geneid | 3678 |
---|---|
ensemblid | ENSG00000161638.11 |
hgncid | 6141 |
symbol | ITGA5 |
name | integrin subunit alpha 5 |
refseq_nuc | NM_002205.5 |
refseq_prot | NP_002196.4 |
ensembl_nuc | ENST00000293379.9 |
ensembl_prot | ENSP00000293379.4 |
mane_status | MANE Select |
chr | chr12 |
start | 54395261 |
end | 54419266 |
strand | - |
ver | v1.2 |
region | chr12:54395261-54419266 |
region5000 | chr12:54390261-54424266 |
regionname0 | ITGA5_chr12_54395261_54419266 |
regionname5000 | ITGA5_chr12_54390261_54424266 |
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 | 1/1 | 1049 | 315 | 85 | 69 | 108 | 12 | 39 | 74 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0002 | 0/0 | 1049 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0003 | 0/0 | 1049 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0004 | 0/0 | 1049 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0005 | 0/0 | 1049 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0006 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0007 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0008 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0009 | 0/0 | 1049 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0010 | 0/0 | 1049 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0011 | 0/0 | 1049 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0012 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0013 | 0/0 | 1049 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0014 | 0/0 | 1049 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
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 | 1/1 | 3150 | 284 | 62 | 69 | 108 | 11 | 32 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0002 | 0/0 | 3150 | 12 | 5 | 0 | 0 | 0 | 7 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0003 | 0/0 | 3150 | 8 | 8 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0004 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0005 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0006 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0007 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0008 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0009 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0010 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0011 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0012 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0013 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0014 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0015 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0016 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0017 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0018 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0019 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0020 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0021 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0022 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
c0023 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1101 | 291 | 76 | 69 | 97 | 12 | 35 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
t0002 | 0/0 | 1101 | 14 | 0 | 0 | 14 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
t0003 | 0/0 | 1093 | 14 | 6 | 0 | 1 | 0 | 7 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
t0004 | 0/0 | 1101 | 7 | 7 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
t0005 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
t0006 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
t0007 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
t0008 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
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 | 46 | 11 | 4 | 27 | 0 | 4 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0002 | 0/0 | 20 | 6 | 6 | 3 | 1 | 4 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0003 | 0/0 | 19 | 1 | 3 | 8 | 5 | 2 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0004 | 0/0 | 16 | 0 | 2 | 11 | 0 | 3 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0005 | 0/0 | 15 | 3 | 6 | 0 | 3 | 3 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0006 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0007 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0008 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0009 | 0/0 | 6 | 1 | 0 | 0 | 0 | 5 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0011 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0013 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0019 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0020 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0032 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
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 | 1/1 | 3150 | 284 | 62 | 69 | 108 | 11 | 32 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0002 | 0/0 | 3150 | 12 | 5 | 0 | 0 | 0 | 7 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0003 | 0/0 | 3150 | 8 | 8 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0005 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0006 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0007 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0015 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0018 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0019 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0021 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0002c0004 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0003c0009 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0004c0011 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0005c0013 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0006c0014 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0007c0016 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0008c0017 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0009c0012 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0010c0010 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0011c0022 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0012c0020 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0013c0008 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0014c0023 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4250 | 268 | 61 | 68 | 94 | 11 | 32 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0001t0002 | 0/0 | 4250 | 14 | 0 | 0 | 14 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0001t0005 | 0/0 | 4250 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0001t0008 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0002t0003 | 0/0 | 4242 | 12 | 5 | 0 | 0 | 0 | 7 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0003t0001 | 0/0 | 4250 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0003t0004 | 0/0 | 4250 | 6 | 6 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0005t0001 | 0/0 | 4250 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0006t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0006t0006 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0007t0001 | 0/0 | 4250 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0015t0003 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0018t0001 | 0/0 | 4250 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0019t0004 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0001c0021t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0002c0004t0001 | 0/0 | 4250 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0003c0009t0001 | 0/0 | 4250 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0004c0011t0001 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0005c0013t0001 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0006c0014t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0007c0016t0007 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0008c0017t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0009c0012t0001 | 0/0 | 4250 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0010c0010t0001 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0011c0022t0003 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0012c0020t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0013c0008t0001 | 0/0 | 4250 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
