geneid | 3658 |
---|---|
ensemblid | ENSG00000136381.13 |
hgncid | 6115 |
symbol | IREB2 |
name | iron responsive element binding protein 2 |
refseq_nuc | NM_004136.4 |
refseq_prot | NP_004127.2 |
ensembl_nuc | ENST00000258886.13 |
ensembl_prot | ENSP00000258886.8 |
mane_status | MANE Select |
chr | chr15 |
start | 78438216 |
end | 78501453 |
strand | + |
ver | v1.2 |
region | chr15:78438216-78501453 |
region5000 | chr15:78433216-78506453 |
regionname0 | IREB2_chr15_78438216_78501453 |
regionname5000 | IREB2_chr15_78433216_78506453 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 963 | 405 | 79 | 65 | 204 | 14 | 42 | 162 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0002 | 0/0 | 963 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0003 | 0/0 | 963 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0004 | 0/0 | 963 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0005 | 1/0 | 963 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0006 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2892 | 240 | 52 | 33 | 124 | 6 | 25 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0002 | 0/1 | 2892 | 151 | 22 | 31 | 72 | 8 | 17 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0003 | 0/0 | 2892 | 7 | 6 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0004 | 0/0 | 2892 | 6 | 0 | 0 | 6 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0005 | 0/0 | 2892 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0006 | 0/0 | 2892 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0007 | 0/0 | 2892 | 2 | 0 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0008 | 0/0 | 2892 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0009 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0010 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0011 | 1/0 | 2892 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
c0012 | 0/0 | 2892 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
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 | 0/0 | 3432 | 97 | 10 | 20 | 50 | 3 | 14 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0002 | 0/0 | 3432 | 65 | 12 | 10 | 34 | 2 | 7 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0003 | 0/0 | 3431 | 59 | 2 | 12 | 39 | 2 | 4 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0004 | 0/0 | 3431 | 41 | 15 | 2 | 19 | 1 | 4 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0005 | 0/1 | 3429 | 32 | 1 | 11 | 7 | 4 | 8 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0006 | 0/0 | 3432 | 18 | 16 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0007 | 0/0 | 3431 | 12 | 0 | 0 | 12 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0008 | 0/0 | 3426 | 9 | 0 | 0 | 9 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0009 | 0/0 | 3431 | 8 | 8 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0010 | 1/0 | 3433 | 8 | 6 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0011 | 0/0 | 3439 | 5 | 2 | 1 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0012 | 0/0 | 3430 | 4 | 2 | 1 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0013 | 0/0 | 3431 | 4 | 0 | 0 | 3 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0014 | 0/0 | 3433 | 4 | 0 | 0 | 2 | 0 | 2 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0015 | 0/0 | 3432 | 4 | 0 | 0 | 4 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0016 | 0/0 | 3433 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0017 | 0/0 | 3430 | 3 | 0 | 2 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0018 | 0/0 | 3431 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0019 | 0/0 | 3432 | 3 | 0 | 2 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0020 | 0/0 | 3432 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0021 | 0/0 | 3432 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0022 | 0/0 | 3432 | 2 | 1 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0023 | 0/0 | 3430 | 2 | 0 | 1 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0024 | 0/0 | 3433 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0025 | 0/0 | 3432 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0026 | 0/0 | 3432 | 2 | 0 | 1 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0027 | 0/0 | 3432 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0028 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0029 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0030 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0031 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0032 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0033 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0034 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0035 | 0/0 | 3431 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0036 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0037 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0038 | 0/0 | 3431 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0039 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0040 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0041 | 0/0 | 3431 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0042 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0043 | 0/0 | 3431 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0044 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0045 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0046 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0047 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0048 | 0/0 | 3431 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
t0049 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 6 | 2 | 0 | 2 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0015 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0023 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0300 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0367 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2892 | 240 | 52 | 33 | 124 | 6 | 25 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002 | 0/1 | 2892 | 151 | 22 | 31 | 72 | 8 | 17 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0004 | 0/0 | 2892 | 6 | 0 | 0 | 6 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0006 | 0/0 | 2892 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0008 | 0/0 | 2892 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0009 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0012 | 0/0 | 2892 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0002c0003 | 0/0 | 2892 | 7 | 6 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0003c0005 | 0/0 | 2892 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0004c0007 | 0/0 | 2892 | 2 | 0 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0005c0011 | 1/0 | 2892 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0006c0010 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6323 | 94 | 9 | 19 | 49 | 3 | 14 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0002 | 0/0 | 6323 | 65 | 12 | 10 | 34 | 2 | 7 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0004 | 0/0 | 6322 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0006 | 0/0 | 6323 | 18 | 16 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0007 | 0/0 | 6322 | 12 | 0 | 0 | 12 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0008 | 0/0 | 6317 | 9 | 0 | 0 | 9 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0009 | 0/0 | 6322 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0011 | 0/0 | 6330 | 5 | 2 | 1 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0013 | 0/0 | 6322 | 4 | 0 | 0 | 3 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0014 | 0/0 | 6324 | 4 | 0 | 0 | 2 | 0 | 2 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0016 | 0/0 | 6324 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0018 | 0/0 | 6322 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0019 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0020 | 0/0 | 6323 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0021 | 0/0 | 6323 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0027 | 0/0 | 6323 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0030 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0031 | 0/0 | 6322 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0032 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0033 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0034 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0035 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0042 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0044 | 0/0 | 6323 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0046 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0047 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0048 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0001t0049 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0003 | 0/0 | 6322 | 57 | 2 | 12 | 37 | 2 | 4 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0004 | 0/0 | 6322 | 39 | 14 | 2 | 19 | 1 | 3 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0005 | 0/1 | 6320 | 32 | 1 | 11 | 7 | 4 | 8 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0012 | 0/0 | 6321 | 4 | 2 | 1 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0017 | 0/0 | 6321 | 3 | 0 | 2 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0022 | 0/0 | 6323 | 2 | 1 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0023 | 0/0 | 6321 | 2 | 0 | 1 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0026 | 0/0 | 6323 | 2 | 0 | 1 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0028 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0029 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0036 | 0/0 | 6322 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0037 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0038 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0039 | 0/0 | 6322 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0040 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0041 | 0/0 | 6322 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0043 | 0/0 | 6322 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0002t0045 | 0/0 | 6322 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0004t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0004t0015 | 0/0 | 6323 | 4 | 0 | 0 | 4 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0004t0016 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0006t0024 | 0/0 | 6324 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0006t0025 | 0/0 | 6323 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0008t0003 | 0/0 | 6322 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0009t0004 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0001c0012t0001 | 0/0 | 6323 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0002c0003t0010 | 0/0 | 6324 | 7 | 6 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0003c0005t0009 | 0/0 | 6322 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0004c0007t0019 | 0/0 | 6323 | 2 | 0 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0005c0011t0010 | 1/0 | 6324 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
a0006c0010t0001 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | copy fasta | chr15 | 78433216 | 78506453 |
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 | 10 | 0 | 6 | 2 | 0 | 2 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0023 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0006g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0007g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0008g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0008g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0008g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0008g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0008g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0008g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0008g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0009g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0011g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0011g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0013g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0013g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0013g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0013g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0014g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0014g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0014g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0016g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0016g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0018g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0018g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0018g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0019g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0020g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0020g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0021g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0021g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0027g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0027g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0030g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0031g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0032g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0033g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0034g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0035g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0042g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0044g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0046g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0047g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0048g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0001t0049g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0003g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0004g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0367 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0005g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0012g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0012g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0017g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0017g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0017g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0022g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0022g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0023g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0023g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0026g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0026g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0028g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0029g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0036g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0037g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0038g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0039g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0040g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0041g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0043g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0002t0045g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0004t0015g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0004t0015g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0004t0015g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0004t0015g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0004t0016g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0006t0024g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0006t0024g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0006t0025g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0006t0025g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0008t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0008t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0009t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0001c0012t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0002c0003t0010g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0002c0003t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0002c0003t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0002c0003t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0002c0003t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0002c0003t0010g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0003c0005t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0003c0005t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0003c0005t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0003c0005t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0004c0007t0019g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0004c0007t0019g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0005c0011t0010g0300 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
a0006c0010t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00099 | hp2 | a0001 | c0002 | t0005 | g0343 | EUR | GBR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00280 | hp1 | a0001 | c0002 | t0004 | g0167 | EUR | FIN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0219 | EUR | FIN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00323 | hp1 | a0001 | c0002 | t0017 | g0221 | EUR | FIN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00323 | hp2 | a0001 | c0002 | t0005 | g0372 | EUR | FIN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00408 | hp1 | a0001 | c0002 | t0005 | g0345 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00408 | hp2 | a0001 | c0001 | t0007 | g0322 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00423 | hp1 | a0001 | c0002 | t0004 | g0159 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00438 | hp1 | a0001 | c0002 | t0004 | g0197 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00544 | hp1 | a0001 | c0002 | t0003 | g0227 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00544 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00558 | hp1 | a0001 | c0002 | t0045 | g0239 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00597 | hp1 | a0001 | c0001 | t0016 | g0058 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0229 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0204 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00609 | hp2 | a0001 | c0002 | t0005 | g0344 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00639 | hp1 | a0001 | c0002 | t0005 | g0354 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00639 | hp2 | a0001 | c0002 | t0017 | g0212 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0210 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00673 | hp2 | a0001 | c0001 | t0030 | g0028 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00733 | hp2 | a0001 | c0002 | t0003 | g0215 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00735 | hp2 | a0001 | c0002 | t0003 | g0106 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00738 | hp1 | a0001 | c0002 | t0005 | g0357 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG00741 | hp2 | a0001 | c0002 | t0012 | g0027 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0226 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01070 | hp2 | a0001 | c0002 | t0043 | g0377 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01081 | hp1 | a0001 | c0002 | t0005 | g0006 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01081 | hp2 | a0001 | c0002 | t0017 | g0216 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01099 | hp1 | a0001 | c0002 | t0005 | g0368 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01099 | hp2 | a0001 | c0012 | t0001 | g0104 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01106 | hp1 | a0001 | c0002 | t0005 | g0006 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01106 | hp2 | a0001 | c0002 | t0003 | g0224 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01109 | hp1 | a0002 | c0003 | t0010 | g0012 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01109 | hp2 | a0001 | c0002 | t0005 | g0353 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01169 | hp1 | a0001 | c0002 | t0005 | g0347 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01175 | hp2 | a0001 | c0002 | t0023 | g0350 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01192 | hp1 | a0001 | c0002 | t0005 | g0369 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01192 | hp2 | a0001 | c0002 | t0003 | g0225 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01243 | hp2 | a0001 | c0002 | t0004 | g0147 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01255 | hp1 | a0001 | c0002 | t0004 | g0153 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01261 | hp1 | a0004 | c0007 | t0019 | g0294 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01346 | hp1 | a0001 | c0002 | t0005 | g0027 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01361 | hp1 | a0001 | c0002 | t0005 | g0373 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01496 | hp1 | a0001 | c0001 | t0011 | g0132 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01496 | hp2 | a0004 | c0007 | t0019 | g0293 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0253 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0021 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01516 | hp2 | a0001 | c0002 | t0005 | g0359 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01884 | hp1 | a0001 | c0002 | t0012 | g0169 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01884 | hp2 | a0001 | c0002 | t0005 | g0360 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01891 | hp1 | a0001 | c0002 | t0004 | g0361 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01891 | hp2 | a0001 | c0002 | t0004 | g0016 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01928 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01934 | hp2 | a0001 | c0002 | t0026 | g0238 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0237 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01981 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0199 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02004 | hp2 | a0001 | c0001 | t0044 | g0295 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02015 | hp1 | a0001 | c0002 | t0003 | g0213 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02027 | hp1 | a0001 | c0002 | t0005 | g0370 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02027 | hp2 | a0001 | c0002 | t0012 | g0154 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0108 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0015 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02056 | hp1 | a0001 | c0002 | t0003 | g0209 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02074 | hp1 | a0001 | c0001 | t0007 | g0324 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02074 | hp2 | a0001 | c0001 | t0027 | g0264 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02080 | hp1 | a0001 | c0002 | t0026 | g0203 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0334 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0228 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0158 