013t0001 | 0/0 | 3691 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0010c0012t0004 | 0/0 | 3691 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0011c0010t0001 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0011c0010t0006 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0012c0009t0001 | 0/0 | 3691 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0013c0025t0001 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0014c0026t0001 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0015c0030t0002 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0016c0024t0001 | 0/0 | 3691 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0017c0021t0001 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0018c0019t0002 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0019c0020t0001 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0020c0018t0001 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
a0021c0023t0001 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | copy fasta | chr5 | 41137116 | 41218532 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0013 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0007g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0012g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0013g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0006t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0006t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0006t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0011t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0022t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0008g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0008g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0008g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0014t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0014t0011g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0015t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0015t0002g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0027t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0028t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0029t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0004c0008t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0004c0008t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0004c0008t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0005c0007t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0005c0007t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0005c0007t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0006c0005t0006g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0006c0005t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0007c0017t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0007c0017t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0008c0016t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0008c0016t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0009c0013t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0009c0013t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0010c0012t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0010c0012t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0011c0010t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0011c0010t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0012c0009t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0012c0009t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0013c0025t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0014c0026t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0015c0030t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0016c0024t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0017c0021t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0018c0019t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0019c0020t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0020c0018t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0021c0023t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0003 | t0001 | g0119 | EUR | GBR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0059 | EUR | GBR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00280 | hp1 | a0002 | c0002 | t0003 | g0103 | EUR | FIN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0028 | EUR | FIN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0246 | EUR | FIN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0050 | EUR | FIN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00609 | hp1 | a0008 | c0016 | t0003 | g0098 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00609 | hp2 | a0003 | c0004 | t0001 | g0160 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0184 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01070 | hp2 | a0002 | c0002 | t0003 | g0096 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0097 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01074 | hp1 | a0001 | c0006 | t0002 | g0144 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01081 | hp1 | a0001 | c0006 | t0002 | g0142 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0018 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01167 | hp2 | a0007 | c0017 | t0004 | g0155 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01168 | hp2 | a0001 | c0011 | t0002 | g0015 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01169 | hp1 | a0007 | c0017 | t0004 | g0154 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01169 | hp2 | a0001 | c0011 | t0002 | g0015 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0210 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0037 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01257 | hp2 | a0016 | c0024 | t0001 | g0317 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0339 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01361 | hp2 | a0004 | c0008 | t0001 | g0153 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0116 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0163 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0026 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0173 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0162 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0174 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01884 | hp1 | a0002 | c0014 | t0009 | g0042 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01934 | hp2 | a0002 | c0002 | t0003 | g0100 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01981 | hp1 | a0002 | c0002 | t0003 | g0095 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02004 | hp1 | a0002 | c0002 | t0008 | g0335 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02004 | hp2 | a0002 | c0002 | t0003 | g0114 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02055 | hp1 | a0002 | c0002 | t0003 | g0089 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02074 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02129 | hp1 | a0002 | c0015 | t0002 | g0230 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0124 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CDX | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | CDX | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02257 | hp2 | a0012 | c0009 | t0001 | g0080 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02258 | hp1 | a0011 | c0010 | t0006 | g0039 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02258 | hp2 | a0019 | c0020 | t0001 | g0341 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02273 | hp2 | a0002 | c0002 | t0008 | g0336 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0121 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0177 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0018 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02451 | hp2 | a0002 | c0014 | t0011 | g0082 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0086 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0147 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02615 | hp2 | a0015 | c0030 | t0002 | g0249 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0167 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02630 | hp1 | a0006 | c0005 | t0006 | g0040 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02630 | hp2 | a0012 | c0009 | t0001 | g0130 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02698 | hp2 | a0001 | c0022 | t0001 | g0307 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02717 | hp1 | a0011 | c0010 | t0001 | g0277 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02723 | hp2 | a0005 | c0007 | t0003 | g0094 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02735 | hp1 | a0002 | c0002 | t0008 | g0337 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02738 | hp1 | a0021 | c0023 | t0001 | g0287 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0211 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0166 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0129 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02895 | hp2 | a0006 | c0005 | t0006 | g0014 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02897 | hp2 | a0006 | c0005 | t0006 | g0014 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0126 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02922 | hp2 | a0010 | c0012 | t0004 | g0138 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0165 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03041 | hp1 | a0002 | c0029 | t0005 | g0338 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03195 | hp1 | a0004 | c0008 | t0001 | g0342 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03195 | hp2 | a0002 | c0002 | t0003 | g0087 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03209 | hp1 | a0010 | c0012 | t0004 | g0136 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03209 | hp2 | a0005 | c0007 | t0003 | g0093 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0127 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03516 | hp1 | a0005 | c0007 | t0003 | g0090 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0242 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03579 | hp2 | a0002 | c0002 | t0010 | g0041 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03688 | hp1 | a0002 | c0027 | t0002 | g0217 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0110 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0122 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0083 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03942 | hp1 | a0014 | c0026 | t0001 | g0194 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0196 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0251 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18522 | hp2 | a0004 | c0008 | t0001 | g0152 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | CHB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18939 | hp1 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18941 | hp1 | a0002 | c0028 | t0001 | g0190 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18943 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18947 | hp2 | a0009 | c0013 | t0001 | g0299 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18949 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18953 | hp2 | a0009 | c0013 | t0001 | g0298 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18959 | hp2 | a0002 | c0002 | t0005 | g0181 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18965 | hp1 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18969 | hp1 | a0003 | c0004 | t0001 | g0158 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18971 | hp2 | a0002 | c0002 | t0003 | g0113 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18974 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18978 | hp1 | a0002 | c0002 | t0003 | g0115 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18983 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18984 | hp1 | a0003 | c0004 | t0001 | g0157 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18985 | hp1 | a0003 | c0004 | t0001 | g0159 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18986 | hp1 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18988 | hp1 | a0002 | c0002 | t0003 | g0085 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18989 | hp2 | a0020 | c0018 | t0001 | g0284 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18994 | hp1 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18995 | hp1 | a0002 | c0002 | t0005 | g0024 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18997 | hp1 | a0002 | c0002 | t0005 | g0183 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18997 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19000 | hp2 | a0002 | c0002 | t0003 | g0112 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19003 | hp2 | a0003 | c0004 | t0001 | g0161 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19004 | hp1 | a0013 | c0025 | t0001 | g0156 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | LWK | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | LWK | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | LWK | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0128 | AFR | LWK | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19054 | hp2 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19056 | hp1 | a0008 | c0016 | t0003 | g0101 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19065 | hp2 | a0002 | c0002 | t0003 | g0108 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19066 | hp2 | a0017 | c0021 | t0001 | g0300 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19077 | hp2 | a0002 | c0002 | t0003 | g0092 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19079 | hp2 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19080 | hp1 | a0002 | c0002 | t0005 | g0182 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19081 | hp2 | a0002 | c0002 | t0005 | g0024 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19082 | hp2 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19084 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19086 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0102 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19089 | hp2 | a0002 | c0002 | t0003 | g0104 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19240 | hp1 | a0002 | c0002 | t0003 | g0091 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | ASW | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20129 | hp2 | a0002 | c0002 | t0003 | g0006 | AFR | ASW | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20752 | hp1 | a0001 | c0001 | t0013 | g0272 | EUR | TSI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0099 | EUR | TSI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0213 | EUR | TSI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | TSI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | GIH | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20905 | hp2 | a0001 | c0006 | t0002 | g0343 | SAS | GIH | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0118 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01123 | hp2 | a0002 | c0002 | t0005 | g0193 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02109 | hp1 | a0002 | c0002 | t0003 | g0088 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0247 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0236 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0244 | AFR | USA | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG06807 | hp2 | a0018 | c0019 | t0002 | g0056 | AFR | USA | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0120 | AFR | USA | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0212 | REF | REF | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
homoSapiens_grch38 | hp1 | a0002 | c0015 | t0002 | g0238 | REF | REF | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:41142830
|
C | T | 2 | a0003a0013 | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
missense_variant | MODERATE | c.2800G>A | p.Ala934Thr | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 2977/3691 | 2800/2805 | 934/934 | chr5 | 41142830 | ||
chr5:41149429
|
G | A | 2 | a0006a0019 | 4 | HG02258.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
missense_variant | MODERATE | c.2435C>T | p.Thr812Ile | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/18 | 2612/3691 | 2435/2805 | 812/934 | chr5 | 41149429 | ||
chr5:41149460
|
C | G | 1 | a0017 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.2404G>C | p.Val802Leu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/18 | 2581/3691 | 2404/2805 | 802/934 | chr5 | 41149460 | ||
chr5:41153812
|
T | C | 1 | a0007 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant&splice_region_variant | MODERATE | c.2288A>G | p.Lys763Arg | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/18 | 2465/3691 | 2288/2805 | 763/934 | chr5 | 41153812 | ||
chr5:41153915
|
C | T | 1 | a0014 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.2185G>A | p.Glu729Lys | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/18 | 2362/3691 | 2185/2805 | 729/934 | chr5 | 41153915 | ||
chr5:41154987
|
C | T | 1 | a0011 | 2 | HG02258.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.2086G>A | p.Asp696Asn | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/18 | 2263/3691 | 2086/2805 | 696/934 | chr5 | 41154987 | ||
chr5:41159090
|
C | T | 2 | a0003a0013 | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
missense_variant | MODERATE | c.1848G>A | p.Met616Ile | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/18 | 2025/3691 | 1848/2805 | 616/934 | chr5 | 41159090 | ||
chr5:41159237
|
C | G | 2 | a0003a0013 | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
missense_variant | MODERATE | c.1701G>C | p.Gln567His | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/18 | 1878/3691 | 1701/2805 | 567/934 | chr5 | 41159237 | ||
chr5:41160271
|
C | T | 3 | a0006a0012a0019 | 6 | HG02257.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
missense_variant | MODERATE | c.1555G>A | p.Asp519Asn | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/18 | 1732/3691 | 1555/2805 | 519/934 | chr5 | 41160271 | ||
chr5:41161764
|
C | G | 1 | a0019 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1387G>C | p.Gly463Arg | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1564/3691 | 1387/2805 | 463/934 | chr5 | 41161764 | ||
chr5:41161796
|
C | T | 1 | a0018 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1355G>A | p.Gly452Glu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1532/3691 | 1355/2805 | 452/934 | chr5 | 41161796 | ||
chr5:41161817
|
C | T | 1 | a0013 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.1334G>A | p.Arg445Gln | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1511/3691 | 1334/2805 | 445/934 | chr5 | 41161817 | ||
chr5:41161850
|
A | T | 1 | a0020 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.1301T>A | p.Ile434Lys | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1478/3691 | 1301/2805 | 434/934 | chr5 | 41161850 | ||
chr5:41161851
|
T | C | 1 | a0008 | 2 | HG00609.hp1 NA19056.hp1 |
missense_variant | MODERATE | c.1300A>G | p.Ile434Val | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1477/3691 | 1300/2805 | 434/934 | chr5 | 41161851 | ||
chr5:41172327
|
T | C | 1 | a0010 | 2 | HG02922.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.1189A>G | p.Lys397Glu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/18 | 1366/3691 | 1189/2805 | 397/934 | chr5 | 41172327 | ||
chr5:41176663
|
G | A | 2 | a0009a0017 | 3 | NA18947.hp2 NA18953.hp2 NA19066.hp2 |
missense_variant | MODERATE | c.980C>T | p.Thr327Met | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/18 | 1157/3691 | 980/2805 | 327/934 | chr5 | 41176663 | ||
chr5:41181379
|
T | C | 1 | a0021 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.907A>G | p.Ile303Val | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 1084/3691 | 907/2805 | 303/934 | chr5 | 41181379 | ||
chr5:41181438
|
A | C | 1 | a0005 | 3 | HG02723.hp2 HG03209.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.848T>G | p.Ile283Ser | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 1025/3691 | 848/2805 | 283/934 | chr5 | 41181438 | ||
chr5:41181465
|
T | C | 1 | a0015 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.821A>G | p.Gln274Arg | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 998/3691 | 821/2805 | 274/934 | chr5 | 41181465 | ||
chr5:41181531
|
G | A | 1 | a0016 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.755C>T | p.Thr252Ile | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 932/3691 | 755/2805 | 252/934 | chr5 | 41181531 | ||
chr5:41186119
|
G | A | 1 | a0007 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.677C>T | p.Thr226Ile | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/18 | 854/3691 | 677/2805 | 226/934 | chr5 | 41186119 | ||
chr5:41199857
|
G | T | 12 | a0001a0006a0009others(9): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
missense_variant | MODERATE | c.356C>A | p.Ala119Glu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/18 | 533/3691 | 356/2805 | 119/934 | chr5 | 41199857 | ||
chr5:41203220
|
C | A | 1 | a0004 | 3 | HG01361.hp2 HG03195.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.11G>T | p.Arg4Leu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/18 | 188/3691 | 11/2805 | 4/934 | chr5 | 41203220 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:41142837
|
C | T | 1 | a0002c0027 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.2793G>A | p.Lys931Lys | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 2970/3691 | 2793/2805 | 931/934 | chr5 | 41142837 | ||
chr5:41153940
|
T | C | 1 | a0002c0028 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.2160A>G | p.Arg720Arg | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/18 | 2337/3691 | 2160/2805 | 720/934 | chr5 | 41153940 | ||
chr5:41155006
|
G | A | 1 | a0002c0029 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.2067C>T | p.Asp689Asp | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/18 | 2244/3691 | 2067/2805 | 689/934 | chr5 | 41155006 | ||
chr5:41155048
|
G | A | 1 | a0001c0011 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.2025C>T | p.Gly675Gly | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/18 | 2202/3691 | 2025/2805 | 675/934 | chr5 | 41155048 | ||
chr5:41158761
|
G | A | 29 | a0001c0001a0001c0003a0001c0006others(26): Show | 400 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(397): Show |
synonymous_variant | LOW | c.1881C>T | p.Asp627Asp | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/18 | 2058/3691 | 1881/2805 | 627/934 | chr5 | 41158761 | ||
chr5:41159243
|
G | A | 2 | a0003c0004a0013c0025 | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
synonymous_variant | LOW | c.1695C>T | p.Asp565Asp | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/18 | 1872/3691 | 1695/2805 | 565/934 | chr5 | 41159243 | ||
chr5:41160191
|
A | G | 1 | a0001c0006 | 3 | HG01074.hp1 HG01081.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.1635T>C | p.Ser545Ser | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/18 | 1812/3691 | 1635/2805 | 545/934 | chr5 | 41160191 | ||
chr5:41160209
|
A | G | 3 | a0002c0014a0003c0004a0013c0025 | 11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
synonymous_variant | LOW | c.1617T>C | p.Cys539Cys | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/18 | 1794/3691 | 1617/2805 | 539/934 | chr5 | 41160209 | ||
chr5:41176593
|
G | A | 1 | a0017c0021 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.1050C>T | p.Asn350Asn | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/18 | 1227/3691 | 1050/2805 | 350/934 | chr5 | 41176593 | ||
chr5:41176710
|
A | G | 2 | a0003c0004a0013c0025 | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
synonymous_variant | LOW | c.933T>C | p.Ser311Ser | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/18 | 1110/3691 | 933/2805 | 311/934 | chr5 | 41176710 | ||
chr5:41181476
|
T | A | 2 | a0001c0022a0021c0023 | 2 | HG02698.hp2 HG02738.hp1 |
synonymous_variant | LOW | c.810A>T | p.Ser270Ser | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 987/3691 | 810/2805 | 270/934 | chr5 | 41181476 | ||
chr5:41186118
|
T | G | 1 | a0001c0003 | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
synonymous_variant | LOW | c.678A>C | p.Thr226Thr | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/18 | 855/3691 | 678/2805 | 226/934 | chr5 | 41186118 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:41142167
|
A | C | 1 | a0002c0002t0008 | 3 | HG02004.hp1 HG02273.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*658T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 658 | chr5 | 41142167 | |||||
chr5:41142188
|
C | G | 6 | a0001c0001t0004a0001c0001t0007a0002c0014t0009others(3): Show | 16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*637G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 637 | chr5 | 41142188 | |||||
chr5:41142249
|
T | C | 1 | a0001c0001t0012 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*576A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 576 | chr5 | 41142249 | |||||
chr5:41142471
|
G | T | 2 | a0002c0002t0005a0002c0029t0005 | 7 | HG01123.hp2 HG03041.hp1 NA18959.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*354C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 354 | chr5 | 41142471 | |||||
chr5:41142504
|
C | T | 33 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(30): Show | 300 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
3_prime_UTR_variant | MODIFIER | c.*321G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 321 | chr5 | 41142504 | |||||
chr5:41142530
|
A | G | 6 | a0001c0001t0004a0001c0001t0007a0002c0014t0009others(3): Show | 16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*295T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 295 | chr5 | 41142530 | |||||
chr5:41142583
|
C | T | 6 | a0001c0001t0004a0001c0001t0007a0002c0014t0009others(3): Show | 16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*242G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 242 | chr5 | 41142583 | |||||
chr5:41142626
|
C | T | 1 | a0001c0001t0012 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*199G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 199 | chr5 | 41142626 | |||||
chr5:41142744
|
T | C | 1 | a0001c0001t0013 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 81 | chr5 | 41142744 | |||||
chr5:41203242
|
C | T | 4 | a0002c0002t0003a0002c0014t0011a0005c0007t0003others(1): Show | 45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-12G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/18 | 12 | chr5 | 41203242 | |||||
chr5:41213435
|
G | T | 2 | a0002c0002t0010a0002c0014t0009 | 2 | HG01884.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-80C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/18 | 10205 | chr5 | 41213435 | |||||
chr5:41213497
|
C | G | 2 | a0006c0005t0006a0011c0010t0006 | 4 | HG02258.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-142G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/18 | 10267 | chr5 | 41213497 | |||||
chr5:41213528
|
A | G | 1 | a0001c0001t0007 | 3 | HG01243.hp2 HG01891.hp2 HG02818.hp2 |