a0014c0023t0001 | 0/0 | 4250 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | copy fasta | chr12 | 54390261 | 54424266 |
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 | 46 | 11 | 4 | 27 | 0 | 4 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0002 | 0/0 | 20 | 6 | 6 | 3 | 1 | 4 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0003 | 0/0 | 19 | 1 | 3 | 8 | 5 | 2 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0004 | 0/0 | 16 | 0 | 2 | 11 | 0 | 3 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0005 | 0/0 | 15 | 3 | 6 | 0 | 3 | 3 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0007 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0008 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0013 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0019 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0020 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0032 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0002g0006 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0002t0003g0009 | 0/0 | 6 | 1 | 0 | 0 | 0 | 5 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0003t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0003t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0003t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0003t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0003t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0006t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0007t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0015t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0018t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0019t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0001c0021t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0002c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0002c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0002c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0003c0009t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0004c0011t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0005c0013t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0006c0014t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0007c0016t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0008c0017t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0009c0012t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0010c0010t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0011c0022t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0012c0020t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0013c0008t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
a0014c0023t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0018 | t0001 | g0108 | EUR | GBR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0091 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01361 | hp2 | a0013 | c0008 | t0001 | g0077 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0037 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02145 | hp1 | a0001 | c0006 | t0006 | g0136 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02145 | hp2 | a0007 | c0016 | t0007 | g0063 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02280 | hp2 | a0001 | c0003 | t0004 | g0021 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02572 | hp2 | a0001 | c0007 | t0001 | g0138 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02615 | hp1 | a0001 | c0002 | t0003 | g0059 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02622 | hp1 | a0001 | c0005 | t0001 | g0135 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02622 | hp2 | a0006 | c0014 | t0001 | g0053 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02630 | hp1 | a0008 | c0017 | t0001 | g0097 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02698 | hp1 | a0001 | c0002 | t0003 | g0058 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02809 | hp1 | a0002 | c0004 | t0001 | g0085 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02886 | hp2 | a0001 | c0005 | t0001 | g0039 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02895 | hp2 | a0001 | c0003 | t0004 | g0145 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02897 | hp2 | a0001 | c0003 | t0004 | g0144 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03041 | hp2 | a0001 | c0021 | t0001 | g0048 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03130 | hp2 | a0001 | c0002 | t0003 | g0057 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03239 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03453 | hp1 | a0001 | c0002 | t0003 | g0061 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03453 | hp2 | a0002 | c0004 | t0001 | g0084 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03490 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03492 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03540 | hp2 | a0001 | c0006 | t0001 | g0094 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03579 | hp1 | a0001 | c0003 | t0004 | g0034 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03579 | hp2 | a0001 | c0005 | t0001 | g0137 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03710 | hp1 | a0009 | c0012 | t0001 | g0036 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03710 | hp2 | a0003 | c0009 | t0001 | g0110 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04115 | hp1 | a0001 | c0002 | t0003 | g0056 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04115 | hp2 | a0014 | c0023 | t0001 | g0147 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18906 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18941 | hp2 | a0010 | c0010 | t0001 | g0045 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18966 | hp1 | a0005 | c0013 | t0001 | g0086 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18972 | hp1 | a0011 | c0022 | t0003 | g0060 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18982 | hp1 | a0004 | c0011 | t0001 | g0081 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19030 | hp1 | a0002 | c0004 | t0001 | g0099 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19030 | hp2 | a0001 | c0003 | t0004 | g0021 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19240 | hp1 | a0001 | c0003 | t0004 | g0146 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA19240 | hp2 | a0001 | c0007 | t0001 | g0139 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ASW | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | GIH | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG02559 | hp2 | a0001 | c0019 | t0004 | g0054 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG03471 | hp2 | a0012 | c0020 | t0001 | g0047 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA21309 | hp1 | a0001 | c0015 | t0003 | g0050 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0032 | REF | REF | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:54401387
|
G | A | 1 | a0007 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2479C>T | p.His827Tyr | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/30 | 2547/4250 | 2479/3150 | 827/1049 | chr12 | 54401387 | ||
chr12:54401420
|
G | A | 1 | a0008 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.2446C>T | p.Pro816Ser | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/30 | 2514/4250 | 2446/3150 | 816/1049 | chr12 | 54401420 | ||
chr12:54403258
|
G | T | 1 | a0006 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1843C>A | p.Gln615Lys | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 18/30 | 1911/4250 | 1843/3150 | 615/1049 | chr12 | 54403258 | ||