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02132 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02135 | hp1 | a0001 | c0001 | t0016 | g0044 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02145 | hp1 | a0002 | c0003 | t0010 | g0127 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0155 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02165 | hp2 | a0001 | c0002 | t0003 | g0201 | EAS | CDX | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02257 | hp1 | a0002 | c0003 | t0010 | g0130 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02258 | hp2 | a0001 | c0001 | t0035 | g0009 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02280 | hp1 | a0006 | c0010 | t0001 | g0297 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02280 | hp2 | a0001 | c0002 | t0004 | g0146 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02451 | hp1 | a0001 | c0001 | t0009 | g0179 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0114 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02615 | hp1 | a0001 | c0001 | t0046 | g0002 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0178 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02630 | hp1 | a0001 | c0006 | t0025 | g0120 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02683 | hp1 | a0001 | c0002 | t0003 | g0233 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02698 | hp2 | a0001 | c0002 | t0005 | g0371 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0112 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02738 | hp1 | a0001 | c0001 | t0014 | g0055 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02738 | hp2 | a0001 | c0002 | t0003 | g0241 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02818 | hp1 | a0001 | c0002 | t0028 | g0138 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02818 | hp2 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02886 | hp1 | a0001 | c0001 | t0048 | g0117 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02886 | hp2 | a0003 | c0005 | t0009 | g0180 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02895 | hp1 | a0001 | c0001 | t0020 | g0124 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02895 | hp2 | a0003 | c0005 | t0009 | g0183 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0165 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02897 | hp1 | a0001 | c0001 | t0020 | g0125 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0149 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02965 | hp2 | a0003 | c0005 | t0009 | g0181 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02970 | hp2 | a0001 | c0002 | t0004 | g0157 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02976 | hp1 | a0001 | c0006 | t0024 | g0122 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0113 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03098 | hp1 | a0001 | c0002 | t0004 | g0173 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03130 | hp1 | a0001 | c0006 | t0024 | g0123 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03139 | hp1 | a0003 | c0005 | t0009 | g0182 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03139 | hp2 | a0001 | c0006 | t0025 | g0121 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03209 | hp1 | a0002 | c0003 | t0010 | g0129 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03225 | hp2 | a0001 | c0002 | t0004 | g0164 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03453 | hp1 | a0001 | c0001 | t0032 | g0008 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0134 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03486 | hp2 | a0002 | c0003 | t0010 | g0126 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03491 | hp1 | a0001 | c0002 | t0041 | g0235 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03491 | hp2 | a0001 | c0002 | t0004 | g0017 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03492 | hp2 | a0001 | c0002 | t0004 | g0017 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03540 | hp1 | a0001 | c0009 | t0004 | g0016 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03654 | hp2 | a0001 | c0002 | t0005 | g0366 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03704 | hp2 | a0001 | c0002 | t0005 | g0348 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03710 | hp1 | a0001 | c0002 | t0005 | g0355 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0223 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0103 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03834 | hp1 | a0001 | c0001 | t0013 | g0332 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0313 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03942 | hp2 | a0001 | c0002 | t0040 | g0236 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04115 | hp2 | a0001 | c0002 | t0005 | g0358 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04184 | hp1 | a0001 | c0002 | t0005 | g0356 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04184 | hp2 | a0001 | c0001 | t0014 | g0063 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04199 | hp1 | a0001 | c0002 | t0005 | g0365 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04228 | hp1 | a0001 | c0002 | t0004 | g0162 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0283 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18612 | hp1 | a0001 | c0002 | t0005 | g0349 | EAS | CHB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0222 | EAS | CHB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18747 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | CHB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0109 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18906 | hp2 | a0001 | c0002 | t0004 | g0168 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18939 | hp1 | a0001 | c0001 | t0007 | g0325 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18939 | hp2 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18941 | hp1 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18942 | hp1 | a0001 | c0002 | t0036 | g0015 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18942 | hp2 | a0001 | c0001 | t0008 | g0321 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18943 | hp1 | a0001 | c0001 | t0007 | g0323 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18943 | hp2 | a0001 | c0001 | t0014 | g0033 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18945 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18947 | hp1 | a0001 | c0001 | t0013 | g0329 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18948 | hp2 | a0001 | c0008 | t0003 | g0218 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18949 | hp1 | a0001 | c0002 | t0029 | g0140 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18950 | hp1 | a0001 | c0001 | t0014 | g0086 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18950 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18951 | hp2 | a0001 | c0002 | t0004 | g0160 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18952 | hp1 | a0001 | c0001 | t0018 | g0327 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18954 | hp2 | a0001 | c0002 | t0039 | g0202 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18956 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18957 | hp1 | a0001 | c0008 | t0003 | g0217 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18959 | hp1 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0336 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18962 | hp1 | a0001 | c0002 | t0003 | g0242 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18967 | hp1 | a0001 | c0002 | t0003 | g0232 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18968 | hp1 | a0001 | c0001 | t0008 | g0025 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18968 | hp2 | a0001 | c0002 | t0004 | g0139 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18969 | hp2 | a0001 | c0002 | t0004 | g0171 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18970 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18971 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18972 | hp1 | a0001 | c0001 | t0013 | g0331 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18972 | hp2 | a0001 | c0001 | t0008 | g0317 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18973 | hp2 | a0001 | c0002 | t0003 | g0205 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18975 | hp1 | a0001 | c0001 | t0008 | g0315 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18975 | hp2 | a0001 | c0001 | t0011 | g0135 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18977 | hp2 | a0001 | c0001 | t0018 | g0328 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18978 | hp2 | a0001 | c0004 | t0015 | g0099 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18980 | hp1 | a0001 | c0002 | t0004 | g0143 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18981 | hp2 | a0001 | c0002 | t0005 | g0364 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18982 | hp1 | a0001 | c0004 | t0015 | g0039 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18983 | hp1 | a0001 | c0002 | t0004 | g0166 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18983 | hp2 | a0001 | c0001 | t0007 | g0335 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18989 | hp1 | a0001 | c0001 | t0021 | g0338 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18990 | hp1 | a0001 | c0002 | t0004 | g0142 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18991 | hp1 | a0001 | c0001 | t0008 | g0320 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18992 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18997 | hp1 | a0001 | c0004 | t0001 | g0093 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0144 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19003 | hp1 | a0001 | c0001 | t0031 | g0072 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19005 | hp1 | a0001 | c0001 | t0018 | g0326 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19005 | hp2 | a0001 | c0001 | t0042 | g0136 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19007 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19007 | hp2 | a0001 | c0002 | t0004 | g0151 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19009 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19009 | hp2 | a0001 | c0002 | t0004 | g0141 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19010 | hp1 | a0001 | c0002 | t0003 | g0240 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19012 | hp1 | a0001 | c0002 | t0004 | g0152 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19012 | hp2 | a0001 | c0001 | t0008 | g0316 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19030 | hp1 | a0001 | c0002 | t0004 | g0156 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19030 | hp2 | a0001 | c0001 | t0049 | g0118 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0148 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19054 | hp1 | a0001 | c0001 | t0007 | g0340 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19054 | hp2 | a0001 | c0004 | t0016 | g0094 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19055 | hp1 | a0001 | c0002 | t0005 | g0363 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19057 | hp2 | a0001 | c0001 | t0011 | g0133 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19058 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19064 | hp1 | a0001 | c0001 | t0007 | g0333 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19066 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19067 | hp1 | a0001 | c0001 | t0008 | g0318 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19067 | hp2 | a0001 | c0002 | t0037 | g0161 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19068 | hp2 | a0001 | c0002 | t0003 | g0231 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19072 | hp2 | a0001 | c0002 | t0003 | g0341 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19074 | hp1 | a0001 | c0002 | t0004 | g0234 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19074 | hp2 | a0001 | c0001 | t0027 | g0245 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19076 | hp1 | a0001 | c0001 | t0033 | g0035 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19076 | hp2 | a0001 | c0002 | t0023 | g0362 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19078 | hp1 | a0001 | c0002 | t0022 | g0163 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19079 | hp1 | a0001 | c0002 | t0004 | g0170 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19079 | hp2 | a0001 | c0001 | t0008 | g0319 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19081 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19082 | hp1 | a0001 | c0004 | t0015 | g0100 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19082 | hp2 | a0001 | c0002 | t0003 | g0211 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19083 | hp1 | a0001 | c0004 | t0015 | g0098 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19084 | hp2 | a0001 | c0001 | t0007 | g0339 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19085 | hp2 | a0001 | c0001 | t0007 | g0337 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19087 | hp1 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19087 | hp2 | a0001 | c0001 | t0021 | g0026 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19088 | hp2 | a0001 | c0001 | t0008 | g0025 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19090 | hp2 | a0001 | c0001 | t0013 | g0330 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19091 | hp1 | a0001 | c0002 | t0005 | g0346 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA19240 | hp2 | a0002 | c0003 | t0010 | g0128 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ASW | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0150 | AFR | ASW | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA20805 | hp1 | a0001 | c0001 | t0019 | g0292 | EUR | TSI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA20805 | hp2 | a0001 | c0002 | t0005 | g0006 | EUR | TSI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA20905 | hp2 | a0001 | c0002 | t0005 | g0374 | SAS | GIH | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01123 | hp1 | a0001 | c0002 | t0005 | g0351 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0220 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02109 | hp2 | a0001 | c0001 | t0034 | g0119 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02486 | hp1 | a0001 | c0002 | t0022 | g0145 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02486 | hp2 | a0001 | c0002 | t0038 | g0352 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0184 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0378 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | USA | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | USA | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA20300 | hp1 | a0001 | c0002 | t0012 | g0172 | AFR | USA | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA20300 | hp2 | a0002 | c0003 | t0010 | g0012 | AFR | USA | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA21309 | hp1 | a0001 | c0001 | t0047 | g0116 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0376 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0005 | g0367 | REF | REF | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
homoSapiens_grch38 | hp1 | a0005 | c0011 | t0010 | g0300 | REF | REF | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:78466335
|
C | G | 1 | a0002 | 7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
missense_variant | MODERATE | c.475C>G | p.Leu159Val | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/22 | 597/6324 | 475/2892 | 159/963 | chr15 | 78466335 | ||
chr15:78487762
|
T | C | 4 | a0001a0003a0004others(1): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
missense_variant | MODERATE | c.1739T>C | p.Ile580Thr | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 14/22 | 1861/6324 | 1739/2892 | 580/963 | chr15 | 78487762 | ||
chr15:78490631
|
A | G | 1 | a0006 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.2194A>G | p.Ile732Val | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/22 | 2316/6324 | 2194/2892 | 732/963 | chr15 | 78490631 | ||
chr15:78490631
|
A | T | 1 | a0003 | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.2194A>T | p.Ile732Phe | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/22 | 2316/6324 | 2194/2892 | 732/963 | chr15 | 78490631 | ||
chr15:78497192
|
A | G | 1 | a0004 | 2 | HG01261.hp1 HG01496.hp2 |
missense_variant | MODERATE | c.2662A>G | p.Ile888Val | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/22 | 2784/6324 | 2662/2892 | 888/963 | chr15 | 78497192 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:78471825
|
A | C | 1 | a0001c0008 | 2 | NA18948.hp2 NA18957.hp1 |
synonymous_variant | LOW | c.784A>C | p.Arg262Arg | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/22 | 906/6324 | 784/2892 | 262/963 | chr15 | 78471825 | ||
chr15:78471845
|
A | G | 1 | a0001c0006 | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.804A>G | p.Lys268Lys | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/22 | 926/6324 | 804/2892 | 268/963 | chr15 | 78471845 | ||
chr15:78478316
|
C | T | 1 | a0001c0012 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.1215C>T | p.Leu405Leu | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/22 | 1337/6324 | 1215/2892 | 405/963 | chr15 | 78478316 | ||
chr15:78484844
|
G | A | 1 | a0001c0004 | 6 | NA18978.hp2 NA18982.hp1 NA18997.hp1 others(3): Show |
synonymous_variant | LOW | c.1497G>A | p.Leu499Leu | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/22 | 1619/6324 | 1497/2892 | 499/963 | chr15 | 78484844 | ||
chr15:78497146
|
C | T | 3 | a0001c0002a0001c0008a0001c0009 | 154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
synonymous_variant | LOW | c.2616C>T | p.Ala872Ala | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/22 | 2738/6324 | 2616/2892 | 872/963 | chr15 | 78497146 | ||
chr15:78497299
|
A | C | 1 | a0001c0009 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.2769A>C | p.Thr923Thr | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/22 | 2891/6324 | 2769/2892 | 923/963 | chr15 | 78497299 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:78438217
|
A | G | 3 | a0001c0001t0047a0001c0001t0048a0001c0001t0049 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-121A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | 121 | chr15 | 78438217 | |||||
chr15:78438227
|
C | T | 1 | a0001c0001t0046 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | 111 | chr15 | 78438227 | |||||
chr15:78438249
|
C | T | 16 | a0001c0001t0002a0001c0001t0018a0001c0001t0019others(13): Show | 144 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(141): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-89C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | chr15 | 78438249 | ||||||
chr15:78438265
|
C | A | 1 | a0001c0002t0039 | 1 | NA18954.hp2 | 5_prime_UTR_variant | MODIFIER | c.-73C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | 73 | chr15 | 78438265 | |||||
chr15:78438330
|
C | T | 1 | a0001c0004t0015 | 4 | NA18978.hp2 NA18982.hp1 NA19082.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | 8 | chr15 | 78438330 | |||||
chr15:78498393
|
TG | T | 44 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(41): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*260delG | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 260 | INFO_REALIGN_3_PRIME | chr15 | 78498393 | ||||
chr15:78498394
|
G | T | 1 | a0001c0001t0027 | 2 | HG02074.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*251G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 251 | chr15 | 78498394 | |||||
chr15:78498397
|
G | T | 1 | a0001c0002t0045 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 254 | chr15 | 78498397 | |||||
chr15:78498430
|
A | G | 1 | a0001c0002t0036 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 287 | chr15 | 78498430 | |||||
chr15:78498499
|
A | G | 6 | a0001c0001t0007a0001c0001t0009a0001c0001t0013others(3): Show | 29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*356A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 356 | chr15 | 78498499 | |||||
chr15:78498708
|
G | A | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(51): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
3_prime_UTR_variant | MODIFIER | c.*565G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 565 | chr15 | 78498708 | |||||
chr15:78498719
|
C | T | 5 | a0001c0001t0002a0001c0001t0019a0001c0001t0027others(2): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*576C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 576 | chr15 | 78498719 | |||||
chr15:78499225
|
A | G | 1 | a0001c0001t0034 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1082A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1082 | chr15 | 78499225 | |||||
chr15:78499390
|
G | A | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(51): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
3_prime_UTR_variant | MODIFIER | c.*1247G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1247 | chr15 | 78499390 | |||||
chr15:78499509
|
G | A | 3 | a0001c0001t0047a0001c0001t0048a0001c0001t0049 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1366G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1366 | chr15 | 78499509 | |||||
chr15:78499569
|
A | G | 1 | a0001c0001t0044 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1426A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1426 | chr15 | 78499569 | |||||
chr15:78499658
|
G | A | 3 | a0001c0001t0006a0001c0001t0035a0001c0001t0046 | 20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1515G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1515 | chr15 | 78499658 | |||||
chr15:78499679
|
C | G | 1 | a0001c0001t0046 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1536C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1536 | chr15 | 78499679 | |||||
chr15:78499757
|
A | G | 1 | a0001c0001t0033 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1614A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1614 | chr15 | 78499757 | |||||
chr15:78499876
|
C | T | 1 | a0001c0001t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1733C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1733 | chr15 | 78499876 | |||||
chr15:78499909
|
A | G | 1 | a0001c0002t0043 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1766A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1766 | chr15 | 78499909 | |||||
chr15:78500056
|
T | C | 21 | a0001c0001t0004a0001c0002t0003a0001c0002t0004others(18): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*1913T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1913 | chr15 | 78500056 | |||||
chr15:78500097
|
G | A | 13 | a0001c0001t0001a0001c0001t0014a0001c0001t0016others(10): Show | 113 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1954G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1954 | chr15 | 78500097 | |||||
chr15:78500145
|
C | T | 1 | a0001c0001t0011 | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2002C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2002 | chr15 | 78500145 | |||||
chr15:78500185
|
T | C | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(20): Show | 192 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*2042T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2042 | chr15 | 78500185 | |||||
