geneid | 4223 |
---|---|
ensemblid | ENSG00000106511.6 |
hgncid | 7014 |
symbol | MEOX2 |
name | mesenchyme homeobox 2 |
refseq_nuc | NM_005924.5 |
refseq_prot | NP_005915.2 |
ensembl_nuc | ENST00000262041.6 |
ensembl_prot | ENSP00000262041.5 |
mane_status | MANE Select |
chr | chr7 |
start | 15611212 |
end | 15686683 |
strand | - |
ver | v1.2 |
region | chr7:15611212-15686683 |
region5000 | chr7:15606212-15691683 |
regionname0 | MEOX2_chr7_15611212_15686683 |
regionname5000 | MEOX2_chr7_15606212_15691683 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 303 | 177 | 72 | 36 | 44 | 7 | 18 | 36 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002 | 1/1 | 304 | 103 | 12 | 27 | 35 | 8 | 19 | 28 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003 | 0/0 | 303 | 58 | 3 | 2 | 52 | 0 | 1 | 43 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0004 | 0/0 | 304 | 7 | 0 | 3 | 4 | 0 | 0 | 2 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0005 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0006 | 0/0 | 303 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0007 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0008 | 0/0 | 303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0009 | 0/0 | 304 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0010 | 0/0 | 303 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0011 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
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 | 912 | 176 | 71 | 36 | 44 | 7 | 18 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0002 | 1/1 | 915 | 103 | 12 | 27 | 35 | 8 | 19 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0003 | 0/0 | 912 | 57 | 3 | 2 | 52 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0004 | 0/0 | 915 | 7 | 0 | 3 | 4 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0005 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0006 | 0/0 | 912 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0007 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0008 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0009 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0010 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0011 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0012 | 0/0 | 915 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
c0013 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
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 | 1459 | 97 | 18 | 25 | 36 | 7 | 11 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0002 | 1/0 | 1457 | 52 | 1 | 11 | 23 | 2 | 14 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0003 | 0/0 | 1459 | 51 | 0 | 2 | 48 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0004 | 0/0 | 1457 | 19 | 4 | 6 | 5 | 1 | 3 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0005 | 0/0 | 1457 | 14 | 0 | 5 | 6 | 2 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0006 | 0/0 | 1459 | 12 | 6 | 1 | 2 | 1 | 2 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0007 | 0/0 | 1459 | 9 | 7 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0008 | 0/0 | 1459 | 9 | 6 | 2 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0009 | 0/0 | 1457 | 8 | 6 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0010 | 0/1 | 1457 | 8 | 2 | 3 | 0 | 1 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0011 | 0/0 | 1457 | 7 | 0 | 3 | 4 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0012 | 0/0 | 1460 | 6 | 4 | 0 | 1 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0013 | 0/0 | 1460 | 5 | 1 | 1 | 0 | 0 | 3 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0014 | 0/0 | 1458 | 5 | 4 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0015 | 0/0 | 1461 | 4 | 3 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0016 | 0/0 | 1461 | 4 | 4 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0017 | 0/0 | 1459 | 4 | 0 | 0 | 4 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0018 | 0/0 | 1459 | 4 | 1 | 0 | 2 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0019 | 0/0 | 1459 | 3 | 2 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0020 | 0/0 | 1457 | 3 | 3 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0021 | 0/0 | 1457 | 3 | 3 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0022 | 0/0 | 1457 | 3 | 1 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0023 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0024 | 0/0 | 1459 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0025 | 0/0 | 1457 | 2 | 0 | 0 | 0 | 2 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0026 | 0/0 | 1457 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0027 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0028 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0029 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0030 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0031 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0032 | 0/0 | 1459 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0033 | 0/0 | 1459 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0034 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0035 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0036 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0037 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0038 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0039 | 0/0 | 1457 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
t0040 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0302 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
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 | 912 | 176 | 71 | 36 | 44 | 7 | 18 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0010 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002 | 1/1 | 915 | 103 | 12 | 27 | 35 | 8 | 19 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003c0003 | 0/0 | 912 | 57 | 3 | 2 | 52 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003c0013 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0004c0004 | 0/0 | 915 | 7 | 0 | 3 | 4 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0005c0011 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0006c0009 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0007c0008 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0008c0007 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0009c0012 | 0/0 | 915 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0010c0006 | 0/0 | 912 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0011c0005 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2370 | 92 | 15 | 25 | 36 | 6 | 10 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0006 | 0/0 | 2370 | 12 | 6 | 1 | 2 | 1 | 2 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0007 | 0/0 | 2370 | 8 | 6 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0008 | 0/0 | 2370 | 8 | 5 | 2 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0009 | 0/0 | 2368 | 8 | 6 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0012 | 0/0 | 2371 | 6 | 4 | 0 | 1 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0013 | 0/0 | 2371 | 5 | 1 | 1 | 0 | 0 | 3 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0014 | 0/0 | 2369 | 5 | 4 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0015 | 0/0 | 2372 | 4 | 3 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0016 | 0/0 | 2372 | 4 | 4 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0018 | 0/0 | 2370 | 4 | 1 | 0 | 2 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0019 | 0/0 | 2370 | 3 | 2 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0020 | 0/0 | 2368 | 3 | 3 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0021 | 0/0 | 2368 | 3 | 3 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0023 | 0/0 | 2372 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0024 | 0/0 | 2370 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0031 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0032 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0033 | 0/0 | 2370 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0034 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0035 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0036 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0001t0037 | 0/0 | 2368 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0001c0010t0029 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0001 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0002 | 1/0 | 2371 | 52 | 1 | 11 | 23 | 2 | 14 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0004 | 0/0 | 2371 | 19 | 4 | 6 | 5 | 1 | 3 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0005 | 0/0 | 2371 | 13 | 0 | 5 | 6 | 2 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0010 | 0/1 | 2371 | 8 | 2 | 3 | 0 | 1 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0022 | 0/0 | 2371 | 3 | 1 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0025 | 0/0 | 2371 | 2 | 0 | 0 | 0 | 2 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0026 | 0/0 | 2371 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0028 | 0/0 | 2374 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0039 | 0/0 | 2371 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0002c0002t0040 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003c0003t0003 | 0/0 | 2370 | 49 | 0 | 2 | 47 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003c0003t0008 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003c0003t0017 | 0/0 | 2370 | 4 | 0 | 0 | 4 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003c0003t0027 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003c0003t0030 | 0/0 | 2371 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003c0003t0038 | 0/0 | 2368 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0003c0013t0003 | 0/0 | 2370 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0004c0004t0011 | 0/0 | 2371 | 7 | 0 | 3 | 4 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0005c0011t0001 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0006c0009t0001 | 0/0 | 2370 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0007c0008t0007 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0008c0007t0003 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0009c0012t0005 | 0/0 | 2371 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0010c0006t0001 | 0/0 | 2370 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
