geneid | 2735 |
---|---|
ensemblid | ENSG00000111087.10 |
hgncid | 4317 |
symbol | GLI1 |
name | GLI family zinc finger 1 |
refseq_nuc | NM_005269.3 |
refseq_prot | NP_005260.1 |
ensembl_nuc | ENST00000228682.7 |
ensembl_prot | ENSP00000228682.2 |
mane_status | MANE Select |
chr | chr12 |
start | 57459785 |
end | 57472268 |
strand | + |
ver | v1.2 |
region | chr12:57459785-57472268 |
region5000 | chr12:57454785-57477268 |
regionname0 | GLI1_chr12_57459785_57472268 |
regionname5000 | GLI1_chr12_57454785_57477268 |
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 | 1/0 | 1106 | 170 | 26 | 34 | 86 | 4 | 19 | 64 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002 | 0/1 | 1106 | 153 | 19 | 30 | 86 | 5 | 12 | 69 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003 | 0/0 | 1106 | 61 | 52 | 5 | 0 | 0 | 4 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0004 | 0/0 | 1106 | 17 | 0 | 0 | 16 | 0 | 1 | 8 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0005 | 0/0 | 1106 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0006 | 0/0 | 1106 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0007 | 0/0 | 1106 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0008 | 0/0 | 1106 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0009 | 0/0 | 1106 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0010 | 0/0 | 1106 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0011 | 0/0 | 1106 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0012 | 0/0 | 1106 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0013 | 0/0 | 1106 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0014 | 0/0 | 188 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0015 | 0/0 | 1106 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0016 | 0/0 | 1106 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
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 | 1/0 | 3321 | 167 | 25 | 33 | 85 | 4 | 19 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0002 | 0/1 | 3321 | 150 | 17 | 30 | 85 | 5 | 12 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0003 | 0/0 | 3321 | 37 | 33 | 3 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0004 | 0/0 | 3321 | 18 | 15 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0005 | 0/0 | 3321 | 16 | 0 | 0 | 15 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0006 | 0/0 | 3321 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0007 | 0/0 | 3321 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0008 | 0/0 | 3321 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0009 | 0/0 | 3321 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0010 | 0/0 | 3321 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0011 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0012 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0013 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0014 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0015 | 0/0 | 3321 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0016 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0017 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0018 | 0/0 | 3321 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0019 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0020 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0021 | 0/0 | 3321 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0022 | 0/0 | 3350 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0023 | 0/0 | 3321 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0024 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0025 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
c0026 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 652 | 370 | 89 | 68 | 168 | 10 | 34 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0002 | 0/0 | 652 | 19 | 0 | 0 | 18 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0003 | 1/0 | 652 | 7 | 5 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0004 | 0/0 | 652 | 2 | 0 | 2 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0005 | 0/0 | 652 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0006 | 0/0 | 652 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0007 | 0/0 | 652 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0008 | 0/0 | 652 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0009 | 0/0 | 652 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0010 | 0/0 | 652 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0011 | 0/0 | 652 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0012 | 0/0 | 652 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0013 | 0/0 | 652 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0014 | 0/0 | 652 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0015 | 0/0 | 652 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
t0016 | 0/0 | 652 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
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 | 1/0 | 109 | 18 | 25 | 48 | 2 | 15 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0002 | 0/1 | 101 | 6 | 23 | 54 | 5 | 12 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0003 | 0/0 | 16 | 1 | 2 | 13 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0004 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0005 | 0/0 | 13 | 10 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0006 | 0/0 | 12 | 0 | 5 | 7 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0007 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0008 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0012 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0015 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
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 | 1/0 | 3321 | 167 | 25 | 33 | 85 | 4 | 19 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0009 | 0/0 | 3321 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0011 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0014 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002 | 0/1 | 3321 | 150 | 17 | 30 | 85 | 5 | 12 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0012 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0013 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0017 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0003 | 0/0 | 3321 | 37 | 33 | 3 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0004 | 0/0 | 3321 | 18 | 15 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0006 | 0/0 | 3321 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0007 | 0/0 | 3321 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0004c0005 | 0/0 | 3321 | 16 | 0 | 0 | 15 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0004c0016 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0005c0008 | 0/0 | 3321 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0006c0025 