chr15:78500186
|
G | T | 2 | a0001c0001t0019a0004c0007t0019 | 3 | HG01261.hp1 HG01496.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2043G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2043 | chr15 | 78500186 | |||||
chr15:78500355
|
A | G | 2 | a0001c0002t0040a0001c0002t0041 | 2 | HG03491.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2212A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2212 | chr15 | 78500355 | |||||
chr15:78500538
|
C | CA | 5 | a0001c0001t0016a0001c0001t0034a0001c0001t0049others(2): Show | 6 | HG00597.hp1 HG02109.hp2 HG02135.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2414dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2415 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | ||||
chr15:78500538
|
CA | C | 26 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(23): Show | 215 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*2414delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2414 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | ||||
chr15:78500538
|
CAA | C | 3 | a0001c0002t0012a0001c0002t0017a0001c0002t0038 | 8 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2413_*2414delAA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2413 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | ||||
chr15:78500538
|
CAAA | C | 2 | a0001c0002t0005a0001c0002t0023 | 34 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2412_*2414delAAA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2412 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | ||||
chr15:78500538
|
CAAAAAA | C | 1 | a0001c0001t0008 | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2409_*2414delAAAA others(2): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2409 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | ||||
chr15:78500552
|
A | G | 4 | a0001c0001t0007a0001c0001t0013a0001c0001t0018others(1): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2409A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2409 | chr15 | 78500552 | |||||
chr15:78500561
|
A | AGTGTAAT others(1): Show |
1 | a0001c0001t0011 | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2419_*2426dupGTGT others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2427 | INFO_REALIGN_3_PRIME | chr15 | 78500561 | ||||
chr15:78500629
|
C | T | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(51): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
3_prime_UTR_variant | MODIFIER | c.*2486C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2486 | chr15 | 78500629 | |||||
chr15:78500659
|
G | A | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(54): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
3_prime_UTR_variant | MODIFIER | c.*2516G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2516 | chr15 | 78500659 | |||||
chr15:78500673
|
A | G | 1 | a0001c0001t0013 | 4 | HG03834.hp1 NA18947.hp1 NA18972.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2530A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2530 | chr15 | 78500673 | |||||
chr15:78500743
|
C | A | 4 | a0001c0001t0007a0001c0001t0013a0001c0001t0018others(1): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2600C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2600 | chr15 | 78500743 | |||||
chr15:78500745
|
A | T | 1 | a0001c0001t0030 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2602A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2602 | chr15 | 78500745 | |||||
chr15:78500767
|
T | C | 5 | a0001c0001t0002a0001c0001t0019a0001c0001t0027others(2): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2624T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2624 | chr15 | 78500767 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:78438627
|
C | G | 1 | a0001c0001t0006g0378 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19+271C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438627 | ||||||
chr15:78438656
|
C | T | 1 | a0001c0002t0043g0377 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.19+300C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438656 | ||||||
chr15:78438679
|
G | A | 1 | a0001c0001t0030g0028 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.19+323G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438679 | ||||||
chr15:78438709
|
C | G | 1 | a0001c0002t0003g0376 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19+353C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438709 | ||||||
chr15:78438753
|
C | T | 1 | a0001c0001t0001g0375 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.19+397C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438753 | ||||||
chr15:78438807
|
C | T | 35 | a0001c0002t0004g0361a0001c0002t0005g0006a0001c0002t0005g0027others(32): Show | 37 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.19+451C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438807 | ||||||
chr15:78438853
|
A | T | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.19+497A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438853 | ||||||
chr15:78438918
|
C | CA | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 98 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.19+575dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr15 | 78438918 | |||||
chr15:78438918
|
CA | C | 22 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(19): Show | 22 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.19+575delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr15 | 78438918 | |||||
chr15:78438946
|
A | G | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+590A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438946 | ||||||
chr15:78439095
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.20-700C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439095 | ||||||
chr15:78439233
|
C | T | 2 | a0001c0002t0003g0106a0001c0002t0003g0313 | 2 | HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.20-562C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439233 | ||||||
chr15:78439398
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.20-397C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439398 | ||||||
chr15:78439419
|
C | T | 1 | a0001c0012t0001g0104 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20-376C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439419 | ||||||
chr15:78439466
|
T | A | 282 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(279): Show | 305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.20-329T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439466 | ||||||
chr15:78439668
|
A | G | 21 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0277others(18): Show | 23 | HG01074.hp2 HG01255.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.20-127A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439668 | ||||||
chr15:78440168
|
G | A | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.106+287G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440168 | ||||||
chr15:78440191
|
T | C | 16 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+310T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440191 | ||||||
chr15:78440370
|
C | CT | 137 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(134): Show | 149 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.106+500dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78440370 | |||||
chr15:78440412
|
A | G | 283 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(280): Show | 306 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.106+531A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440412 | ||||||
chr15:78440533
|
A | G | 3 | a0001c0002t0005g0371a0001c0002t0005g0372a0001c0002t0005g0373 | 3 | HG00323.hp2 HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.106+652A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440533 | ||||||
chr15:78440555
|
T | C | 1 | a0001c0001t0047g0116 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+674T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440555 | ||||||
chr15:78440736
|
A | G | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+855A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440736 | ||||||
chr15:78440798
|
C | A | 1 | a0001c0001t0002g0278 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.106+917C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440798 | ||||||
chr15:78441048
|
A | T | 78 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(75): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.106+1167A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441048 | ||||||
chr15:78441239
|
AAC | A | 37 | a0001c0001t0002g0022a0001c0001t0002g0029a0001c0001t0002g0244others(34): Show | 38 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.106+1360_106+1361d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78441239 | |||||
chr15:78441389
|
T | C | 78 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(75): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.106+1508T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441389 | ||||||
chr15:78441474
|
T | C | 1 | a0001c0002t0028g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.106+1593T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441474 | ||||||
chr15:78441514
|
ATAAAT | A | 8 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0139others(5): Show | 10 | NA18944.hp1 NA18949.hp1 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+1638_106+1642d others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78441514 | |||||
chr15:78441712
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 6 | HG00423.hp2 HG02056.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+1831G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441712 | ||||||
chr15:78441916
|
T | C | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2035T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441916 | ||||||
chr15:78441950
|
A | G | 133 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(130): Show | 144 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.106+2069A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441950 | ||||||
chr15:78441954
|
T | C | 1 | a0001c0002t0005g0343 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.106+2073T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441954 | ||||||
chr15:78441980
|
C | A | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+2099C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441980 | ||||||
chr15:78441997
|
C | G | 21 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(18): Show | 25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.106+2116C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441997 | ||||||
chr15:78442243
|
A | G | 78 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(75): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.106+2362A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442243 | ||||||
chr15:78442246
|
ATTAC | A | 78 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(75): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.106+2369_106+2372d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78442246 | |||||
chr15:78442415
|
G | T | 1 | a0001c0002t0003g0137 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.106+2534G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442415 | ||||||
chr15:78442463
|
C | T | 1 | a0001c0002t0005g0370 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.106+2582C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442463 | ||||||
chr15:78442491
|
T | A | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.106+2610T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442491 | ||||||
chr15:78442546
|
C | T | 1 | a0001c0001t0044g0295 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.106+2665C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442546 | ||||||
chr15:78442582
|
T | C | 1 | a0001c0001t0007g0322 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.106+2701T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442582 | ||||||
chr15:78442667
|
C | G | 380 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(377): Show | 415 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(412): Show |
intron_variant | MODIFIER | c.106+2786C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442667 | ||||||
chr15:78442728
|
A | C | 133 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(130): Show | 144 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.106+2847A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442728 | ||||||
chr15:78442758
|
C | T | 6 | a0002c0003t0010g0012a0002c0003t0010g0126a0002c0003t0010g0127others(3): Show | 7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+2877C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442758 | ||||||
chr15:78442808
|
A | C | 1 | a0001c0002t0004g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.106+2927A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442808 | ||||||
chr15:78442816
|
T | C | 3 | a0001c0002t0004g0146a0001c0002t0004g0147a0001c0002t0022g0145 | 3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.106+2935T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442816 | ||||||
chr15:78442927
|
C | T | 78 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(75): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.106+3046C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442927 | ||||||
chr15:78443013
|
C | G | 133 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(130): Show | 144 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.106+3132C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443013 | ||||||
chr15:78443096
|
G | C | 78 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(75): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.106+3215G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443096 | ||||||
chr15:78443194
|
G | A | 1 | a0002c0003t0010g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.106+3313G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443194 | ||||||
chr15:78443384
|
G | A | 11 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(8): Show | 11 | HG02074.hp1 HG03834.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+3503G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443384 | ||||||
chr15:78443532
|
T | C | 3 | a0001c0001t0047g0116a0001c0001t0048g0117a0001c0001t0049g0118 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.106+3651T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443532 | ||||||
chr15:78443534
|
T | C | 1 | a0001c0002t0004g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.106+3653T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443534 | ||||||
chr15:78443626
|
G | T | 1 | a0001c0002t0003g0241 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.106+3745G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443626 | ||||||
chr15:78443657
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.106+3776G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443657 | ||||||
chr15:78443842
|
C | T | 61 | a0001c0001t0042g0136a0001c0002t0003g0003a0001c0002t0003g0005others(58): Show | 69 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.106+3961C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443842 | ||||||
chr15:78443983
|
G | A | 61 | a0001c0001t0042g0136a0001c0002t0003g0003a0001c0002t0003g0005others(58): Show | 69 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.106+4102G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443983 | ||||||
chr15:78444080
|
G | A | 1 | a0001c0001t0007g0334 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.106+4199G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78444080 | ||||||
chr15:78444251
|
T | A | 282 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(279): Show | 305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.106+4370T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78444251 | ||||||
chr15:78444523
|
C | G | 1 | a0001c0001t0008g0321 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.106+4642C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78444523 | ||||||
chr15:78444665
|
T | C | 382 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(379): Show | 417 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.106+4784T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78444665 | ||||||
chr15:78445136
|
AT | A | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG01070.hp1 HG02735.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+5274delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78445136 | |||||
chr15:78445136
|
ATT | A | 18 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(15): Show | 18 | HG00408.hp2 HG01243.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.106+5273_106+5274d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78445136 | |||||
chr15:78445138
|
T | TTTA | 63 | a0001c0001t0004g0103a0001c0001t0042g0136a0001c0002t0003g0003others(60): Show | 71 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.106+5259_106+5260i others(5): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78445138 | |||||
chr15:78445139
|
T | TA | 4 | a0003c0005t0009g0180a0003c0005t0009g0181a0003c0005t0009g0182others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+5258_106+5259i others(3): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445139 | ||||||
chr15:78445140
|
T | A | 4 | a0001c0001t0001g0034a0001c0001t0009g0018a0001c0001t0009g0178others(1): Show | 5 | HG00099.hp1 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+5259T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445140 | ||||||
chr15:78445140
|
T | TA | 5 | a0001c0002t0005g0369a0001c0006t0024g0122a0001c0006t0024g0123others(2): Show | 5 | HG01192.hp1 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+5259_106+5260i others(3): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445140 | ||||||
chr15:78445141
|
T | A | 105 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(102): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.106+5260T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445141 | ||||||
chr15:78445141
|
T | TA | 3 | a0001c0001t0002g0290a0001c0001t0002g0291a0001c0001t0044g0295 | 3 | HG01978.hp2 HG02004.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.106+5260_106+5261i others(3): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445141 | ||||||
chr15:78445142
|
T | A | 69 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(66): Show | 72 | HG00438.hp1 HG00738.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.106+5261T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445142 | ||||||
chr15:78445143
|
T | A | 1 | a0001c0002t0003g0199 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.106+5262T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445143 | ||||||
chr15:78445146
|
T | A | 43 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(40): Show | 46 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.106+5265T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445146 | ||||||
chr15:78445319
|
G | C | 1 | a0001c0001t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.106+5438G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445319 | ||||||
chr15:78445485
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.106+5604A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445485 | ||||||
chr15:78445495
|
A | G | 1 | a0001c0001t0002g0289 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.106+5614A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445495 | ||||||
chr15:78445600
|
G | T | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+5719G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445600 | ||||||
chr15:78445932
|
A | T | 1 | a0001c0001t0034g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.106+6051A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445932 | ||||||
chr15:78446028
|
T | C | 279 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(276): Show | 302 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.106+6147T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446028 | ||||||
chr15:78446079
|
C | T | 6 | a0002c0003t0010g0012a0002c0003t0010g0126a0002c0003t0010g0127others(3): Show | 7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+6198C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446079 | ||||||
chr15:78446293
|
A | G | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+6412A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446293 | ||||||
chr15:78446438
|
C | T | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.106+6557C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446438 | ||||||
chr15:78446716
|
C | A | 1 | a0001c0001t0009g0178 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+6835C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446716 | ||||||
chr15:78446778
|
G | A | 15 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(12): Show | 17 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.106+6897G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446778 | ||||||
chr15:78446891
|
C | CAGT | 284 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(281): Show | 307 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.106+7011_106+7013d others(5): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78446891 | |||||
chr15:78447129
|
T | C | 283 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(280): Show | 306 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.106+7248T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447129 | ||||||
chr15:78447167
|
TTTTC | T | 3 | a0001c0002t0003g0003a0001c0002t0003g0237a0001c0002t0026g0238 | 6 | HG01928.hp2 HG01934.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+7298_106+7301d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447167 | |||||
chr15:78447179
|
C | CT | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(12): Show | 15 | HG00438.hp2 HG01167.hp1 NA18952.hp1 others(12): Show |
intron_variant | MODIFIER | c.106+7313dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447179 | |||||
chr15:78447179
|
CT | C | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0002g0244others(4): Show | 7 | NA18941.hp1 NA18959.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+7313delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447179 | |||||
chr15:78447320
|
T | A | 1 | a0001c0001t0002g0278 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.106+7439T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447320 | ||||||
chr15:78447332
|
A | AT | 108 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0312others(105): Show | 120 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+7467dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447332 | |||||
chr15:78447332
|
A | ATT | 35 | a0001c0001t0002g0022a0001c0001t0002g0029a0001c0001t0002g0244others(32): Show | 36 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.106+7466_106+7467d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447332 | |||||
chr15:78447332
|
AT | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0302a0001c0001t0048g0117others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+7467delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447332 | |||||
chr15:78447421
|