a0011c0005t0001 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | copy fasta | chr7 | 15606212 | 15691683 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0007g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0008g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0008g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0009g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0009g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0012g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0012g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0013g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0013g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0013g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0014g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0014g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0014g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0014g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0014g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0015g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0016g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0016g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0016g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0016g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0018g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0018g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0018g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0018g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0019g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0019g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0019g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0020g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0020g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0020g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0021g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0021g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0021g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0023g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0024g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0024g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0031g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0032g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0033g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0034g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0035g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0036g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0001t0037g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0001c0010t0029g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0302 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0004g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0010g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0010g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0010g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0010g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0010g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0010g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0010g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0022g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0022g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0022g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0025g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0025g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0026g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0026g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0028g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0039g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0002c0002t0040g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0017g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0017g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0017g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0027g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0030g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0003t0038g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0003c0013t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0004c0004t0011g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0004c0004t0011g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0004c0004t0011g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0004c0004t0011g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0004c0004t0011g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0004c0004t0011g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0004c0004t0011g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0005c0011t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0006c0009t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0007c0008t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0008c0007t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0009c0012t0005g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0010c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
a0011c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0322 | EUR | GBR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0135 | EUR | FIN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00323 | hp1 | a0010 | c0006 | t0001 | g0035 | EUR | FIN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00323 | hp2 | a0002 | c0002 | t0010 | g0307 | EUR | FIN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00408 | hp2 | a0003 | c0003 | t0003 | g0161 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00558 | hp1 | a0004 | c0004 | t0011 | g0312 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00558 | hp2 | a0003 | c0003 | t0003 | g0192 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00609 | hp1 | a0003 | c0003 | t0003 | g0156 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0291 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0301 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00639 | hp1 | a0001 | c0001 | t0009 | g0226 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0222 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00673 | hp1 | a0004 | c0004 | t0011 | g0277 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0292 | EAS | CHS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00735 | hp1 | a0002 | c0002 | t0004 | g0328 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00735 | hp2 | a0002 | c0002 | t0005 | g0267 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0323 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00741 | hp1 | a0004 | c0004 | t0011 | g0315 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG00741 | hp2 | a0002 | c0002 | t0022 | g0320 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01074 | hp1 | a0001 | c0001 | t0019 | g0118 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01074 | hp2 | a0002 | c0002 | t0005 | g0263 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0071 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01099 | hp2 | a0002 | c0002 | t0005 | g0274 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01106 | hp1 | a0002 | c0002 | t0004 | g0333 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01109 | hp1 | a0002 | c0002 | t0004 | g0255 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01109 | hp2 | a0002 | c0002 | t0022 | g0256 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0041 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0136 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01169 | hp2 | a0001 | c0001 | t0008 | g0042 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01175 | hp2 | a0002 | c0002 | t0010 | g0304 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01192 | hp2 | a0004 | c0004 | t0011 | g0314 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0180 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0278 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01261 | hp1 | a0001 | c0001 | t0013 | g0023 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01358 | hp2 | a0002 | c0002 | t0010 | g0310 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0332 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01361 | hp2 | a0002 | c0002 | t0005 | g0268 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01433 | hp2 | a0002 | c0002 | t0004 | g0324 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0283 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01515 | hp1 | a0002 | c0002 | t0004 | g0241 | EUR | IBS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01515 | hp2 | a0002 | c0002 | t0025 | g0335 | EUR | IBS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01517 | hp1 | a0002 | c0002 | t0025 | g0334 | EUR | IBS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01884 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01891 | hp1 | a0001 | c0001 | t0016 | g0014 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01928 | hp1 | a0003 | c0003 | t0003 | g0128 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0331 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0305 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01934 | hp2 | a0002 | c0002 | t0004 | g0339 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01943 | hp2 | a0004 | c0004 | t0011 | g0311 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01952 | hp1 | a0002 | c0002 | t0010 | g0270 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01993 | hp1 | a0001 | c0001 | t0033 | g0213 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0293 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02015 | hp1 | a0003 | c0003 | t0003 | g0155 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02055 | hp2 | a0003 | c0003 | t0008 | g0112 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02056 | hp2 | a0001 | c0001 | t0018 | g0101 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02071 | hp1 | a0003 | c0003 | t0003 | g0057 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02071 | hp2 | a0003 | c0003 | t0003 | g0099 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02074 | hp2 | a0002 | c0002 | t0005 | g0266 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02129 | hp1 | a0002 | c0002 | t0005 | g0258 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02129 | hp2 | a0003 | c0003 | t0003 | g0086 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02132 | hp1 | a0003 | c0003 | t0003 | g0076 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02145 | hp1 | a0001 | c0001 | t0013 | g0022 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02145 | hp2 | a0001 | c0001 | t0034 | g0217 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0306 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | CDX | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02258 | hp2 | a0002 | c0002 | t0022 | g0303 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02273 | hp1 | a0002 | c0002 | t0004 | g0238 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02273 | hp2 | a0003 | c0003 | t0003 | g0164 | AMR | PEL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02280 | hp1 | a0005 | c0011 | t0001 | g0211 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02280 | hp2 | a0001 | c0001 | t0014 | g0220 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02451 | hp1 | a0001 | c0001 | t0009 | g0224 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02572 | hp1 | a0001 | c0001 | t0021 | g0237 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0182 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02602 | hp1 | a0001 | c0001 | t0013 | g0020 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02602 | hp2 | a0006 | c0009 | t0001 | g0078 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02615 | hp1 | a0001 | c0001 | t0019 | g0117 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0031 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0179 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02647 | hp1 | a0002 | c0002 | t0004 | g0244 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02647 | hp2 | a0001 | c0001 | t0032 | g0079 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0318 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0068 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02717 | hp1 | a0001 | c0001 | t0020 | g0227 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0321 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02809 | hp1 | a0001 | c0001 | t0016 | g0018 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0013 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02818 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0176 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0229 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02886 | hp2 | a0001 | c0001 | t0021 | g0236 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02896 | hp1 | a0003 | c0003 | t0038 | g0234 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02897 | hp1 | a0011 | c0005 | t0001 | g0034 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02922 | hp1 | a0002 | c0002 | t0004 | g0246 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02965 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0183 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03017 | hp1 | a0001 | c0001 | t0008 | g0072 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0325 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03098 | hp1 | a0002 | c0002 | t0010 | g0247 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03139 | hp1 | a0001 | c0001 | t0014 | g0215 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0231 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0232 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03195 | hp2 | a0002 | c0002 | t0040 | g0252 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03209 | hp1 | a0001 | c0001 | t0037 | g0235 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03209 | hp2 | a0001 | c0001 | t0018 | g0177 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03225 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0319 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03453 | hp1 | a0007 | c0008 | t0007 | g0178 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0012 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03486 | hp1 | a0002 | c0002 | t0026 | g0243 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03486 | hp2 | a0001 | c0001 | t0016 | g0016 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0275 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03490 | hp2 | a0002 | c0002 | t0004 | g0257 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03491 | hp1 | a0001 | c0001 | t0018 | g0075 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0317 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0276 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0316 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03516 | hp1 | a0002 | c0002 | t0026 | g0250 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0120 | AFR | ESN | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0032 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03540 | hp2 | a0001 | c0001 | t0021 | g0225 | AFR | GWD | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03579 | hp1 | a0003 | c0003 | t0027 | g0025 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03579 | hp2 | a0001 | c0001 | t0014 | g0218 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03654 | hp1 | a0009 | c0012 | t0005 | g0340 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0326 | SAS | PJL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03688 | hp2 | a0001 | c0001 | t0006 | g0173 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03831 | hp2 | a0003 | c0013 | t0003 | g0212 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03927 | hp1 | a0001 | c0001 | t0013 | g0021 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0265 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0327 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03942 | hp2 | a0002 | c0002 | t0028 | g0026 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04115 | hp1 | a0002 | c0002 | t0010 | g0309 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04184 | hp1 | a0002 | c0002 | t0004 | g0308 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0329 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04204 | hp2 | a0001 | c0001 | t0012 | g0029 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04228 | hp1 | a0001 | c0001 | t0013 | g0024 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0336 | SAS | STU | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0039 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18612 | hp1 | a0003 | c0003 | t0003 | g0123 | EAS | CHB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | CHB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18906 | hp1 | a0002 | c0002 | t0004 | g0254 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0230 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18939 | hp1 | a0003 | c0003 | t0003 | g0106 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18940 | hp1 | a0003 | c0003 | t0003 | g0197 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18941 | hp1 | a0003 | c0003 | t0017 | g0008 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18944 | hp1 | a0002 | c0002 | t0004 | g0296 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18944 | hp2 | a0002 | c0002 | t0005 | g0272 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18947 | hp1 | a0001 | c0001 | t0015 | g0019 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18948 | hp2 | a0003 | c0003 | t0003 | g0157 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18949 | hp1 | a0003 | c0003 | t0003 | g0105 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18949 | hp2 | a0004 | c0004 | t0011 | g0240 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18950 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18954 | hp1 | a0008 | c0007 | t0003 | g0037 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18956 | hp2 | a0003 | c0003 | t0003 | g0195 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18957 | hp2 | a0003 | c0003 | t0003 | g0144 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18960 | hp1 | a0003 | c0003 | t0003 | g0104 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18961 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18962 | hp2 | a0003 | c0003 | t0003 | g0152 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18963 | hp2 | a0003 | c0003 | t0003 | g0107 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18964 | hp1 | a0002 | c0002 | t0004 | g0287 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18964 | hp2 | a0003 | c0003 | t0003 | g0198 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18965 | hp1 | a0003 | c0003 | t0003 | g0207 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18965 | hp2 | a0002 | c0002 | t0005 | g0261 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18968 | hp1 | a0003 | c0003 | t0003 | g0209 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18969 | hp2 | a0003 | c0003 | t0003 | g0205 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18975 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18977 | hp1 | a0003 | c0003 | t0003 | g0049 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18977 | hp2 | a0003 | c0003 | t0003 | g0119 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18978 | hp2 | a0003 | c0003 | t0017 | g0210 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18983 | hp1 | a0001 | c0001 | t0024 | g0141 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18986 | hp1 | a0002 | c0002 | t0004 | g0239 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0338 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18988 | hp2 | a0003 | c0003 | t0003 | g0203 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18990 | hp1 | a0001 | c0001 | t0018 | g0102 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18990 | hp2 | a0003 | c0003 | t0003 | g0208 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18992 | hp2 | a0003 | c0003 | t0003 | g0199 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18993 | hp1 | a0003 | c0003 | t0003 | g0158 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18995 | hp1 | a0003 | c0003 | t0003 | g0096 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18998 | hp1 | a0003 | c0003 | t0003 | g0201 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19000 | hp2 | a0003 | c0003 | t0030 | g0033 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19001 | hp1 | a0003 | c0003 | t0003 | g0159 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19002 | hp1 | a0002 | c0002 | t0039 | g0300 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19003 | hp1 | a0003 | c0003 | t0003 | g0098 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19004 | hp1 | a0003 | c0003 | t0003 | g0202 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19004 | hp2 | a0001 | c0001 | t0012 | g0030 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19007 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19007 | hp2 | a0002 | c0002 | t0004 | g0260 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19012 | hp2 | a0001 | c0001 | t0006 | g0081 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0181 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0233 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0015 