chr12:54403702
|
G | T | 1 | a0005 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.1699C>A | p.Gln567Lys | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/30 | 1767/4250 | 1699/3150 | 567/1049 | chr12 | 54403702 | ||
chr12:54404227
|
C | T | 1 | a0002 | 3 | HG02809.hp1 HG03453.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.1483G>A | p.Ala495Thr | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 15/30 | 1551/4250 | 1483/3150 | 495/1049 | chr12 | 54404227 | ||
chr12:54404469
|
A | G | 1 | a0009 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1424T>C | p.Ile475Thr | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/30 | 1492/4250 | 1424/3150 | 475/1049 | chr12 | 54404469 | ||
chr12:54404841
|
C | T | 1 | a0004 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1279G>A | p.Val427Ile | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 13/30 | 1347/4250 | 1279/3150 | 427/1049 | chr12 | 54404841 | ||
chr12:54405193
|
C | T | 1 | a0010 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.1198G>A | p.Gly400Arg | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 12/30 | 1266/4250 | 1198/3150 | 400/1049 | chr12 | 54405193 | ||
chr12:54405369
|
T | C | 1 | a0011 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.1022A>G | p.Asp341Gly | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 12/30 | 1090/4250 | 1022/3150 | 341/1049 | chr12 | 54405369 | ||
chr12:54405665
|
C | T | 1 | a0012 | 1 | HG03471.hp2 | missense_variant&splice_region_variant | MODERATE | c.1015G>A | p.Gly339Arg | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 11/30 | 1083/4250 | 1015/3150 | 339/1049 | chr12 | 54405665 | ||
chr12:54405898
|
C | T | 1 | a0003 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.935G>A | p.Arg312Gln | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 10/30 | 1003/4250 | 935/3150 | 312/1049 | chr12 | 54405898 | ||
chr12:54408904
|
C | T | 1 | a0013 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.634G>A | p.Glu212Lys | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 5/30 | 702/4250 | 634/3150 | 212/1049 | chr12 | 54408904 | ||
chr12:54419099
|
G | A | 1 | a0014 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.100C>T | p.Pro34Ser | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/30 | 168/4250 | 100/3150 | 34/1049 | chr12 | 54419099 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:54399717
|
G | A | 3 | a0001c0005a0001c0021a0012c0020 | 5 | HG02622.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.2769C>T | p.Leu923Leu | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/30 | 2837/4250 | 2769/3150 | 923/1049 | chr12 | 54399717 | ||
chr12:54401626
|
A | G | 5 | a0001c0002a0001c0003a0001c0015others(2): Show | 23 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(20): Show |
synonymous_variant | LOW | c.2346T>C | p.Phe782Phe | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 23/30 | 2414/4250 | 2346/3150 | 782/1049 | chr12 | 54401626 | ||
chr12:54402061
|
G | A | 1 | a0001c0019 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.2166C>T | p.Ala722Ala | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 21/30 | 2234/4250 | 2166/3150 | 722/1049 | chr12 | 54402061 | ||
chr12:54403214
|
A | G | 4 | a0001c0002a0001c0015a0001c0019others(1): Show | 15 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(12): Show |
synonymous_variant | LOW | c.1887T>C | p.Tyr629Tyr | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 18/30 | 1955/4250 | 1887/3150 | 629/1049 | chr12 | 54403214 | ||
chr12:54403238
|
G | A | 1 | a0001c0018 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1863C>T | p.His621His | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 18/30 | 1931/4250 | 1863/3150 | 621/1049 | chr12 | 54403238 | ||
chr12:54404225
|
A | G | 3 | a0001c0006a0001c0007a0001c0019 | 5 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
synonymous_variant | LOW | c.1485T>C | p.Ala495Ala | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 15/30 | 1553/4250 | 1485/3150 | 495/1049 | chr12 | 54404225 | ||
chr12:54404228
|
G | A | 3 | a0001c0006a0001c0007a0001c0019 | 5 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
synonymous_variant | LOW | c.1482C>T | p.Ser494Ser | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 15/30 | 1550/4250 | 1482/3150 | 494/1049 | chr12 | 54404228 | ||
chr12:54405666
|
G | A | 1 | a0001c0007 | 2 | HG02572.hp2 NA19240.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1014C>T | p.Asp338Asp | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 11/30 | 1082/4250 | 1014/3150 | 338/1049 | chr12 | 54405666 | ||
chr12:54408796
|
G | A | 4 | a0001c0002a0001c0021a0011c0022others(1): Show | 15 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(12): Show |
synonymous_variant | LOW | c.651C>T | p.Gly217Gly | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/30 | 719/4250 | 651/3150 | 217/1049 | chr12 | 54408796 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:54395372
|
T | G | 5 | a0001c0002t0003a0001c0003t0004a0001c0015t0003others(2): Show | 21 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*921A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 921 | chr12 | 54395372 | |||||
chr12:54395710
|
TCTGGGCC | T | 3 | a0001c0002t0003a0001c0015t0003a0011c0022t0003 | 14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*576_*582delGGCCCA others(1): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 576 | chr12 | 54395710 | |||||
chr12:54395839
|
C | T | 1 | a0007c0016t0007 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 454 | chr12 | 54395839 | |||||
chr12:54395952
|
A | G | 1 | a0001c0006t0006 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 341 | chr12 | 54395952 | |||||
chr12:54395969
|
TC | T | 3 | a0001c0002t0003a0001c0015t0003a0011c0022t0003 | 14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*323delG | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 323 | chr12 | 54395969 | |||||
chr12:54396057
|
T | C | 1 | a0001c0001t0008 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*236A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 236 | chr12 | 54396057 | |||||
chr12:54396183
|
C | T | 1 | a0001c0001t0002 | 14 | HG00597.hp2 HG02056.hp2 HG02523.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*110G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 110 | chr12 | 54396183 | |||||
chr12:54396189
|
C | T | 1 | a0001c0001t0005 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*104G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 104 | chr12 | 54396189 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:54396517
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3067-141T>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396517 | ||||||
chr12:54396526
|
C | T | 1 | a0001c0005t0001g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3067-150G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396526 | ||||||
chr12:54396858
|
G | GT | 9 | a0001c0001t0001g0051a0001c0001t0001g0088a0001c0002t0003g0009others(6): Show | 14 | HG02135.hp1 HG02135.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.3067-483dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396858 | ||||||
chr12:54396879
|
T | C | 1 | a0001c0001t0001g0030 | 2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3066+486A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396879 | ||||||
chr12:54396885
|
T | C | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3066+480A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396885 | ||||||
chr12:54397199
|
A | AG | 7 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0057others(4): Show | 12 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.3066+165dupC | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54397199 | ||||||