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0007c0024 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0008c0021 | 0/0 | 3321 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0009c0020 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0010c0019 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0011c0018 | 0/0 | 3321 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0012c0010 | 0/0 | 3321 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0013c0015 | 0/0 | 3321 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0014c0022 | 0/0 | 3350 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0015c0023 | 0/0 | 3321 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0016c0026 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3972 | 154 | 19 | 32 | 81 | 4 | 18 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0001t0002 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0001t0003 | 1/0 | 3972 | 7 | 5 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0001t0007 | 0/0 | 3972 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0001t0011 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0001t0012 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0001t0015 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0009t0001 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0011t0001 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0001c0014t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002t0001 | 0/1 | 3972 | 138 | 14 | 28 | 80 | 5 | 10 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002t0002 | 0/0 | 3972 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002t0004 | 0/0 | 3972 | 2 | 0 | 2 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002t0006 | 0/0 | 3972 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002t0008 | 0/0 | 3972 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002t0009 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002t0010 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002t0013 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0002t0014 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0012t0001 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0013t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0002c0017t0001 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0003t0001 | 0/0 | 3972 | 36 | 33 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0003t0016 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0004t0001 | 0/0 | 3972 | 16 | 13 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0004t0005 | 0/0 | 3972 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0006t0001 | 0/0 | 3972 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0003c0007t0001 | 0/0 | 3972 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0004c0005t0002 | 0/0 | 3972 | 16 | 0 | 0 | 15 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0004c0016t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0005c0008t0001 | 0/0 | 3972 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0006c0025t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0007c0024t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0008c0021t0001 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0009c0020t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0010c0019t0001 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0011c0018t0001 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0012c0010t0001 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0013c0015t0001 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0014c0022t0001 | 0/0 | 4001 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0015c0023t0001 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
a0016c0026t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | copy fasta | chr12 | 57454785 | 57477268 |
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 | 92 | 11 | 20 | 45 | 2 | 14 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0003 | 0/0 | 16 | 1 | 2 | 13 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0006 | 0/0 | 12 | 0 | 5 | 7 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0012 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0003g0001 | 1/0 | 7 | 5 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0009t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0011t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0001c0014t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0002 | 0/1 | 93 | 4 | 23 | 51 | 5 | 9 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0004 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0008g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0002t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0012t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0013t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0002c0017t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0008 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0003t0016g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0004t0001g0005 | 0/0 | 11 | 8 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0004t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0004t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0006t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0003c0007t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0004c0005t0002g0007 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0004c0005t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0004c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0004c0016t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0005c0008t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0006c0025t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0007c0024t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0008c0021t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0009c0020t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0010c0019t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0011c0018t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0012c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0013c0015t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0014c0022t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0015c0023t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