A | G | 34 | a0001c0002t0004g0361a0001c0002t0005g0006a0001c0002t0005g0027others(31): Show | 36 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.106+7540A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447421 | ||||||
chr15:78447523
|
A | G | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+7642A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447523 | ||||||
chr15:78447524
|
T | C | 1 | a0001c0002t0022g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.106+7643T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447524 | ||||||
chr15:78447538
|
C | G | 5 | a0002c0003t0010g0012a0002c0003t0010g0126a0002c0003t0010g0128others(2): Show | 6 | HG01109.hp1 HG02257.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+7657C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447538 | ||||||
chr15:78447592
|
A | G | 1 | a0001c0002t0004g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.106+7711A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447592 | ||||||
chr15:78447617
|
C | T | 1 | a0001c0002t0004g0170 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.106+7736C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447617 | ||||||
chr15:78447626
|
C | T | 3 | a0001c0001t0001g0298a0001c0002t0040g0236a0001c0002t0041g0235 | 3 | HG02723.hp2 HG03491.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.106+7745C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447626 | ||||||
chr15:78447709
|
C | A | 2 | a0001c0006t0025g0120a0001c0006t0025g0121 | 2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.106+7828C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447709 | ||||||
chr15:78447775
|
T | C | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.106+7894T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447775 | ||||||
chr15:78447780
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.106+7899C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447780 | ||||||
chr15:78447827
|
A | AGGTATCA others(19): Show |
1 | a0001c0002t0004g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.106+7947_106+7972d others(28): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447827 | |||||
chr15:78447891
|
G | A | 277 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(274): Show | 300 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.106+8010G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447891 | ||||||
chr15:78447908
|
G | C | 1 | a0001c0002t0003g0201 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.106+8027G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447908 | ||||||
chr15:78448126
|
AATGTATG others(1): Show |
A | 3 | a0001c0001t0047g0116a0001c0001t0048g0117a0001c0001t0049g0118 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.106+8260_106+8267d others(10): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78448126 | |||||
chr15:78448184
|
A | G | 16 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+8303A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448184 | ||||||
chr15:78448293
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.106+8412C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448293 | ||||||
chr15:78448296
|
C | T | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+8415C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448296 | ||||||
chr15:78448306
|
G | T | 1 | a0001c0001t0002g0276 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.106+8425G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448306 | ||||||
chr15:78448346
|
T | G | 111 | a0001c0001t0001g0043a0001c0001t0006g0002a0001c0001t0006g0009others(108): Show | 122 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.106+8465T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448346 | ||||||
chr15:78448369
|
T | C | 22 | a0001c0002t0003g0005a0001c0002t0003g0019a0001c0002t0003g0020others(19): Show | 26 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.106+8488T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448369 | ||||||
chr15:78448437
|
G | A | 3 | a0001c0002t0004g0146a0001c0002t0004g0147a0001c0002t0022g0145 | 3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.106+8556G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448437 | ||||||
chr15:78448590
|
A | C | 110 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(107): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.106+8709A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448590 | ||||||
chr15:78448622
|
G | A | 110 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(107): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.106+8741G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448622 | ||||||
chr15:78448692
|
C | T | 2 | a0001c0002t0004g0197a0001c0002t0004g0234 | 2 | HG00438.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.106+8811C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448692 | ||||||
chr15:78449003
|
C | A | 35 | a0001c0001t0002g0022a0001c0001t0002g0029a0001c0001t0002g0244others(32): Show | 36 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.106+9122C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449003 | ||||||
chr15:78449040
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.106+9159G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449040 | ||||||
chr15:78449042
|
T | C | 279 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(276): Show | 302 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.106+9161T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449042 | ||||||
chr15:78449043
|
G | A | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+9162G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449043 | ||||||
chr15:78449230
|
T | C | 2 | a0001c0002t0003g0242a0001c0002t0003g0243 | 2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.106+9349T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449230 | ||||||
chr15:78449276
|
T | C | 77 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(74): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.106+9395T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449276 | ||||||
chr15:78449290
|
G | T | 3 | a0001c0002t0004g0146a0001c0002t0004g0147a0001c0002t0022g0145 | 3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.106+9409G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449290 | ||||||
chr15:78449550
|
C | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0192 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.106+9669C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449550 | ||||||
chr15:78449773
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.106+9892C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449773 | ||||||
chr15:78449787
|
A | G | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+9906A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449787 | ||||||
chr15:78449834
|
T | C | 3 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316 | 4 | NA18968.hp1 NA18975.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+9953T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449834 | ||||||
chr15:78449902
|
G | A | 5 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG00558.hp2 HG02015.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+10021G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449902 | ||||||
chr15:78449904
|
A | G | 1 | a0001c0001t0002g0275 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.106+10023A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449904 | ||||||
chr15:78449933
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.106+10052A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449933 | ||||||
chr15:78449934
|
T | G | 278 | a0001c0001t0001g0043a0001c0001t0002g0022a0001c0001t0002g0023others(275): Show | 301 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.106+10053T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449934 | ||||||
chr15:78450034
|
G | A | 77 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(74): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.106+10153G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450034 | ||||||
chr15:78450048
|
T | A | 1 | a0001c0001t0016g0044 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.106+10167T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450048 | ||||||
chr15:78450237
|
A | G | 77 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(74): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.106+10356A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450237 | ||||||
chr15:78450412
|
C | A | 132 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(129): Show | 143 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.106+10531C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450412 | ||||||
chr15:78450596
|
G | A | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+10715G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450596 | ||||||
chr15:78450687
|
G | A | 277 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(274): Show | 300 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.106+10806G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450687 | ||||||
chr15:78450707
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.106+10826C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450707 | ||||||
chr15:78450824
|
T | TTG | 34 | a0001c0001t0001g0085a0001c0001t0001g0101a0001c0001t0001g0298others(31): Show | 36 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.106+10991_106+1099 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
T | TTGTG | 14 | a0001c0001t0001g0087a0001c0001t0001g0307a0001c0001t0006g0010others(11): Show | 17 | HG00438.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.106+10989_106+1099 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
T | TTGTGTG | 3 | a0001c0001t0006g0115a0001c0002t0003g0196a0001c0002t0003g0198 | 3 | HG02723.hp1 NA18970.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.106+10987_106+1099 others(10): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
TTG | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(76): Show | 94 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.106+10991_106+1099 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
TTGTG | T | 70 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0052others(67): Show | 74 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.106+10989_106+1099 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
TTGTGTG | T | 48 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0002g0022others(45): Show | 50 | HG00280.hp1 HG00609.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.106+10987_106+1099 others(10): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
TTGTGTGT others(1): Show |
T | 54 | a0001c0001t0001g0048a0001c0001t0002g0023a0001c0001t0002g0024others(51): Show | 58 | HG00423.hp1 HG00639.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.106+10985_106+1099 others(12): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
TTGTGTGT others(3): Show |
T | 9 | a0001c0001t0001g0047a0001c0001t0002g0249a0001c0001t0002g0250others(6): Show | 9 | HG01175.hp2 HG01257.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+10983_106+1099 others(14): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
TTGTGTGT others(5): Show |
T | 3 | a0001c0002t0004g0147a0001c0002t0004g0148a0001c0002t0004g0150 | 3 | HG01243.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.106+10981_106+1099 others(16): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
TTGTGTGT others(7): Show |
T | 3 | a0001c0002t0004g0146a0001c0002t0005g0347a0001c0002t0005g0348 | 3 | HG01169.hp1 HG02280.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.106+10979_106+1099 others(18): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
TTGTGTGT others(11): Show |
T | 4 | a0001c0001t0001g0091a0001c0001t0047g0116a0001c0001t0048g0117others(1): Show | 4 | HG00438.hp2 HG02886.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+10975_106+1099 others(22): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450824
|
TTGTGTGT others(13): Show |
T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.106+10973_106+1099 others(24): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | |||||
chr15:78450870
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.106+10989G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450870 | ||||||
chr15:78450874
|
A | G | 4 | a0003c0005t0009g0180a0003c0005t0009g0181a0003c0005t0009g0182others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+10993A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450874 | ||||||
chr15:78450918
|
A | G | 132 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(129): Show | 143 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.106+11037A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450918 | ||||||
chr15:78450958
|
A | C | 160 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(157): Show | 172 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.106+11077A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450958 | ||||||
chr15:78450959
|
A | T | 3 | a0001c0002t0003g0209a0001c0002t0003g0210a0001c0002t0003g0341 | 3 | HG00673.hp1 HG02056.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.106+11078A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450959 | ||||||
chr15:78451110
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.106+11229G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451110 | ||||||
chr15:78451215
|
C | G | 1 | a0001c0002t0003g0240 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.106+11334C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451215 | ||||||
chr15:78451494
|
C | T | 16 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.107-11428C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451494 | ||||||
chr15:78451588
|
G | A | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-11334G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451588 | ||||||
chr15:78451909
|
C | T | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-11013C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451909 | ||||||
chr15:78451928
|
G | A | 28 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(25): Show | 29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.107-10994G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451928 | ||||||
chr15:78451950
|
A | G | 277 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(274): Show | 300 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.107-10972A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451950 | ||||||
chr15:78452097
|
G | A | 1 | a0001c0001t0011g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.107-10825G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452097 | ||||||
chr15:78452151
|
T | C | 2 | a0001c0001t0011g0133a0001c0001t0011g0135 | 2 | NA18975.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.107-10771T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452151 | ||||||
chr15:78452182
|
G | A | 62 | a0001c0001t0042g0136a0001c0002t0003g0003a0001c0002t0003g0005others(59): Show | 70 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.107-10740G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452182 | ||||||
chr15:78452200
|
C | T | 11 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(8): Show | 13 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(10): Show |
intron_variant | MODIFIER | c.107-10722C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452200 | ||||||
chr15:78452258
|
G | A | 62 | a0001c0001t0042g0136a0001c0002t0003g0003a0001c0002t0003g0005others(59): Show | 70 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.107-10664G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452258 | ||||||
chr15:78452515
|
G | A | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-10407G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452515 | ||||||
chr15:78452623
|
G | A | 22 | a0001c0002t0003g0005a0001c0002t0003g0019a0001c0002t0003g0020others(19): Show | 26 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.107-10299G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452623 | ||||||
chr15:78452729
|
A | G | 1 | a0001c0002t0003g0194 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.107-10193A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452729 | ||||||
chr15:78452947
|
A | G | 1 | a0001c0002t0005g0348 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.107-9975A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452947 | ||||||
chr15:78452992
|
T | C | 2 | a0001c0002t0003g0242a0001c0002t0003g0243 | 2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.107-9930T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452992 | ||||||
chr15:78453001
|
T | A | 282 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(279): Show | 305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.107-9921T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453001 | ||||||
chr15:78453074
|
C | T | 35 | a0001c0001t0002g0022a0001c0001t0002g0029a0001c0001t0002g0244others(32): Show | 36 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.107-9848C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453074 | ||||||
chr15:78453365
|
C | T | 277 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(274): Show | 300 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.107-9557C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453365 | ||||||
chr15:78453437
|
A | G | 1 | a0001c0001t0002g0024 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.107-9485A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453437 | ||||||
chr15:78453574
|
G | A | 1 | a0001c0002t0005g0358 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.107-9348G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453574 | ||||||
chr15:78453627
|
C | T | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-9295C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453627 | ||||||
chr15:78453710
|
C | T | 5 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-9212C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453710 | ||||||
chr15:78453722
|
A | G | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.107-9200A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453722 | ||||||
chr15:78453776
|
T | G | 25 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(22): Show | 25 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.107-9146T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453776 | ||||||
chr15:78453952
|
C | G | 9 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(6): Show | 11 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-8970C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453952 | ||||||
chr15:78454092
|
A | G | 16 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.107-8830A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454092 | ||||||
chr15:78454317
|
T | C | 6 | a0002c0003t0010g0012a0002c0003t0010g0126a0002c0003t0010g0127others(3): Show | 7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-8605T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454317 | ||||||
chr15:78454340
|
G | A | 15 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(12): Show | 17 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-8582G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454340 | ||||||
chr15:78454356
|
T | G | 1 | a0002c0003t0010g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.107-8566T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454356 | ||||||
chr15:78454497
|
G | C | 2 | a0001c0002t0004g0146a0001c0002t0004g0147 | 2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.107-8425G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454497 | ||||||
chr15:78454613
|
C | T | 21 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(18): Show | 25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.107-8309C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454613 | ||||||
chr15:78454713
|
A | G | 28 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(25): Show | 29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.107-8209A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454713 | ||||||
chr15:78454841
|
A | C | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-8081A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454841 | ||||||
chr15:78455012
|
A | AGAGAATA others(313): Show |
1 | a0001c0001t0034g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.107-7897_107-7896i others(322): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78455012 | |||||
chr15:78455057
|
G | T | 1 | a0001c0001t0002g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.107-7865G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455057 | ||||||
chr15:78455064
|
C | T | 1 | a0001c0002t0004g0167 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.107-7858C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455064 | ||||||
chr15:78455097
|
T | C | 1 | a0001c0001t0009g0178 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.107-7825T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455097 | ||||||
chr15:78455226
|
A | G | 70 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(67): Show | 73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.107-7696A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455226 | ||||||
chr15:78455539
|
T | A | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.107-7383T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455539 | ||||||
chr15:78455569
|
G | GA | 29 | a0001c0001t0001g0092a0001c0001t0007g0026a0001c0001t0007g0322others(26): Show | 30 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.107-7343dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78455569 | |||||
chr15:78455574
|
AAAAAAG | A | 139 | a0001c0001t0042g0136a0001c0002t0003g0003a0001c0002t0003g0005others(136): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.107-7342_107-7337d others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78455574 | |||||
chr15:78455695
|
T | G | 1 | a0001c0001t0002g0251 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.107-7227T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455695 | ||||||
chr15:78455704
|
T | G | 4 | a0001c0001t0011g0132a0001c0001t0011g0133a0001c0001t0011g0134others(1): Show | 4 | HG01496.hp1 HG03486.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-7218T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455704 | ||||||
chr15:78455769
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.107-7153A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455769 | ||||||
chr15:78455778
|
G | A | 2 | a0001c0002t0004g0013a0001c0002t0004g0139 | 3 | NA18944.hp1 NA18968.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.107-7144G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455778 | ||||||
chr15:78455897
|
C | T | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-7025C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455897 | ||||||
chr15:78456060
|
CTT | C | 15 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(12): Show | 17 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-6859_107-6858d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78456060 | |||||
chr15:78456104
|
A | G | 1 | a0001c0002t0004g0017 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.107-6818A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456104 | ||||||
chr15:78456161
|