chr12:54397213
|
T | C | 5 | a0001c0002t0003g0009a0001c0002t0003g0056a0001c0002t0003g0058others(2): Show | 10 | HG02698.hp1 HG03017.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.3066+152A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54397213 | ||||||
chr12:54397321
|
G | C | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3066+44C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54397321 | ||||||
chr12:54397712
|
C | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(17): Show | 65 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2944-225G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397712 | ||||||
chr12:54397844
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0122 | 2 | HG00423.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2944-357A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397844 | ||||||
chr12:54397902
|
A | AT | 17 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 39 | HG00733.hp1 HG00741.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.2944-416dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397902 | ||||||
chr12:54397902
|
AT | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0070a0001c0001t0001g0092others(7): Show | 13 | HG00423.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2944-416delA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397902 | ||||||
chr12:54397924
|
G | T | 1 | a0001c0002t0003g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2944-437C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397924 | ||||||
chr12:54398279
|
T | G | 4 | a0001c0003t0004g0021a0001c0003t0004g0034a0001c0003t0004g0144others(1): Show | 5 | HG02280.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2943+318A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54398279 | ||||||
chr12:54398294
|
C | T | 2 | a0001c0002t0003g0057a0001c0002t0003g0059 | 2 | HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2943+303G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54398294 | ||||||
chr12:54398402
|
T | A | 1 | a0001c0001t0001g0042 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2943+195A>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54398402 | ||||||
chr12:54398409
|
A | G | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2943+188T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54398409 | ||||||
chr12:54398789
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2842-91G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398789 | ||||||
chr12:54398833
|
C | CTT | 6 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(3): Show | 11 | HG01884.hp2 HG02698.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.2842-136_2842-135i others(4): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398833 | ||||||
chr12:54398834
|
TC | T | 8 | a0001c0001t0001g0031a0001c0001t0001g0123a0001c0003t0004g0146others(5): Show | 9 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2842-137delG | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398834 | ||||||
chr12:54398835
|
C | CT | 8 | a0001c0001t0001g0051a0001c0001t0001g0072a0001c0001t0001g0087others(5): Show | 8 | HG01175.hp2 HG02135.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.2842-138dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398835 | ||||||
chr12:54398835
|
C | T | 16 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(13): Show | 21 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.2842-137G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398835 | ||||||
chr12:54398835
|
CT | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0022others(18): Show | 46 | HG00558.hp2 HG00733.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2842-138delA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398835 | ||||||
chr12:54398837
|
T | C | 1 | a0001c0003t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2842-139A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398837 | ||||||
chr12:54398860
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2842-162C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398860 | ||||||
chr12:54399237
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2841+408A>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54399237 | ||||||
chr12:54399247
|
A | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0025others(13): Show | 36 | HG00099.hp1 HG00558.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.2841+398T>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54399247 | ||||||
chr12:54399450
|
A | G | 1 | a0001c0001t0001g0014 | 4 | HG00673.hp1 NA18747.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2841+195T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54399450 | ||||||
chr12:54399962
|
G | T | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2644-15C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54399962 | ||||||
chr12:54400046
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2644-99T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400046 | ||||||
chr12:54400202
|
A | C | 11 | a0001c0001t0008g0141a0001c0002t0003g0009a0001c0002t0003g0037others(8): Show | 16 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.2644-255T>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400202 | ||||||
chr12:54400457
|
C | T | 9 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(6): Show | 14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.2643+389G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400457 | ||||||
chr12:54400553
|
G | T | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2643+293C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400553 | ||||||
chr12:54400663
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2643+183G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400663 | ||||||
chr12:54400805
|
G | A | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2643+41C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400805 | ||||||
chr12:54400806
|
A | G | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2643+40T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400806 | ||||||
chr12:54401049
|
A | G | 12 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(9): Show | 17 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.2494-54T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401049 | ||||||
chr12:54401143
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2494-148G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401143 | ||||||
chr12:54401170
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2494-175G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401170 | ||||||
chr12:54401197
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2493+176A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401197 | ||||||
chr12:54401251
|
A | G | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2493+122T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401251 | ||||||
chr12:54401483
|
G | GGAGGAGG others(8): Show |
1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.2388-20_2388-6dupT others(14): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 23/29 | chr12 | 54401483 | ||||||
chr12:54401489
|
G | GGGTGGTT others(7): Show |
9 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(6): Show | 14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.2388-25_2388-12dup others(14): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 23/29 | chr12 | 54401489 | ||||||
chr12:54401935
|
G | A | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2226+66C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 21/29 | chr12 | 54401935 | ||||||
chr12:54402168
|
G | A | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2133+12C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 20/29 | chr12 | 54402168 | ||||||
chr12:54402361