a0016c0026t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00544 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00544 | hp2 | a0004 | c0016 | t0001 | g0014 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00673 | hp2 | a0009 | c0020 | t0001 | g0019 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00738 | hp2 | a0011 | c0018 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0036 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01175 | hp1 | a0002 | c0002 | t0004 | g0072 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01192 | hp1 | a0001 | c0009 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01243 | hp2 | a0003 | c0003 | t0016 | g0008 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01255 | hp1 | a0003 | c0004 | t0001 | g0005 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01257 | hp1 | a0002 | c0002 | t0004 | g0073 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01261 | hp1 | a0003 | c0004 | t0001 | g0005 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01515 | hp1 | a0014 | c0022 | t0001 | g0065 | EUR | IBS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01891 | hp1 | a0002 | c0012 | t0001 | g0015 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01891 | hp2 | a0003 | c0003 | t0001 | g0033 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01928 | hp1 | a0013 | c0015 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01978 | hp1 | a0008 | c0021 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02015 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02027 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02040 | hp2 | a0001 | c0001 | t0011 | g0061 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02055 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02055 | hp2 | a0003 | c0004 | t0001 | g0034 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02071 | hp2 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02129 | hp2 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02145 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02165 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | CDX | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02257 | hp1 | a0005 | c0008 | t0001 | g0026 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02257 | hp2 | a0003 | c0003 | t0001 | g0010 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02451 | hp1 | a0003 | c0006 | t0001 | g0013 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02523 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02572 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02572 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02615 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02622 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02630 | hp1 | a0003 | c0003 | t0001 | g0049 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02630 | hp2 | a0002 | c0002 | t0006 | g0002 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02647 | hp2 | a0003 | c0004 | t0001 | g0021 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02683 | hp1 | a0015 | c0023 | t0001 | g0046 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02698 | hp1 | a0003 | c0007 | t0001 | g0030 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02717 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02723 | hp1 | a0002 | c0002 | t0006 | g0002 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02723 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02809 | hp1 | a0003 | c0006 | t0001 | g0013 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02809 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02818 | hp1 | a0003 | c0003 | t0001 | g0031 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02818 | hp2 | a0003 | c0006 | t0001 | g0013 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02886 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0053 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02896 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02897 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02922 | hp1 | a0003 | c0004 | t0001 | g0021 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02922 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02965 | hp2 | a0003 | c0003 | t0001 | g0050 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02970 | hp1 | a0005 | c0008 | t0001 | g0026 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02970 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02976 | hp1 | a0003 | c0004 | t0005 | g0005 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03041 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03041 | hp2 | a0003 | c0006 | t0001 | g0013 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0082 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0083 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03130 | hp2 | a0001 | c0011 | t0001 | g0041 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03139 | hp2 | a0003 | c0003 | t0001 | g0023 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03195 | hp1 | a0003 | c0004 | t0001 | g0021 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03195 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03209 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03239 | hp1 | a0003 | c0004 | t0001 | g0005 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03453 | hp2 | a0003 | c0004 | t0001 | g0078 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03486 | hp1 | a0003 | c0004 | t0005 | g0005 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03490 | hp2 | a0002 | c0002 | t0008 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03492 | hp2 | a0002 | c0002 | t0008 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0010 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03704 | hp2 | a0012 | c0010 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03834 | hp1 | a0003 | c0007 | t0001 | g0030 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03927 | hp1 | a0004 | c0005 | t0002 | g0007 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG04115 | hp2 | a0001 | c0001 | t0015 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG04204 | hp1 | a0003 | c0003 | t0001 | g0079 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18906 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18948 | hp1 | a0002 | c0013 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18960 | hp2 | a0004 | c0005 | t0002 | g0007 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18967 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18978 | hp1 | a0002 | c0002 | t0013 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18979 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18980 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18984 | hp1 | a0006 | c0025 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19003 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19006 | hp1 | a0002 | c0002 | t0009 | g0040 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19011 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19030 | hp1 | a0002 | c0002 | t0014 | g0080 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19030 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19043 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19054 | hp1 | a0002 | c0002 | t0010 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19058 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19060 | hp1 | a0001 | c0014 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19064 | hp2 | a0004 | c0005 | t0002 | g0007 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19068 | hp1 | a0007 | c0024 | t0001 | g0075 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19078 | hp2 | a0016 | c0026 | t0001 | g0035 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19082 | hp1 | a0004 | c0005 | t0002 | g0077 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0023 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | ASW | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02109 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02109 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03471 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG03471 | hp2 | a0003 | c0003 | t0001 | g0010 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | USA | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