5_prime_UTR_variant | MODIFIER | c.-173T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/18 | 10298 | chr5 | 41213528 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:41143214
|
C | T | 1 | a0001c0001t0004g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-208G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143214 | ||||||
chr5:41143320
|
C | T | 3 | a0002c0002t0002g0209a0002c0002t0002g0216a0002c0002t0002g0225 | 3 | NA18951.hp2 NA19077.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2624-314G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143320 | ||||||
chr5:41143321
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2624-315C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143321 | ||||||
chr5:41143477
|
G | T | 1 | a0001c0001t0001g0325 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2624-471C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143477 | ||||||
chr5:41143545
|
G | A | 7 | a0001c0001t0001g0140a0002c0002t0001g0031a0002c0002t0001g0148others(4): Show | 8 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2624-539C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143545 | ||||||
chr5:41143654
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(127): Show | 155 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.2624-648C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143654 | ||||||
chr5:41143736
|
C | T | 15 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(12): Show | 16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2624-730G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143736 | ||||||
chr5:41143835
|
C | T | 6 | a0002c0002t0005g0024a0002c0002t0005g0181a0002c0002t0005g0182others(3): Show | 7 | HG01123.hp2 HG03041.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.2624-829G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143835 | ||||||
chr5:41144223
|
T | C | 1 | a0001c0001t0001g0321 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2624-1217A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144223 | ||||||
chr5:41144237
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2624-1231C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144237 | ||||||
chr5:41144267
|
G | A | 6 | a0002c0002t0005g0024a0002c0002t0005g0181a0002c0002t0005g0182others(3): Show | 7 | HG01123.hp2 HG03041.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.2624-1261C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144267 | ||||||
chr5:41144294
|
G | A | 6 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(3): Show | 6 | HG00140.hp1 HG01123.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.2624-1288C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144294 | ||||||
chr5:41144352
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0318 | 2 | HG01928.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.2624-1346G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144352 | ||||||
chr5:41144353
|
G | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(44): Show | 55 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.2624-1347C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144353 | ||||||
chr5:41144363
|
G | C | 1 | a0002c0002t0001g0025 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2624-1357C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144363 | ||||||
chr5:41144387
|
C | G | 1 | a0015c0030t0002g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2624-1381G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144387 | ||||||
chr5:41144513
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2624-1507A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144513 | ||||||
chr5:41144574
|
C | A | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2624-1568G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144574 | ||||||
chr5:41144751
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(113): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2624-1745A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144751 | ||||||
chr5:41144787
|
C | T | 1 | a0002c0002t0002g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2624-1781G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144787 | ||||||
chr5:41144792
|
G | A | 5 | a0001c0003t0001g0123a0001c0003t0001g0124a0001c0003t0001g0125others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2624-1786C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144792 | ||||||
chr5:41144875
|
G | A | 15 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(12): Show | 16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2624-1869C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144875 | ||||||
chr5:41144889
|
T | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2624-1883A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144889 | ||||||
chr5:41144901
|
C | A | 15 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(12): Show | 16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2624-1895G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144901 | ||||||
chr5:41144940
|
A | G | 5 | a0006c0005t0006g0014a0006c0005t0006g0040a0012c0009t0001g0080others(2): Show | 6 | HG02257.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2624-1934T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144940 | ||||||
chr5:41144948
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(209): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.2624-1942C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144948 | ||||||
chr5:41144959
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2624-1953G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144959 | ||||||
chr5:41145041
|
A | C | 1 | a0004c0008t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2624-2035T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145041 | ||||||
chr5:41145106
|
G | A | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2624-2100C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145106 | ||||||
chr5:41145182
|
A | G | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2624-2176T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145182 | ||||||
chr5:41145411
|
C | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG01167.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2624-2405G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145411 | ||||||
chr5:41145412
|
G | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0265others(7): Show | 13 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.2624-2406C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145412 | ||||||
chr5:41145458
|
G | T | 1 | a0002c0002t0002g0225 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2624-2452C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145458 | ||||||
chr5:41145523
|
G | A | 1 | a0001c0001t0004g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-2517C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145523 | ||||||
chr5:41145620
|
A | G | 10 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0051others(7): Show | 16 | HG00438.hp2 HG00558.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.2624-2614T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145620 | ||||||
chr5:41145643
|
G | A | 1 | a0001c0001t0007g0037 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2624-2637C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145643 | ||||||
chr5:41145692
|
C | T | 8 | a0002c0014t0009g0042a0003c0004t0001g0008a0003c0004t0001g0157others(5): Show | 10 | HG00609.hp2 HG01884.hp1 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.2624-2686G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145692 | ||||||
chr5:41145701
|
C | T | 3 | a0002c0002t0003g0018a0002c0002t0003g0089a0002c0002t0003g0091 | 4 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-2695G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145701 | ||||||
chr5:41145816
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2624-2810C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145816 | ||||||
chr5:41145849
|
T | A | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2624-2843A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145849 | ||||||
chr5:41145864
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2624-2858A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145864 | ||||||
chr5:41145921
|
A | G | 2 | a0012c0009t0001g0080a0012c0009t0001g0130 | 2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2624-2915T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145921 | ||||||
chr5:41146152
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2623+3089C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146152 | ||||||
chr5:41146175
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(112): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2623+3066G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146175 | ||||||
chr5:41146176
|
G | A | 15 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(12): Show | 16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2623+3065C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146176 | ||||||
chr5:41146178
|
T | C | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2623+3063A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146178 | ||||||
chr5:41146274
|
TG | T | 62 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(59): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2623+2966delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146274 | ||||||
chr5:41146322
|
A | T | 15 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(12): Show | 16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2623+2919T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146322 | ||||||
chr5:41146357
|
C | T | 2 | a0002c0002t0001g0163a0002c0002t0001g0174 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2623+2884G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146357 | ||||||
chr5:41146529
|
A | T | 4 | a0001c0001t0001g0135a0004c0008t0001g0152a0004c0008t0001g0153others(1): Show | 4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+2712T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146529 | ||||||
chr5:41146531
|
C | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2623+2710G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146531 | ||||||
chr5:41146676
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2623+2565A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146676 | ||||||
chr5:41146748
|
C | CT | 11 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(8): Show | 13 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2623+2492dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146748 | ||||||
chr5:41146888
|
T | C | 13 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(10): Show | 14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+2353A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146888 | ||||||
chr5:41146899
|
A | T | 1 | a0002c0002t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2623+2342T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146899 | ||||||
chr5:41146921
|
C | CA | 8 | a0002c0002t0002g0236a0002c0002t0002g0247a0002c0002t0005g0183others(5): Show | 10 | HG00609.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2623+2319dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146921 | ||||||
chr5:41146921
|
C | T | 1 | a0002c0014t0009g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2623+2320G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146921 | ||||||
chr5:41146921
|
CA | C | 18 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(15): Show | 19 | HG00140.hp1 HG01123.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.2623+2319delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146921 | ||||||
chr5:41147076
|
C | T | 1 | a0015c0030t0002g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2623+2165G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147076 | ||||||
chr5:41147198
|
G | A | 13 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(10): Show | 14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+2043C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147198 | ||||||
chr5:41147232
|
G | T | 10 | a0002c0002t0001g0022a0002c0002t0001g0163a0002c0002t0001g0165others(7): Show | 11 | HG01515.hp1 HG01517.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2623+2009C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147232 | ||||||
chr5:41147426
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(112): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2623+1815C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147426 | ||||||
chr5:41147542
|
C | T | 3 | a0002c0002t0002g0010a0002c0002t0002g0218a0002c0002t0002g0224 | 5 | NA18945.hp1 NA18959.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.2623+1699G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147542 | ||||||
chr5:41147555
|
A | G | 3 | a0002c0002t0005g0024a0002c0002t0005g0182a0002c0002t0005g0183 | 4 | NA18995.hp1 NA18997.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+1686T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147555 | ||||||
chr5:41147613
|
T | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2623+1628A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147613 | ||||||
chr5:41147739
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2623+1502C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147739 | ||||||
chr5:41147778
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2623+1463G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147778 | ||||||
chr5:41147869
|
C | T | 6 | a0002c0002t0001g0027a0002c0002t0001g0220a0002c0002t0001g0221others(3): Show | 7 | HG00408.hp1 HG00673.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2623+1372G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147869 | ||||||
chr5:41148023
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(88): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.2623+1218G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148023 | ||||||
chr5:41148097
|
T | A | 1 | a0001c0001t0001g0340 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2623+1144A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148097 | ||||||
chr5:41148127
|
T | G | 1 | a0001c0001t0001g0321 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2623+1114A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148127 | ||||||
chr5:41148395
|
T | G | 13 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(10): Show | 14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+846A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148395 | ||||||
chr5:41148400
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(292): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.2623+841T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148400 | ||||||
chr5:41148401
|
C | T | 2 | a0002c0002t0002g0237a0002c0002t0002g0239 | 2 | NA18974.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2623+840G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148401 | ||||||
chr5:41148408
|
A | C | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2623+833T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148408 | ||||||
chr5:41148441
|
T | A | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2623+800A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148441 | ||||||
chr5:41148477
|
A | G | 1 | a0002c0002t0002g0248 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2623+764T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148477 | ||||||
chr5:41148757
|
C | T | 13 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(10): Show | 14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+484G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148757 | ||||||
chr5:41148793
|
C | G | 1 | a0002c0002t0008g0335 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2623+448G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148793 | ||||||
chr5:41148802
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2623+439C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148802 | ||||||
chr5:41148851
|
T | C | 4 | a0001c0001t0001g0135a0004c0008t0001g0152a0004c0008t0001g0153others(1): Show | 4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+390A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148851 | ||||||
chr5:41148978
|
C | T | 15 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0162others(12): Show | 17 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2623+263G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148978 | ||||||
chr5:41149040
|
A | G | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2623+201T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149040 | ||||||
chr5:41149045
|
C | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(112): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2623+196G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149045 | ||||||
chr5:41149133
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(112): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2623+108T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149133 | ||||||
chr5:41149156
|
G | C | 5 | a0001c0003t0001g0123a0001c0003t0001g0124a0001c0003t0001g0125others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2623+85C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149156 | ||||||
chr5:41149182
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(80): Show | 103 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.2623+59C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149182 | ||||||
chr5:41149618
|
T | A | 1 | a0005c0007t0003g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2382-136A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149618 | ||||||
chr5:41149636
|
A | C | 1 | a0002c0014t0009g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2382-154T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149636 | ||||||
chr5:41149701
|
T | G | 1 | a0017c0021t0001g0300 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2382-219A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149701 | ||||||
chr5:41149808
|
A | G | 13 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(10): Show | 14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2381+127T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149808 | ||||||
chr5:41149818
|
T | C | 1 | a0001c0003t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2381+117A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149818 | ||||||
chr5:41149858
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2381+77G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149858 | ||||||
chr5:41150080
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2291-55T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150080 | ||||||
chr5:41150324
|
T | A | 8 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0273others(5): Show | 8 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.2291-299A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150324 | ||||||
chr5:41150684
|
C | T | 1 | a0002c0002t0002g0226 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2291-659G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150684 | ||||||
chr5:41150687
|
G | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(44): Show | 55 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.2291-662C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150687 | ||||||
chr5:41150812
|
G | A | 1 | a0011c0010t0001g0277 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2291-787C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150812 | ||||||
chr5:41150844
|
GC | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(88): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.2291-820delG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150844 | ||||||
chr5:41150852
|
A | AC | 135 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(132): Show | 162 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.2291-828dupG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150852 | ||||||
chr5:41150884
|
T | TA | 31 | a0001c0001t0002g0052a0001c0001t0004g0020a0001c0001t0004g0079others(28): Show | 33 | HG00140.hp1 HG01123.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.2291-860dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150884 | ||||||
chr5:41150884
|
TA | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(112): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2291-860delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150884 | ||||||
chr5:41150913
|
G | T | 1 | a0001c0001t0002g0073 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2291-888C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150913 | ||||||
chr5:41150974
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2291-949T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150974 | ||||||
chr5:41151061
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2291-1036T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151061 | ||||||
chr5:41151177
|
A | AT | 2 | a0002c0002t0001g0021a0002c0002t0001g0149 | 3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2291-1153dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151177 | ||||||
chr5:41151178
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(88): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.2291-1153A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151178 | ||||||
chr5:41151200
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2291-1175C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151200 | ||||||
chr5:41151307
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2291-1282G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151307 | ||||||
chr5:41151459
|
G | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2291-1434C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151459 | ||||||
chr5:41151507
|
C | A | 1 | a0004c0008t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2291-1482G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151507 | ||||||
chr5:41151859
|
G | GA | 12 | a0002c0002t0001g0027a0002c0002t0001g0220a0002c0002t0001g0221others(9): Show | 15 | HG00408.hp1 HG00609.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.2291-1835dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151859 | ||||||
chr5:41151859
|
GA | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(100): Show | 126 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2291-1835delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151859 | ||||||
chr5:41151863
|
A | G | 1 | a0002c0002t0001g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2291-1838T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151863 | ||||||
chr5:41152005
|
G | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2290+1805C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152005 | ||||||
chr5:41152097
|
A | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2290+1713T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152097 | ||||||
chr5:41152159
|
A | C | 2 | a0002c0002t0001g0021a0002c0002t0001g0149 | 3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2290+1651T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152159 | ||||||
chr5:41152197
|
A | G | 1 | a0001c0001t0002g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2290+1613T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152197 | ||||||
chr5:41152243
|
A | T | 11 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(8): Show | 13 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2290+1567T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152243 | ||||||
chr5:41152267
|
C | A | 1 | a0002c0002t0003g0109 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2290+1543G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152267 | ||||||
chr5:41152319
|
G | A | 2 | a0002c0002t0003g0019a0002c0002t0003g0109 | 3 | NA18939.hp1 NA18986.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2290+1491C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152319 | ||||||
chr5:41152465
|
C | T | 1 | a0002c0002t0002g0184 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2290+1345G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152465 | ||||||
chr5:41152493
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2290+1317G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152493 | ||||||
chr5:41152555
|
G | A | 2 | a0001c0001t0001g0309a0001c0001t0001g0334 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2290+1255C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152555 | ||||||
chr5:41152563
|
C | T | 4 | a0001c0001t0001g0135a0004c0008t0001g0152a0004c0008t0001g0153others(1): Show | 4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2290+1247G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152563 | ||||||
chr5:41152587
|
A | G | 110 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0134others(107): Show | 126 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2290+1223T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152587 | ||||||
chr5:41152658
|
CT | C | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2290+1151delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152658 | ||||||
chr5:41152661
|
G | C | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2290+1149C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152661 | ||||||
chr5:41152717
|
A | G | 32 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(29): Show | 35 | HG00140.hp1 HG01123.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.2290+1093T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152717 | ||||||
chr5:41152727
|
A | T | 81 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(78): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2290+1083T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152727 | ||||||
chr5:41152846
|
G | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(46): Show | 57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.2290+964C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152846 | ||||||
chr5:41152937
|
A | G | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2290+873T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152937 | ||||||
chr5:41152973
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2290+837G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152973 | ||||||
chr5:41152983
|
T | C | 5 | a0006c0005t0006g0014a0006c0005t0006g0040a0012c0009t0001g0080others(2): Show | 6 | HG02257.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2290+827A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152983 | ||||||
chr5:41153183
|
T | C | 1 | a0002c0002t0001g0243 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2290+627A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153183 | ||||||
chr5:41153259
|
T | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(44): Show | 55 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.2290+551A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153259 | ||||||
chr5:41153341
|
G | T | 1 | a0001c0001t0012g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2290+469C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153341 | ||||||
chr5:41153344
|
T | C | 1 | a0002c0002t0001g0178 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2290+466A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153344 | ||||||
chr5:41153357
|