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1983-31C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402361 | ||||||
chr12:54402658
|
C | T | 1 | a0001c0001t0008g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1982+325G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402658 | ||||||
chr12:54402696
|
G | A | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1982+287C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402696 | ||||||
chr12:54402743
|
C | T | 12 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(9): Show | 17 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.1982+240G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402743 | ||||||
chr12:54402809
|
C | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0130others(3): Show | 15 | HG00735.hp1 HG01346.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.1982+174G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402809 | ||||||
chr12:54402859
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0080a0001c0001t0001g0101others(1): Show | 12 | HG02257.hp2 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1982+124T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402859 | ||||||
chr12:54402973
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0041others(3): Show | 22 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1982+10G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402973 | ||||||
chr12:54403531
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1776+94A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403531 | ||||||
chr12:54403543
|
G | A | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1776+82C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403543 | ||||||
chr12:54403544
|
T | C | 9 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(6): Show | 14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.1776+81A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403544 | ||||||
chr12:54403556
|
C | T | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1776+69G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403556 | ||||||
chr12:54403609
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0041 | 4 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1776+16C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403609 | ||||||
chr12:54403787
|
C | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0025others(12): Show | 35 | HG00099.hp1 HG00558.hp2 HG00673.hp1 others(32): Show |
splice_region_variant&intron_variant | LOW | c.1622-8G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 16/29 | chr12 | 54403787 | ||||||
chr12:54403797
|
T | A | 1 | a0001c0006t0006g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1622-18A>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 16/29 | chr12 | 54403797 | ||||||
chr12:54404264
|
G | A | 9 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(6): Show | 14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.1464-18C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/29 | chr12 | 54404264 | ||||||
chr12:54404303
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0098 | 2 | HG02165.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1464-57T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/29 | chr12 | 54404303 | ||||||
chr12:54404353
|
C | T | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1463+77G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/29 | chr12 | 54404353 | ||||||
chr12:54404380
|
C | T | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1463+50G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/29 | chr12 | 54404380 | ||||||
chr12:54404507
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1418-32G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 13/29 | chr12 | 54404507 | ||||||
chr12:54404909
|
A | G | 9 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(6): Show | 14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.1226-15T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 12/29 | chr12 | 54404909 | ||||||
chr12:54404968
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1226-74C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 12/29 | chr12 | 54404968 | ||||||
chr12:54405451
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1017-77C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 11/29 | chr12 | 54405451 | ||||||
chr12:54405939
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.907-13C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54405939 | ||||||
chr12:54406080
|
A | G | 2 | a0001c0015t0003g0050a0001c0019t0004g0054 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.907-154T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406080 | ||||||
chr12:54406126
|
C | G | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.907-200G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406126 | ||||||
chr12:54406140
|
C | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0128 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.907-214G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406140 | ||||||
chr12:54406140
|
C | T | 2 | a0001c0003t0004g0144a0001c0003t0004g0145 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.907-214G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406140 | ||||||
chr12:54406329
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.907-403G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406329 | ||||||
chr12:54406764
|
T | C | 8 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(5): Show | 13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-838A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406764 | ||||||
chr12:54406830
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.906+819T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406830 | ||||||
chr12:54406881
|
G | A | 1 | a0008c0017t0001g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.906+768C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406881 | ||||||
chr12:54406887
|
C | T | 11 | a0001c0001t0002g0124a0001c0002t0003g0009a0001c0002t0003g0037others(8): Show | 16 | HG01884.hp2 HG02523.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.906+762G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406887 | ||||||
chr12:54406902
|
T | C | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.906+747A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406902 | ||||||
chr12:54407076
|
G | T | 7 | a0001c0002t0003g0009a0001c0002t0003g0056a0001c0002t0003g0057others(4): Show | 12 | HG02615.hp1 HG02698.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.906+573C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407076 | ||||||
chr12:54407393
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.906+256G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407393 | ||||||
chr12:54407420
|
G | A | 8 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(5): Show | 13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.906+229C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407420 | ||||||
chr12:54407495
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.906+154C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407495 | ||||||
chr12:54407591
|
C | T | 2 | a0001c0015t0003g0050a0001c0019t0004g0054 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.906+58G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407591 | ||||||
chr12:54407592
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.906+57C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407592 | ||||||
chr12:54407592
|
G | T | 3 | a0001c0003t0004g0144a0001c0003t0004g0145a0001c0003t0004g0146 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.906+57C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407592 | ||||||
chr12:54407741
|
A | G | 10 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(7): Show | 15 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-49T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 8/29 | chr12 | 54407741 | ||||||