HG06807 | hp2 | a0002 | c0017 | t0001 | g0069 | AFR | USA | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | USA | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA21309 | hp1 | a0010 | c0019 | t0001 | g0001 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0002 | REF | REF | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0001 | REF | REF | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:57464023
|
A | T | 1 | a0016 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.125A>T | p.His42Leu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/12 | 569/3972 | 125/3321 | 42/1106 | chr12 | 57464023 | ||
chr12:57464730
|
C | T | 1 | a0006 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.251C>T | p.Ser84Phe | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/12 | 695/3972 | 251/3321 | 84/1106 | chr12 | 57464730 | ||
chr12:57464777
|
C | G | 1 | a0007 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.298C>G | p.Arg100Gly | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/12 | 742/3972 | 298/3321 | 100/1106 | chr12 | 57464777 | ||
chr12:57464778
|
G | C | 1 | a0007 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.299G>C | p.Arg100Pro | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/12 | 743/3972 | 299/3321 | 100/1106 | chr12 | 57464778 | ||
chr12:57465224
|
C | G | 1 | a0015 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.503C>G | p.Pro168Arg | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 5/12 | 947/3972 | 503/3321 | 168/1106 | chr12 | 57465224 | ||
chr12:57465242
|
T | TGCAACTA others(22): Show |
1 | a0014 | 1 | HG01515.hp1 | frameshift_variant | HIGH | c.521_522insGCAACTAG others(21): Show |
p.Phe174fs | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 5/12 | 966/3972 | 522/3321 | 174/1106 | chr12 | 57465242 | ||
chr12:57465245
|
C | A | 1 | a0014 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.524C>A | p.Pro175Gln | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 5/12 | 968/3972 | 524/3321 | 175/1106 | chr12 | 57465245 | ||
chr12:57466297
|
G | C | 1 | a0013 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.820G>C | p.Gly274Arg | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/12 | 1264/3972 | 820/3321 | 274/1106 | chr12 | 57466297 | ||
chr12:57468130
|
G | A | 1 | a0005 | 2 | HG02257.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.1214G>A | p.Arg405Gln | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/12 | 1658/3972 | 1214/3321 | 405/1106 | chr12 | 57468130 | ||
chr12:57470361
|
C | T | 1 | a0008 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1621C>T | p.Arg541Cys | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2065/3972 | 1621/3321 | 541/1106 | chr12 | 57470361 | ||
chr12:57470409
|
C | T | 1 | a0009 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.1669C>T | p.Arg557Cys | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2113/3972 | 1669/3321 | 557/1106 | chr12 | 57470409 | ||
chr12:57470995
|
C | T | 1 | a0010 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.2255C>T | p.Pro752Leu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2699/3972 | 2255/3321 | 752/1106 | chr12 | 57470995 | ||
chr12:57471063
|
C | G | 1 | a0011 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.2323C>G | p.Pro775Ala | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2767/3972 | 2323/3321 | 775/1106 | chr12 | 57471063 | ||
chr12:57471538
|
G | A | 6 | a0002a0006a0007others(3): Show | 158 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
missense_variant | MODERATE | c.2798G>A | p.Gly933Asp | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3242/3972 | 2798/3321 | 933/1106 | chr12 | 57471538 | ||
chr12:57471775
|
G | T | 1 | a0004 | 17 | HG00544.hp1 HG00544.hp2 HG02015.hp1 others(14): Show |
missense_variant | MODERATE | c.3035G>T | p.Gly1012Val | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3479/3972 | 3035/3321 | 1012/1106 | chr12 | 57471775 | ||
chr12:57471942
|
C | T | 1 | a0012 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.3202C>T | p.Arg1068Trp | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3646/3972 | 3202/3321 | 1068/1106 | chr12 | 57471942 | ||
chr12:57472038
|
G | C | 9 | a0002a0003a0004others(6): Show | 238 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(235): Show |
missense_variant | MODERATE | c.3298G>C | p.Glu1100Gln | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3742/3972 | 3298/3321 | 1100/1106 | chr12 | 57472038 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:57464770
|
G | A | 1 | a0001c0009 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.291G>A | p.Thr97Thr | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/12 | 735/3972 | 291/3321 | 97/1106 | chr12 | 57464770 | ||
chr12:57465648
|
G | A | 9 | a0001c0011a0002c0002a0002c0012others(6): Show | 158 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
synonymous_variant | LOW | c.576G>A | p.Glu192Glu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 6/12 | 1020/3972 | 576/3321 | 192/1106 | chr12 | 57465648 | ||
chr12:57465829
|
G | A | 1 | a0001c0014 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.666G>A | p.Glu222Glu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/12 | 1110/3972 | 666/3321 | 222/1106 | chr12 | 57465829 | ||
chr12:57466263
|
C | T | 1 | a0003c0004 | 18 | HG01255.hp1 HG01261.hp1 HG02055.hp2 others(15): Show |
synonymous_variant | LOW | c.786C>T | p.His262His | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/12 | 1230/3972 | 786/3321 | 262/1106 | chr12 | 57466263 | ||
chr12:57467356
|
C | T | 1 | a0002c0013 | 1 | NA18948.hp1 | synonymous_variant | LOW | c.936C>T | p.Tyr312Tyr | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/12 | 1380/3972 | 936/3321 | 312/1106 | chr12 | 57467356 | ||
chr12:57468002
|
T | C | 1 | a0003c0007 | 2 | HG02698.hp1 HG03834.hp1 |
synonymous_variant | LOW | c.1086T>C | p.Tyr362Tyr | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/12 | 1530/3972 | 1086/3321 | 362/1106 | chr12 | 57468002 | ||