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19043 | hp2 | a0002 | c0002 | t0004 | g0245 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19056 | hp2 | a0003 | c0003 | t0003 | g0191 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19058 | hp2 | a0003 | c0003 | t0003 | g0200 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19062 | hp1 | a0003 | c0003 | t0017 | g0008 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19063 | hp2 | a0003 | c0003 | t0003 | g0194 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19065 | hp1 | a0003 | c0003 | t0003 | g0174 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19066 | hp2 | a0002 | c0002 | t0005 | g0273 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19068 | hp1 | a0004 | c0004 | t0011 | g0313 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19074 | hp1 | a0003 | c0003 | t0003 | g0204 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19077 | hp2 | a0003 | c0003 | t0017 | g0206 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19083 | hp1 | a0003 | c0003 | t0003 | g0137 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19083 | hp2 | a0001 | c0001 | t0024 | g0196 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19084 | hp1 | a0002 | c0002 | t0004 | g0259 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19084 | hp2 | a0003 | c0003 | t0003 | g0150 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19086 | hp1 | a0003 | c0003 | t0003 | g0103 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19086 | hp2 | a0003 | c0003 | t0003 | g0154 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19089 | hp1 | a0003 | c0003 | t0003 | g0151 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19089 | hp2 | a0002 | c0002 | t0005 | g0279 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0040 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0248 | AFR | YRI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20129 | hp1 | a0002 | c0002 | t0010 | g0249 | AFR | ASW | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ASW | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20752 | hp1 | a0002 | c0002 | t0005 | g0262 | EUR | TSI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0330 | EUR | TSI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20805 | hp2 | a0002 | c0002 | t0005 | g0264 | EUR | TSI | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0337 | SAS | GIH | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20905 | hp2 | a0002 | c0002 | t0004 | g0242 | SAS | GIH | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01123 | hp1 | a0002 | c0002 | t0005 | g0269 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG01123 | hp2 | a0001 | c0001 | t0014 | g0221 | AMR | CLM | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02109 | hp1 | a0001 | c0001 | t0015 | g0017 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0189 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02486 | hp1 | a0001 | c0001 | t0014 | g0216 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02486 | hp2 | a0001 | c0001 | t0009 | g0223 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG02559 | hp2 | a0001 | c0001 | t0035 | g0214 | AFR | ACB | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03471 | hp1 | a0001 | c0001 | t0031 | g0028 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | MSL | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG06807 | hp1 | a0001 | c0001 | t0036 | g0219 | AFR | USA | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
HG06807 | hp2 | a0001 | c0001 | t0019 | g0126 | AFR | USA | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA18955 | hp2 | a0003 | c0003 | t0003 | g0190 | EAS | JPT | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | USA | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA20300 | hp2 | a0001 | c0001 | t0020 | g0228 | AFR | USA | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA21309 | hp1 | a0001 | c0010 | t0029 | g0027 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0010 | g0251 | REF | REF | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0302 | REF | REF | MEOX2_chr7_15606212_15691683 | MEOX2 | chr7 | 15606212 | 15691683 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:15612428
|
T | A | 1 | a0006 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.874A>T | p.Ser292Cys | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 1155/2371 | 874/915 | 292/304 | chr7 | 15612428 | ||
chr7:15612442
|
A | G | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.860T>C | p.Ile287Thr | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 1141/2371 | 860/915 | 287/304 | chr7 | 15612442 | ||
chr7:15612443
|
T | G | 3 | a0003a0004a0008 | 66 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(63): Show |
missense_variant | MODERATE | c.859A>C | p.Ile287Leu | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 1140/2371 | 859/915 | 287/304 | chr7 | 15612443 | ||
chr7:15686064
|
G | T | 1 | a0008 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.339C>A | p.Asp113Glu | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 620/2371 | 339/915 | 113/304 | chr7 | 15686064 | ||
chr7:15686105
|
G | C | 1 | a0005 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.298C>G | p.Pro100Ala | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 579/2371 | 298/915 | 100/304 | chr7 | 15686105 | ||
chr7:15686172
|
ATGG | A | 8 | a0001a0003a0005others(5): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
disruptive_inframe_deletion | MODERATE | c.228_230delCCA | p.His77del | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 511/2371 | 228/915 | 76/304 | chr7 | 15686172 | ||
chr7:15686191
|
T | C | 1 | a0009 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.212A>G | p.His71Arg | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 493/2371 | 212/915 | 71/304 | chr7 | 15686191 | ||
chr7:15686198
|
G | T | 1 | a0010 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.205C>A | p.His69Asn | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 486/2371 | 205/915 | 69/304 | chr7 | 15686198 | ||
chr7:15686342
|
G | T | 1 | a0011 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.61C>A | p.Pro21Thr | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 342/2371 | 61/915 | 21/304 | chr7 | 15686342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:15626848
|
T | C | 1 | a0001c0010 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.588A>G | p.Lys196Lys | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/3 | 869/2371 | 588/915 | 196/304 | chr7 | 15626848 | ||
chr7:15686343
|
G | A | 1 | a0003c0013 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.60C>T | p.His20His | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 341/2371 | 60/915 | 20/304 | chr7 | 15686343 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:15611372
|
C | T | 1 | a0001c0001t0019 | 3 | HG01074.hp1 HG02615.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1015G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 1015 | chr7 | 15611372 | |||||
chr7:15611505
|
G | C | 1 | a0002c0002t0025 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*882C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 882 | chr7 | 15611505 | |||||
chr7:15611533
|
G | T | 43 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(40): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*854C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 854 | chr7 | 15611533 | |||||
chr7:15611966
|
T | C | 1 | a0002c0002t0040 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*421A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 421 | chr7 | 15611966 | |||||
chr7:15611973
|
C | T | 1 | a0003c0003t0017 | 4 | NA18941.hp1 NA18978.hp2 NA19062.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 414 | chr7 | 15611973 | |||||
chr7:15611974
|
C | G | 5 | a0001c0001t0018a0001c0001t0024a0002c0002t0005others(2): Show | 21 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*413G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 413 | chr7 | 15611974 | |||||
chr7:15612067
|
T | C | 7 | a0003c0003t0003a0003c0003t0017a0003c0003t0030others(4): Show | 64 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*320A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 320 | chr7 | 15612067 | |||||
chr7:15612145
|
C | T | 26 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(23): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*242G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 242 | chr7 | 15612145 | |||||
chr7:15612276
|
A | T | 27 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(24): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*111T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 111 | chr7 | 15612276 | |||||
chr7:15612279
|
A | G | 1 | a0001c0001t0032 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 3/3 | 108 | chr7 | 15612279 | |||||
chr7:15686408
|
G | A | 1 | a0001c0001t0033 | 1 | HG01993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 6 | chr7 | 15686408 | |||||
chr7:15686433
|
A | G | 1 | a0001c0010t0029 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 31 | chr7 | 15686433 | |||||
chr7:15686441
|
G | A | 38 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(35): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
5_prime_UTR_variant | MODIFIER | c.-39C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 39 | chr7 | 15686441 | |||||
chr7:15686492
|
A | AT | 4 | a0001c0001t0014a0001c0001t0034a0001c0001t0035others(1): Show | 8 | HG01123.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-91dupA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 91 | chr7 | 15686492 | |||||
chr7:15686492
|
A | ATT | 20 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(17): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
5_prime_UTR_variant | MODIFIER | c.-92_-91dupAA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 91 | chr7 | 15686492 | |||||
chr7:15686492
|
A | ATTT | 7 | a0001c0001t0012a0001c0001t0013a0001c0001t0031others(4): Show | 16 | HG01261.hp1 HG02145.hp1 HG02602.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-93_-91dupAAA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 91 | chr7 | 15686492 | |||||
chr7:15686492
|
A | ATTTT | 3 | a0001c0001t0015a0001c0001t0016a0001c0001t0023 | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-94_-91dupAAAA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 91 | chr7 | 15686492 | |||||
chr7:15686504
|
A | C | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(36): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
5_prime_UTR_variant | MODIFIER | c.-102T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 102 | chr7 | 15686504 | |||||