A | C | 1 | a0001c0001t0002g0247 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.107-6761A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456161 | ||||||
chr15:78456204
|
T | A | 3 | a0001c0001t0047g0116a0001c0001t0048g0117a0001c0001t0049g0118 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.107-6718T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456204 | ||||||
chr15:78456253
|
G | A | 7 | a0001c0001t0002g0244a0001c0001t0002g0258a0001c0001t0002g0259others(4): Show | 7 | NA18952.hp2 NA18959.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.107-6669G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456253 | ||||||
chr15:78456271
|
T | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0192 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.107-6651T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456271 | ||||||
chr15:78456287
|
G | A | 2 | a0001c0001t0027g0245a0001c0001t0027g0264 | 2 | HG02074.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.107-6635G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456287 | ||||||
chr15:78456302
|
T | C | 1 | a0001c0002t0005g0369 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.107-6620T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456302 | ||||||
chr15:78456432
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0048a0001c0001t0001g0059 | 5 | NA18961.hp2 NA18963.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-6490G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456432 | ||||||
chr15:78456479
|
A | G | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-6443A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456479 | ||||||
chr15:78456513
|
G | A | 21 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(18): Show | 25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.107-6409G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456513 | ||||||
chr15:78456665
|
C | CA | 30 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0006g0002others(27): Show | 33 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.107-6242dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78456665 | |||||
chr15:78456665
|
CA | C | 27 | a0001c0001t0001g0037a0001c0001t0001g0078a0001c0001t0002g0244others(24): Show | 27 | HG00408.hp2 HG01243.hp2 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.107-6242delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78456665 | |||||
chr15:78456764
|
A | G | 4 | a0001c0004t0015g0039a0001c0004t0015g0098a0001c0004t0015g0099others(1): Show | 4 | NA18978.hp2 NA18982.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-6158A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456764 | ||||||
chr15:78456893
|
C | T | 2 | a0001c0001t0001g0077a0001c0012t0001g0104 | 2 | HG01069.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.107-6029C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456893 | ||||||
chr15:78456968
|
T | A | 2 | a0001c0004t0001g0093a0001c0004t0016g0094 | 2 | NA18997.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.107-5954T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456968 | ||||||
chr15:78457156
|
T | G | 1 | a0001c0002t0003g0237 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.107-5766T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457156 | ||||||
chr15:78457266
|
T | C | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-5656T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457266 | ||||||
chr15:78457437
|
A | T | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-5485A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457437 | ||||||
chr15:78457476
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.107-5446T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457476 | ||||||
chr15:78457710
|
T | C | 70 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(67): Show | 73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.107-5212T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457710 | ||||||
chr15:78457993
|
T | C | 3 | a0001c0002t0005g0344a0001c0002t0005g0345a0001c0002t0005g0370 | 3 | HG00408.hp1 HG00609.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.107-4929T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457993 | ||||||
chr15:78458046
|
A | T | 1 | a0001c0001t0001g0312 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.107-4876A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458046 | ||||||
chr15:78458187
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0083 | 2 | NA18946.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.107-4735A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458187 | ||||||
chr15:78458206
|
G | C | 1 | a0001c0001t0034g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.107-4716G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458206 | ||||||
chr15:78458207
|
G | A | 141 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(138): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.107-4715G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458207 | ||||||
chr15:78458564
|
C | T | 15 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(12): Show | 17 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-4358C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458564 | ||||||
chr15:78458761
|
T | A | 1 | a0001c0001t0002g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.107-4161T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458761 | ||||||
chr15:78458778
|
G | T | 2 | a0001c0002t0004g0152a0001c0002t0004g0166 | 2 | NA18983.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.107-4144G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458778 | ||||||
chr15:78458779
|
G | T | 2 | a0001c0002t0004g0152a0001c0002t0004g0166 | 2 | NA18983.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.107-4143G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458779 | ||||||
chr15:78458810
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.107-4112G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458810 | ||||||
chr15:78458957
|
C | T | 1 | a0001c0002t0003g0211 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.107-3965C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458957 | ||||||
chr15:78459196
|
A | T | 7 | a0001c0001t0034g0119a0002c0003t0010g0012a0002c0003t0010g0126others(4): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-3726A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459196 | ||||||
chr15:78459198
|
A | T | 7 | a0001c0001t0034g0119a0002c0003t0010g0012a0002c0003t0010g0126others(4): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-3724A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459198 | ||||||
chr15:78459308
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107-3614T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459308 | ||||||
chr15:78459340
|
G | GT | 34 | a0001c0002t0004g0361a0001c0002t0005g0006a0001c0002t0005g0027others(31): Show | 36 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-3578dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78459340 | |||||
chr15:78459380
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.107-3542C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459380 | ||||||
chr15:78459416
|
C | G | 2 | a0001c0002t0004g0143a0001c0002t0004g0144 | 2 | NA18980.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.107-3506C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459416 | ||||||
chr15:78459419
|
C | T | 1 | a0001c0002t0004g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107-3503C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459419 | ||||||
chr15:78459420
|
G | A | 2 | a0001c0002t0005g0371a0001c0002t0005g0372 | 2 | HG00323.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.107-3502G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459420 | ||||||
chr15:78459549
|
C | T | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-3373C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459549 | ||||||
chr15:78459619
|
C | T | 141 | a0001c0001t0042g0136a0001c0002t0003g0003a0001c0002t0003g0005others(138): Show | 154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.107-3303C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459619 | ||||||
chr15:78459620
|
G | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 98 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.107-3302G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459620 | ||||||
chr15:78459630
|
G | A | 1 | a0001c0002t0003g0242 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.107-3292G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459630 | ||||||
chr15:78459650
|
C | T | 1 | a0001c0002t0005g0347 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.107-3272C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459650 | ||||||
chr15:78459772
|
C | T | 282 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(279): Show | 305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.107-3150C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459772 | ||||||
chr15:78459812
|
CCT | C | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.107-3107_107-3106d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78459812 | |||||
chr15:78459846
|
C | G | 34 | a0001c0002t0004g0361a0001c0002t0005g0006a0001c0002t0005g0027others(31): Show | 36 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-3076C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459846 | ||||||
chr15:78460001
|
G | A | 277 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(274): Show | 300 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.107-2921G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460001 | ||||||
chr15:78460021
|
G | A | 380 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(377): Show | 415 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(412): Show |
intron_variant | MODIFIER | c.107-2901G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460021 | ||||||
chr15:78460050
|
T | A | 2 | a0001c0001t0027g0245a0001c0001t0027g0264 | 2 | HG02074.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.107-2872T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460050 | ||||||
chr15:78460124
|
C | G | 1 | a0001c0001t0002g0289 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.107-2798C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460124 | ||||||
chr15:78460265
|
T | G | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.107-2657T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460265 | ||||||
chr15:78460405
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.107-2517A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460405 | ||||||
chr15:78460551
|
C | G | 1 | a0001c0002t0005g0357 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.107-2371C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460551 | ||||||
chr15:78460800
|
C | G | 1 | a0001c0002t0003g0240 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.107-2122C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460800 | ||||||
chr15:78461029
|
A | G | 132 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(129): Show | 143 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.107-1893A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461029 | ||||||
chr15:78461101
|
GAT | G | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1819_107-1818d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78461101 | |||||
chr15:78461103
|
T | G | 1 | a0001c0001t0042g0136 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.107-1819T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461103 | ||||||
chr15:78461133
|
A | G | 6 | a0002c0003t0010g0012a0002c0003t0010g0126a0002c0003t0010g0127others(3): Show | 7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-1789A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461133 | ||||||
chr15:78461199
|
C | G | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1723C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461199 | ||||||
chr15:78461225
|
CAGGACAT others(14): Show |
C | 1 | a0004c0007t0019g0294 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.107-1696_107-1676d others(23): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461225 | ||||||
chr15:78461330
|
A | G | 2 | a0001c0001t0011g0133a0001c0001t0011g0135 | 2 | NA18975.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.107-1592A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461330 | ||||||
chr15:78461361
|
T | TAAAG | 4 | a0003c0005t0009g0180a0003c0005t0009g0181a0003c0005t0009g0182others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1559_107-1556d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78461361 | |||||
chr15:78461604
|
G | A | 6 | a0002c0003t0010g0012a0002c0003t0010g0126a0002c0003t0010g0127others(3): Show | 7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-1318G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461604 | ||||||
chr15:78461658
|
A | G | 142 | a0001c0001t0004g0103a0001c0001t0016g0058a0001c0001t0042g0136others(139): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.107-1264A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461658 | ||||||
chr15:78461672
|
G | T | 1 | a0001c0001t0016g0044 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.107-1250G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461672 | ||||||
chr15:78461760
|
A | G | 75 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(72): Show | 80 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.107-1162A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461760 | ||||||
chr15:78462027
|
T | A | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.107-895T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462027 | ||||||
chr15:78462052
|
A | G | 4 | a0001c0002t0004g0016a0001c0002t0004g0149a0001c0002t0004g0165others(1): Show | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-870A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462052 | ||||||
chr15:78462095
|
A | G | 1 | a0001c0002t0003g0376 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.107-827A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462095 | ||||||
chr15:78462233
|
T | C | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-689T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462233 | ||||||
chr15:78462239
|
T | C | 1 | a0001c0006t0025g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.107-683T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462239 | ||||||
chr15:78462366
|
A | T | 1 | a0001c0002t0003g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.107-556A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462366 | ||||||
chr15:78462388
|
A | G | 5 | a0001c0001t0001g0037a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG02165.hp1 NA18946.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-534A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462388 | ||||||
chr15:78462521
|
T | C | 70 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(67): Show | 73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.107-401T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462521 | ||||||
chr15:78462660
|
C | A | 5 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-262C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462660 | ||||||
chr15:78462779
|
C | T | 1 | a0001c0002t0003g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.107-143C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462779 | ||||||
chr15:78462820
|
A | G | 2 | a0001c0001t0002g0185a0001c0001t0002g0190 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.107-102A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462820 | ||||||
chr15:78462827
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.107-95A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462827 | ||||||
chr15:78462853
|
T | G | 1 | a0001c0001t0001g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.107-69T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462853 | ||||||
chr15:78462900
|
T | G | 3 | a0001c0002t0004g0146a0001c0002t0004g0147a0001c0002t0022g0145 | 3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.107-22T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462900 | ||||||
chr15:78463341
|
T | C | 2 | a0001c0002t0003g0215a0001c0002t0017g0216 | 2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.272+254T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463341 | ||||||
chr15:78463376
|
G | A | 1 | a0001c0002t0003g0206 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.272+289G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463376 | ||||||
chr15:78463406
|
A | C | 1 | a0001c0001t0001g0304 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.272+319A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463406 | ||||||
chr15:78463490
|
G | GT | 9 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(6): Show | 10 | HG00673.hp1 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.272+404dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr15 | 78463490 | |||||
chr15:78463492
|
G | T | 348 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(345): Show | 377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.272+405G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463492 | ||||||
chr15:78463895
|
A | T | 16 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.272+808A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463895 | ||||||
chr15:78464167
|
A | G | 16 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.272+1080A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78464167 | ||||||
chr15:78464220
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.273-1031G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78464220 | ||||||
chr15:78464829
|
C | T | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.273-422C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78464829 | ||||||
chr15:78464890
|
G | A | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-361G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78464890 | ||||||
chr15:78465028
|
T | C | 1 | a0001c0001t0034g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.273-223T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78465028 | ||||||
chr15:78465033
|
A | G | 1 | a0001c0001t0002g0272 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.273-218A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78465033 | ||||||
chr15:78465088
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.273-163T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78465088 | ||||||
chr15:78465530
|
C | G | 3 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257 | 3 | HG00738.hp2 HG00741.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.410+142C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465530 | ||||||
chr15:78465550
|
T | C | 70 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(67): Show | 73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.410+162T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465550 | ||||||
chr15:78465571
|
C | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.410+183C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465571 | ||||||
chr15:78465617
|
C | T | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+229C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465617 | ||||||
chr15:78465635
|
C | A | 1 | a0001c0001t0008g0317 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.410+247C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465635 | ||||||
chr15:78465871
|
G | A | 347 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(344): Show | 376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.411-400G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465871 | ||||||
chr15:78465915
|
T | A | 1 | a0001c0001t0034g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.411-356T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465915 | ||||||
chr15:78465956
|
T | A | 2 | a0001c0002t0005g0359a0001c0002t0005g0360 | 2 | HG01516.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.411-315T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465956 | ||||||
chr15:78465970
|
TA | T | 6 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0139others(3): Show | 8 | NA18944.hp1 NA18949.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-300delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465970 | ||||||
chr15:78465982
|
A | G | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-289A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465982 | ||||||
chr15:78466099
|
T | A | 5 | a0001c0001t0006g0011a0001c0006t0024g0122a0001c0006t0024g0123others(2): Show | 6 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.411-172T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78466099 | ||||||
chr15:78466105
|
A | G | 1 | a0001c0002t0003g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.411-166A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78466105 | ||||||
chr15:78466136
|
G | C | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-135G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78466136 | ||||||
chr15:78466239
|
G | A | 2 | a0001c0001t0047g0116a0001c0001t0049g0118 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.411-32G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78466239 | ||||||
chr15:78466496
|
G | T | 3 | a0001c0001t0047g0116a0001c0001t0048g0117a0001c0001t0049g0118 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.629+7G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466496 | ||||||
chr15:78466511
|
A | C | 377 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(374): Show | 411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.629+22A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466511 | ||||||
chr15:78466560
|
T | TC | 378 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(375): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.629+72dupC | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78466560 | |||||
chr15:78466578
|
A | T | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.629+89A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466578 | ||||||
chr15:78466913
|
A | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0192 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.629+424A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466913 | ||||||
chr15:78466922
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.629+433A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466922 | ||||||
chr15:78466986
|
GCAGGTGG others(12): Show |
G | 70 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(67): Show | 73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.629+502_629+520del others(19): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78466986 | |||||
chr15:78466989
|
G | A | 1 | a0001c0002t0004g0361 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.629+500G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466989 | ||||||
chr15:78467006
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(97): Show | 112 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.629+517C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467006 | ||||||
chr15:78467012
|
T | G | 1 | a0004c0007t0019g0294 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.629+523T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467012 | ||||||
chr15:78467034
|