chr12:57469607
|
T | C | 1 | a0004c0016 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.1485T>C | p.Leu495Leu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 11/12 | 1929/3972 | 1485/3321 | 495/1106 | chr12 | 57469607 | ||
chr12:57469682
|
C | T | 1 | a0002c0012 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1560C>T | p.Pro520Pro | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 11/12 | 2004/3972 | 1560/3321 | 520/1106 | chr12 | 57469682 | ||
chr12:57470876
|
C | T | 1 | a0005c0008 | 2 | HG02257.hp1 HG02970.hp1 |
synonymous_variant | LOW | c.2136C>T | p.Ser712Ser | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2580/3972 | 2136/3321 | 712/1106 | chr12 | 57470876 | ||
chr12:57472058
|
C | T | 1 | a0003c0006 | 4 | HG02451.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
synonymous_variant | LOW | c.3318C>T | p.Ala1106Ala | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3762/3972 | 3318/3321 | 1106/1106 | chr12 | 57472058 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:57459785
|
G | T | 1 | a0002c0002t0008 | 2 | HG03490.hp2 HG03492.hp2 |
5_prime_UTR_variant | MODIFIER | c.-444G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3907 | chr12 | 57459785 | |||||
chr12:57459816
|
G | A | 1 | a0002c0002t0004 | 2 | HG01175.hp1 HG01257.hp1 |
5_prime_UTR_variant | MODIFIER | c.-413G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3876 | chr12 | 57459816 | |||||
chr12:57459838
|
G | T | 1 | a0003c0003t0016 | 1 | HG01243.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-391G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | chr12 | 57459838 | ||||||
chr12:57459848
|
C | G | 1 | a0001c0001t0015 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-381C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3844 | chr12 | 57459848 | |||||
chr12:57459993
|
A | G | 1 | a0002c0002t0014 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-236A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3699 | chr12 | 57459993 | |||||
chr12:57460025
|
C | T | 1 | a0002c0002t0013 | 1 | NA18978.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-204C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | chr12 | 57460025 | ||||||
chr12:57460083
|
T | G | 1 | a0002c0002t0009 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-146T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3609 | chr12 | 57460083 | |||||
chr12:57460094
|
T | G | 1 | a0003c0004t0005 | 2 | HG02976.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-135T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3598 | chr12 | 57460094 | |||||
chr12:57460124
|
C | T | 1 | a0001c0001t0012 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3568 | chr12 | 57460124 | |||||
chr12:57460125
|
C | G | 1 | a0001c0001t0007 | 2 | HG02129.hp1 NA19011.hp2 |
5_prime_UTR_variant | MODIFIER | c.-104C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3567 | chr12 | 57460125 | |||||
chr12:57460159
|
C | A | 1 | a0002c0002t0010 | 1 | NA19054.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3533 | chr12 | 57460159 | |||||
chr12:57460171
|
C | G | 3 | a0001c0001t0002a0002c0002t0002a0004c0005t0002 | 19 | HG00544.hp1 HG02015.hp1 HG02027.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-58C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3521 | chr12 | 57460171 | |||||
chr12:57472078
|
T | G | 1 | a0002c0002t0006 | 2 | HG02630.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 17 | chr12 | 57472078 | |||||
chr12:57472145
|
A | C | 41 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(38): Show | 407 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(404): Show |
3_prime_UTR_variant | MODIFIER | c.*84A>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 84 | chr12 | 57472145 | |||||
chr12:57472172
|
G | A | 1 | a0001c0001t0011 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*111G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 111 | chr12 | 57472172 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:57460206
|
GA | G | 11 | a0002c0002t0001g0015a0002c0002t0001g0081a0002c0002t0014g0080others(8): Show | 23 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
splice_region_variant&intron_variant | LOW | c.-28+7delA | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 57460206 | |||||
chr12:57460208
|
A | AG | 8 | a0001c0001t0001g0076a0001c0001t0002g0074a0002c0002t0002g0029others(5): Show | 22 | HG00544.hp1 HG00544.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.-28+14dupG | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 57460208 | |||||
chr12:57460302
|
A | G | 2 | a0002c0002t0004g0072a0002c0002t0004g0073 | 2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.-28+101A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460302 | ||||||
chr12:57460338
|
C | T | 1 | a0002c0002t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-28+137C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460338 | ||||||
chr12:57460374
|
C | T | 1 | a0004c0005t0002g0077 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-28+173C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460374 | ||||||
chr12:57460500
|
T | G | 63 | a0001c0001t0001g0047a0001c0001t0002g0074a0001c0011t0001g0041others(60): Show | 229 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.-28+299T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460500 | ||||||
chr12:57460528
|
G | T | 51 | a0001c0001t0001g0047a0001c0011t0001g0041a0002c0002t0001g0002others(48): Show | 199 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.-28+327G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460528 | ||||||
chr12:57460542
|
A | G | 4 | a0004c0005t0002g0007a0004c0005t0002g0014a0004c0005t0002g0077others(1): Show | 17 | HG00544.hp1 HG00544.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28+341A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460542 | ||||||
chr12:57460779
|
G | C | 1 | a0001c0001t0001g0006 | 12 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28+578G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460779 | ||||||
chr12:57460863
|
G | A | 1 | a0003c0004t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-28+662G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460863 | ||||||
chr12:57460870
|
A | G | 2 | a0003c0003t0001g0013a0003c0006t0001g0013 | 5 | HG02451.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+669A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460870 | ||||||
chr12:57460879
|
C | T | 1 | a0003c0007t0001g0030 | 2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28+678C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460879 | ||||||
chr12:57460999
|
G | T | 1 | a0003c0007t0001g0030 | 2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28+798G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460999 | ||||||