chr7:15686672
|
A | G | 5 | a0001c0001t0013a0001c0001t0015a0001c0001t0016others(2): Show | 16 | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-270T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/3 | 270 | chr7 | 15686672 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:15612789
|
A | C | 225 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-178T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15612789 | ||||||
chr7:15612852
|
T | G | 135 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0044others(132): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.691-241A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15612852 | ||||||
chr7:15612898
|
A | G | 1 | a0002c0002t0002g0293 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.691-287T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15612898 | ||||||
chr7:15613028
|
A | T | 7 | a0001c0001t0001g0044a0001c0001t0012g0003a0001c0001t0012g0031others(4): Show | 8 | HG01109.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-417T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613028 | ||||||
chr7:15613070
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.691-459T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613070 | ||||||
chr7:15613095
|
C | G | 2 | a0003c0003t0008g0112a0003c0003t0027g0025 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-484G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613095 | ||||||
chr7:15613158
|
T | G | 225 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-547A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613158 | ||||||
chr7:15613273
|
G | C | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691-662C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613273 | ||||||
chr7:15613282
|
C | T | 1 | a0002c0002t0010g0270 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.691-671G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613282 | ||||||
chr7:15613285
|
C | T | 1 | a0002c0002t0002g0318 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.691-674G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613285 | ||||||
chr7:15613310
|
G | T | 1 | a0003c0003t0003g0203 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.691-699C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613310 | ||||||
chr7:15613395
|
C | CA | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.691-785dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613395 | ||||||
chr7:15613429
|
A | C | 225 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-818T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613429 | ||||||
chr7:15613435
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.691-824A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613435 | ||||||
chr7:15613509
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0139others(2): Show | 6 | HG01192.hp1 HG01256.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-898T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613509 | ||||||
chr7:15613516
|
T | C | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-905A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613516 | ||||||
chr7:15613544
|
T | C | 2 | a0001c0001t0023g0002a0001c0001t0034g0217 | 3 | HG01884.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.691-933A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613544 | ||||||
chr7:15613861
|
T | A | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.691-1250A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613861 | ||||||
chr7:15613914
|
G | A | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691-1303C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15613914 | ||||||
chr7:15614022
|
T | C | 1 | a0001c0001t0035g0214 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.691-1411A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614022 | ||||||
chr7:15614024
|
A | T | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-1413T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614024 | ||||||
chr7:15614053
|
TTG | T | 15 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0097others(12): Show | 15 | HG01106.hp1 HG01261.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.691-1444_691-1443d others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614053 | ||||||
chr7:15614054
|
TG | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0044others(117): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.691-1444delC | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614054 | ||||||
chr7:15614059
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-1448G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614059 | ||||||
chr7:15614081
|
T | C | 1 | a0002c0002t0002g0336 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.691-1470A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614081 | ||||||
chr7:15614118
|
T | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0077others(8): Show | 12 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.691-1507A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614118 | ||||||
chr7:15614132
|
G | A | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.691-1521C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614132 | ||||||
chr7:15614136
|
C | G | 2 | a0002c0002t0026g0243a0002c0002t0026g0250 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.691-1525G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614136 | ||||||
chr7:15614148
|
G | T | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691-1537C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614148 | ||||||
chr7:15614201
|
A | T | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-1590T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614201 | ||||||
chr7:15614202
|
G | GATAAA | 14 | a0001c0001t0006g0135a0001c0001t0016g0015a0002c0002t0002g0011others(11): Show | 15 | HG00280.hp1 HG00738.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-1596_691-1592d others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | ||||||
chr7:15614202
|
G | GATAAAAT others(3): Show |
6 | a0001c0001t0016g0014a0002c0002t0002g0283a0002c0002t0002g0305others(3): Show | 6 | HG00099.hp2 HG01361.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-1601_691-1592d others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | ||||||
chr7:15614202
|
GATAAA | G | 20 | a0001c0001t0006g0058a0001c0001t0006g0068a0001c0001t0006g0080others(17): Show | 20 | HG00639.hp2 HG01074.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.691-1596_691-1592d others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | ||||||
chr7:15614202
|
GATAAAAT others(3): Show |
G | 65 | a0001c0001t0006g0056a0001c0001t0006g0060a0001c0001t0006g0061others(62): Show | 66 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.691-1601_691-1592d others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | ||||||
chr7:15614202
|
GATAAAAT others(8): Show |
G | 4 | a0001c0001t0008g0189a0001c0001t0021g0236a0001c0001t0021g0237others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-1606_691-1592d others(17): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | ||||||
chr7:15614202
|
GATAAAAT others(13): Show |
G | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.691-1611_691-1592d others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | ||||||
chr7:15614202
|
GATAAAAT others(18): Show |
G | 1 | a0001c0001t0007g0180 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.691-1616_691-1592d others(27): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614202 | ||||||
chr7:15614240
|
A | G | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.691-1629T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614240 | ||||||
chr7:15614315
|
A | G | 2 | a0003c0003t0008g0112a0003c0003t0027g0025 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-1704T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614315 | ||||||
chr7:15614316
|
G | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-1705C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614316 | ||||||
chr7:15614356
|
G | T | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.691-1745C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614356 | ||||||
chr7:15614399
|
G | T | 1 | a0003c0003t0003g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.691-1788C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614399 | ||||||
chr7:15614416
|
A | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-1805T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614416 | ||||||
chr7:15614419
|
G | GA | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.691-1809dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614419 | ||||||
chr7:15614495
|
G | A | 3 | a0001c0001t0007g0071a0001c0001t0023g0002a0001c0001t0034g0217 | 4 | HG01081.hp1 HG01884.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-1884C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614495 | ||||||
chr7:15614536
|
C | A | 1 | a0002c0002t0004g0246 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.691-1925G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614536 | ||||||
chr7:15614537
|
A | T | 2 | a0003c0003t0008g0112a0003c0003t0027g0025 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-1926T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614537 | ||||||
chr7:15614670
|
T | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2059A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614670 | ||||||
chr7:15614692
|
T | C | 1 | a0001c0001t0020g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.691-2081A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614692 | ||||||
chr7:15614755
|
G | A | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.691-2144C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614755 | ||||||
chr7:15614794
|
A | G | 1 | a0003c0003t0003g0203 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.691-2183T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614794 | ||||||
chr7:15614804
|
A | T | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-2193T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614804 | ||||||
chr7:15614989
|
T | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0077others(8): Show | 12 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.691-2378A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15614989 | ||||||
chr7:15615031
|
T | A | 3 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218 | 3 | HG02486.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.691-2420A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615031 | ||||||
chr7:15615180
|