A | G | 1 | a0009c0013t0001g0298 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2290+453T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153357 | ||||||
chr5:41153435
|
CACTT | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG01167.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2290+371_2290+374d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153435 | ||||||
chr5:41153579
|
C | G | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2290+231G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153579 | ||||||
chr5:41153593
|
C | T | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2290+217G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153593 | ||||||
chr5:41153626
|
A | C | 2 | a0001c0001t0001g0140a0002c0002t0001g0148 | 2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2290+184T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153626 | ||||||
chr5:41153685
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0252 | 3 | HG02976.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2290+125T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153685 | ||||||
chr5:41153696
|
T | C | 2 | a0002c0014t0009g0042a0002c0014t0011g0082 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2290+114A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153696 | ||||||
chr5:41153756
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2290+54G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153756 | ||||||
chr5:41154048
|
A | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(289): Show | 342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.2102-50T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154048 | ||||||
chr5:41154113
|
C | T | 1 | a0002c0002t0001g0151 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2102-115G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154113 | ||||||
chr5:41154282
|
A | G | 1 | a0002c0002t0003g0095 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2102-284T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154282 | ||||||
chr5:41154334
|
A | G | 81 | a0001c0001t0001g0035a0001c0001t0001g0134a0001c0001t0001g0320others(78): Show | 94 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.2102-336T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154334 | ||||||
chr5:41154342
|
A | G | 7 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2102-344T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154342 | ||||||
chr5:41154401
|
TC | T | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2102-404delG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154401 | ||||||
chr5:41154426
|
T | C | 94 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(91): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.2102-428A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154426 | ||||||
chr5:41154648
|
G | A | 2 | a0002c0002t0001g0021a0002c0002t0001g0149 | 3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2101+324C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154648 | ||||||
chr5:41154925
|
A | G | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2101+47T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154925 | ||||||
chr5:41155147
|
A | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-43T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155147 | ||||||
chr5:41155220
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1969-116G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155220 | ||||||
chr5:41155331
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-227G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155331 | ||||||
chr5:41155563
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-459G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155563 | ||||||
chr5:41155612
|
C | G | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1969-508G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155612 | ||||||
chr5:41155641
|
A | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-537T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155641 | ||||||
chr5:41155744
|
A | C | 2 | a0002c0014t0009g0042a0002c0014t0011g0082 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1969-640T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155744 | ||||||
chr5:41155772
|
C | CA | 10 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(7): Show | 11 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1969-669dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155772 | ||||||
chr5:41155791
|
A | C | 1 | a0001c0001t0002g0049 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1969-687T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155791 | ||||||
chr5:41155806
|
A | G | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-702T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155806 | ||||||
chr5:41155810
|
G | C | 1 | a0001c0003t0001g0122 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1969-706C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155810 | ||||||
chr5:41155875
|
AATAAT | A | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-776_1969-772d others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155875 | ||||||
chr5:41155906
|
T | C | 58 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(55): Show | 68 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1969-802A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155906 | ||||||
chr5:41156063
|
T | C | 1 | a0002c0002t0001g0339 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1969-959A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156063 | ||||||
chr5:41156111
|
C | T | 2 | a0011c0010t0001g0277a0011c0010t0006g0039 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1969-1007G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156111 | ||||||
chr5:41156129
|
T | C | 1 | a0003c0004t0001g0161 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1969-1025A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156129 | ||||||
chr5:41156173
|
A | G | 12 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(9): Show | 12 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1969-1069T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156173 | ||||||
chr5:41156285
|
T | A | 1 | a0002c0002t0001g0339 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1969-1181A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156285 | ||||||
chr5:41156457
|
A | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0265others(8): Show | 14 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1969-1353T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156457 | ||||||
chr5:41156498
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1969-1394G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156498 | ||||||
chr5:41156569
|
A | G | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1969-1465T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156569 | ||||||
chr5:41156611
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1969-1507G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156611 | ||||||
chr5:41156688
|
T | C | 1 | a0002c0002t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1969-1584A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156688 | ||||||
chr5:41156787
|
C | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1969-1683G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156787 | ||||||
chr5:41156821
|
T | A | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-1717A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156821 | ||||||
chr5:41157122
|
T | G | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968+1552A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157122 | ||||||
chr5:41157165
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1968+1509C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157165 | ||||||
chr5:41157238
|
C | T | 89 | a0001c0001t0001g0035a0001c0001t0001g0134a0001c0001t0001g0320others(86): Show | 104 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1968+1436G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157238 | ||||||
chr5:41157298
|
G | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(7): Show | 12 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1968+1376C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157298 | ||||||
chr5:41157398
|
G | A | 1 | a0002c0002t0001g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1968+1276C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157398 | ||||||
chr5:41157410
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1968+1264C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157410 | ||||||
chr5:41157412
|
G | A | 1 | a0002c0002t0003g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1968+1262C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157412 | ||||||
chr5:41157975
|
G | C | 2 | a0002c0002t0003g0085a0002c0002t0003g0108 | 2 | NA18988.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1968+699C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157975 | ||||||
chr5:41157983
|
T | C | 1 | a0002c0002t0002g0250 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1968+691A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157983 | ||||||
chr5:41158009
|
A | G | 1 | a0002c0002t0001g0220 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1968+665T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158009 | ||||||
chr5:41158067
|
G | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1968+607C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158067 | ||||||
chr5:41158069
|
A | G | 9 | a0002c0014t0009g0042a0002c0014t0011g0082a0003c0004t0001g0008others(6): Show | 11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1968+605T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158069 | ||||||
chr5:41158076
|
A | T | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 5 | HG01346.hp1 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968+598T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158076 | ||||||
chr5:41158165
|
TA | T | 3 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339 | 4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1968+508delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158165 | ||||||
chr5:41158197
|
T | TA | 12 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0265others(9): Show | 15 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1968+476dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158197 | ||||||
chr5:41158197
|
TA | T | 8 | a0001c0001t0001g0140a0002c0002t0001g0031a0002c0002t0001g0148others(5): Show | 9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1968+476delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158197 | ||||||
chr5:41158250
|
G | C | 1 | a0010c0012t0004g0136 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1968+424C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158250 | ||||||
chr5:41158347
|
A | G | 2 | a0001c0001t0001g0273a0001c0001t0013g0272 | 2 | HG01243.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1968+327T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158347 | ||||||
chr5:41158387
|
A | G | 83 | a0001c0001t0001g0035a0001c0001t0001g0134a0001c0001t0001g0320others(80): Show | 96 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968+287T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158387 | ||||||
chr5:41158404
|
A | G | 1 | a0002c0002t0002g0245 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1968+270T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158404 | ||||||
chr5:41158465
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1968+209C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158465 | ||||||
chr5:41158470
|
A | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(288): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1968+204T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158470 | ||||||
chr5:41158473
|
T | A | 3 | a0003c0004t0001g0008a0003c0004t0001g0160a0013c0025t0001g0156 | 5 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968+201A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158473 | ||||||
chr5:41158515
|
A | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1968+159T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158515 | ||||||
chr5:41158569
|
T | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(288): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1968+105A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158569 | ||||||
chr5:41158640
|
A | C | 2 | a0002c0002t0001g0021a0002c0002t0001g0149 | 3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1968+34T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158640 | ||||||
chr5:41158650
|
A | G | 2 | a0002c0014t0009g0042a0002c0014t0011g0082 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1968+24T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158650 | ||||||
chr5:41158807
|
G | A | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1857-22C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/17 | chr5 | 41158807 | ||||||
chr5:41158865
|
A | G | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(1): Show | 4 | HG00741.hp2 HG01256.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857-80T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/17 | chr5 | 41158865 | ||||||
chr5:41158884
|
A | G | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069 | 3 | HG01256.hp1 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1857-99T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/17 | chr5 | 41158884 | ||||||
chr5:41159014
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0252 | 3 | HG02976.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1856+68T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/17 | chr5 | 41159014 | ||||||
chr5:41159407
|
C | T | 81 | a0001c0001t0001g0035a0001c0001t0001g0134a0001c0001t0001g0320others(78): Show | 94 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1685-154G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159407 | ||||||
chr5:41159427
|
C | T | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(1): Show | 4 | HG00741.hp2 HG01256.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685-174G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159427 | ||||||
chr5:41159551
|
T | C | 82 | a0001c0001t0001g0035a0001c0001t0001g0134a0001c0001t0001g0320others(79): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1685-298A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159551 | ||||||
chr5:41159573
|
T | C | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1685-320A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159573 | ||||||
chr5:41159620
|
G | T | 82 | a0001c0001t0001g0035a0001c0001t0001g0134a0001c0001t0001g0320others(79): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1685-367C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159620 | ||||||
chr5:41159643
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1685-390G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159643 | ||||||
chr5:41159646
|
G | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1685-393C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159646 | ||||||
chr5:41159647
|
C | A | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1685-394G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159647 | ||||||
chr5:41159648
|
C | CTAACTAT others(13): Show |
1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1685-396_1685-395i others(22): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159648 | ||||||
chr5:41159868
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1684+274T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159868 | ||||||
chr5:41159963
|
A | G | 82 | a0001c0001t0001g0035a0001c0001t0001g0134a0001c0001t0001g0320others(79): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1684+179T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159963 | ||||||
chr5:41160006
|
G | A | 1 | a0001c0001t0007g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1684+136C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41160006 | ||||||
chr5:41160016
|
C | T | 3 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339 | 4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+126G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41160016 | ||||||
chr5:41160463
|
A | C | 1 | a0002c0002t0001g0150 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1459-96T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160463 | ||||||
chr5:41160604
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459-237C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160604 | ||||||
chr5:41160714
|
G | A | 9 | a0002c0014t0009g0042a0002c0014t0011g0082a0003c0004t0001g0008others(6): Show | 11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1459-347C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160714 | ||||||
chr5:41160963
|
G | T | 1 | a0002c0002t0010g0041 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1459-596C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160963 | ||||||
chr5:41160970
|
A | G | 9 | a0002c0014t0009g0042a0002c0014t0011g0082a0003c0004t0001g0008others(6): Show | 11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1459-603T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160970 | ||||||
chr5:41161120
|
C | T | 1 | a0002c0002t0001g0234 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1458+573G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161120 | ||||||
chr5:41161150
|
A | G | 1 | a0001c0001t0004g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1458+543T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161150 | ||||||
chr5:41161178
|
G | A | 1 | a0002c0014t0009g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1458+515C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161178 | ||||||
chr5:41161387
|
A | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(62): Show | 81 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1458+306T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161387 | ||||||
chr5:41161419
|
A | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(288): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1458+274T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161419 | ||||||
chr5:41161422
|
G | A | 2 | a0001c0001t0007g0037a0001c0001t0007g0038 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1458+271C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161422 | ||||||
chr5:41162144
|
G | T | 1 | a0001c0001t0001g0279 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1292-285C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162144 | ||||||
chr5:41162170
|
C | T | 1 | a0002c0002t0001g0242 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1292-311G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162170 | ||||||
chr5:41162268
|
T | A | 1 | a0003c0004t0001g0157 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1292-409A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162268 | ||||||
chr5:41162382
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1292-523G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162382 | ||||||
chr5:41162461
|
G | A | 9 | a0002c0014t0009g0042a0002c0014t0011g0082a0003c0004t0001g0008others(6): Show | 11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-602C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162461 | ||||||
chr5:41162574
|
TCTAA | T | 3 | a0006c0005t0006g0014a0006c0005t0006g0040a0019c0020t0001g0341 | 4 | HG02258.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-719_1292-716d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162574 | ||||||
chr5:41162577
|
A | G | 81 | a0001c0001t0001g0035a0001c0001t0001g0134a0001c0001t0001g0320others(78): Show | 94 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1292-718T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162577 | ||||||
chr5:41162662
|
G | C | 8 | a0001c0001t0001g0140a0002c0002t0001g0031a0002c0002t0001g0148others(5): Show | 9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-803C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162662 | ||||||
chr5:41162813
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1292-954G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162813 | ||||||
chr5:41162828
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-969C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162828 | ||||||
chr5:41163163
|
GA | G | 34 | a0001c0001t0001g0032a0001c0001t0001g0133a0001c0001t0001g0252others(31): Show | 37 | HG00140.hp1 HG01123.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.1292-1305delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163163 | ||||||
chr5:41163163
|
GAA | G | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-1306_1292-130 others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163163 | ||||||
chr5:41163219
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0283a0001c0001t0001g0297 | 5 | NA18960.hp2 NA18973.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-1360T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163219 | ||||||
chr5:41163310
|
C | CT | 8 | a0001c0001t0004g0117a0001c0001t0007g0036a0001c0001t0007g0037others(5): Show | 10 | HG01071.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1292-1452dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | ||||||
chr5:41163310
|
C | CTTT | 17 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0265others(14): Show | 20 | HG00323.hp1 HG00597.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1292-1454_1292-145 others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | ||||||
chr5:41163310
|
C | CTTTT | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(57): Show | 76 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-1455_1292-145 others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | ||||||
chr5:41163310
|
CT | C | 18 | a0001c0001t0002g0066a0001c0001t0004g0020a0001c0001t0004g0137others(15): Show | 20 | HG01192.hp2 HG01257.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1292-1452delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | ||||||
chr5:41163310
|
CTTT | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-1454_1292-145 others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | ||||||
chr5:41163340
|
T | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-1481A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163340 | ||||||
chr5:41163356
|
A | C | 1 | a0002c0002t0002g0251 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1292-1497T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163356 | ||||||
chr5:41163395
|
C | T | 1 | a0002c0002t0001g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1292-1536G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163395 | ||||||
chr5:41163459
|
T | A | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-1600A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163459 | ||||||
chr5:41163463
|
T | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(288): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1292-1604A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163463 | ||||||
chr5:41163473
|
T | C | 31 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(28): Show | 34 | HG00140.hp1 HG00609.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.1292-1614A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163473 | ||||||
chr5:41163649
|
G | A | 2 | a0011c0010t0001g0277a0011c0010t0006g0039 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1292-1790C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163649 | ||||||
chr5:41163773
|
T | C | 1 | a0003c0004t0001g0160 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1292-1914A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163773 | ||||||
chr5:41163994
|
T | C | 1 | a0001c0003t0001g0122 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1292-2135A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163994 | ||||||
chr5:41164021
|
C | T | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-2162G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164021 | ||||||
chr5:41164025
|
A | G | 15 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(12): Show | 18 | HG00609.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1292-2166T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164025 | ||||||
chr5:41164114
|
A | G | 1 | a0002c0002t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1292-2255T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164114 | ||||||
chr5:41164144
|
A | G | 2 | a0011c0010t0001g0277a0011c0010t0006g0039 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1292-2285T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164144 | ||||||
chr5:41164165
|
TA | T | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-2307delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164165 | ||||||
chr5:41164168
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1292-2309T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164168 | ||||||
chr5:41164176
|
A | G | 4 | a0001c0001t0001g0134a0002c0002t0003g0086a0002c0002t0003g0087others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-2317T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164176 | ||||||
chr5:41164179
|
A | C | 65 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(62): Show | 76 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-2320T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164179 | ||||||
chr5:41164193
|
T | G | 15 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(12): Show | 18 | HG00609.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1292-2334A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164193 | ||||||
chr5:41164232
|
G | A | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1292-2373C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164232 | ||||||
chr5:41164282
|
G | T | 2 | a0011c0010t0001g0277a0011c0010t0006g0039 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1292-2423C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164282 | ||||||
chr5:41164294
|
G | A | 1 | a0002c0002t0002g0026 | 2 | HG01516.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1292-2435C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164294 | ||||||
chr5:41164413
|
C | T | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-2554G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164413 | ||||||
chr5:41164423
|
T | C | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-2564A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164423 | ||||||
chr5:41164547
|
G | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069 | 3 | HG01256.hp1 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1292-2688C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164547 | ||||||
chr5:41164692
|
A | C | 1 | a0002c0002t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1292-2833T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164692 | ||||||
chr5:41164721
|
G | C | 2 | a0002c0014t0009g0042a0002c0014t0011g0082 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1292-2862C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164721 | ||||||
chr5:41164839
|
T | C | 1 | a0001c0001t0001g0314 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1292-2980A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164839 | ||||||
chr5:41165082
|