chr12:57461017
|
C | G | 1 | a0003c0003t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-28+816C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57461017 | ||||||
chr12:57461353
|
C | A | 1 | a0001c0001t0001g0027 | 2 | HG01106.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-28+1152C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57461353 | ||||||
chr12:57461397
|
G | A | 45 | a0001c0001t0001g0047a0001c0011t0001g0041a0002c0002t0001g0002others(42): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.-28+1196G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57461397 | ||||||
chr12:57461887
|
A | T | 2 | a0001c0001t0001g0070a0002c0017t0001g0069 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-28+1686A>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57461887 | ||||||
chr12:57462057
|
CAGCTAGG others(18): Show |
C | 1 | a0016c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-1606_-27-1582d others(27): Show |
GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 57462057 | |||||
chr12:57462084
|
C | G | 7 | a0003c0003t0001g0008a0003c0003t0001g0048a0003c0003t0001g0050others(4): Show | 16 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-27-1581C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462084 | ||||||
chr12:57462192
|
C | A | 1 | a0016c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-1473C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462192 | ||||||
chr12:57462231
|
C | T | 35 | a0001c0001t0001g0047a0001c0011t0001g0041a0002c0002t0001g0002others(32): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.-27-1434C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462231 | ||||||
chr12:57462252
|
G | T | 1 | a0001c0001t0001g0068 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-27-1413G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462252 | ||||||
chr12:57462285
|
T | C | 1 | a0003c0003t0001g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-27-1380T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462285 | ||||||
chr12:57462404
|
T | C | 1 | a0002c0002t0001g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-27-1261T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462404 | ||||||
chr12:57462413
|
GCGCCGGC others(10): Show |
G | 1 | a0003c0003t0001g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-27-1248_-27-1232d others(19): Show |
GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 57462413 | |||||
chr12:57462434
|
T | A | 1 | a0016c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-1231T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462434 | ||||||
chr12:57462710
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0066others(2): Show | 20 | HG01358.hp1 HG01952.hp2 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.-27-955A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462710 | ||||||
chr12:57462849
|
CACTGCAG others(23): Show |
C | 1 | a0014c0022t0001g0065 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-27-815_-27-786del others(30): Show |
GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462849 | ||||||
chr12:57462884
|
G | C | 34 | a0001c0011t0001g0041a0002c0002t0001g0002a0002c0002t0001g0004others(31): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.-27-781G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462884 | ||||||
chr12:57462962
|
C | T | 1 | a0003c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-27-703C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462962 | ||||||
chr12:57462993
|
C | G | 42 | a0001c0011t0001g0041a0002c0002t0001g0002a0002c0002t0001g0004others(39): Show | 166 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.-27-672C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462993 | ||||||
chr12:57463012
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-27-653G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463012 | ||||||
chr12:57463150
|
C | T | 42 | a0001c0011t0001g0041a0002c0002t0001g0002a0002c0002t0001g0004others(39): Show | 166 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.-27-515C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463150 | ||||||
chr12:57463177
|
T | G | 1 | a0016c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-488T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463177 | ||||||
chr12:57463217
|
G | A | 36 | a0001c0011t0001g0041a0002c0002t0001g0002a0002c0002t0001g0004others(33): Show | 158 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.-27-448G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463217 | ||||||
chr12:57463335
|
AGCCTTCC others(6): Show |
A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-27-329_-27-317del others(13): Show |
GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463335 | ||||||
chr12:57463517
|
G | A | 1 | a0001c0001t0001g0011 | 5 | NA18945.hp1 NA18951.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-148G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463517 | ||||||
chr12:57463555
|
T | A | 1 | a0016c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-110T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463555 | ||||||
chr12:57463571
|
T | C | 64 | a0001c0011t0001g0041a0002c0002t0001g0002a0002c0002t0001g0004others(61): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.-27-94T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463571 | ||||||
chr12:57464228
|
C | G | 1 | a0015c0023t0001g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.193+137C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464228 | ||||||
chr12:57464232
|
G | T | 5 | a0003c0003t0001g0008a0003c0003t0001g0013a0003c0003t0001g0082others(2): Show | 16 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+141G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464232 | ||||||
chr12:57464233
|
A | G | 5 | a0003c0003t0001g0008a0003c0003t0001g0013a0003c0003t0001g0082others(2): Show | 16 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+142A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464233 | ||||||
chr12:57464247
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.193+156G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464247 | ||||||
chr12:57464265
|
T | A | 1 | a0016c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.193+174T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464265 | ||||||
chr12:57464290
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.193+199G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464290 | ||||||
chr12:57464305
|
T | A | 3 | a0003c0003t0001g0048a0003c0003t0001g0050a0005c0008t0001g0026 | 4 | HG02257.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+214T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464305 | ||||||
chr12:57464489
|
T | G | 1 | a0003c0003t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.194-184T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464489 | ||||||