C | T | 348 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(345): Show | 377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.629+545C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467034 | ||||||
chr15:78467085
|
C | G | 2 | a0001c0001t0002g0248a0001c0001t0002g0274 | 2 | NA18961.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.629+596C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467085 | ||||||
chr15:78467208
|
C | CA | 148 | a0001c0001t0001g0051a0001c0001t0001g0064a0001c0001t0001g0065others(145): Show | 161 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.629+736dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78467208 | |||||
chr15:78467538
|
A | T | 1 | a0004c0007t0019g0294 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.629+1049A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467538 | ||||||
chr15:78467662
|
C | A | 1 | a0001c0001t0002g0190 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.629+1173C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467662 | ||||||
chr15:78467945
|
G | A | 70 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(67): Show | 73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.629+1456G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467945 | ||||||
chr15:78468002
|
G | A | 70 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(67): Show | 73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.629+1513G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468002 | ||||||
chr15:78468232
|
C | T | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.629+1743C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468232 | ||||||
chr15:78468271
|
G | T | 1 | a0001c0001t0034g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.629+1782G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468271 | ||||||
chr15:78468493
|
CT | C | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.629+2006delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78468493 | |||||
chr15:78468509
|
G | A | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.629+2020G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468509 | ||||||
chr15:78468542
|
C | CT | 85 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(82): Show | 92 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(89): Show |
intron_variant | MODIFIER | c.630-1977dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78468542 | |||||
chr15:78468568
|
A | G | 2 | a0001c0002t0003g0223a0001c0002t0003g0241 | 2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.630-1964A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468568 | ||||||
chr15:78468568
|
A | T | 1 | a0001c0002t0012g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.630-1964A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468568 | ||||||
chr15:78468576
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(223): Show | 246 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.630-1956G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468576 | ||||||
chr15:78468942
|
T | A | 1 | a0004c0007t0019g0294 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.630-1590T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468942 | ||||||
chr15:78468969
|
A | T | 1 | a0001c0001t0002g0252 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.630-1563A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468969 | ||||||
chr15:78469072
|
C | G | 35 | a0001c0002t0004g0361a0001c0002t0005g0006a0001c0002t0005g0027others(32): Show | 37 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.630-1460C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469072 | ||||||
chr15:78469124
|
A | C | 1 | a0001c0001t0002g0252 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.630-1408A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469124 | ||||||
chr15:78469137
|
T | G | 1 | a0001c0001t0014g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.630-1395T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469137 | ||||||
chr15:78469164
|
T | A | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.630-1368T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469164 | ||||||
chr15:78469282
|
G | C | 1 | a0001c0002t0005g0347 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.630-1250G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469282 | ||||||
chr15:78469318
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.630-1214G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469318 | ||||||
chr15:78469338
|
C | G | 1 | a0001c0001t0002g0251 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.630-1194C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469338 | ||||||
chr15:78469355
|
A | G | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.630-1177A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469355 | ||||||
chr15:78469442
|
G | A | 6 | a0001c0002t0003g0220a0001c0002t0003g0224a0001c0002t0003g0225others(3): Show | 6 | HG01069.hp2 HG01106.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.630-1090G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469442 | ||||||
chr15:78469491
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.630-1041G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469491 | ||||||
chr15:78469501
|
G | A | 379 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(376): Show | 414 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(411): Show |
intron_variant | MODIFIER | c.630-1031G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469501 | ||||||
chr15:78469533
|
G | C | 3 | a0001c0001t0042g0136a0001c0002t0003g0227a0001c0002t0003g0240 | 3 | HG00544.hp1 NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.630-999G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469533 | ||||||
chr15:78469550
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.630-982C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469550 | ||||||
chr15:78469611
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.630-921T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469611 | ||||||
chr15:78469859
|
G | A | 1 | a0001c0002t0039g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.630-673G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469859 | ||||||
chr15:78469971
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(102): Show | 117 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.630-561A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469971 | ||||||
chr15:78469973
|
A | G | 4 | a0003c0005t0009g0180a0003c0005t0009g0181a0003c0005t0009g0182others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.630-559A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469973 | ||||||
chr15:78470006
|
A | C | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-526A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470006 | ||||||
chr15:78470049
|
T | C | 2 | a0001c0002t0040g0236a0001c0002t0041g0235 | 2 | HG03491.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.630-483T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470049 | ||||||
chr15:78470142
|
A | G | 377 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(374): Show | 411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.630-390A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470142 | ||||||
chr15:78470174
|
A | G | 5 | a0001c0001t0020g0124a0001c0001t0020g0125a0001c0001t0047g0116others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-358A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470174 | ||||||
chr15:78470286
|
T | C | 2 | a0001c0002t0003g0242a0001c0002t0003g0243 | 2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.630-246T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470286 | ||||||
chr15:78470689
|
C | CT | 148 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0073others(145): Show | 160 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.699+111dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr15 | 78470689 | |||||
chr15:78470689
|
C | CTT | 12 | a0001c0001t0001g0041a0001c0001t0002g0246a0001c0002t0003g0137others(9): Show | 12 | HG01081.hp2 HG01123.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.699+110_699+111dup others(2): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr15 | 78470689 | |||||
chr15:78470689
|
C | T | 1 | a0004c0007t0019g0294 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.699+88C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470689 | ||||||
chr15:78470689
|
CT | C | 21 | a0001c0001t0001g0045a0001c0001t0001g0077a0001c0001t0001g0312others(18): Show | 25 | HG01069.hp1 HG01243.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.699+111delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr15 | 78470689 | |||||
chr15:78470726
|
G | A | 1 | a0001c0002t0017g0212 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.699+125G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470726 | ||||||
chr15:78470758
|
G | C | 1 | a0001c0001t0008g0315 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.699+157G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470758 | ||||||
chr15:78470840
|
G | A | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.699+239G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470840 | ||||||
chr15:78470848
|
G | C | 378 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(375): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.699+247G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470848 | ||||||
chr15:78470901
|
G | A | 3 | a0001c0002t0003g0228a0001c0002t0003g0229a0001c0002t0003g0232 | 3 | HG00597.hp2 HG02129.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.699+300G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470901 | ||||||
chr15:78470931
|
G | A | 5 | a0001c0001t0007g0333a0001c0001t0013g0329a0001c0001t0013g0330others(2): Show | 5 | HG03834.hp1 NA18947.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.699+330G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470931 | ||||||
chr15:78470933
|
A | G | 1 | a0001c0002t0004g0017 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.699+332A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470933 | ||||||
chr15:78470946
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.699+345C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470946 | ||||||
chr15:78470947
|
G | A | 3 | a0001c0001t0002g0290a0001c0001t0002g0291a0001c0001t0044g0295 | 3 | HG01978.hp2 HG02004.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.699+346G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470947 | ||||||
chr15:78470951
|
C | T | 2 | a0001c0002t0017g0212a0001c0002t0017g0221 | 2 | HG00323.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.699+350C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470951 | ||||||
chr15:78470955
|
C | G | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+354C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470955 | ||||||
chr15:78470999
|
T | G | 1 | a0004c0007t0019g0294 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.699+398T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470999 | ||||||
chr15:78471275
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(102): Show | 117 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.700-466C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471275 | ||||||
chr15:78471302
|
C | T | 1 | a0001c0001t0011g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.700-439C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471302 | ||||||
chr15:78471387
|
G | A | 1 | a0001c0001t0008g0320 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.700-354G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471387 | ||||||
chr15:78471467
|
C | T | 378 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(375): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.700-274C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471467 | ||||||
chr15:78471554
|
T | G | 1 | a0001c0002t0012g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.700-187T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471554 | ||||||
chr15:78471597
|
T | C | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.700-144T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471597 | ||||||
chr15:78471673
|
T | C | 16 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.700-68T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471673 | ||||||
chr15:78471943
|
A | G | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.883+19A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78471943 | ||||||
chr15:78471982
|
G | A | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.883+58G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78471982 | ||||||
chr15:78472179
|
T | C | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.883+255T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472179 | ||||||
chr15:78472237
|
G | C | 1 | a0001c0002t0003g0209 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.883+313G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472237 | ||||||
chr15:78472407
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.883+483C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472407 | ||||||
chr15:78472524
|
G | A | 5 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+600G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472524 | ||||||
chr15:78472557
|
C | T | 2 | a0001c0001t0020g0124a0001c0001t0020g0125 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.883+633C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472557 | ||||||
chr15:78472567
|
A | G | 5 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+643A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472567 | ||||||
chr15:78472780
|
G | T | 78 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(75): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.884-462G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472780 | ||||||
chr15:78472847
|
C | T | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.884-395C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472847 | ||||||
chr15:78472927
|
A | C | 1 | a0001c0002t0005g0355 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.884-315A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472927 | ||||||
chr15:78472944
|
A | G | 5 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-298A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472944 | ||||||
chr15:78472948
|
T | G | 142 | a0001c0001t0004g0103a0001c0002t0003g0003a0001c0002t0003g0005others(139): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.884-294T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472948 | ||||||
chr15:78473051
|
G | GT | 3 | a0001c0001t0001g0067a0001c0001t0001g0307a0001c0002t0003g0232 | 3 | HG01175.hp1 NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.884-186dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr15 | 78473051 | |||||
chr15:78473120
|
A | G | 1 | a0001c0002t0004g0167 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.884-122A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78473120 | ||||||
chr15:78473404
|
C | T | 2 | a0001c0002t0004g0151a0001c0002t0004g0160 | 2 | NA18951.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1023+23C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473404 | ||||||
chr15:78473611
|
T | C | 1 | a0001c0002t0003g0240 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1023+230T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473611 | ||||||
chr15:78473852
|
T | A | 140 | a0001c0001t0004g0103a0001c0002t0003g0003a0001c0002t0003g0005others(137): Show | 153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1023+471T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473852 | ||||||
chr15:78473853
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1023+472A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473853 | ||||||
chr15:78473866
|
A | T | 39 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(36): Show | 42 | HG00280.hp1 HG00423.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.1023+485A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473866 | ||||||
chr15:78473908
|
A | G | 35 | a0001c0002t0004g0361a0001c0002t0005g0006a0001c0002t0005g0027others(32): Show | 37 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.1023+527A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473908 | ||||||
chr15:78473969
|
T | C | 1 | a0001c0002t0017g0221 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1023+588T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473969 | ||||||
chr15:78474084
|
C | T | 1 | a0001c0001t0031g0072 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1023+703C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474084 | ||||||
chr15:78474287
|
C | T | 139 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(136): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1023+906C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474287 | ||||||
chr15:78474345
|
T | C | 4 | a0001c0001t0011g0132a0001c0001t0011g0133a0001c0001t0011g0134others(1): Show | 4 | HG01496.hp1 HG03486.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+964T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474345 | ||||||
chr15:78474396
|
A | G | 21 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(18): Show | 25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1023+1015A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474396 | ||||||
chr15:78474400
|
A | G | 4 | a0003c0005t0009g0180a0003c0005t0009g0181a0003c0005t0009g0182others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+1019A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474400 | ||||||
chr15:78474558
|
A | G | 1 | a0001c0002t0004g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1023+1177A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474558 | ||||||
chr15:78474918
|
G | A | 1 | a0001c0002t0004g0017 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1024-1270G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474918 | ||||||
chr15:78474980
|
G | A | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1024-1208G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474980 | ||||||
chr15:78475004
|
G | A | 129 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(126): Show | 141 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1024-1184G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475004 | ||||||
chr15:78475049
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1024-1139G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475049 | ||||||
chr15:78475061
|
C | CA | 28 | a0001c0001t0002g0022a0001c0001t0002g0177a0001c0001t0002g0246others(25): Show | 29 | HG00741.hp2 HG01123.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1024-1102dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | |||||
chr15:78475061
|
C | CAAA | 10 | a0001c0001t0006g0002a0001c0001t0006g0010a0001c0001t0006g0107others(7): Show | 13 | HG01346.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1024-1104_1024-110 others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | |||||
chr15:78475061
|
C | CAAAA | 5 | a0001c0001t0006g0009a0001c0001t0006g0011a0001c0001t0006g0108others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-1105_1024-110 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | |||||
chr15:78475061
|
C | CAAAAA | 5 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(2): Show | 6 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-1106_1024-110 others(9): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | |||||
chr15:78475061
|
CA | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(198): Show | 225 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1024-1102delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | |||||
chr15:78475061
|
CAA | C | 6 | a0001c0001t0001g0097a0001c0001t0001g0314a0001c0002t0004g0165others(3): Show | 6 | HG00280.hp1 HG01099.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-1103_1024-110 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | |||||
chr15:78475164
|
C | T | 1 | a0001c0002t0004g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1024-1024C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475164 | ||||||
chr15:78475206
|
C | G | 1 | a0001c0002t0012g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1024-982C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475206 | ||||||
chr15:78475285
|
A | G | 4 | a0003c0005t0009g0180a0003c0005t0009g0181a0003c0005t0009g0182others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-903A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475285 | ||||||
chr15:78475345
|
A | G | 16 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1024-843A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475345 | ||||||
chr15:78475508
|
C | T | 139 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(136): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1024-680C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475508 | ||||||
chr15:78475682
|
C | CA | 70 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(67): Show | 73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.1024-494dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475682 | |||||
chr15:78475765
|
T | G | 3 | a0001c0002t0005g0371a0001c0002t0005g0372a0001c0002t0005g0373 | 3 | HG00323.hp2 HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1024-423T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475765 | ||||||
chr15:78475801
|
G | A | 1 | a0002c0003t0010g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1024-387G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475801 | ||||||
chr15:78475817
|
G | A | 2 | a0001c0002t0040g0236a0001c0002t0041g0235 | 2 | HG03491.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1024-371G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475817 | ||||||
chr15:78475825
|
C | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(101): Show | 116 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1024-363C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475825 | ||||||
chr15:78475974
|
C | A | 1 | a0001c0002t0005g0366 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1024-214C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475974 | ||||||
chr15:78476043
|
T | C | 1 | a0001c0002t0003g0206 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1024-145T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78476043 | ||||||
chr15:78476529
|
C | G | 139 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(136): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1195+170C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476529 | ||||||
chr15:78476536
|
T | C | 3 | a0001c0001t0047g0116a0001c0001t0048g0117a0001c0001t0049g0118 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1195+177T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476536 | ||||||
chr15:78476752
|
C | T | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.1195+393C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476752 | ||||||
chr15:78476771
|
A | C | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+412A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476771 | ||||||
chr15:78476788
|
A | G | 141 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(138): Show | 154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1195+429A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476788 | ||||||