T | A | 19 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(16): Show | 20 | HG00140.hp1 HG01123.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1292-3223A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165082 | ||||||
chr5:41165172
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1292-3313T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165172 | ||||||
chr5:41165222
|
AT | A | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-3364delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165222 | ||||||
chr5:41165228
|
G | A | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-3369C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165228 | ||||||
chr5:41165282
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-3423C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165282 | ||||||
chr5:41165287
|
T | C | 8 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(5): Show | 9 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1292-3428A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165287 | ||||||
chr5:41165319
|
T | G | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1292-3460A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165319 | ||||||
chr5:41165324
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0069 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1292-3465C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165324 | ||||||
chr5:41165402
|
A | G | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-3543T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165402 | ||||||
chr5:41165642
|
C | T | 50 | a0001c0001t0001g0035a0001c0001t0001g0320a0001c0001t0001g0321others(47): Show | 58 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1292-3783G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165642 | ||||||
chr5:41165652
|
A | G | 1 | a0001c0003t0001g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1292-3793T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165652 | ||||||
chr5:41165669
|
G | A | 2 | a0011c0010t0001g0277a0011c0010t0006g0039 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1292-3810C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165669 | ||||||
chr5:41165832
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1292-3973G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165832 | ||||||
chr5:41165884
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1292-4025A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165884 | ||||||
chr5:41166067
|
A | T | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-4208T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166067 | ||||||
chr5:41166075
|
A | G | 3 | a0002c0002t0001g0177a0002c0002t0001g0189a0002c0002t0001g0198 | 3 | HG02293.hp2 NA18948.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1292-4216T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166075 | ||||||
chr5:41166080
|
G | A | 5 | a0006c0005t0006g0014a0006c0005t0006g0040a0012c0009t0001g0080others(2): Show | 6 | HG02257.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-4221C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166080 | ||||||
chr5:41166153
|
G | T | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-4294C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166153 | ||||||
chr5:41166255
|
A | C | 4 | a0002c0002t0001g0195a0002c0002t0008g0335a0002c0002t0008g0336others(1): Show | 4 | HG02004.hp1 HG02273.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-4396T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166255 | ||||||
chr5:41166377
|
C | CT | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG01167.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1292-4519dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166377 | ||||||
chr5:41166382
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1292-4523A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166382 | ||||||
chr5:41166571
|
A | AT | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-4713dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166571 | ||||||
chr5:41166591
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(250): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1292-4732A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166591 | ||||||
chr5:41166598
|
C | T | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-4739G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166598 | ||||||
chr5:41166672
|
TG | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0265others(10): Show | 16 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1292-4814delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166672 | ||||||
chr5:41166751
|
C | A | 2 | a0002c0014t0009g0042a0002c0014t0011g0082 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1292-4892G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166751 | ||||||
chr5:41166798
|
ATTTCAAT others(9): Show |
A | 4 | a0001c0001t0001g0135a0004c0008t0001g0152a0004c0008t0001g0153others(1): Show | 4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-4955_1292-494 others(20): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166798 | ||||||
chr5:41166923
|
C | T | 1 | a0002c0002t0002g0233 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1292-5064G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166923 | ||||||
chr5:41166954
|
A | G | 12 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0162others(9): Show | 14 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-5095T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166954 | ||||||
chr5:41166988
|
C | A | 1 | a0015c0030t0002g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1292-5129G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166988 | ||||||
chr5:41167100
|
G | A | 1 | a0001c0001t0012g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1291+5125C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167100 | ||||||
chr5:41167143
|
G | A | 1 | a0014c0026t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1291+5082C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167143 | ||||||
chr5:41167143
|
G | C | 2 | a0003c0004t0001g0158a0003c0004t0001g0159 | 2 | NA18969.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1291+5082C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167143 | ||||||
chr5:41167157
|
A | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0265others(8): Show | 14 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1291+5068T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167157 | ||||||
chr5:41167274
|
G | T | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 5 | HG01346.hp1 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+4951C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167274 | ||||||
chr5:41167302
|
A | G | 6 | a0001c0001t0002g0141a0001c0001t0002g0143a0001c0001t0002g0145others(3): Show | 6 | HG01074.hp1 HG01081.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+4923T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167302 | ||||||
chr5:41167364
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1291+4861T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167364 | ||||||
chr5:41167450
|
C | T | 1 | a0015c0030t0002g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1291+4775G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167450 | ||||||
chr5:41167472
|
C | T | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+4753G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167472 | ||||||
chr5:41167476
|
A | T | 1 | a0001c0001t0007g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1291+4749T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167476 | ||||||
chr5:41168124
|
G | C | 1 | a0001c0001t0002g0055 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1291+4101C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168124 | ||||||
chr5:41168210
|
G | T | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+4015C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168210 | ||||||
chr5:41168389
|
G | T | 93 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(90): Show | 106 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1291+3836C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168389 | ||||||
chr5:41168499
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1291+3726G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168499 | ||||||
chr5:41168655
|
A | G | 10 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(7): Show | 12 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1291+3570T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168655 | ||||||
chr5:41168673
|
T | C | 1 | a0002c0002t0001g0167 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1291+3552A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168673 | ||||||
chr5:41168710
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1291+3515G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168710 | ||||||
chr5:41168820
|
C | T | 3 | a0002c0002t0001g0177a0002c0002t0001g0189a0002c0002t0001g0198 | 3 | HG02293.hp2 NA18948.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1291+3405G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168820 | ||||||
chr5:41169002
|
C | T | 50 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(47): Show | 58 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1291+3223G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169002 | ||||||
chr5:41169065
|
G | A | 1 | a0002c0002t0003g0102 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1291+3160C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169065 | ||||||
chr5:41169121
|
C | T | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1291+3104G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169121 | ||||||
chr5:41169183
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0145 | 2 | HG03927.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1291+3042C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169183 | ||||||
chr5:41169220
|
G | A | 2 | a0001c0003t0001g0124a0001c0003t0001g0125 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1291+3005C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169220 | ||||||
chr5:41169300
|
T | C | 16 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(13): Show | 19 | HG00609.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1291+2925A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169300 | ||||||
chr5:41169317
|
G | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0262 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1291+2908C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169317 | ||||||
chr5:41169328
|
C | T | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+2897G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169328 | ||||||
chr5:41169427
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(61): Show | 80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1291+2798G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169427 | ||||||
chr5:41169433
|
C | T | 1 | a0012c0009t0001g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1291+2792G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169433 | ||||||
chr5:41169466
|
T | A | 1 | a0002c0002t0001g0172 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1291+2759A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169466 | ||||||
chr5:41169486
|
T | C | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1291+2739A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169486 | ||||||
chr5:41169756
|
C | T | 6 | a0002c0002t0001g0023a0002c0002t0001g0162a0002c0002t0001g0171others(3): Show | 7 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1291+2469G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169756 | ||||||
chr5:41169757
|
G | A | 2 | a0002c0002t0003g0018a0002c0002t0003g0089 | 3 | HG01109.hp2 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1291+2468C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169757 | ||||||
chr5:41169785
|
A | G | 1 | a0002c0002t0001g0195 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1291+2440T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169785 | ||||||
chr5:41169951
|
C | T | 2 | a0002c0014t0009g0042a0002c0014t0011g0082 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1291+2274G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169951 | ||||||
chr5:41169985
|
GT | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1291+2239delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169985 | ||||||
chr5:41170025
|
T | G | 2 | a0007c0017t0004g0154a0007c0017t0004g0155 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1291+2200A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170025 | ||||||
chr5:41170060
|
G | A | 1 | a0002c0002t0003g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1291+2165C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170060 | ||||||
chr5:41170113
|
A | G | 62 | a0001c0001t0001g0134a0001c0001t0004g0020a0001c0001t0004g0081others(59): Show | 69 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1291+2112T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170113 | ||||||
chr5:41170121
|
T | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+2104A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170121 | ||||||
chr5:41170166
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1291+2059G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170166 | ||||||
chr5:41170205
|
C | T | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+2020G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170205 | ||||||
chr5:41170249
|
A | T | 1 | a0003c0004t0001g0157 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1291+1976T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170249 | ||||||
chr5:41170261
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+1964G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170261 | ||||||
chr5:41170508
|
C | T | 50 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(47): Show | 58 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1291+1717G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170508 | ||||||
chr5:41170645
|
A | T | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+1580T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170645 | ||||||
chr5:41170709
|
A | G | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+1516T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170709 | ||||||
chr5:41170977
|
A | C | 1 | a0002c0002t0001g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1291+1248T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170977 | ||||||
chr5:41171323
|
A | G | 1 | a0005c0007t0003g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1291+902T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171323 | ||||||
chr5:41171386
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1291+839G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171386 | ||||||
chr5:41171400
|
C | A | 1 | a0002c0002t0002g0251 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1291+825G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171400 | ||||||
chr5:41171410
|
G | T | 2 | a0002c0002t0001g0021a0002c0002t0001g0149 | 3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1291+815C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171410 | ||||||
chr5:41171450
|
T | C | 3 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339 | 4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+775A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171450 | ||||||
chr5:41171464
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+761G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171464 | ||||||
chr5:41171492
|
T | C | 1 | a0002c0002t0001g0191 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1291+733A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171492 | ||||||
chr5:41171512
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+713C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171512 | ||||||
chr5:41171735
|
T | C | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1291+490A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171735 | ||||||
chr5:41171772
|
A | G | 1 | a0001c0003t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+453T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171772 | ||||||
chr5:41171787
|
C | T | 1 | a0002c0002t0002g0208 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1291+438G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171787 | ||||||
chr5:41171852
|
A | G | 1 | a0002c0002t0002g0214 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1291+373T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171852 | ||||||
chr5:41171971
|
T | A | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+254A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171971 | ||||||
chr5:41172351
|
G | A | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | HG00597.hp1 HG02040.hp1 |
splice_region_variant&intron_variant | LOW | c.1169-4C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172351 | ||||||
chr5:41172416
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1169-69G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172416 | ||||||
chr5:41172531
|
C | A | 1 | a0012c0009t0001g0080 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1169-184G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172531 | ||||||
chr5:41172563
|
T | G | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169-216A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172563 | ||||||
chr5:41172698
|
C | T | 2 | a0007c0017t0004g0154a0007c0017t0004g0155 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1169-351G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172698 | ||||||
chr5:41172868
|
G | T | 1 | a0012c0009t0001g0080 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1169-521C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172868 | ||||||
chr5:41172889
|
A | G | 1 | a0001c0001t0004g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1169-542T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172889 | ||||||
chr5:41172900
|
T | C | 1 | a0006c0005t0006g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1169-553A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172900 | ||||||
chr5:41173071
|
T | G | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169-724A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173071 | ||||||
chr5:41173151
|
T | C | 1 | a0002c0002t0002g0219 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1169-804A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173151 | ||||||
chr5:41173188
|
T | C | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169-841A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173188 | ||||||
chr5:41173192
|
C | T | 2 | a0007c0017t0004g0154a0007c0017t0004g0155 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1169-845G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173192 | ||||||
chr5:41173203
|
C | T | 7 | a0002c0002t0001g0022a0002c0002t0001g0164a0002c0002t0001g0165others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1169-856G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173203 | ||||||
chr5:41173263
|
T | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169-916A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173263 | ||||||
chr5:41173509
|
A | G | 1 | a0001c0001t0002g0017 | 2 | HG01515.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1169-1162T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173509 | ||||||
chr5:41173585
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1169-1238A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173585 | ||||||
chr5:41173728
|
C | T | 1 | a0001c0001t0002g0017 | 2 | HG01515.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1169-1381G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173728 | ||||||
chr5:41173729
|
G | A | 1 | a0002c0002t0002g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1169-1382C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173729 | ||||||
chr5:41173740
|
AG | A | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1169-1394delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173740 | ||||||
chr5:41173785
|
A | G | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169-1438T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173785 | ||||||
chr5:41174055
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169-1708C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174055 | ||||||
chr5:41174176
|
T | C | 4 | a0002c0002t0003g0019a0002c0002t0003g0104a0002c0002t0003g0105others(1): Show | 5 | NA18939.hp1 NA18986.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1169-1829A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174176 | ||||||
chr5:41174258
|
G | T | 1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1169-1911C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174258 | ||||||
chr5:41174323
|
C | G | 22 | a0001c0001t0004g0020a0001c0001t0004g0079a0001c0001t0004g0081others(19): Show | 23 | HG00140.hp1 HG01123.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1169-1976G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174323 | ||||||
chr5:41174388
|
G | A | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1169-2041C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174388 | ||||||
chr5:41174420
|
C | T | 1 | a0002c0002t0002g0227 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1168+2055G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174420 | ||||||
chr5:41174465
|
G | A | 1 | a0001c0001t0007g0037 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1168+2010C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174465 | ||||||
chr5:41174570
|
T | G | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1168+1905A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174570 | ||||||
chr5:41174636
|
G | A | 1 | a0002c0002t0002g0233 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1168+1839C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174636 | ||||||
chr5:41174834
|
T | C | 1 | a0001c0003t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1168+1641A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174834 | ||||||
chr5:41174985
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1168+1490T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174985 | ||||||
chr5:41174995
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1168+1480G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174995 | ||||||
chr5:41175137
|
C | T | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+1338G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175137 | ||||||
chr5:41175156
|
G | A | 1 | a0002c0002t0001g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1168+1319C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175156 | ||||||
chr5:41175171
|
T | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168+1304A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175171 | ||||||
chr5:41175223
|
C | A | 2 | a0002c0002t0002g0236a0002c0002t0002g0247 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1168+1252G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175223 | ||||||
chr5:41175257
|
T | C | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+1218A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175257 | ||||||
chr5:41175322
|
G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(291): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1168+1153C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175322 | ||||||
chr5:41175361
|
T | TATGTATG others(10): Show |
1 | a0001c0001t0001g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1168+1097_1168+111 others(21): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175361 | ||||||
chr5:41175377
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1168+1098C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175377 | ||||||
chr5:41175383
|
A | G | 1 | a0002c0002t0003g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1168+1092T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175383 | ||||||
chr5:41175454
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168+1021G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175454 | ||||||
chr5:41175517
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+958C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175517 | ||||||
chr5:41175978
|
T | G | 1 | a0001c0001t0002g0059 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1168+497A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175978 | ||||||
chr5:41175998
|
T | C | 2 | a0002c0002t0003g0096a0002c0002t0003g0097 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1168+477A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175998 | ||||||
chr5:41176088
|
T | C | 2 | a0002c0002t0001g0221a0002c0002t0001g0235 | 2 | HG00408.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1168+387A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41176088 | ||||||
chr5:41176218
|
T | TAGGAAAT others(1215): Show |
1 | a0001c0001t0001g0328 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1168+256_1168+257i others(1224): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41176218 | ||||||
chr5:41176233
|
C | A | 2 | a0002c0002t0001g0021a0002c0002t0001g0149 | 3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1168+242G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41176233 | ||||||
chr5:41176247
|
A | C | 1 | a0001c0001t0001g0296 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1168+228T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41176247 | ||||||
chr5:41176914
|
AG | A | 48 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(45): Show | 56 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.928-200delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41176914 | ||||||
chr5:41177158
|
T | C | 2 | a0005c0007t0003g0090a0005c0007t0003g0093 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.928-443A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177158 | ||||||
chr5:41177197
|
T | C | 1 | a0003c0004t0001g0159 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.928-482A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177197 | ||||||
chr5:41177215
|
G | T | 1 | a0001c0001t0001g0264 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.928-500C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177215 | ||||||
chr5:41177323
|
C | A | 1 | a0002c0002t0001g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.928-608G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177323 | ||||||
chr5:41177595
|
ATAACTGT others(7): Show |
A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-894_928-881del others(14): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177595 | ||||||
chr5:41177925
|
A | G | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-1210T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177925 | ||||||
chr5:41177959
|
A | G | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-1244T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177959 | ||||||
chr5:41178267
|
A | G | 1 | a0002c0002t0003g0109 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.928-1552T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178267 | ||||||
chr5:41178300
|
C | A | 1 | a0002c0002t0005g0193 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928-1585G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178300 | ||||||