GT | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2570delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615180 | ||||||
chr7:15615284
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.691-2673T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615284 | ||||||
chr7:15615364
|
G | T | 1 | a0001c0001t0015g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.691-2753C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615364 | ||||||
chr7:15615426
|
T | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2815A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615426 | ||||||
chr7:15615429
|
TA | T | 210 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0044others(207): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.691-2819delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615429 | ||||||
chr7:15615438
|
AG | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0043others(11): Show | 15 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.691-2828delC | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615438 | ||||||
chr7:15615467
|
G | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2856C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615467 | ||||||
chr7:15615510
|
G | T | 5 | a0002c0002t0004g0241a0002c0002t0004g0242a0002c0002t0022g0256others(2): Show | 5 | HG00741.hp2 HG01109.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-2899C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615510 | ||||||
chr7:15615540
|
T | C | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-2929A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615540 | ||||||
chr7:15615568
|
T | C | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-2957A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615568 | ||||||
chr7:15615640
|
G | T | 1 | a0001c0001t0035g0214 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.691-3029C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615640 | ||||||
chr7:15615668
|
T | C | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.691-3057A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615668 | ||||||
chr7:15615892
|
T | C | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-3281A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615892 | ||||||
chr7:15615923
|
T | C | 1 | a0001c0001t0034g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.691-3312A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15615923 | ||||||
chr7:15616049
|
T | G | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.691-3438A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616049 | ||||||
chr7:15616228
|
T | A | 1 | a0003c0003t0008g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.691-3617A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616228 | ||||||
chr7:15616371
|
A | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-3760T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616371 | ||||||
chr7:15616444
|
T | C | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.691-3833A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616444 | ||||||
chr7:15616465
|
A | G | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.691-3854T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616465 | ||||||
chr7:15616477
|
G | A | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.691-3866C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616477 | ||||||
chr7:15616562
|
A | T | 135 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0044others(132): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.691-3951T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616562 | ||||||
chr7:15616641
|
C | G | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.691-4030G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616641 | ||||||
chr7:15616680
|
T | A | 18 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(15): Show | 18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-4069A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616680 | ||||||
chr7:15616765
|
T | C | 6 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032others(3): Show | 7 | HG01109.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-4154A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616765 | ||||||
chr7:15616825
|
C | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4214G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616825 | ||||||
chr7:15616851
|
G | T | 2 | a0003c0003t0003g0096a0003c0003t0003g0098 | 2 | NA18995.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.691-4240C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616851 | ||||||
chr7:15616867
|
A | G | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691-4256T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616867 | ||||||
chr7:15616908
|
A | G | 18 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(15): Show | 18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-4297T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616908 | ||||||
chr7:15616937
|
T | A | 7 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(4): Show | 8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-4326A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616937 | ||||||
chr7:15616981
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4370G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616981 | ||||||
chr7:15616984
|
T | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4373A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15616984 | ||||||
chr7:15617031
|
C | G | 1 | a0001c0001t0006g0068 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.691-4420G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617031 | ||||||
chr7:15617082
|
A | G | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.691-4471T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617082 | ||||||
chr7:15617103
|
A | C | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4492T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617103 | ||||||
chr7:15617188
|
A | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4577T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617188 | ||||||
chr7:15617337
|
A | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-4726T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617337 | ||||||
chr7:15617429
|
G | A | 18 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(15): Show | 18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-4818C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617429 | ||||||
chr7:15617499
|
T | C | 225 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-4888A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617499 | ||||||
chr7:15617500
|
G | T | 158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.691-4889C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617500 | ||||||
chr7:15617619
|
C | G | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.691-5008G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617619 | ||||||
chr7:15617647
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.691-5036G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617647 | ||||||
chr7:15617681
|
G | T | 2 | a0001c0001t0023g0002a0001c0001t0034g0217 | 3 | HG01884.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.691-5070C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617681 | ||||||
chr7:15617682
|
T | C | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.691-5071A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617682 | ||||||
chr7:15617697
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.691-5086A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617697 | ||||||
chr7:15617734
|
C | T | 18 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(15): Show | 18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-5123G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617734 | ||||||
chr7:15617803
|
C | A | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.691-5192G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617803 | ||||||
chr7:15617839
|
G | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-5228C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617839 | ||||||
chr7:15617867
|
T | G | 2 | a0002c0002t0001g0036a0002c0002t0004g0324 | 2 | HG01433.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.691-5256A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617867 | ||||||
chr7:15617874
|
T | A | 1 | a0001c0001t0009g0222 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.691-5263A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617874 | ||||||
chr7:15617890
|
T | C | 19 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(16): Show | 19 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.691-5279A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617890 | ||||||
chr7:15617903
|
A | G | 290 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(287): Show | 299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.691-5292T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617903 | ||||||
chr7:15617948
|
G | C | 1 | a0003c0003t0003g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.691-5337C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617948 | ||||||
chr7:15617970
|
G | A | 1 | a0003c0003t0008g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.691-5359C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15617970 | ||||||
chr7:15618027
|
C | G | 1 | a0003c0003t0003g0192 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.691-5416G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618027 | ||||||
chr7:15618038
|
C | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-5427G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618038 | ||||||
chr7:15618124
|
G | C | 1 | a0001c0001t0009g0222 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.691-5513C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618124 | ||||||
chr7:15618157
|
T | C | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-5546A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618157 | ||||||
chr7:15618173
|
G | A | 1 | a0001c0001t0006g0153 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.691-5562C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618173 | ||||||
chr7:15618324
|
T | A | 8 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(5): Show | 9 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-5713A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618324 | ||||||
chr7:15618350
|
C | CT | 4 | a0001c0001t0006g0056a0001c0001t0006g0060a0001c0001t0006g0061others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-5740dupA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618350 | ||||||