chr15:78476957
|
C | T | 2 | a0001c0002t0005g0359a0001c0002t0005g0360 | 2 | HG01516.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1195+598C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476957 | ||||||
chr15:78476964
|
A | G | 1 | a0001c0001t0013g0332 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1195+605A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476964 | ||||||
chr15:78476964
|
A | T | 1 | a0001c0001t0001g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1195+605A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476964 | ||||||
chr15:78477187
|
C | T | 2 | a0001c0001t0020g0124a0001c0001t0020g0125 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1195+828C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477187 | ||||||
chr15:78477344
|
T | G | 1 | a0001c0001t0002g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1196-953T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477344 | ||||||
chr15:78477401
|
T | C | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-896T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477401 | ||||||
chr15:78477460
|
T | C | 1 | a0001c0002t0017g0221 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1196-837T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477460 | ||||||
chr15:78477560
|
A | G | 1 | a0001c0001t0007g0340 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1196-737A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477560 | ||||||
chr15:78477628
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1196-669T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477628 | ||||||
chr15:78477677
|
C | T | 378 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(375): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.1196-620C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477677 | ||||||
chr15:78477690
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1196-607C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477690 | ||||||
chr15:78478020
|
G | A | 2 | a0001c0001t0020g0124a0001c0001t0020g0125 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1196-277G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78478020 | ||||||
chr15:78478076
|
A | G | 64 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(61): Show | 67 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.1196-221A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78478076 | ||||||
chr15:78478081
|
T | TA | 44 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0029others(41): Show | 45 | HG00738.hp2 HG00741.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.1196-198dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr15 | 78478081 | |||||
chr15:78478081
|
TA | T | 28 | a0001c0001t0001g0057a0001c0001t0001g0077a0001c0001t0001g0305others(25): Show | 32 | HG00323.hp2 HG01069.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1196-198delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr15 | 78478081 | |||||
chr15:78478212
|
C | T | 1 | a0001c0002t0005g0368 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1196-85C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78478212 | ||||||
chr15:78478575
|
G | A | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1296+178G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78478575 | ||||||
chr15:78478829
|
C | T | 2 | a0001c0001t0006g0110a0001c0001t0006g0112 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1296+432C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78478829 | ||||||
chr15:78478831
|
C | CA | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+435dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78478831 | |||||
chr15:78478844
|
T | C | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1296+447T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78478844 | ||||||
chr15:78479093
|
T | G | 1 | a0001c0001t0008g0320 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1296+696T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479093 | ||||||
chr15:78479204
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(104): Show | 119 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1296+807C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479204 | ||||||
chr15:78479399
|
A | AT | 14 | a0001c0001t0001g0032a0001c0001t0002g0023a0001c0001t0002g0024others(11): Show | 16 | HG01074.hp2 HG01255.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1296+1018dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479399 | |||||
chr15:78479399
|
A | ATT | 15 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(12): Show | 19 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1296+1017_1296+101 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479399 | |||||
chr15:78479657
|
T | C | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1296+1260T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479657 | ||||||
chr15:78479728
|
T | G | 377 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(374): Show | 411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.1296+1331T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479728 | ||||||
chr15:78479748
|
T | G | 1 | a0001c0002t0004g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1296+1351T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479748 | ||||||
chr15:78479818
|
G | A | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(8): Show | 11 | HG00438.hp2 NA18956.hp2 NA18978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1296+1421G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479818 | ||||||
chr15:78479832
|
G | A | 1 | a0001c0002t0004g0170 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1296+1435G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479832 | ||||||
chr15:78479919
|
T | TA | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(142): Show | 164 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1296+1539dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479919 | |||||
chr15:78479919
|
T | TAA | 63 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0002g0022others(60): Show | 66 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.1296+1538_1296+153 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479919 | |||||
chr15:78479919
|
T | TAAA | 6 | a0001c0001t0001g0071a0001c0001t0002g0029a0001c0001t0002g0273others(3): Show | 6 | HG01261.hp1 NA18973.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1296+1537_1296+153 others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479919 | |||||
chr15:78480298
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0031g0072 | 2 | NA19003.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1296+1901T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480298 | ||||||
chr15:78480334
|
A | G | 35 | a0001c0002t0004g0361a0001c0002t0005g0006a0001c0002t0005g0027others(32): Show | 37 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.1296+1937A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480334 | ||||||
chr15:78480464
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(104): Show | 119 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1296+2067C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480464 | ||||||
chr15:78480564
|
C | A | 1 | a0001c0002t0003g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1296+2167C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480564 | ||||||
chr15:78480603
|
C | T | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1296+2206C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480603 | ||||||
chr15:78480604
|
G | A | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1296+2207G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480604 | ||||||
chr15:78480618
|
G | A | 5 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG00558.hp2 HG02015.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296+2221G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480618 | ||||||
chr15:78480663
|
T | C | 7 | a0001c0002t0005g0344a0001c0002t0005g0345a0001c0002t0005g0346others(4): Show | 7 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1296+2266T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480663 | ||||||
chr15:78480674
|
A | G | 369 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(366): Show | 402 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(399): Show |
intron_variant | MODIFIER | c.1296+2277A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480674 | ||||||
chr15:78480686
|
T | TA | 19 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0054others(16): Show | 23 | HG01243.hp1 HG01256.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.1296+2309dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | |||||
chr15:78480686
|
T | TAA | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(91): Show | 107 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1296+2308_1296+230 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | |||||
chr15:78480686
|
T | TAAA | 175 | a0001c0001t0001g0032a0001c0001t0001g0051a0001c0001t0001g0065others(172): Show | 189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1296+2307_1296+230 others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | |||||
chr15:78480686
|
T | TAAAA | 52 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0174others(49): Show | 54 | HG00673.hp1 HG01074.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1296+2306_1296+230 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | |||||
chr15:78480686
|
T | TAAAAA | 33 | a0001c0001t0002g0022a0001c0001t0002g0175a0001c0001t0002g0177others(30): Show | 34 | HG00738.hp2 HG00741.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.1296+2305_1296+230 others(9): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | |||||
chr15:78480716
|
G | A | 1 | a0001c0002t0004g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1296+2319G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480716 | ||||||
chr15:78480720
|
G | T | 2 | a0001c0002t0005g0359a0001c0002t0005g0360 | 2 | HG01516.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1296+2323G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480720 | ||||||
chr15:78480731
|
C | T | 8 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1296+2334C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480731 | ||||||
chr15:78480776
|
G | A | 4 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0301others(1): Show | 4 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296+2379G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480776 | ||||||
chr15:78480801
|
A | T | 1 | a0001c0001t0002g0285 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1296+2404A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480801 | ||||||
chr15:78481008
|
C | CA | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0002g0247others(7): Show | 10 | HG01175.hp1 HG01952.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1297-2295dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481008 | |||||
chr15:78481078
|
G | A | 2 | a0001c0002t0003g0223a0001c0002t0003g0241 | 2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1297-2240G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481078 | ||||||
chr15:78481093
|
A | T | 21 | a0001c0001t0006g0002a0001c0001t0006g0009a0001c0001t0006g0010others(18): Show | 25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1297-2225A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481093 | ||||||
chr15:78481174
|
C | A | 378 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(375): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.1297-2144C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481174 | ||||||
chr15:78481204
|
G | A | 3 | a0001c0002t0004g0146a0001c0002t0004g0147a0001c0002t0022g0145 | 3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1297-2114G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481204 | ||||||
chr15:78481210
|
A | G | 1 | a0001c0002t0003g0376 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1297-2108A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481210 | ||||||
chr15:78481246
|
A | G | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1297-2072A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481246 | ||||||
chr15:78481332
|
A | C | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297-1986A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481332 | ||||||
chr15:78481346
|
A | G | 377 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(374): Show | 411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.1297-1972A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481346 | ||||||
chr15:78481347
|
C | T | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297-1971C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481347 | ||||||
chr15:78481351
|
C | T | 64 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(61): Show | 67 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.1297-1967C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481351 | ||||||
chr15:78481363
|
C | T | 2 | a0001c0002t0003g0215a0001c0002t0017g0216 | 2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1297-1955C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481363 | ||||||
chr15:78481366
|
C | CT | 8 | a0001c0001t0002g0246a0001c0001t0007g0325a0001c0001t0047g0116others(5): Show | 8 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1297-1942dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481366 | |||||
chr15:78481388
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1297-1930G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481388 | ||||||
chr15:78481522
|
A | AT | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(82): Show | 97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1297-1780dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481522 | |||||
chr15:78481522
|
A | ATT | 189 | a0001c0001t0001g0054a0001c0001t0001g0095a0001c0001t0001g0296others(186): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1297-1781_1297-178 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481522 | |||||
chr15:78481522
|
A | ATTT | 84 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(81): Show | 88 | HG00597.hp2 HG00738.hp2 HG01074.hp2 others(85): Show |
intron_variant | MODIFIER | c.1297-1782_1297-178 others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481522 | |||||
chr15:78481522
|
A | ATTTT | 11 | a0001c0001t0002g0177a0001c0001t0002g0255a0001c0001t0002g0265others(8): Show | 11 | HG00741.hp1 HG02083.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.1297-1783_1297-178 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481522 | |||||
chr15:78481566
|
C | T | 62 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(59): Show | 70 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1297-1752C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481566 | ||||||
chr15:78481591
|
T | C | 2 | a0001c0001t0002g0187a0001c0001t0002g0192 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1297-1727T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481591 | ||||||
chr15:78481592
|
C | T | 2 | a0001c0001t0002g0187a0001c0001t0002g0192 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1297-1726C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481592 | ||||||
chr15:78481781
|
T | C | 1 | a0001c0002t0005g0343 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1297-1537T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481781 | ||||||
chr15:78481929
|
C | T | 141 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(138): Show | 154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1297-1389C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481929 | ||||||
chr15:78482032
|
A | G | 141 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(138): Show | 154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1297-1286A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482032 | ||||||
chr15:78482090
|
C | T | 2 | a0001c0001t0002g0185a0001c0001t0002g0190 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1297-1228C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482090 | ||||||
chr15:78482334
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 114 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1297-984A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482334 | ||||||
chr15:78482395
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(9): Show | 12 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1297-923A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482395 | ||||||
chr15:78482640
|
AT | A | 8 | a0001c0002t0004g0361a0001c0002t0005g0006a0001c0002t0005g0343others(5): Show | 10 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1297-675delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78482640 | |||||
chr15:78482643
|
T | C | 2 | a0001c0006t0025g0120a0001c0006t0025g0121 | 2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1297-675T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482643 | ||||||
chr15:78482722
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0053 | 3 | HG03490.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1297-596T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482722 | ||||||
chr15:78482751
|
G | GT | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(105): Show | 120 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1297-553dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78482751 | |||||
chr15:78482751
|
G | GTT | 6 | a0001c0001t0001g0032a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG00438.hp2 HG01928.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297-554_1297-553d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78482751 | |||||
chr15:78482826
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1297-492C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482826 | ||||||
chr15:78482834
|
G | A | 2 | a0001c0001t0002g0248a0001c0001t0002g0274 | 2 | NA18961.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1297-484G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482834 | ||||||
chr15:78482892
|
C | T | 3 | a0001c0001t0047g0116a0001c0001t0048g0117a0001c0001t0049g0118 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1297-426C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482892 | ||||||
chr15:78482929
|
C | T | 2 | a0001c0001t0002g0187a0001c0001t0002g0192 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1297-389C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482929 | ||||||
chr15:78482987
|
C | T | 1 | a0001c0002t0045g0239 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1297-331C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482987 | ||||||
chr15:78483039
|
C | G | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1297-279C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78483039 | ||||||
chr15:78483130
|
G | T | 2 | a0001c0001t0001g0077a0001c0012t0001g0104 | 2 | HG01069.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1297-188G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78483130 | ||||||
chr15:78483178
|
G | A | 2 | a0001c0001t0002g0185a0001c0001t0002g0190 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1297-140G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78483178 | ||||||
chr15:78483210
|
A | C | 2 | a0001c0001t0001g0032a0001c0001t0014g0033 | 2 | NA18943.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1297-108A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78483210 | ||||||
chr15:78483576
|
T | A | 3 | a0001c0001t0007g0335a0001c0001t0007g0337a0001c0001t0007g0339 | 3 | NA18983.hp2 NA19084.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1413+142T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483576 | ||||||
chr15:78483756
|
A | G | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+322A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483756 | ||||||
chr15:78483785
|
C | CT | 6 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(3): Show | 7 | HG00438.hp1 HG01169.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1413+367dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr15 | 78483785 | |||||
chr15:78483785
|
CT | C | 16 | a0001c0001t0001g0309a0001c0001t0002g0279a0001c0001t0008g0025others(13): Show | 17 | HG01496.hp1 HG03491.hp1 NA18942.hp2 others(14): Show |
intron_variant | MODIFIER | c.1413+367delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr15 | 78483785 | |||||
chr15:78483810
|
G | A | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1413+376G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483810 | ||||||
chr15:78483867
|
TC | T | 384 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(381): Show | 419 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(416): Show |
intron_variant | MODIFIER | c.1413+439delC | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr15 | 78483867 | |||||
chr15:78483888
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0073 | 2 | NA18949.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1413+454G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483888 | ||||||
chr15:78483975
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1413+541G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483975 | ||||||
chr15:78484007
|
A | T | 1 | a0001c0006t0024g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1413+573A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484007 | ||||||
chr15:78484014
|
A | T | 2 | a0001c0001t0020g0124a0001c0001t0020g0125 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1413+580A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484014 | ||||||
chr15:78484114
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(98): Show | 113 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1414-647C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484114 | ||||||
chr15:78484115
|
G | A | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-646G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484115 | ||||||
chr15:78484384
|
C | T | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-377C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484384 | ||||||
chr15:78484970
|
G | A | 378 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(375): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.1573+50G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78484970 | ||||||
chr15:78485015
|
G | T | 4 | a0001c0001t0002g0244a0001c0001t0002g0258a0001c0001t0002g0261others(1): Show | 4 | NA18952.hp2 NA18959.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573+95G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78485015 | ||||||
chr15:78485350
|
A | T | 4 | a0003c0005t0009g0180a0003c0005t0009g0181a0003c0005t0009g0182others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1574-355A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78485350 | ||||||
chr15:78485398
|
G | T | 1 | a0001c0001t0009g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1574-307G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78485398 | ||||||
chr15:78485420
|
G | GA | 377 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(374): Show | 411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.1574-279dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr15 | 78485420 | |||||