chr12:57464525
|
C | CA | 13 | a0001c0001t0001g0028a0002c0002t0001g0024a0002c0002t0004g0072others(10): Show | 23 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-131dupA | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 57464525 | |||||
chr12:57464525
|
CA | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0068a0002c0002t0001g0020others(7): Show | 17 | HG00323.hp1 HG01167.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.194-131delA | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 57464525 | |||||
chr12:57464631
|
A | G | 37 | a0001c0001t0001g0062a0001c0011t0001g0041a0002c0002t0001g0002others(34): Show | 159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.194-42A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464631 | ||||||
chr12:57464638
|
T | C | 5 | a0003c0003t0001g0008a0003c0003t0001g0013a0003c0003t0001g0082others(2): Show | 16 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.194-35T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464638 | ||||||
chr12:57464650
|
G | A | 1 | a0002c0002t0001g0038 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.194-23G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464650 | ||||||
chr12:57464655
|
C | T | 1 | a0001c0001t0011g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.194-18C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464655 | ||||||
chr12:57464656
|
G | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0060a0009c0020t0001g0019 | 5 | HG00673.hp2 NA18941.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-17G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464656 | ||||||
chr12:57464894
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.389+26C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/11 | chr12 | 57464894 | ||||||
chr12:57464950
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.389+82C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/11 | chr12 | 57464950 | ||||||
chr12:57465047
|
A | G | 1 | a0003c0003t0001g0023 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.390-64A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/11 | chr12 | 57465047 | ||||||
chr12:57465052
|
G | A | 36 | a0001c0011t0001g0041a0002c0002t0001g0002a0002c0002t0001g0004others(33): Show | 158 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.390-59G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/11 | chr12 | 57465052 | ||||||
chr12:57465376
|
G | T | 1 | a0002c0002t0001g0044 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.534+121G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 5/11 | chr12 | 57465376 | ||||||
chr12:57465985
|
A | G | 1 | a0001c0001t0001g0012 | 5 | HG02280.hp2 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+60A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/11 | chr12 | 57465985 | ||||||
chr12:57466097
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.763-143T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/11 | chr12 | 57466097 | ||||||
chr12:57466143
|
G | C | 2 | a0002c0002t0001g0022a0002c0002t0001g0025 | 5 | HG01884.hp2 HG02451.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.763-97G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/11 | chr12 | 57466143 | ||||||
chr12:57466149
|
G | A | 40 | a0001c0011t0001g0041a0002c0002t0001g0002a0002c0002t0001g0004others(37): Show | 175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.763-91G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/11 | chr12 | 57466149 | ||||||
chr12:57466593
|
T | C | 8 | a0003c0003t0001g0010a0003c0003t0001g0018a0003c0003t0001g0023others(5): Show | 16 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.912+204T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466593 | ||||||
chr12:57466688
|
G | A | 1 | a0002c0002t0001g0039 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.912+299G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466688 | ||||||
chr12:57466809
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.912+420C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466809 | ||||||
chr12:57466839
|
G | A | 8 | a0003c0003t0001g0016a0003c0003t0001g0032a0003c0003t0001g0036others(5): Show | 24 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.912+450G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466839 | ||||||
chr12:57466861
|
G | A | 1 | a0002c0002t0009g0040 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.912+472G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466861 | ||||||
chr12:57466882
|
C | T | 36 | a0001c0011t0001g0041a0002c0002t0001g0002a0002c0002t0001g0004others(33): Show | 158 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.913-451C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466882 | ||||||
chr12:57466898
|
C | T | 1 | a0005c0008t0001g0026 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.913-435C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466898 | ||||||
chr12:57466913
|
A | T | 9 | a0001c0001t0001g0067a0003c0003t0001g0016a0003c0003t0001g0032others(6): Show | 25 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.913-420A>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466913 | ||||||
chr12:57466914
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.913-419T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466914 | ||||||
chr12:57466921
|
T | A | 2 | a0003c0003t0001g0016a0003c0003t0001g0036 | 5 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-412T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466921 | ||||||
chr12:57466922
|
A | T | 8 | a0003c0003t0001g0010a0003c0003t0001g0018a0003c0003t0001g0023others(5): Show | 16 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.913-411A>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466922 | ||||||
chr12:57466945
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.913-388G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466945 | ||||||
chr12:57467008
|
C | A | 2 | a0002c0002t0004g0072a0002c0002t0004g0073 | 2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.913-325C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467008 | ||||||
chr12:57467027
|
G | A | 2 | a0002c0002t0004g0072a0002c0002t0004g0073 | 2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.913-306G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467027 | ||||||
chr12:57467030
|
C | T | 1 | a0003c0003t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.913-303C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467030 | ||||||
chr12:57467043
|
T | C | 60 | a0001c0001t0001g0062a0001c0011t0001g0041a0002c0002t0001g0002others(57): Show | 220 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.913-290T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467043 | ||||||
chr12:57467088
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.913-245G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467088 | ||||||