chr7:15618352
|
T | G | 2 | a0002c0002t0004g0244a0002c0002t0004g0245 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.691-5741A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618352 | ||||||
chr7:15618358
|
C | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-5747G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618358 | ||||||
chr7:15618395
|
G | A | 1 | a0003c0003t0003g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.691-5784C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618395 | ||||||
chr7:15618488
|
C | T | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691-5877G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618488 | ||||||
chr7:15618510
|
C | T | 1 | a0002c0002t0002g0253 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.691-5899G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618510 | ||||||
chr7:15618555
|
T | C | 1 | a0002c0002t0002g0253 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.691-5944A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618555 | ||||||
chr7:15618681
|
T | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6070A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618681 | ||||||
chr7:15618750
|
A | C | 225 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.691-6139T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618750 | ||||||
chr7:15618800
|
A | T | 1 | a0003c0003t0003g0099 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.691-6189T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618800 | ||||||
chr7:15618819
|
A | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6208T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618819 | ||||||
chr7:15618896
|
C | T | 2 | a0003c0003t0008g0112a0003c0003t0027g0025 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-6285G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618896 | ||||||
chr7:15618918
|
G | A | 1 | a0002c0002t0002g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.691-6307C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618918 | ||||||
chr7:15618943
|
C | T | 338 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(335): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.691-6332G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618943 | ||||||
chr7:15618958
|
T | C | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6347A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618958 | ||||||
chr7:15618974
|
A | C | 1 | a0001c0001t0015g0013 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.691-6363T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618974 | ||||||
chr7:15618976
|
C | T | 339 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(336): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.691-6365G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618976 | ||||||
chr7:15618978
|
G | A | 2 | a0003c0003t0008g0112a0003c0003t0027g0025 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-6367C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15618978 | ||||||
chr7:15619003
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0193 | 2 | HG02155.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.691-6392C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619003 | ||||||
chr7:15619038
|
G | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6427C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619038 | ||||||
chr7:15619039
|
T | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6428A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619039 | ||||||
chr7:15619041
|
G | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6430C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619041 | ||||||
chr7:15619160
|
T | C | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6549A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619160 | ||||||
chr7:15619175
|
A | C | 3 | a0001c0001t0019g0117a0001c0001t0019g0118a0001c0010t0029g0027 | 3 | HG01074.hp1 HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.691-6564T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619175 | ||||||
chr7:15619197
|
G | C | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6586C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619197 | ||||||
chr7:15619332
|
G | A | 18 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(15): Show | 18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-6721C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619332 | ||||||
chr7:15619356
|
G | C | 2 | a0003c0003t0008g0112a0003c0003t0027g0025 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.691-6745C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619356 | ||||||
chr7:15619369
|
A | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6758T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619369 | ||||||
chr7:15619412
|
A | G | 1 | a0002c0002t0004g0308 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.691-6801T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619412 | ||||||
chr7:15619418
|
A | G | 13 | a0001c0001t0007g0007a0001c0001t0007g0071a0001c0001t0007g0179others(10): Show | 15 | HG01081.hp1 HG01255.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.691-6807T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619418 | ||||||
chr7:15619453
|
A | C | 1 | a0001c0001t0016g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.691-6842T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619453 | ||||||
chr7:15619455
|
A | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6844T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619455 | ||||||
chr7:15619576
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.691-6965G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619576 | ||||||
chr7:15619596
|
G | A | 1 | a0002c0002t0004g0328 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.691-6985C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619596 | ||||||
chr7:15619647
|
T | A | 1 | a0001c0001t0015g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.691-7036A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619647 | ||||||
chr7:15619674
|
A | G | 1 | a0001c0001t0018g0177 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.691-7063T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619674 | ||||||
chr7:15619695
|
C | T | 18 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(15): Show | 18 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+7051G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619695 | ||||||
chr7:15619714
|
A | G | 1 | a0001c0001t0014g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690+7032T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619714 | ||||||
chr7:15619763
|
G | C | 7 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(4): Show | 8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+6983C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619763 | ||||||
chr7:15619975
|
A | G | 1 | a0002c0002t0004g0238 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.690+6771T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15619975 | ||||||
chr7:15620121
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+6625G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620121 | ||||||
chr7:15620125
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.690+6621C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620125 | ||||||
chr7:15620341
|
A | G | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+6405T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620341 | ||||||
chr7:15620424
|
C | T | 2 | a0002c0002t0004g0244a0002c0002t0004g0245 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+6322G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620424 | ||||||
chr7:15620466
|
G | A | 3 | a0002c0002t0002g0280a0002c0002t0002g0281a0002c0002t0002g0282 | 3 | NA18940.hp2 NA18955.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.690+6280C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620466 | ||||||
chr7:15620476
|
G | C | 2 | a0003c0003t0008g0112a0003c0003t0027g0025 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+6270C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620476 | ||||||
chr7:15620496
|
T | G | 1 | a0006c0009t0001g0078 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.690+6250A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620496 | ||||||
chr7:15620505
|
G | A | 7 | a0001c0001t0014g0220a0001c0001t0015g0017a0001c0001t0019g0117others(4): Show | 7 | HG01074.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+6241C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620505 | ||||||
chr7:15620521
|
C | T | 3 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079 | 3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.690+6225G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620521 | ||||||
chr7:15620555
|
A | AAAC | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+6188_690+6190d others(5): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620555 | ||||||
chr7:15620576
|
A | C | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+6170T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620576 | ||||||
chr7:15620604
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.690+6142T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620604 | ||||||
chr7:15620719
|
A | G | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 6 | HG01071.hp2 HG01167.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+6027T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620719 | ||||||
chr7:15620761
|
T | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0043others(14): Show | 18 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+5985A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620761 | ||||||
chr7:15620820
|
T | C | 2 | a0002c0002t0026g0243a0002c0002t0026g0250 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.690+5926A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620820 | ||||||
chr7:15620854
|
A | G | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.690+5892T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620854 | ||||||
chr7:15620862
|
A | G | 266 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.690+5884T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620862 | ||||||
chr7:15620939
|
ACT | A | 22 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(19): Show | 22 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.690+5805_690+5806d others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620939 | ||||||
chr7:15620954
|