chr15:78485552
|
A | G | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1574-153A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78485552 | ||||||
chr15:78485857
|
G | A | 1 | a0001c0006t0025g0121 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1709+17G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78485857 | ||||||
chr15:78485910
|
C | G | 1 | a0001c0001t0002g0268 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1709+70C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78485910 | ||||||
chr15:78486301
|
G | C | 3 | a0001c0001t0047g0116a0001c0001t0048g0117a0001c0001t0049g0118 | 3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1709+461G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486301 | ||||||
chr15:78486335
|
G | A | 1 | a0001c0001t0006g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1709+495G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486335 | ||||||
chr15:78486536
|
C | T | 2 | a0001c0001t0001g0047a0001c0002t0017g0212 | 2 | HG00639.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1709+696C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486536 | ||||||
chr15:78486541
|
G | T | 1 | a0001c0001t0034g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1709+701G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486541 | ||||||
chr15:78486552
|
C | T | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1709+712C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486552 | ||||||
chr15:78486582
|
G | A | 1 | a0001c0001t0034g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1709+742G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486582 | ||||||
chr15:78486610
|
GA | G | 9 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(6): Show | 10 | HG02109.hp2 NA18942.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1709+782delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr15 | 78486610 | |||||
chr15:78486611
|
A | G | 170 | a0001c0001t0004g0103a0001c0001t0007g0026a0001c0001t0007g0322others(167): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1709+771A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486611 | ||||||
chr15:78486612
|
A | G | 9 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(6): Show | 10 | HG02109.hp2 NA18942.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1709+772A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486612 | ||||||
chr15:78486616
|
A | G | 4 | a0003c0005t0009g0180a0003c0005t0009g0181a0003c0005t0009g0182others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1709+776A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486616 | ||||||
chr15:78486630
|
A | G | 179 | a0001c0001t0004g0103a0001c0001t0007g0026a0001c0001t0007g0322others(176): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1709+790A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486630 | ||||||
chr15:78486653
|
A | G | 8 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(5): Show | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.1709+813A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486653 | ||||||
chr15:78486748
|
CA | C | 3 | a0001c0002t0005g0353a0001c0002t0005g0354a0001c0002t0038g0352 | 3 | HG00639.hp1 HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1709+909delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486748 | ||||||
chr15:78486885
|
G | A | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1710-848G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486885 | ||||||
chr15:78487042
|
C | T | 179 | a0001c0001t0004g0103a0001c0001t0007g0026a0001c0001t0007g0322others(176): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1710-691C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487042 | ||||||
chr15:78487168
|
T | A | 142 | a0001c0001t0004g0103a0001c0002t0003g0003a0001c0002t0003g0005others(139): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1710-565T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487168 | ||||||
chr15:78487192
|
ACAAT | A | 357 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(354): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1710-536_1710-533d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr15 | 78487192 | |||||
chr15:78487459
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1710-274C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487459 | ||||||
chr15:78487591
|
A | G | 28 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(25): Show | 29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.1710-142A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487591 | ||||||
chr15:78487596
|
T | C | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1710-137T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487596 | ||||||
chr15:78487967
|
T | C | 1 | a0001c0001t0002g0252 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1794+150T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 14/21 | chr15 | 78487967 | ||||||
chr15:78488039
|
A | G | 1 | a0001c0002t0003g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1795-141A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 14/21 | chr15 | 78488039 | ||||||
chr15:78488442
|
G | A | 3 | a0001c0002t0005g0371a0001c0002t0005g0372a0001c0002t0005g0373 | 3 | HG00323.hp2 HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1951+106G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 15/21 | chr15 | 78488442 | ||||||
chr15:78488817
|
G | T | 4 | a0001c0002t0003g0224a0001c0002t0003g0225a0001c0002t0003g0226others(1): Show | 4 | HG01069.hp2 HG01106.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076+46G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78488817 | ||||||
chr15:78488909
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2076+138C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78488909 | ||||||
chr15:78488970
|
G | A | 22 | a0001c0001t0002g0186a0001c0001t0007g0026a0001c0001t0007g0322others(19): Show | 22 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.2076+199G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78488970 | ||||||
chr15:78488974
|
C | A | 4 | a0001c0001t0011g0132a0001c0001t0011g0133a0001c0001t0011g0134others(1): Show | 4 | HG01496.hp1 HG03486.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076+203C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78488974 | ||||||
chr15:78489163
|
G | A | 7 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(4): Show | 10 | HG01928.hp2 HG01934.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076+392G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489163 | ||||||
chr15:78489222
|
C | CA | 7 | a0001c0001t0002g0266a0001c0001t0011g0131a0001c0001t0011g0132others(4): Show | 7 | HG01496.hp1 HG02135.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2076+467dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr15 | 78489222 | |||||
chr15:78489222
|
CA | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(135): Show | 151 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.2076+467delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr15 | 78489222 | |||||
chr15:78489282
|
G | C | 1 | a0001c0001t0014g0086 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2076+511G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489282 | ||||||
chr15:78489339
|
C | T | 1 | a0001c0001t0011g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2076+568C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489339 | ||||||
chr15:78489345
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(98): Show | 113 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.2076+574G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489345 | ||||||
chr15:78489378
|
A | C | 1 | a0001c0002t0022g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2076+607A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489378 | ||||||
chr15:78489395
|
A | C | 1 | a0001c0001t0011g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2076+624A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489395 | ||||||
chr15:78489425
|
A | G | 1 | a0001c0002t0003g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2076+654A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489425 | ||||||
chr15:78489511
|
T | C | 1 | a0001c0002t0003g0195 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2076+740T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489511 | ||||||
chr15:78489584
|
C | T | 1 | a0001c0002t0004g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2076+813C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489584 | ||||||
chr15:78489647
|
T | TG | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.2077-771dupG | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr15 | 78489647 | |||||
chr15:78489659
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2077-763C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489659 | ||||||
chr15:78489681
|
A | T | 1 | a0001c0001t0002g0281 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2077-741A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489681 | ||||||
chr15:78489753
|
C | T | 142 | a0001c0001t0004g0103a0001c0002t0003g0003a0001c0002t0003g0005others(139): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.2077-669C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489753 | ||||||
chr15:78489936
|
A | G | 1 | a0001c0002t0003g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2077-486A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489936 | ||||||
chr15:78489956
|
T | C | 2 | a0001c0004t0001g0093a0001c0004t0016g0094 | 2 | NA18997.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2077-466T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489956 | ||||||
chr15:78489984
|
T | G | 70 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(67): Show | 73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.2077-438T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489984 | ||||||
chr15:78490243
|
A | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0062a0001c0001t0001g0080others(2): Show | 5 | NA18747.hp2 NA18944.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.2077-179A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490243 | ||||||
chr15:78490250
|
A | T | 41 | a0001c0001t0002g0022a0001c0001t0002g0029a0001c0001t0002g0244others(38): Show | 42 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.2077-172A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490250 | ||||||
chr15:78490326
|
T | G | 1 | a0001c0001t0002g0280 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2077-96T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490326 | ||||||
chr15:78490357
|
A | T | 2 | a0001c0006t0025g0120a0001c0006t0025g0121 | 2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2077-65A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490357 | ||||||
chr15:78490390
|
C | T | 19 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0247others(16): Show | 19 | HG02074.hp2 HG02083.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.2077-32C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490390 | ||||||
chr15:78490765
|
T | C | 1 | a0001c0001t0002g0249 | 1 | NA19084.hp1 | splice_region_variant&intron_variant | LOW | c.2324+4T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78490765 | ||||||
chr15:78490857
|
A | G | 3 | a0002c0003t0010g0012a0002c0003t0010g0128a0002c0003t0010g0130 | 4 | HG01109.hp1 HG02257.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2324+96A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78490857 | ||||||
chr15:78490935
|
G | A | 37 | a0001c0002t0004g0147a0001c0002t0004g0361a0001c0002t0005g0006others(34): Show | 39 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.2324+174G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78490935 | ||||||
chr15:78490952
|
C | T | 1 | a0001c0002t0005g0343 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2324+191C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78490952 | ||||||
chr15:78491106
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2324+345G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491106 | ||||||
chr15:78491157
|
A | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0066 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2324+396A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491157 | ||||||
chr15:78491341
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(104): Show | 119 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2324+580C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491341 | ||||||
chr15:78491382
|
G | A | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2324+621G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491382 | ||||||
chr15:78491470
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0177 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2324+709A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491470 | ||||||
chr15:78491490
|
GTATGTAT others(5): Show |
G | 140 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(137): Show | 153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2324+743_2324+754d others(14): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78491490 | |||||
chr15:78491539
|
C | G | 11 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(8): Show | 11 | HG00438.hp2 NA18956.hp2 NA18978.hp2 others(8): Show |
intron_variant | MODIFIER | c.2324+778C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491539 | ||||||
chr15:78491607
|
C | T | 1 | a0001c0001t0002g0275 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2324+846C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491607 | ||||||
chr15:78492036
|
T | G | 5 | a0001c0001t0008g0317a0001c0001t0008g0318a0001c0001t0008g0319others(2): Show | 5 | NA18942.hp2 NA18972.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.2324+1275T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492036 | ||||||
chr15:78492256
|
A | ACCCAGAT others(327): Show |
1 | a0001c0002t0012g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2324+1512_2324+151 others(338): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78492256 | |||||
chr15:78492362
|
C | CAAAAATT others(13): Show |
206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 222 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.2325-1542_2325-152 others(24): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78492362 | |||||
chr15:78492409
|
T | A | 4 | a0003c0005t0009g0180a0003c0005t0009g0181a0003c0005t0009g0182others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-1500T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492409 | ||||||
chr15:78492561
|
A | ATTTG | 39 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(36): Show | 42 | HG00280.hp1 HG00423.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.2325-1332_2325-132 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78492561 | |||||
chr15:78492577
|
G | T | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-1332G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492577 | ||||||
chr15:78492640
|
G | T | 5 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2325-1269G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492640 | ||||||
chr15:78492651
|
G | A | 4 | a0001c0002t0004g0016a0001c0002t0004g0149a0001c0002t0004g0165others(1): Show | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-1258G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492651 | ||||||
chr15:78492919
|
T | C | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.2325-990T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492919 | ||||||
chr15:78493202
|
CAGAT | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(107): Show | 122 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2325-703_2325-700d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78493202 | |||||
chr15:78493460
|
T | G | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.2325-449T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493460 | ||||||
chr15:78493602
|
A | AT | 40 | a0001c0002t0004g0361a0001c0002t0005g0006a0001c0002t0005g0027others(37): Show | 42 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.2325-295dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78493602 | |||||
chr15:78493602
|
AT | A | 67 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(64): Show | 70 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.2325-295delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78493602 | |||||
chr15:78493642
|
A | G | 1 | a0001c0001t0018g0327 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2325-267A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493642 | ||||||
chr15:78493724
|
G | A | 2 | a0001c0001t0047g0116a0001c0001t0049g0118 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2325-185G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493724 | ||||||
chr15:78493769
|
G | T | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-140G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493769 | ||||||
chr15:78493851
|
A | G | 6 | a0001c0002t0004g0159a0001c0002t0004g0162a0001c0002t0004g0167others(3): Show | 6 | HG00280.hp1 HG00423.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.2325-58A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493851 | ||||||
chr15:78494068
|
A | C | 378 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(375): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.2472+12A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 19/21 | chr15 | 78494068 | ||||||
chr15:78494496
|
T | A | 2 | a0001c0006t0025g0120a0001c0006t0025g0121 | 2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2595+232T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494496 | ||||||
chr15:78494501
|
A | G | 10 | a0001c0002t0003g0005a0001c0002t0003g0019a0001c0002t0003g0193others(7): Show | 13 | HG00544.hp2 HG00673.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2595+237A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494501 | ||||||
chr15:78494756
|
A | G | 2 | a0001c0001t0027g0245a0001c0001t0027g0264 | 2 | HG02074.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2595+492A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494756 | ||||||
chr15:78494820
|
G | A | 1 | a0001c0001t0034g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2595+556G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494820 | ||||||
chr15:78494858
|
C | A | 7 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179others(4): Show | 8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2595+594C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494858 | ||||||
chr15:78494867
|
C | T | 1 | a0001c0006t0024g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2595+603C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494867 | ||||||
chr15:78495076
|
GA | G | 9 | a0001c0001t0008g0025a0001c0001t0008g0315a0001c0001t0008g0316others(6): Show | 10 | HG02109.hp2 NA18942.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.2595+814delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr15 | 78495076 | |||||
chr15:78495238
|
G | A | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(351): Show | 383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.2595+974G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78495238 | ||||||
chr15:78495918
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0016g0058 | 2 | HG00597.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2596-1208T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78495918 | ||||||
chr15:78496158
|
G | C | 62 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(59): Show | 70 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.2596-968G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496158 | ||||||
chr15:78496231
|
G | T | 4 | a0001c0001t0002g0244a0001c0001t0002g0258a0001c0001t0002g0261others(1): Show | 4 | NA18952.hp2 NA18959.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.2596-895G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496231 | ||||||
chr15:78496307
|
G | T | 5 | a0002c0003t0010g0012a0002c0003t0010g0126a0002c0003t0010g0128others(2): Show | 6 | HG01109.hp1 HG02257.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2596-819G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496307 | ||||||
chr15:78496415
|
C | CA | 4 | a0001c0006t0024g0122a0001c0006t0024g0123a0001c0006t0025g0120others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2596-710dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr15 | 78496415 | |||||
chr15:78496465
|
A | G | 378 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(375): Show | 412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.2596-661A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496465 | ||||||
chr15:78496506
|
G | T | 3 | a0001c0001t0007g0335a0001c0001t0007g0337a0001c0001t0007g0339 | 3 | NA18983.hp2 NA19084.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2596-620G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496506 | ||||||
chr15:78496637
|
C | G | 2 | a0001c0006t0024g0122a0001c0006t0024g0123 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2596-489C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496637 | ||||||
chr15:78496722
|
G | T | 3 | a0001c0001t0002g0290a0001c0001t0002g0291a0001c0001t0044g0295 | 3 | HG01978.hp2 HG02004.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2596-404G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496722 | ||||||
chr15:78496784
|
A | G | 3 | a0001c0001t0009g0018a0001c0001t0009g0178a0001c0001t0009g0179 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2596-342A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496784 | ||||||
chr15:78496849
|
G | A | 28 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(25): Show | 29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.2596-277G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496849 | ||||||
chr15:78496881
|
G | A | 141 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0019others(138): Show | 154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2596-245G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496881 | ||||||
chr15:78496921
|
C | T | 1 | a0001c0001t0011g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2596-205C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496921 | ||||||
chr15:78497330
|
A | G | 21 | a0001c0001t0007g0026a0001c0001t0007g0322a0001c0001t0007g0323others(18): Show | 21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.2781+19A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497330 | ||||||
chr15:78497334
|
T | C | 68 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(65): Show | 71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.2781+23T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497334 | ||||||
chr15:78497420
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2781+109A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497420 | ||||||
chr15:78497759
|
G | A | 362 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(359): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.2782-274G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497759 | ||||||
chr15:78497847
|
A | G | 35 | a0001c0001t0002g0022a0001c0001t0002g0029a0001c0001t0002g0244others(32): Show | 36 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.2782-186A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497847 |