chr12:54408246
|
T | G | 12 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(9): Show | 17 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.692-11A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408246 | ||||||
chr12:54408306
|
C | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 35 | HG00733.hp1 HG00741.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.692-71G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408306 | ||||||
chr12:54408392
|
T | C | 1 | a0001c0003t0004g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.692-157A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408392 | ||||||
chr12:54408482
|
C | T | 8 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(5): Show | 13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.692-247G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408482 | ||||||
chr12:54408666
|
T | C | 12 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(9): Show | 17 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.691+90A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408666 | ||||||
chr12:54408709
|
C | CA | 20 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0069others(17): Show | 22 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.691+46dupT | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408709 | ||||||
chr12:54408709
|
C | CAA | 5 | a0001c0001t0001g0044a0001c0003t0004g0021a0001c0003t0004g0034others(2): Show | 6 | HG01109.hp1 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.691+45_691+46dupTT | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408709 | ||||||
chr12:54408709
|
C | CAAAA | 3 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0061 | 8 | HG01884.hp2 HG03017.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.691+43_691+46dupTT others(2): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408709 | ||||||
chr12:54408854
|
A | G | 10 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(7): Show | 15 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.645+39T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 5/29 | chr12 | 54408854 | ||||||
chr12:54408875
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.645+18G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 5/29 | chr12 | 54408875 | ||||||
chr12:54408886
|
C | G | 10 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(7): Show | 15 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.645+7G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 5/29 | chr12 | 54408886 | ||||||
chr12:54408983
|
G | A | 10 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(7): Show | 15 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.584-29C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54408983 | ||||||
chr12:54409056
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.584-102C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54409056 | ||||||
chr12:54409067
|
G | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0025others(13): Show | 36 | HG00099.hp1 HG00558.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.584-113C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54409067 | ||||||
chr12:54409088
|
G | C | 8 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(5): Show | 13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.584-134C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54409088 | ||||||
chr12:54409144
|
T | C | 1 | a0001c0005t0001g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.583+88A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54409144 | ||||||
chr12:54409478
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02523.hp2 | splice_region_variant&intron_variant | LOW | c.462+7G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 3/29 | chr12 | 54409478 | ||||||
chr12:54409611
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0075 | 4 | HG00735.hp2 HG00738.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-14C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409611 | ||||||
chr12:54409820
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.350-223T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409820 | ||||||
chr12:54409843
|
C | T | 3 | a0001c0019t0004g0054a0001c0021t0001g0048a0012c0020t0001g0047 | 3 | HG02559.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.350-246G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409843 | ||||||
chr12:54409913
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.350-316C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409913 | ||||||
chr12:54409918
|
A | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.350-321T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409918 | ||||||
chr12:54409927
|
G | A | 8 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(5): Show | 13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.350-330C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409927 | ||||||
chr12:54409942
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0015t0003g0050 | 7 | HG01071.hp1 HG01243.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-345G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409942 | ||||||
chr12:54410014
|
A | G | 15 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(12): Show | 20 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.350-417T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410014 | ||||||
chr12:54410095
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.350-498G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410095 | ||||||
chr12:54410153
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.350-556C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410153 | ||||||
chr12:54410188
|
G | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.350-591C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410188 | ||||||
chr12:54410234
|
C | T | 12 | a0001c0002t0003g0009a0001c0002t0003g0037a0001c0002t0003g0056others(9): Show | 17 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-637G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410234 | ||||||
chr12:54410331
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.350-734G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410331 | ||||||
chr12:54410347
|
C | CT | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.350-751dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410347 | ||||||
chr12:54410347
|
C | CTT | 12 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(9): Show | 17 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.350-752_350-751dup others(2): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410347 | ||||||
chr12:54410503
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.350-906C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410503 | ||||||
chr12:54410552
|
A | AT | 9 | a0001c0001t0001g0072a0001c0002t0003g0009a0001c0002t0003g0056others(6): Show | 14 | HG02145.hp1 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-956dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410552 | ||||||
chr12:54410552
|
AT | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0118others(3): Show | 6 | HG02922.hp2 HG02976.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-956delA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410552 | ||||||
chr12:54410679
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.350-1082G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410679 | ||||||
chr12:54410725
|
A | AT | 17 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0071others(14): Show | 25 | HG01256.hp2 HG01258.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.349+1108dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410725 | ||||||
chr12:54410898
|