chr5:41178301
|
T | A | 1 | a0002c0002t0005g0193 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928-1586A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178301 | ||||||
chr5:41178302
|
G | A | 1 | a0002c0002t0005g0193 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928-1587C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178302 | ||||||
chr5:41178339
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.928-1624G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178339 | ||||||
chr5:41178433
|
T | G | 1 | a0001c0022t0001g0307 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.928-1718A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178433 | ||||||
chr5:41178442
|
ATTTTC | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-1732_928-1728d others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178442 | ||||||
chr5:41178466
|
C | CT | 16 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0257others(13): Show | 16 | HG01346.hp1 HG01361.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.928-1752dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178466 | ||||||
chr5:41178466
|
CT | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(159): Show | 192 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.928-1752delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178466 | ||||||
chr5:41178472
|
T | C | 2 | a0007c0017t0004g0154a0007c0017t0004g0155 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.928-1757A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178472 | ||||||
chr5:41178495
|
G | A | 42 | a0001c0001t0001g0134a0002c0002t0001g0206a0002c0002t0003g0006others(39): Show | 48 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.928-1780C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178495 | ||||||
chr5:41178497
|
G | A | 42 | a0001c0001t0001g0134a0002c0002t0001g0206a0002c0002t0003g0006others(39): Show | 48 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.928-1782C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178497 | ||||||
chr5:41178497
|
GACAGA | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(235): Show | 282 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.928-1787_928-1783d others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178497 | ||||||
chr5:41178503
|
G | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(235): Show | 282 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.928-1788C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178503 | ||||||
chr5:41178549
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0324 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.928-1834G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178549 | ||||||
chr5:41178578
|
T | C | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-1863A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178578 | ||||||
chr5:41178596
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.928-1881G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178596 | ||||||
chr5:41178632
|
C | T | 1 | a0002c0002t0001g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-1917G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178632 | ||||||
chr5:41178766
|
G | A | 1 | a0002c0002t0001g0339 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.928-2051C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178766 | ||||||
chr5:41178767
|
C | T | 46 | a0001c0001t0001g0134a0001c0001t0001g0135a0002c0002t0001g0206others(43): Show | 52 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.928-2052G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178767 | ||||||
chr5:41178768
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.928-2053C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178768 | ||||||
chr5:41178917
|
G | A | 7 | a0001c0001t0001g0140a0002c0002t0001g0031a0002c0002t0001g0148others(4): Show | 8 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-2202C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178917 | ||||||
chr5:41178923
|
C | T | 17 | a0001c0001t0001g0304a0002c0002t0001g0022a0002c0002t0001g0023others(14): Show | 19 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.928-2208G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178923 | ||||||
chr5:41178998
|
C | T | 2 | a0001c0001t0007g0037a0001c0001t0007g0038 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.928-2283G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178998 | ||||||
chr5:41179015
|
G | A | 1 | a0002c0002t0003g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.928-2300C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179015 | ||||||
chr5:41179054
|
G | A | 2 | a0002c0002t0001g0211a0002c0002t0002g0026 | 3 | HG01516.hp1 HG01952.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.927+2305C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179054 | ||||||
chr5:41179117
|
G | A | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.927+2242C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179117 | ||||||
chr5:41179300
|
T | G | 4 | a0001c0001t0001g0135a0004c0008t0001g0152a0004c0008t0001g0153others(1): Show | 4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+2059A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179300 | ||||||
chr5:41179418
|
A | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0268a0001c0001t0001g0312others(4): Show | 9 | HG01081.hp2 HG01257.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+1941T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179418 | ||||||
chr5:41179447
|
C | T | 1 | a0014c0026t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.927+1912G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179447 | ||||||
chr5:41179537
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.927+1822C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179537 | ||||||
chr5:41179583
|
C | T | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1776G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179583 | ||||||
chr5:41179735
|
T | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+1624A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179735 | ||||||
chr5:41179760
|
T | C | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1599A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179760 | ||||||
chr5:41179823
|
TAAAG | T | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.927+1532_927+1535d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179823 | ||||||
chr5:41179960
|
G | A | 3 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036 | 3 | HG01891.hp2 HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.927+1399C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179960 | ||||||
chr5:41180015
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(292): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.927+1344C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180015 | ||||||
chr5:41180085
|
G | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(292): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.927+1274C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180085 | ||||||
chr5:41180149
|
A | G | 1 | a0002c0002t0001g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.927+1210T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180149 | ||||||
chr5:41180269
|
T | C | 75 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(72): Show | 85 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.927+1090A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180269 | ||||||
chr5:41180307
|
C | T | 58 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(55): Show | 67 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.927+1052G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180307 | ||||||
chr5:41180407
|
T | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(66): Show | 87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.927+952A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180407 | ||||||
chr5:41180490
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.927+869C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180490 | ||||||
chr5:41180498
|
T | TGAAGAAT others(11): Show |
6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+860_927+861ins others(18): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180498 | ||||||
chr5:41180595
|
A | G | 1 | a0002c0002t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.927+764T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180595 | ||||||
chr5:41180699
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.927+660G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180699 | ||||||
chr5:41180832
|
T | TA | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(82): Show | 106 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.927+526dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180832 | ||||||
chr5:41180832
|
TA | T | 12 | a0001c0001t0001g0133a0001c0001t0004g0079a0001c0001t0004g0117others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.927+526delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180832 | ||||||
chr5:41181049
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+310G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41181049 | ||||||
chr5:41181078
|
G | A | 9 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(6): Show | 10 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.927+281C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41181078 | ||||||
chr5:41181080
|
A | G | 1 | a0002c0002t0001g0228 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+279T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41181080 | ||||||
chr5:41181236
|
C | T | 4 | a0001c0001t0001g0135a0004c0008t0001g0152a0004c0008t0001g0153others(1): Show | 4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+123G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41181236 | ||||||
chr5:41181610
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.727-51C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181610 | ||||||
chr5:41181657
|
A | G | 1 | a0002c0002t0002g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.727-98T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181657 | ||||||
chr5:41181797
|
C | T | 1 | a0002c0002t0003g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.727-238G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181797 | ||||||
chr5:41181877
|
G | T | 1 | a0002c0002t0002g0209 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.727-318C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181877 | ||||||
chr5:41181915
|
G | A | 1 | a0002c0002t0001g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.727-356C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181915 | ||||||
chr5:41181940
|
C | A | 1 | a0002c0014t0009g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.727-381G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181940 | ||||||
chr5:41182031
|
C | T | 1 | a0001c0001t0007g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.727-472G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182031 | ||||||
chr5:41182241
|
G | A | 3 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339 | 4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-682C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182241 | ||||||
chr5:41182262
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(84): Show | 108 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.727-703G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182262 | ||||||
chr5:41182266
|
T | C | 1 | a0001c0003t0001g0122 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.727-707A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182266 | ||||||
chr5:41182302
|
G | T | 1 | a0002c0002t0001g0201 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.727-743C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182302 | ||||||
chr5:41182318
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-759C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182318 | ||||||
chr5:41182344
|
G | C | 1 | a0001c0001t0002g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.727-785C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182344 | ||||||
chr5:41182546
|
T | C | 2 | a0001c0001t0001g0309a0001c0001t0001g0334 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.727-987A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182546 | ||||||
chr5:41182630
|
T | A | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0018c0019t0002g0056 | 3 | HG00140.hp2 HG01074.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.727-1071A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182630 | ||||||
chr5:41182849
|
CAG | C | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.727-1292_727-1291d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182849 | ||||||
chr5:41182942
|
T | G | 1 | a0002c0002t0003g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.727-1383A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182942 | ||||||
chr5:41182963
|
T | C | 1 | a0002c0002t0001g0202 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.727-1404A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182963 | ||||||
chr5:41182995
|
C | T | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069 | 3 | HG01256.hp1 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.727-1436G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182995 | ||||||
chr5:41183066
|
C | T | 2 | a0001c0001t0001g0285a0001c0001t0001g0303 | 2 | HG02083.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.727-1507G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183066 | ||||||
chr5:41183156
|
T | C | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-1597A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183156 | ||||||
chr5:41183394
|
A | G | 1 | a0020c0018t0001g0284 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.727-1835T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183394 | ||||||
chr5:41183517
|
A | C | 8 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(5): Show | 8 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.727-1958T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183517 | ||||||
chr5:41183539
|
A | G | 4 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(1): Show | 4 | HG02015.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-1980T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183539 | ||||||
chr5:41183661
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.727-2102G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183661 | ||||||
chr5:41183677
|
A | G | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-2118T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183677 | ||||||
chr5:41183976
|
TA | T | 12 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(9): Show | 14 | HG00609.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.726+2093delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183976 | ||||||
chr5:41183977
|
AG | A | 17 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0162others(14): Show | 19 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.726+2092delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183977 | ||||||
chr5:41183978
|
G | C | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+2092C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183978 | ||||||
chr5:41183979
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0081a0001c0001t0004g0137others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.726+2091C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183979 | ||||||
chr5:41184140
|
G | GA | 66 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0252others(63): Show | 76 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.726+1929dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184140 | ||||||
chr5:41184274
|
T | G | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+1796A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184274 | ||||||
chr5:41184296
|
T | A | 1 | a0002c0002t0003g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.726+1774A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184296 | ||||||
chr5:41184342
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(46): Show | 57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.726+1728A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184342 | ||||||
chr5:41184376
|
G | T | 2 | a0002c0002t0002g0227a0002c0002t0002g0245 | 2 | HG02040.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.726+1694C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184376 | ||||||
chr5:41184462
|
ATTTTCTT others(3): Show |
A | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.726+1598_726+1607d others(12): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184462 | ||||||
chr5:41184482
|
C | CT | 73 | a0001c0001t0001g0032a0001c0001t0001g0135a0001c0001t0001g0252others(70): Show | 83 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.726+1587dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184482 | ||||||
chr5:41184533
|
G | A | 6 | a0002c0002t0003g0018a0002c0002t0003g0086a0002c0002t0003g0087others(3): Show | 7 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+1537C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184533 | ||||||
chr5:41184537
|
T | C | 1 | a0002c0002t0002g0210 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.726+1533A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184537 | ||||||
chr5:41184726
|
G | A | 71 | a0001c0001t0001g0032a0001c0001t0001g0135a0001c0001t0001g0252others(68): Show | 82 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.726+1344C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184726 | ||||||
chr5:41184752
|
A | G | 1 | a0001c0001t0002g0261 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.726+1318T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184752 | ||||||
chr5:41184953
|
T | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0262 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.726+1117A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184953 | ||||||
chr5:41185049
|
G | T | 1 | a0002c0002t0003g0110 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.726+1021C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185049 | ||||||
chr5:41185070
|
C | A | 88 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(85): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.726+1000G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185070 | ||||||
chr5:41185143
|
A | G | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.726+927T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185143 | ||||||
chr5:41185195
|
G | A | 6 | a0002c0002t0001g0031a0002c0002t0001g0148a0002c0002t0001g0207others(3): Show | 7 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+875C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185195 | ||||||
chr5:41185259
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(277): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.726+811A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185259 | ||||||
chr5:41185274
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.726+796G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185274 | ||||||
chr5:41185406
|
A | G | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.726+664T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185406 | ||||||
chr5:41185416
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.726+654C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185416 | ||||||
chr5:41185418
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.726+652G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185418 | ||||||
chr5:41185505
|
G | A | 9 | a0001c0001t0002g0141a0001c0001t0002g0145a0001c0001t0012g0129others(6): Show | 9 | HG01074.hp1 HG01081.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.726+565C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185505 | ||||||
chr5:41185544
|
C | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(37): Show | 48 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.726+526G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185544 | ||||||
chr5:41185575
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0275 | 3 | HG02602.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.726+495A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185575 | ||||||
chr5:41185629
|
G | C | 1 | a0002c0002t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.726+441C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185629 | ||||||
chr5:41185697
|
C | G | 7 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0112others(4): Show | 11 | HG01496.hp2 HG02004.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.726+373G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185697 | ||||||
chr5:41185744
|
G | A | 3 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339 | 4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+326C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185744 | ||||||
chr5:41185767
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.726+303T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185767 | ||||||
chr5:41185792
|
C | T | 1 | a0008c0016t0003g0098 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.726+278G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185792 | ||||||
chr5:41185796
|
G | T | 1 | a0002c0002t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.726+274C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185796 | ||||||
chr5:41185810
|
A | C | 41 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(38): Show | 47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.726+260T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185810 | ||||||
chr5:41185818
|
C | A | 2 | a0002c0002t0001g0021a0002c0002t0001g0149 | 3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.726+252G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185818 | ||||||
chr5:41186270
|
A | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-62T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186270 | ||||||
chr5:41186347
|
C | CT | 87 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(84): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.588-140dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186347 | ||||||
chr5:41186412
|
G | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-204C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186412 | ||||||
chr5:41186470
|
A | G | 1 | a0005c0007t0003g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.588-262T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186470 | ||||||
chr5:41186664
|
A | G | 88 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(85): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-456T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186664 | ||||||
chr5:41186692
|
T | C | 88 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(85): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-484A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186692 | ||||||
chr5:41186772
|
A | G | 88 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(85): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-564T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186772 | ||||||
chr5:41186907
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588-699A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186907 | ||||||
chr5:41186918
|
T | TA | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-711dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186918 | ||||||
chr5:41186940
|
T | C | 2 | a0001c0001t0002g0260a0001c0001t0002g0262 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.588-732A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186940 | ||||||
chr5:41186942
|
A | T | 1 | a0018c0019t0002g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.588-734T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186942 | ||||||
chr5:41187002
|
T | C | 2 | a0002c0002t0001g0179a0002c0002t0001g0180 | 2 | NA18961.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.588-794A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187002 | ||||||
chr5:41187094
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.588-886G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187094 | ||||||
chr5:41187137
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.588-929T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187137 | ||||||
chr5:41187155
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.588-947T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187155 | ||||||
chr5:41187234
|
T | C | 1 | a0002c0002t0003g0110 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.588-1026A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187234 | ||||||
chr5:41187392
|
G | A | 1 | a0002c0002t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.588-1184C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187392 | ||||||
chr5:41187466
|
A | G | 1 | a0002c0002t0001g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.588-1258T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187466 | ||||||
chr5:41187526
|
C | T | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.588-1318G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187526 | ||||||
chr5:41187547
|
G | C | 1 | a0002c0002t0003g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.588-1339C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187547 | ||||||
chr5:41187560
|
T | G | 2 | a0002c0002t0001g0021a0002c0002t0001g0149 | 3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.588-1352A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187560 | ||||||
chr5:41187581
|
T | A | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.588-1373A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187581 | ||||||
chr5:41187699
|
T | TAC | 17 | a0001c0001t0001g0140a0001c0001t0001g0281a0001c0001t0001g0313others(14): Show | 18 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-1493_588-1492d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | ||||||
chr5:41187699
|
T | TACAC | 81 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(78): Show | 100 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.588-1495_588-1492d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | ||||||
chr5:41187699
|
T | TACACAC | 70 | a0001c0001t0001g0340a0002c0002t0001g0003a0002c0002t0001g0009others(67): Show | 81 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.588-1497_588-1492d others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | ||||||
chr5:41187699
|
T | TACACACA others(1): Show |
18 | a0002c0002t0001g0162a0002c0002t0001g0163a0002c0002t0001g0170others(15): Show | 22 | HG01496.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.588-1499_588-1492d others(10): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | ||||||
chr5:41187699
|
TAC | T | 5 | a0002c0002t0001g0021a0002c0002t0001g0149a0003c0004t0001g0008others(2): Show | 8 | HG00609.hp2 HG01192.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.588-1493_588-1492d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | ||||||
chr5:41187699
|
TACACAC | T | 6 | a0002c0002t0001g0031a0002c0002t0001g0148a0002c0002t0001g0207others(3): Show | 7 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-1497_588-1492d others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | ||||||