chr12:57467124
|
T | C | 1 | a0002c0002t0004g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.913-209T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467124 | ||||||
chr12:57467126
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-207T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467126 | ||||||
chr12:57467130
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-203C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467130 | ||||||
chr12:57467131
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-202A>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467131 | ||||||
chr12:57467134
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-199G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467134 | ||||||
chr12:57467140
|
G | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-193G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467140 | ||||||
chr12:57467142
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-191G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467142 | ||||||
chr12:57467152
|
G | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-181G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467152 | ||||||
chr12:57467156
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-177C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467156 | ||||||
chr12:57467159
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-174T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467159 | ||||||
chr12:57467170
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-163C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467170 | ||||||
chr12:57467172
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-161T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467172 | ||||||
chr12:57467173
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-160G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467173 | ||||||
chr12:57467177
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-156G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467177 | ||||||
chr12:57467178
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-155C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467178 | ||||||
chr12:57467179
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-154C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467179 | ||||||
chr12:57467189
|
T | C | 8 | a0003c0003t0001g0016a0003c0003t0001g0032a0003c0003t0001g0036others(5): Show | 24 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.913-144T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467189 | ||||||
chr12:57467192
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-141T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467192 | ||||||
chr12:57467198
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-135G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467198 | ||||||
chr12:57467199
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-134A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467199 | ||||||
chr12:57467200
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-133A>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467200 | ||||||
chr12:57467207
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-126C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467207 | ||||||
chr12:57467214
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-119C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467214 | ||||||
chr12:57467227
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-106T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467227 | ||||||
chr12:57467228
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-105C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467228 | ||||||
chr12:57467234
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-99T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467234 | ||||||
chr12:57467236
|
A | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-97A>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467236 | ||||||
chr12:57467237
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-96T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467237 | ||||||
chr12:57467238
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-95A>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467238 | ||||||
chr12:57467536
|
G | C | 2 | a0004c0005t0002g0007a0004c0005t0002g0077 | 12 | HG00544.hp1 HG02015.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1077+39G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467536 | ||||||
chr12:57467558
|
C | T | 1 | a0002c0002t0002g0029 | 2 | NA18971.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1077+61C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467558 | ||||||
chr12:57467621
|
C | T | 1 | a0002c0002t0001g0017 | 4 | NA18944.hp1 NA18960.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+124C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467621 | ||||||
chr12:57467701
|
A | G | 62 | a0001c0001t0001g0062a0002c0002t0001g0002a0002c0002t0001g0004others(59): Show | 233 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1077+204A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467701 | ||||||
chr12:57467875
|
C | A | 1 | a0003c0003t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1078-119C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467875 | ||||||
chr12:57468443
|
C | T | 1 | a0003c0004t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1308+219C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57468443 | ||||||
chr12:57468823
|
C | T | 7 | a0003c0003t0001g0010a0003c0003t0001g0018a0003c0003t0001g0031others(4): Show | 14 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1308+599C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57468823 | ||||||
chr12:57469134
|
T | G | 10 | a0003c0003t0001g0013a0003c0003t0001g0016a0003c0003t0001g0032others(7): Show | 29 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1309-297T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469134 | ||||||
chr12:57469171
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1309-260C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469171 | ||||||
chr12:57469233
|
T | C | 1 | a0002c0002t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1309-198T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469233 | ||||||
chr12:57469293
|
T | G | 1 | a0002c0002t0001g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1309-138T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469293 | ||||||
chr12:57469353
|
G | A | 1 | a0002c0002t0001g0043 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1309-78G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469353 | ||||||
chr12:57470015
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1577-302C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 11/11 | chr12 | 57470015 |