T | A | 3 | a0001c0003t0004g0144a0001c0003t0004g0145a0001c0003t0004g0146 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.349+936A>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410898 | ||||||
chr12:54411031
|
C | G | 1 | a0001c0006t0006g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+803G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411031 | ||||||
chr12:54411160
|
C | T | 9 | a0001c0001t0001g0015a0001c0002t0003g0009a0001c0002t0003g0037others(6): Show | 16 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.349+674G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411160 | ||||||
chr12:54411209
|
T | G | 9 | a0001c0003t0004g0021a0001c0003t0004g0034a0001c0003t0004g0144others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.349+625A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411209 | ||||||
chr12:54411590
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0121 | 6 | HG00099.hp2 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+244A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411590 | ||||||
chr12:54411731
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.349+103G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411731 | ||||||
chr12:54411969
|
G | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
splice_region_variant&intron_variant | LOW | c.219-5C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54411969 | ||||||
chr12:54411981
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.219-17G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54411981 | ||||||
chr12:54412085
|
C | A | 1 | a0001c0003t0004g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.219-121G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412085 | ||||||
chr12:54412086
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.219-122C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412086 | ||||||
chr12:54412158
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0123 | 3 | HG01109.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.219-194C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412158 | ||||||
chr12:54412165
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.219-201G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412165 | ||||||
chr12:54412253
|
T | C | 1 | a0001c0001t0001g0020 | 3 | HG01192.hp1 HG04199.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.219-289A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412253 | ||||||
chr12:54412283
|
C | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02280.hp2 HG02572.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-319G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412283 | ||||||
chr12:54412328
|
A | G | 2 | a0001c0001t0002g0124a0001c0002t0003g0037 | 2 | HG01884.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.219-364T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412328 | ||||||
chr12:54412584
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.219-620C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412584 | ||||||
chr12:54412754
|
A | G | 2 | a0001c0001t0001g0022a0001c0005t0001g0039 | 3 | HG02559.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.219-790T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412754 | ||||||
chr12:54412834
|
C | A | 10 | a0001c0001t0001g0140a0001c0002t0003g0037a0001c0003t0004g0144others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-870G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412834 | ||||||
chr12:54412834
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.219-870G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412834 | ||||||
chr12:54412925
|
C | G | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.219-961G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412925 | ||||||
chr12:54412943
|
T | C | 2 | a0001c0003t0004g0144a0001c0003t0004g0145 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.219-979A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412943 | ||||||
chr12:54412985
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.219-1021G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412985 | ||||||
chr12:54412992
|
C | G | 1 | a0001c0001t0001g0067 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.219-1028G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412992 | ||||||
chr12:54413081
|
G | GGTTTCTG others(314): Show |
1 | a0001c0001t0002g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.219-1118_219-1117i others(323): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413081 | ||||||
chr12:54413169
|
A | G | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.219-1205T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413169 | ||||||
chr12:54413261
|
C | T | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.219-1297G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413261 | ||||||
chr12:54413420
|
T | C | 1 | a0001c0001t0001g0020 | 3 | HG01192.hp1 HG04199.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.219-1456A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413420 | ||||||
chr12:54413511
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.219-1547T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413511 | ||||||
chr12:54413646
|
C | T | 7 | a0001c0001t0001g0140a0001c0002t0003g0037a0001c0005t0001g0135others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-1682G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413646 | ||||||
chr12:54413709
|
A | C | 1 | a0001c0001t0001g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.219-1745T>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413709 | ||||||
chr12:54413830
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.219-1866A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413830 | ||||||
chr12:54414102
|
G | T | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.219-2138C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414102 | ||||||
chr12:54414119
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.219-2155A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414119 | ||||||
chr12:54414175
|
C | T | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.219-2211G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414175 | ||||||
chr12:54414212
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219-2248G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414212 | ||||||
chr12:54414226
|
C | T | 1 | a0001c0005t0001g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219-2262G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414226 | ||||||
chr12:54414557
|
G | T | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.219-2593C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414557 | ||||||
chr12:54414587
|
CTGTAATC others(295): Show |
C | 7 | a0001c0002t0003g0009a0001c0002t0003g0056a0001c0002t0003g0057others(4): Show | 12 | HG02615.hp1 HG02698.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-2925_219-2624d others(2): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414587 | ||||||
chr12:54414618
|
GGGCAGAT others(295): Show |
G | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.219-2956_219-2655d others(2): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414618 | ||||||
chr12:54414673
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.219-2709G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414673 | ||||||
chr12:54414676
|
C | T | 1 | a0007c0016t0007g0063 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.219-2712G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414676 | ||||||
chr12:54414708
|
G | A | 6 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 7 | HG02280.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-2744C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414708 | ||||||
chr12:54414803
|
C | T | 2 | a0001c0003t0004g0144a0001c0003t0004g0145 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.219-2839G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414803 | ||||||