chr5:41187708
|
AC | A | 87 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(84): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.588-1501delG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187708 | ||||||
chr5:41187728
|
C | T | 2 | a0012c0009t0001g0080a0012c0009t0001g0130 | 2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.588-1520G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187728 | ||||||
chr5:41187855
|
T | A | 137 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(134): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.588-1647A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187855 | ||||||
chr5:41188189
|
G | A | 129 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(126): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.588-1981C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188189 | ||||||
chr5:41188392
|
G | C | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.588-2184C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188392 | ||||||
chr5:41188413
|
T | A | 6 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(3): Show | 6 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.588-2205A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188413 | ||||||
chr5:41188465
|
AC | A | 39 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0025others(36): Show | 46 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.588-2258delG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188465 | ||||||
chr5:41188546
|
C | T | 6 | a0002c0002t0001g0031a0002c0002t0001g0148a0002c0002t0001g0207others(3): Show | 7 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-2338G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188546 | ||||||
chr5:41188602
|
T | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0052a0001c0001t0002g0054others(2): Show | 10 | HG00438.hp2 HG00558.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-2394A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188602 | ||||||
chr5:41188653
|
G | GA | 6 | a0002c0002t0003g0018a0002c0002t0003g0086a0002c0002t0003g0087others(3): Show | 7 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-2446dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188653 | ||||||
chr5:41188734
|
T | C | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.588-2526A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188734 | ||||||
chr5:41189069
|
C | T | 1 | a0002c0002t0001g0150 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.588-2861G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189069 | ||||||
chr5:41189187
|
A | G | 3 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339 | 4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-2979T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189187 | ||||||
chr5:41189336
|
G | A | 2 | a0002c0002t0010g0041a0002c0014t0009g0042 | 2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.588-3128C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189336 | ||||||
chr5:41189357
|
A | C | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.588-3149T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189357 | ||||||
chr5:41189367
|
C | G | 1 | a0001c0001t0001g0302 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.588-3159G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189367 | ||||||
chr5:41189466
|
T | A | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.588-3258A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189466 | ||||||
chr5:41189567
|
A | G | 1 | a0002c0002t0003g0091 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.588-3359T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189567 | ||||||
chr5:41189603
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.588-3395G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189603 | ||||||
chr5:41189774
|
C | G | 1 | a0002c0002t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.588-3566G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189774 | ||||||
chr5:41189809
|
A | C | 137 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(134): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.588-3601T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189809 | ||||||
chr5:41189843
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.588-3635C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189843 | ||||||
chr5:41189984
|
A | C | 129 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(126): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.588-3776T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189984 | ||||||
chr5:41190038
|
G | C | 88 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(85): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-3830C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190038 | ||||||
chr5:41190099
|
C | T | 1 | a0002c0002t0002g0226 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.588-3891G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190099 | ||||||
chr5:41190184
|
C | G | 7 | a0002c0002t0001g0022a0002c0002t0001g0164a0002c0002t0001g0165others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-3976G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190184 | ||||||
chr5:41190275
|
A | G | 3 | a0002c0002t0002g0209a0002c0002t0002g0216a0002c0002t0002g0225 | 3 | NA18951.hp2 NA19077.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.588-4067T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190275 | ||||||
chr5:41190297
|
A | C | 88 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0132others(85): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-4089T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190297 | ||||||
chr5:41190352
|
C | A | 58 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(55): Show | 67 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.588-4144G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190352 | ||||||
chr5:41190493
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-4285G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190493 | ||||||
chr5:41190597
|
A | C | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.588-4389T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190597 | ||||||
chr5:41190681
|
A | T | 2 | a0001c0001t0002g0061a0001c0001t0002g0062 | 2 | HG02698.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.588-4473T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190681 | ||||||
chr5:41190778
|
A | G | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.588-4570T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190778 | ||||||
chr5:41190836
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.588-4628G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190836 | ||||||
chr5:41191011
|
A | AACATGTA others(2): Show |
9 | a0001c0001t0002g0017a0001c0001t0002g0049a0001c0001t0002g0050others(6): Show | 10 | HG00323.hp2 HG01192.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+4772_587+4780d others(11): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191011 | ||||||
chr5:41191067
|
C | CTTT | 42 | a0001c0001t0001g0032a0001c0001t0001g0254a0001c0001t0001g0255others(39): Show | 51 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.587+4722_587+4724d others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | ||||||
chr5:41191067
|
C | CTTTT | 30 | a0001c0001t0001g0135a0001c0001t0001g0252a0001c0001t0001g0253others(27): Show | 31 | HG00140.hp1 HG00735.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.587+4721_587+4724d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | ||||||
chr5:41191067
|
C | CTTTTT | 10 | a0001c0001t0001g0133a0001c0001t0002g0044a0001c0001t0002g0046others(7): Show | 10 | HG00621.hp1 HG01167.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.587+4720_587+4724d others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | ||||||
chr5:41191067
|
CT | C | 41 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(38): Show | 48 | HG00323.hp2 HG00597.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.587+4724delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | ||||||
chr5:41191067
|
CTT | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(152): Show | 187 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.587+4723_587+4724d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | ||||||
chr5:41191067
|
CTTT | C | 6 | a0001c0001t0001g0301a0002c0002t0001g0192a0002c0002t0003g0103others(3): Show | 6 | HG00280.hp1 HG01361.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.587+4722_587+4724d others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | ||||||
chr5:41191159
|
C | T | 41 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(38): Show | 47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.587+4633G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191159 | ||||||
chr5:41191221
|
C | T | 1 | a0001c0006t0002g0142 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.587+4571G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191221 | ||||||
chr5:41191316
|
C | T | 3 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339 | 4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+4476G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191316 | ||||||
chr5:41191335
|
C | A | 1 | a0001c0001t0001g0326 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.587+4457G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191335 | ||||||
chr5:41191451
|
A | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(285): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.587+4341T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191451 | ||||||
chr5:41191511
|
C | T | 3 | a0002c0002t0010g0041a0002c0014t0009g0042a0002c0014t0011g0082 | 3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.587+4281G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191511 | ||||||
chr5:41191678
|
G | T | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.587+4114C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191678 | ||||||
chr5:41191793
|
C | CT | 15 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0079others(12): Show | 16 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.587+3998dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191793 | ||||||
chr5:41191793
|
C | CTT | 16 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(13): Show | 16 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.587+3997_587+3998d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191793 | ||||||
chr5:41191793
|
CT | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(7): Show | 11 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.587+3998delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191793 | ||||||
chr5:41191799
|
T | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+3993A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191799 | ||||||
chr5:41191826
|
G | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(291): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.587+3966C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191826 | ||||||
chr5:41191887
|
A | T | 1 | a0001c0001t0004g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.587+3905T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191887 | ||||||
chr5:41192052
|
C | T | 3 | a0004c0008t0001g0152a0004c0008t0001g0153a0004c0008t0001g0342 | 3 | HG01361.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.587+3740G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192052 | ||||||
chr5:41192079
|
A | G | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587+3713T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192079 | ||||||
chr5:41192214
|
C | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0034others(16): Show | 24 | HG00597.hp2 HG01081.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.587+3578G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192214 | ||||||
chr5:41192217
|
T | A | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.587+3575A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192217 | ||||||
chr5:41192258
|
T | C | 6 | a0002c0002t0001g0027a0002c0002t0001g0220a0002c0002t0001g0221others(3): Show | 7 | HG00408.hp1 HG00673.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+3534A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192258 | ||||||
chr5:41192313
|
A | G | 1 | a0002c0002t0001g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.587+3479T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192313 | ||||||
chr5:41192332
|
A | G | 1 | a0001c0001t0007g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.587+3460T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192332 | ||||||
chr5:41192399
|
A | G | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.587+3393T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192399 | ||||||
chr5:41192406
|
G | A | 1 | a0002c0002t0002g0250 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.587+3386C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192406 | ||||||
chr5:41192463
|
T | A | 1 | a0002c0002t0001g0025 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.587+3329A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192463 | ||||||
chr5:41192511
|
C | T | 3 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339 | 4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+3281G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192511 | ||||||
chr5:41192603
|
G | GT | 13 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(10): Show | 14 | HG01243.hp2 HG01891.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.587+3188dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192603 | ||||||
chr5:41192623
|
A | C | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+3169T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192623 | ||||||
chr5:41192828
|
G | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(46): Show | 57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.587+2964C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192828 | ||||||
chr5:41192897
|
A | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(83): Show | 106 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.587+2895T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192897 | ||||||
chr5:41192905
|
T | C | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+2887A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192905 | ||||||
chr5:41192986
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.587+2806G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192986 | ||||||
chr5:41193189
|
A | G | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | NA19011.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.587+2603T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193189 | ||||||
chr5:41193204
|
C | G | 1 | a0002c0029t0005g0338 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.587+2588G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193204 | ||||||
chr5:41193311
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+2481C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193311 | ||||||
chr5:41193422
|
G | A | 2 | a0001c0003t0001g0123a0001c0003t0001g0126 | 2 | HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.587+2370C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193422 | ||||||
chr5:41193590
|
A | G | 3 | a0004c0008t0001g0152a0004c0008t0001g0153a0004c0008t0001g0342 | 3 | HG01361.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.587+2202T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193590 | ||||||
chr5:41193591
|
T | G | 3 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339 | 4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+2201A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193591 | ||||||
chr5:41193795
|
A | AT | 29 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0035others(26): Show | 39 | HG00140.hp1 HG00408.hp2 HG01981.hp2 others(36): Show |
intron_variant | MODIFIER | c.587+1996dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193795 | ||||||
chr5:41193795
|
A | ATT | 113 | a0001c0001t0001g0032a0001c0001t0001g0135a0001c0001t0001g0252others(110): Show | 131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.587+1995_587+1996d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193795 | ||||||
chr5:41193795
|
A | ATTT | 6 | a0001c0001t0002g0060a0001c0001t0004g0079a0001c0001t0007g0037others(3): Show | 6 | HG01243.hp2 HG01981.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.587+1994_587+1996d others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193795 | ||||||
chr5:41193795
|
AT | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0021others(51): Show | 63 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.587+1996delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193795 | ||||||
chr5:41193816
|
G | A | 38 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(35): Show | 44 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.587+1976C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193816 | ||||||
chr5:41193882
|
G | T | 1 | a0002c0002t0002g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.587+1910C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193882 | ||||||
chr5:41193984
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.587+1808C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193984 | ||||||
chr5:41194208
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+1584G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194208 | ||||||
chr5:41194213
|
A | T | 2 | a0012c0009t0001g0080a0012c0009t0001g0130 | 2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.587+1579T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194213 | ||||||
chr5:41194243
|
G | A | 52 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0022others(49): Show | 60 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.587+1549C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194243 | ||||||
chr5:41194418
|
T | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(281): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.587+1374A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194418 | ||||||
chr5:41194431
|
C | T | 1 | a0001c0001t0004g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.587+1361G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194431 | ||||||
chr5:41194554
|
G | T | 1 | a0001c0001t0002g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.587+1238C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194554 | ||||||
chr5:41194717
|
T | C | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.587+1075A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194717 | ||||||
chr5:41194722
|
A | AT | 65 | a0001c0001t0001g0032a0001c0001t0001g0135a0001c0001t0001g0252others(62): Show | 75 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.587+1069dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194722 | ||||||
chr5:41194780
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587+1012A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194780 | ||||||
chr5:41195111
|
T | G | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.587+681A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195111 | ||||||
chr5:41195207
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.587+585G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195207 | ||||||
chr5:41195278
|
A | G | 2 | a0002c0002t0002g0146a0002c0002t0002g0223 | 2 | NA18960.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.587+514T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195278 | ||||||
chr5:41195311
|
A | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+481T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195311 | ||||||
chr5:41195382
|
C | T | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+410G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195382 | ||||||
chr5:41195598
|
C | T | 41 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(38): Show | 47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.587+194G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195598 | ||||||
chr5:41195977
|
T | C | 1 | a0001c0001t0002g0017 | 2 | HG01515.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.446-44A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41195977 | ||||||
chr5:41196011
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-78G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196011 | ||||||
chr5:41196088
|
C | T | 4 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059others(1): Show | 4 | HG00140.hp2 HG01074.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-155G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196088 | ||||||
chr5:41196110
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.446-177A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196110 | ||||||
chr5:41196128
|
C | T | 41 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(38): Show | 47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.446-195G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196128 | ||||||
chr5:41196171
|
A | G | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.446-238T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196171 | ||||||
chr5:41196209
|
A | G | 61 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0021others(58): Show | 71 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.446-276T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196209 | ||||||
chr5:41196273
|
G | A | 3 | a0004c0008t0001g0152a0004c0008t0001g0153a0004c0008t0001g0342 | 3 | HG01361.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.446-340C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196273 | ||||||
chr5:41196433
|
T | C | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-500A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196433 | ||||||
chr5:41196508
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0295 | 2 | HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.446-575T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196508 | ||||||
chr5:41196549
|
G | A | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-616C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196549 | ||||||
chr5:41196658
|
A | G | 1 | a0001c0001t0004g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.446-725T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196658 | ||||||
chr5:41196680
|
A | G | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.446-747T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196680 | ||||||
chr5:41196967
|
T | C | 2 | a0001c0001t0004g0020a0001c0001t0004g0137 | 3 | HG01884.hp2 HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.446-1034A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196967 | ||||||
chr5:41196973
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(148): Show | 181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.446-1040T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196973 | ||||||
chr5:41197278
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-1345G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197278 | ||||||
chr5:41197282
|
A | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-1349T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197282 | ||||||
chr5:41197370
|
A | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(148): Show | 181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.446-1437T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197370 | ||||||
chr5:41197467
|
C | A | 7 | a0002c0002t0001g0031a0002c0002t0001g0148a0002c0002t0001g0207others(4): Show | 8 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-1534G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197467 | ||||||
chr5:41197639
|
A | G | 1 | a0002c0002t0002g0222 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.446-1706T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197639 | ||||||
chr5:41198015
|
A | G | 17 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0162others(14): Show | 19 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.445+1753T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198015 | ||||||
chr5:41198045
|
C | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+1723G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198045 | ||||||
chr5:41198060
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.445+1708G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198060 | ||||||
chr5:41198099
|
A | G | 58 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0022others(55): Show | 67 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.445+1669T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198099 | ||||||
chr5:41198122
|
C | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(291): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.445+1646G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198122 | ||||||
chr5:41198136
|
C | T | 9 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(6): Show | 10 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+1632G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198136 | ||||||
chr5:41198137
|
G | A | 2 | a0002c0002t0003g0104a0002c0002t0003g0105 | 2 | NA18994.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.445+1631C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198137 | ||||||
chr5:41198402
|
A | T | 6 | a0002c0002t0003g0018a0002c0002t0003g0086a0002c0002t0003g0087others(3): Show | 7 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.445+1366T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198402 | ||||||
chr5:41198665
|
A | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(82): Show | 105 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.445+1103T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198665 | ||||||
chr5:41198667
|
A | G | 3 | a0001c0001t0001g0288a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG00408.hp2 NA18968.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.445+1101T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198667 | ||||||
chr5:41198720
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.445+1048G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198720 | ||||||
chr5:41198749
|
T | C | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.445+1019A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198749 | ||||||
chr5:41198855
|
C | T | 2 | a0002c0002t0001g0179a0002c0002t0001g0180 | 2 | NA18961.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.445+913G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198855 | ||||||
chr5:41198891
|
C | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0265others(7): Show | 13 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.445+877G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198891 | ||||||
chr5:41198910
|
G | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(171): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.445+858C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198910 | ||||||
chr5:41198966
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(170): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.445+802T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198966 | ||||||
chr5:41199020
|
G | C | 1 | a0001c0001t0001g0319 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.445+748C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199020 | ||||||
chr5:41199038
|
C | T | 1 | a0005c0007t0003g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.445+730G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199038 | ||||||
chr5:41199056
|
A | G | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+712T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199056 | ||||||
chr5:41199093
|
C | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+675G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199093 | ||||||
chr5:41199136
|
A | G | 41 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(38): Show | 47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.445+632T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199136 | ||||||
chr5:41199303
|
C | T | 1 | a0001c0001t0001g0288 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.445+465G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199303 | ||||||
chr5:41199314
|
C | T | 2 | a0002c0002t0001g0028a0002c0002t0001g0246 | 3 | HG00280.hp2 HG00323.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445+454G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199314 | ||||||
chr5:41199379
|
A | G | 1 | a0001c0001t0002g0055 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.445+389T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199379 | ||||||
chr5:41199474
|
T | C | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.445+294A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199474 | ||||||
chr5:41199514
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(148): Show | 181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.445+254A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199514 | ||||||
chr5:41199527
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(171): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.445+241A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199527 | ||||||
chr5:41199747
|
C | T | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.445+21G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199747 | ||||||
chr5:41200024
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301-112G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200024 | ||||||
chr5:41200180
|
C | T | 5 | a0006c0005t0006g0014a0006c0005t0006g0040a0011c0010t0001g0277others(2): Show | 6 | HG02258.hp1 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-268G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200180 | ||||||
chr5:41200211
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.301-299A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200211 | ||||||
chr5:41200251
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(171): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.301-339G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200251 | ||||||
chr5:41200256
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(171): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.301-344C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200256 | ||||||
chr5:41200281
|
T | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-369A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200281 | ||||||
chr5:41200307
|
G | A | 3 | a0005c0007t0003g0090a0005c0007t0003g0093a0005c0007t0003g0094 | 3 | HG02723.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.301-395C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200307 | ||||||
chr5:41200360
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-448G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200360 | ||||||
chr5:41200446
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(46): Show | 57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.301-534A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200446 | ||||||
chr5:41200624
|
T | C | 2 | a0002c0002t0001g0168a0002c0002t0001g0169 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.301-712A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200624 | ||||||
chr5:41200658
|
G | T | 1 | a0001c0001t0007g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.301-746C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200658 | ||||||
chr5:41200693
|
T | C | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG00140.hp1 HG01123.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-781A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200693 | ||||||
chr5:41200724
|
G | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(46): Show | 57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.301-812C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200724 | ||||||
chr5:41200863
|
C | A | 1 | a0002c0002t0008g0337 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.300+695G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200863 | ||||||
chr5:41200870
|
TTTGTTG | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134 | 3 | HG02809.hp1 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.300+682_300+687del others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200870 | ||||||
chr5:41200888
|
GTTGTT | G | 6 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0124others(3): Show | 6 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+665_300+669del others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200888 | ||||||
chr5:41200888
|
GTTGTTT | G | 11 | a0001c0001t0012g0129a0001c0003t0001g0120a0001c0003t0001g0123others(8): Show | 11 | HG02055.hp1 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.300+664_300+669del others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200888 | ||||||
chr5:41200888
|
GTTGTTTT | G | 20 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0079others(17): Show | 22 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.300+663_300+669del others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200888 | ||||||
chr5:41200888
|
GTTGTTTT others(1): Show |
G | 27 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0019others(24): Show | 32 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.300+662_300+669del others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200888 | ||||||
chr5:41200891
|
G | GT | 33 | a0002c0002t0001g0025a0002c0002t0001g0028a0002c0002t0001g0029others(30): Show | 42 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.300+666dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
G | GTT | 39 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0027others(36): Show | 46 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.300+665_300+666dup others(2): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
G | GTTT | 16 | a0002c0002t0001g0185a0002c0002t0001g0199a0002c0002t0001g0241others(13): Show | 19 | HG00597.hp1 HG00738.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.300+664_300+666dup others(3): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
G | GTTTTGTT others(3): Show |
1 | a0002c0002t0001g0023 | 2 | HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.300+666_300+667ins others(10): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
G | GTTTTTTT | 7 | a0002c0002t0001g0022a0002c0002t0001g0162a0002c0002t0001g0164others(4): Show | 8 | HG00738.hp1 HG01517.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+660_300+666dup others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
G | GTTTTTTT others(3): Show |
2 | a0002c0002t0001g0173a0002c0002t0001g0174 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.300+657_300+666dup others(10): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
G | GTTTTTTT others(4): Show |
2 | a0002c0002t0001g0171a0002c0002t0001g0172 | 2 | HG00741.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.300+656_300+666dup others(11): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
G | T | 1 | a0002c0002t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.300+667C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
GTT | G | 9 | a0001c0001t0001g0280a0001c0001t0002g0043a0001c0001t0002g0053others(6): Show | 9 | HG00621.hp1 HG02135.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+665_300+666del others(2): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
GTTT | G | 36 | a0001c0001t0001g0263a0001c0001t0001g0271a0001c0001t0001g0281others(33): Show | 44 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.300+664_300+666del others(3): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
GTTTT | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(68): Show | 90 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.300+663_300+666del others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200891
|
GTTTTT | G | 26 | a0001c0001t0001g0032a0001c0001t0001g0140a0001c0001t0001g0252others(23): Show | 28 | HG00323.hp2 HG00423.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+662_300+666del others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | ||||||
chr5:41200895
|
T | G | 1 | a0001c0001t0001g0278 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.300+663A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200895 | ||||||
chr5:41200915
|
T | A | 1 | a0010c0012t0004g0138 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.300+643A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200915 | ||||||
chr5:41200924
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.300+634C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200924 | ||||||
chr5:41201013
|
T | A | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.300+545A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201013 | ||||||
chr5:41201017
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(141): Show | 173 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.300+541C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201017 | ||||||
chr5:41201055
|
A | G | 41 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(38): Show | 47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.300+503T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201055 | ||||||
chr5:41201084
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG01358.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.300+474G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201084 | ||||||
chr5:41201097
|
G | A | 1 | a0002c0002t0001g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.300+461C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201097 | ||||||
chr5:41201104
|
G | A | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.300+454C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201104 | ||||||
chr5:41201237
|
G | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+321C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201237 | ||||||
chr5:41201269
|
C | T | 2 | a0002c0002t0001g0179a0002c0002t0001g0180 | 2 | NA18961.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.300+289G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201269 | ||||||
chr5:41201324
|
T | C | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.300+234A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201324 | ||||||
chr5:41201463
|
G | A | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.300+95C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201463 | ||||||
chr5:41201526
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+32G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201526 | ||||||
chr5:41201530
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.300+28A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201530 | ||||||
chr5:41201744
|
A | C | 1 | a0001c0001t0001g0275 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.144-30T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201744 | ||||||
chr5:41201769
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-55G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201769 | ||||||
chr5:41201785
|
T | G | 1 | a0001c0001t0001g0325 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.144-71A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201785 | ||||||
chr5:41201831
|
T | C | 4 | a0002c0002t0003g0007a0002c0002t0003g0112a0002c0002t0003g0113others(1): Show | 6 | NA18971.hp2 NA18974.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-117A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201831 | ||||||
chr5:41201845
|
A | G | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-131T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201845 | ||||||
chr5:41201850
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-136C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201850 | ||||||
chr5:41202211
|
A | G | 5 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339others(2): Show | 6 | HG01192.hp2 HG01261.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-497T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202211 | ||||||
chr5:41202237
|
C | T | 1 | a0001c0006t0002g0343 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.144-523G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202237 | ||||||
chr5:41202292
|
AG | A | 8 | a0002c0002t0001g0211a0002c0002t0001g0212a0002c0002t0002g0026others(5): Show | 9 | HG01168.hp1 HG01175.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.144-579delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202292 | ||||||
chr5:41202366
|
T | G | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-652A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202366 | ||||||
chr5:41202595
|
T | G | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143+493A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202595 | ||||||
chr5:41202656
|
C | G | 1 | a0001c0001t0002g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.143+432G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202656 | ||||||
chr5:41202768
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.143+320G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202768 | ||||||
chr5:41202809
|
A | AAAGCTTG others(1): Show |
9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.143+271_143+278dup others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202809 | ||||||
chr5:41202869
|
T | C | 1 | a0002c0002t0001g0170 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.143+219A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202869 | ||||||
chr5:41202894
|
C | T | 1 | a0006c0005t0006g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.143+194G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202894 | ||||||
chr5:41202904
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.143+184C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202904 | ||||||
chr5:41203445
|
A | G | 15 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 15 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20-195T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203445 | ||||||
chr5:41203855
|
G | T | 1 | a0001c0001t0012g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-20-605C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203855 | ||||||
chr5:41203902
|
G | A | 39 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(36): Show | 45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-20-652C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203902 | ||||||
chr5:41203994
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-744G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203994 | ||||||
chr5:41203995
|
G | A | 5 | a0002c0002t0003g0085a0002c0002t0003g0106a0002c0002t0003g0107others(2): Show | 5 | NA18988.hp1 NA19054.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-745C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203995 | ||||||
chr5:41204071
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-20-821C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204071 | ||||||
chr5:41204199
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-949C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204199 | ||||||
chr5:41204201
|
C | T | 63 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0021others(60): Show | 73 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-20-951G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204201 | ||||||
chr5:41204230
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-20-980T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204230 | ||||||
chr5:41204241
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-991C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204241 | ||||||
chr5:41204446
|
G | T | 1 | a0002c0002t0001g0178 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-20-1196C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204446 | ||||||
chr5:41204459
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1209G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204459 | ||||||
chr5:41204559
|
G | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(77): Show | 99 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-20-1309C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204559 | ||||||
chr5:41204659
|
C | CT | 133 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(130): Show | 161 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.-20-1410dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204659 | ||||||
chr5:41204664
|
T | C | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-20-1414A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204664 | ||||||
chr5:41204670
|
C | T | 5 | a0001c0001t0001g0254a0001c0001t0001g0278a0001c0001t0001g0334others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1420G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204670 | ||||||
chr5:41204670
|
CT | C | 31 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(28): Show | 32 | HG00140.hp1 HG00323.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.-20-1421delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204670 | ||||||
chr5:41204671
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-20-1421A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204671 | ||||||
chr5:41204675
|
T | C | 7 | a0002c0002t0001g0021a0002c0002t0001g0023a0002c0002t0001g0171others(4): Show | 9 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20-1425A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204675 | ||||||
chr5:41204677
|
T | C | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG02056.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-20-1427A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204677 | ||||||
chr5:41204737
|
T | A | 1 | a0002c0002t0002g0214 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-20-1487A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204737 | ||||||
chr5:41204739
|
G | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(46): Show | 57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-20-1489C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204739 | ||||||
chr5:41204806
|
A | T | 15 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 15 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20-1556T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204806 | ||||||
chr5:41204872
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1622G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204872 | ||||||
chr5:41205016
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1766C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205016 | ||||||
chr5:41205030
|
G | A | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | HG00597.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.-20-1780C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205030 | ||||||
chr5:41205060
|
A | G | 1 | a0002c0002t0002g0215 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-20-1810T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205060 | ||||||
chr5:41205126
|
T | C | 39 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(36): Show | 45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-20-1876A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205126 | ||||||
chr5:41205174
|
C | T | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20-1924G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205174 | ||||||
chr5:41205190
|
A | G | 1 | a0001c0003t0001g0118 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-20-1940T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205190 | ||||||
chr5:41205242
|
G | A | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-1992C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205242 | ||||||
chr5:41205297
|
C | T | 1 | a0011c0010t0001g0277 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20-2047G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205297 | ||||||
chr5:41205376
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2126C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205376 | ||||||
chr5:41205386
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-2136G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205386 | ||||||
chr5:41205387
|
G | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-2137C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205387 | ||||||
chr5:41205418
|
G | A | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-2168C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205418 | ||||||
chr5:41205446
|
G | A | 1 | a0002c0002t0001g0201 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-20-2196C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205446 | ||||||
chr5:41205506
|
C | T | 63 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0021others(60): Show | 73 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-20-2256G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205506 | ||||||
chr5:41205508
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2258C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205508 | ||||||
chr5:41205577
|
C | T | 1 | a0002c0002t0002g0251 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-20-2327G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205577 | ||||||
chr5:41205582
|
C | A | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20-2332G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205582 | ||||||
chr5:41205589
|
G | A | 5 | a0001c0003t0001g0123a0001c0003t0001g0124a0001c0003t0001g0125others(2): Show | 5 | HG00544.hp1 HG02145.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-2339C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205589 | ||||||
chr5:41205680
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-20-2430G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205680 | ||||||
chr5:41205681
|
C | A | 3 | a0002c0002t0001g0339a0002c0002t0010g0041a0002c0014t0009g0042 | 3 | HG01261.hp1 HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-20-2431G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205681 | ||||||
chr5:41205682
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-2432C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205682 | ||||||
chr5:41205706
|
A | T | 1 | a0001c0001t0001g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-20-2456T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205706 | ||||||
chr5:41205713
|
G | C | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2463C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205713 | ||||||
chr5:41205760
|
G | A | 1 | a0015c0030t0002g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20-2510C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205760 | ||||||
chr5:41205787
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-20-2537G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205787 | ||||||
chr5:41205818
|
C | G | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-2568G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205818 | ||||||
chr5:41205884
|
C | T | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-20-2634G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205884 | ||||||
chr5:41205905
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2655C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205905 | ||||||
chr5:41205958
|
A | G | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2708T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205958 | ||||||
chr5:41205963
|
C | T | 3 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0011t0002g0015 | 4 | HG00735.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2713G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205963 | ||||||
chr5:41205972
|
C | T | 1 | a0002c0002t0002g0251 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-20-2722G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205972 | ||||||
chr5:41206000
|
G | C | 2 | a0002c0002t0003g0083a0002c0002t0003g0110 | 2 | HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-20-2750C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206000 | ||||||
chr5:41206059
|
C | A | 3 | a0006c0005t0006g0014a0006c0005t0006g0040a0011c0010t0006g0039 | 4 | HG02258.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2809G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206059 | ||||||
chr5:41206083
|
C | T | 1 | a0001c0003t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-20-2833G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206083 | ||||||
chr5:41206277
|
C | T | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-20-3027G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206277 | ||||||
chr5:41206329
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-3079G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206329 | ||||||
chr5:41206330
|
G | A | 2 | a0001c0003t0001g0118a0001c0003t0001g0119 | 2 | HG00140.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-20-3080C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206330 | ||||||
chr5:41206404
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0275 | 3 | HG02602.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-20-3154G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206404 | ||||||
chr5:41206420
|
A | G | 2 | a0002c0002t0003g0112a0002c0002t0003g0113 | 2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-20-3170T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206420 | ||||||
chr5:41206575
|
G | A | 2 | a0002c0002t0010g0041a0002c0014t0009g0042 | 2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-20-3325C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206575 | ||||||
chr5:41206630
|
T | C | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-20-3380A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206630 | ||||||
chr5:41206699
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-3449C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206699 | ||||||
chr5:41206759
|
C | A | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-20-3509G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206759 | ||||||
chr5:41206770
|
A | G | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3520T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206770 | ||||||
chr5:41206774
|
C | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3524G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206774 | ||||||
chr5:41206774
|
C | T | 1 | a0001c0003t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20-3524G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206774 | ||||||
chr5:41206777
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3527C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206777 | ||||||
chr5:41206783
|
C | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3533G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206783 | ||||||
chr5:41206785
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3535C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206785 | ||||||
chr5:41206787
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3537C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206787 | ||||||
chr5:41206787
|
G | T | 17 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0162others(14): Show | 19 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20-3537C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206787 | ||||||
chr5:41206909
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(218): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-20-3659A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206909 | ||||||
chr5:41206930
|
A | T | 6 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(3): Show | 6 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-3680T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206930 | ||||||
chr5:41206933
|
C | T | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-20-3683G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206933 | ||||||
chr5:41206940
|
T | C | 39 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(36): Show | 45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-20-3690A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206940 | ||||||
chr5:41206945
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-20-3695A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206945 | ||||||
chr5:41207027
|
C | T | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-3777G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207027 | ||||||
chr5:41207062
|
G | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-3812C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207062 | ||||||
chr5:41207063
|
G | T | 3 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045 | 3 | HG02015.hp1 HG02074.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-20-3813C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207063 | ||||||
chr5:41207064
|
C | T | 1 | a0002c0002t0001g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-20-3814G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207064 | ||||||
chr5:41207071
|
A | G | 1 | a0002c0002t0003g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-20-3821T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207071 | ||||||
chr5:41207101
|
C | A | 1 | a0001c0001t0004g0139 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-20-3851G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207101 | ||||||
chr5:41207111
|
G | A | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(1): Show | 4 | HG00741.hp2 HG01256.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-3861C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207111 | ||||||
chr5:41207254
|
T | C | 1 | a0001c0001t0001g0333 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-20-4004A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207254 | ||||||
chr5:41207297
|
T | G | 58 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0022others(55): Show | 67 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.-20-4047A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207297 | ||||||
chr5:41207302
|
G | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-4052C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207302 | ||||||
chr5:41207358
|
T | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(281): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.-20-4108A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207358 | ||||||
chr5:41207574
|
G | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(281): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.-20-4324C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207574 | ||||||
chr5:41207660
|
T | C | 41 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0025others(38): Show | 48 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-20-4410A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207660 | ||||||
chr5:41207695
|
G | T | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20-4445C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207695 | ||||||
chr5:41207834
|
A | G | 1 | a0002c0002t0001g0176 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-20-4584T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207834 | ||||||
chr5:41207882
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-20-4632A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207882 | ||||||
chr5:41208040
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-4790C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208040 | ||||||
chr5:41208072
|
C | T | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-20-4822G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208072 | ||||||
chr5:41208157
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-4907C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208157 | ||||||
chr5:41208190
|
A | C | 2 | a0002c0002t0001g0162a0002c0002t0001g0163 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-20-4940T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208190 | ||||||
chr5:41208259
|
G | C | 1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-20-5009C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208259 | ||||||
chr5:41208260
|
A | G | 46 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(43): Show | 53 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.-20-5010T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208260 | ||||||
chr5:41208272
|
A | G | 1 | a0002c0002t0003g0084 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-20-5022T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208272 | ||||||
chr5:41208333
|
A | G | 7 | a0002c0002t0001g0211a0002c0002t0001g0212a0002c0002t0002g0026others(4): Show | 8 | HG01168.hp1 HG01175.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+5043T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208333 | ||||||
chr5:41208348
|
G | T | 1 | a0001c0001t0012g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-21+5028C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208348 | ||||||
chr5:41208391
|
A | G | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+4985T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208391 | ||||||
chr5:41208418
|
A | G | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+4958T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208418 | ||||||
chr5:41208449
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-21+4927T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208449 | ||||||
chr5:41208470
|
C | T | 1 | a0002c0002t0003g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-21+4906G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208470 | ||||||
chr5:41208584
|
T | C | 46 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(43): Show | 53 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.-21+4792A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208584 | ||||||
chr5:41208598
|
C | T | 41 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0025others(38): Show | 48 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+4778G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208598 | ||||||
chr5:41208648
|
A | G | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+4728T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208648 | ||||||
chr5:41208718
|
G | A | 3 | a0002c0002t0001g0339a0002c0002t0010g0041a0002c0014t0009g0042 | 3 | HG01261.hp1 HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-21+4658C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208718 | ||||||
chr5:41208742
|
C | CA | 7 | a0003c0004t0001g0008a0003c0004t0001g0157a0003c0004t0001g0158others(4): Show | 9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21+4633dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208742 | ||||||
chr5:41208751
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-21+4625A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208751 | ||||||
chr5:41208798
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0252 | 3 | HG02976.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-21+4578T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208798 | ||||||
chr5:41208915
|
C | T | 39 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0025others(36): Show | 46 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.-21+4461G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208915 | ||||||
chr5:41208916
|
G | A | 69 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(66): Show | 76 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.-21+4460C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208916 | ||||||
chr5:41208955
|
C | T | 58 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0022others(55): Show | 67 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.-21+4421G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208955 | ||||||
chr5:41209183
|
A | C | 39 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(36): Show | 45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-21+4193T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209183 | ||||||
chr5:41209193
|
A | G | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+4183T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209193 | ||||||
chr5:41209283
|
T | A | 16 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0162others(13): Show | 18 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+4093A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209283 | ||||||
chr5:41209344
|
C | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+4032G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209344 | ||||||
chr5:41209444
|
G | C | 39 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(36): Show | 45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-21+3932C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209444 | ||||||
chr5:41209481
|
C | G | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+3895G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209481 | ||||||
chr5:41209484
|
T | C | 69 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(66): Show | 76 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.-21+3892A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209484 | ||||||
chr5:41209494
|
C | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(284): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-21+3882G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209494 | ||||||
chr5:41209512
|
C | A | 39 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0025others(36): Show | 46 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.-21+3864G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209512 | ||||||
chr5:41209533
|
C | A | 1 | a0002c0002t0003g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-21+3843G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209533 | ||||||
chr5:41209573
|
C | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(281): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.-21+3803G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209573 | ||||||
chr5:41209734
|
A | T | 1 | a0002c0002t0001g0151 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-21+3642T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209734 | ||||||
chr5:41209771
|
C | T | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+3605G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209771 | ||||||
chr5:41209772
|
G | A | 2 | a0002c0002t0001g0204a0002c0002t0001g0205 | 2 | HG03579.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-21+3604C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209772 | ||||||
chr5:41209833
|
A | C | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+3543T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209833 | ||||||
chr5:41209946
|
T | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(284): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-21+3430A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209946 | ||||||
chr5:41210004
|
G | T | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+3372C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210004 | ||||||
chr5:41210096
|
G | A | 1 | a0002c0002t0003g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-21+3280C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210096 | ||||||
chr5:41210111
|
T | C | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+3265A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210111 | ||||||
chr5:41210114
|
G | A | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+3262C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210114 | ||||||
chr5:41210147
|
G | T | 3 | a0002c0002t0001g0339a0002c0002t0010g0041a0002c0014t0009g0042 | 3 | HG01261.hp1 HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-21+3229C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210147 | ||||||
chr5:41210156
|
C | G | 1 | a0002c0002t0002g0209 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-21+3220G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210156 | ||||||
chr5:41210180
|
C | G | 1 | a0001c0001t0007g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-21+3196G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210180 | ||||||
chr5:41210182
|
G | C | 1 | a0002c0002t0002g0208 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-21+3194C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210182 | ||||||
chr5:41210183
|
G | T | 1 | a0002c0002t0002g0208 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-21+3193C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210183 | ||||||
chr5:41210281
|
C | A | 1 | a0002c0002t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-21+3095G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210281 | ||||||
chr5:41210295
|
A | C | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+3081T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210295 | ||||||
chr5:41210349
|
A | T | 1 | a0001c0001t0004g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-21+3027T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210349 | ||||||
chr5:41210378
|
A | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+2998T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210378 | ||||||
chr5:41210400
|
C | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(128): Show | 157 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-21+2976G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210400 | ||||||
chr5:41210470
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | NA19000.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-21+2906G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210470 | ||||||
chr5:41210508
|
A | G | 1 | a0002c0002t0001g0150 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-21+2868T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210508 | ||||||
chr5:41210571
|
C | A | 23 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(20): Show | 23 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.-21+2805G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210571 | ||||||
chr5:41210611
|
A | T | 2 | a0001c0003t0001g0118a0001c0003t0001g0119 | 2 | HG00140.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-21+2765T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210611 | ||||||
chr5:41210616
|
G | A | 1 | a0001c0003t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-21+2760C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210616 | ||||||
chr5:41210649
|
G | A | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+2727C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210649 | ||||||
chr5:41210714
|
C | T | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+2662G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210714 | ||||||
chr5:41210765
|
T | C | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+2611A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210765 | ||||||
chr5:41210820
|
G | T | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21+2556C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210820 | ||||||
chr5:41210891
|
C | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(284): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-21+2485G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210891 | ||||||
chr5:41210937
|
C | A | 1 | a0002c0002t0001g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-21+2439G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210937 | ||||||
chr5:41211034
|
A | G | 5 | a0002c0002t0001g0021a0002c0002t0001g0149a0002c0002t0001g0339others(2): Show | 6 | HG01192.hp2 HG01261.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+2342T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211034 | ||||||
chr5:41211047
|
C | T | 1 | a0002c0002t0001g0207 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-21+2329G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211047 | ||||||
chr5:41211101
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0004g0117a0001c0001t0007g0036others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+2275C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211101 | ||||||
chr5:41211131
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21+2245T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211131 | ||||||
chr5:41211170
|
A | G | 38 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(35): Show | 44 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-21+2206T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211170 | ||||||
chr5:41211202
|
A | G | 1 | a0002c0002t0001g0207 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-21+2174T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211202 | ||||||
chr5:41211217
|
T | C | 1 | a0002c0002t0002g0250 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-21+2159A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211217 | ||||||
chr5:41211263
|
G | T | 1 | a0001c0001t0004g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-21+2113C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211263 | ||||||
chr5:41211268
|
A | C | 11 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(8): Show | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+2108T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211268 | ||||||
chr5:41211269
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-21+2107C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211269 | ||||||
chr5:41211272
|
C | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(284): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-21+2104G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211272 | ||||||
chr5:41211293
|
C | G | 1 | a0002c0014t0011g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+2083G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211293 | ||||||
chr5:41211294
|
G | A | 1 | a0001c0003t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-21+2082C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211294 | ||||||
chr5:41211310
|
T | C | 3 | a0001c0001t0012g0129a0012c0009t0001g0080a0012c0009t0001g0130 | 3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-21+2066A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211310 | ||||||
chr5:41211318
|
C | CATGGCAT | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(141): Show | 173 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.-21+2051_-21+2057d others(9): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211318 | ||||||
chr5:41211353
|
G | A | 7 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0112others(4): Show | 11 | HG01496.hp2 HG02004.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+2023C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211353 | ||||||
chr5:41211459
|
C | G | 1 | a0001c0001t0004g0020 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-21+1917G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211459 | ||||||
chr5:41211504
|
C | A | 1 | a0012c0009t0001g0080 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-21+1872G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211504 | ||||||
chr5:41211547
|
T | G | 1 | a0002c0002t0002g0251 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-21+1829A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211547 | ||||||
chr5:41211687
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(82): Show | 105 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.-21+1689C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211687 | ||||||
chr5:41211732
|
T | A | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+1644A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211732 | ||||||
chr5:41211751
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(141): Show | 173 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.-21+1625A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211751 | ||||||
chr5:41211782
|
C | CT | 69 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(66): Show | 76 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.-21+1593_-21+1594i others(3): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211782 | ||||||
chr5:41211795
|
G | A | 18 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+1581C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211795 | ||||||
chr5:41211847
|
A | G | 1 | a0002c0002t0001g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-21+1529T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211847 | ||||||
chr5:41211932
|
T | A | 1 | a0001c0001t0002g0078 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-21+1444A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211932 | ||||||
chr5:41211978
|
A | C | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+1398T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211978 | ||||||
chr5:41212025
|
G | A | 20 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(17): Show | 20 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+1351C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212025 | ||||||
chr5:41212114
|
T | A | 3 | a0002c0002t0008g0335a0002c0002t0008g0336a0002c0002t0008g0337 | 3 | HG02004.hp1 HG02273.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-21+1262A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212114 | ||||||
chr5:41212169
|
T | C | 1 | a0002c0029t0005g0338 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-21+1207A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212169 | ||||||
chr5:41212260
|
C | T | 1 | a0002c0002t0002g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-21+1116G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212260 | ||||||
chr5:41212263
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(37): Show | 48 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+1113C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212263 | ||||||
chr5:41212285
|
C | T | 1 | a0002c0002t0002g0146 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-21+1091G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212285 | ||||||
chr5:41212291
|
G | A | 3 | a0002c0002t0001g0339a0002c0002t0010g0041a0002c0014t0009g0042 | 3 | HG01261.hp1 HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-21+1085C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212291 | ||||||
chr5:41212333
|
G | C | 1 | a0001c0001t0001g0340 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-21+1043C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212333 | ||||||
chr5:41212349
|
C | T | 12 | a0001c0001t0001g0135a0001c0001t0002g0141a0001c0001t0002g0143others(9): Show | 13 | HG01074.hp1 HG01081.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21+1027G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212349 | ||||||
chr5:41212350
|
G | T | 3 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0038 | 3 | HG01243.hp2 HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-21+1026C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212350 | ||||||
chr5:41212361
|
A | T | 3 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0038 | 3 | HG01243.hp2 HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-21+1015T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212361 | ||||||
chr5:41212410
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-21+966G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212410 | ||||||
chr5:41212439
|
G | A | 1 | a0019c0020t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21+937C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212439 | ||||||
chr5:41212509
|
G | C | 20 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(17): Show | 20 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+867C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212509 | ||||||
chr5:41212560
|
C | G | 4 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(1): Show | 4 | HG02015.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+816G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212560 | ||||||
chr5:41212628
|
C | A | 1 | a0004c0008t0001g0342 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-21+748G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212628 | ||||||
chr5:41212634
|
T | C | 7 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(4): Show | 8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+742A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212634 | ||||||
chr5:41212669
|
A | G | 46 | a0001c0001t0001g0135a0001c0001t0004g0020a0001c0001t0004g0081others(43): Show | 53 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.-21+707T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212669 | ||||||
chr5:41212699
|
G | A | 3 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0038 | 3 | HG01243.hp2 HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-21+677C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212699 | ||||||
chr5:41212931
|
G | T | 2 | a0001c0001t0004g0079a0012c0009t0001g0080 | 2 | HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-21+445C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212931 | ||||||
chr5:41212970
|
C | T | 20 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(17): Show | 20 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+406G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212970 | ||||||
chr5:41213006
|
A | AT | 39 | a0002c0002t0003g0006a0002c0002t0003g0007a0002c0002t0003g0018others(36): Show | 45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-21+369dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213006 | ||||||
chr5:41213006
|
A | T | 1 | a0001c0001t0004g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-21+370T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213006 | ||||||
chr5:41213071
|
G | A | 1 | a0001c0006t0002g0343 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-21+305C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213071 | ||||||
chr5:41213144
|
A | C | 2 | a0001c0001t0004g0079a0012c0009t0001g0080 | 2 | HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-21+232T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213144 | ||||||
chr5:41213233
|
C | G | 40 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(37): Show | 48 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+143G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213233 |