chr12:54414827
|
C | T | 10 | a0001c0001t0001g0140a0001c0002t0003g0037a0001c0005t0001g0135others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-2863G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414827 | ||||||
chr12:54414829
|
G | C | 6 | a0001c0001t0001g0140a0001c0005t0001g0135a0001c0005t0001g0137others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-2865C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414829 | ||||||
chr12:54414832
|
C | T | 3 | a0001c0003t0004g0144a0001c0003t0004g0145a0001c0003t0004g0146 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.219-2868G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414832 | ||||||
chr12:54415008
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.219-3044G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415008 | ||||||
chr12:54415143
|
C | T | 2 | a0001c0001t0002g0006a0001c0001t0002g0035 | 13 | HG00597.hp2 HG02056.hp2 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.219-3179G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415143 | ||||||
chr12:54415144
|
G | A | 2 | a0001c0021t0001g0048a0012c0020t0001g0047 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219-3180C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415144 | ||||||
chr12:54415401
|
G | A | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.219-3437C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415401 | ||||||
chr12:54415404
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.219-3440C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415404 | ||||||
chr12:54415513
|
C | T | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.218+3468G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415513 | ||||||
chr12:54415615
|
T | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 36 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.218+3366A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415615 | ||||||
chr12:54415711
|
G | A | 21 | a0001c0001t0001g0015a0001c0001t0001g0140a0001c0002t0003g0009others(18): Show | 28 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+3270C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415711 | ||||||
chr12:54415774
|
A | G | 1 | a0001c0002t0003g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.218+3207T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415774 | ||||||
chr12:54415800
|
T | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0140a0001c0002t0003g0009others(18): Show | 28 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+3181A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415800 | ||||||
chr12:54415880
|
GGAGCT | G | 6 | a0001c0001t0001g0140a0001c0005t0001g0135a0001c0005t0001g0137others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+3096_218+3100d others(7): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415880 | ||||||
chr12:54416195
|
G | A | 8 | a0001c0002t0003g0009a0001c0002t0003g0056a0001c0002t0003g0057others(5): Show | 13 | HG02615.hp1 HG02698.hp1 HG03017.hp2 others(10): Show |
intron_variant | MODIFIER | c.218+2786C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416195 | ||||||
chr12:54416236
|
A | C | 2 | a0001c0003t0001g0142a0001c0003t0001g0143 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.218+2745T>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416236 | ||||||
chr12:54416542
|
G | GGAGAACT others(4): Show |
21 | a0001c0001t0001g0015a0001c0001t0001g0140a0001c0002t0003g0009others(18): Show | 28 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+2438_218+2439i others(13): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416542 | ||||||
chr12:54416546
|
C | T | 21 | a0001c0001t0001g0015a0001c0001t0001g0140a0001c0002t0003g0009others(18): Show | 28 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+2435G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416546 | ||||||
chr12:54416551
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.218+2430G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416551 | ||||||
chr12:54416609
|
G | A | 2 | a0001c0021t0001g0048a0012c0020t0001g0047 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.218+2372C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416609 | ||||||
chr12:54416735
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.218+2246G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416735 | ||||||
chr12:54416981
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 12 | HG00735.hp1 HG01346.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+2000C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416981 | ||||||
chr12:54416981
|
G | T | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.218+2000C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416981 | ||||||
chr12:54416991
|
C | T | 1 | a0006c0014t0001g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.218+1990G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416991 | ||||||
chr12:54417053
|
A | T | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.218+1928T>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417053 | ||||||
chr12:54417070
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.218+1911C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417070 | ||||||
chr12:54417220
|
C | G | 2 | a0001c0003t0001g0142a0001c0003t0001g0143 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.218+1761G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417220 | ||||||
chr12:54417331
|
G | A | 6 | a0001c0001t0001g0140a0001c0005t0001g0135a0001c0005t0001g0137others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+1650C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417331 | ||||||
chr12:54417439
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.218+1542G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417439 | ||||||
chr12:54417538
|
T | C | 1 | a0001c0001t0008g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+1443A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417538 | ||||||
chr12:54417671
|
A | C | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218+1310T>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417671 | ||||||
chr12:54417688
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 39 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.218+1293C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417688 | ||||||
chr12:54417700
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.218+1281T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417700 | ||||||
chr12:54417881
|
C | T | 1 | a0009c0012t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.218+1100G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417881 | ||||||
chr12:54417924
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 39 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.218+1057G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417924 | ||||||
chr12:54418016
|
T | C | 2 | a0001c0003t0001g0142a0001c0003t0001g0143 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.218+965A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418016 | ||||||
chr12:54418175
|
A | T | 1 | a0001c0001t0002g0035 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.218+806T>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418175 | ||||||
chr12:54418585
|
G | C | 3 | a0001c0003t0004g0144a0001c0003t0004g0145a0001c0003t0004g0146 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+396C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418585 | ||||||
chr12:54418691
|
C | T | 2 | a0001c0003t0004g0021a0001c0003t0004g0034 | 3 | HG02280.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+290G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418691 | ||||||
chr12:54418919
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+62G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418919 |