C | G | 1 | a0003c0003t0003g0190 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.690+5792G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15620954 | ||||||
chr7:15621012
|
G | A | 4 | a0001c0001t0006g0056a0001c0001t0006g0060a0001c0001t0006g0061others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+5734C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621012 | ||||||
chr7:15621046
|
G | C | 1 | a0003c0003t0008g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.690+5700C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621046 | ||||||
chr7:15621121
|
A | C | 1 | a0003c0003t0003g0202 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.690+5625T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621121 | ||||||
chr7:15621275
|
C | T | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.690+5471G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621275 | ||||||
chr7:15621363
|
G | C | 2 | a0003c0003t0008g0112a0003c0003t0027g0025 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+5383C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621363 | ||||||
chr7:15621435
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.690+5311C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621435 | ||||||
chr7:15621450
|
C | G | 1 | a0002c0002t0002g0286 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.690+5296G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621450 | ||||||
chr7:15621515
|
T | C | 1 | a0002c0002t0005g0272 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.690+5231A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621515 | ||||||
chr7:15621608
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.690+5138C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621608 | ||||||
chr7:15621630
|
T | A | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+5116A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621630 | ||||||
chr7:15621651
|
T | C | 2 | a0001c0001t0023g0002a0001c0001t0034g0217 | 3 | HG01884.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.690+5095A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621651 | ||||||
chr7:15621702
|
A | G | 1 | a0002c0002t0002g0286 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.690+5044T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621702 | ||||||
chr7:15621766
|
A | C | 1 | a0001c0001t0035g0214 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.690+4980T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621766 | ||||||
chr7:15621899
|
A | C | 2 | a0002c0002t0026g0243a0002c0002t0026g0250 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.690+4847T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15621899 | ||||||
chr7:15622053
|
G | T | 1 | a0002c0002t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.690+4693C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622053 | ||||||
chr7:15622135
|
C | A | 1 | a0002c0002t0005g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.690+4611G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622135 | ||||||
chr7:15622144
|
T | C | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.690+4602A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622144 | ||||||
chr7:15622262
|
T | C | 8 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(5): Show | 9 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.690+4484A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622262 | ||||||
chr7:15622373
|
C | G | 1 | a0001c0001t0007g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.690+4373G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622373 | ||||||
chr7:15622524
|
T | G | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+4222A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622524 | ||||||
chr7:15622580
|
A | C | 1 | a0001c0001t0015g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.690+4166T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622580 | ||||||
chr7:15622696
|
A | T | 195 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0044others(192): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.690+4050T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622696 | ||||||
chr7:15622747
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA18998.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.690+3999A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622747 | ||||||
chr7:15622807
|
C | T | 55 | a0001c0001t0009g0233a0003c0003t0003g0001a0003c0003t0003g0049others(52): Show | 58 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.690+3939G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622807 | ||||||
chr7:15622840
|
T | C | 17 | a0001c0001t0001g0043a0001c0001t0007g0007a0001c0001t0007g0071others(14): Show | 19 | HG01074.hp1 HG01081.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.690+3906A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15622840 | ||||||
chr7:15623014
|
C | G | 1 | a0001c0001t0037g0235 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.690+3732G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623014 | ||||||
chr7:15623385
|
T | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+3361A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623385 | ||||||
chr7:15623526
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+3220G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623526 | ||||||
chr7:15623529
|
C | G | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.690+3217G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623529 | ||||||
chr7:15623634
|
T | A | 2 | a0002c0002t0004g0244a0002c0002t0004g0245 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+3112A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623634 | ||||||
chr7:15623803
|
C | T | 4 | a0001c0001t0008g0189a0001c0001t0021g0236a0001c0001t0021g0237others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+2943G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623803 | ||||||
chr7:15623824
|
A | T | 7 | a0002c0002t0005g0262a0002c0002t0005g0263a0002c0002t0005g0264others(4): Show | 7 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+2922T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623824 | ||||||
chr7:15623828
|
C | A | 2 | a0002c0002t0026g0243a0002c0002t0026g0250 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.690+2918G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623828 | ||||||
chr7:15623887
|
A | G | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+2859T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623887 | ||||||
chr7:15623970
|
G | A | 1 | a0001c0001t0014g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.690+2776C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15623970 | ||||||
chr7:15624346
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+2400G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624346 | ||||||
chr7:15624354
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+2392G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624354 | ||||||
chr7:15624470
|
G | A | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+2276C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624470 | ||||||
chr7:15624541
|
A | G | 1 | a0001c0001t0016g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.690+2205T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624541 | ||||||
chr7:15624592
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.690+2154T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624592 | ||||||
chr7:15624625
|
A | G | 1 | a0003c0003t0003g0190 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.690+2121T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624625 | ||||||
chr7:15624629
|
C | G | 3 | a0003c0003t0003g0105a0003c0003t0003g0128a0003c0003t0003g0164 | 3 | HG01928.hp1 HG02273.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.690+2117G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624629 | ||||||
chr7:15624735
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+2011G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624735 | ||||||
chr7:15624823
|
G | A | 1 | a0002c0002t0005g0273 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.690+1923C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624823 | ||||||
chr7:15624946
|
G | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+1800C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15624946 | ||||||
chr7:15625144
|
A | G | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+1602T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625144 | ||||||
chr7:15625181
|
A | G | 2 | a0001c0001t0019g0117a0001c0001t0019g0118 | 2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.690+1565T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625181 | ||||||
chr7:15625240
|
G | A | 2 | a0001c0001t0016g0014a0001c0001t0016g0015 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.690+1506C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625240 | ||||||
chr7:15625257
|
A | C | 7 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0087others(4): Show | 7 | HG01243.hp1 HG01258.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+1489T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625257 | ||||||
chr7:15625461
|
C | G | 208 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(205): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.690+1285G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625461 | ||||||
chr7:15625465
|
T | C | 20 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+1281A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625465 | ||||||
chr7:15625748
|
G | A | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.690+998C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15625748 | ||||||
chr7:15626179
|
A | G | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.690+567T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626179 | ||||||
chr7:15626242
|
G | C | 1 | a0003c0003t0008g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.690+504C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626242 | ||||||
chr7:15626354
|
C | G | 1 | a0002c0002t0002g0280 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.690+392G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626354 | ||||||
chr7:15626392
|
T | G | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+354A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626392 | ||||||
chr7:15626463
|
C | G | 1 | a0002c0002t0026g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.690+283G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626463 | ||||||
chr7:15626546
|
A | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+200T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626546 | ||||||
chr7:15626598
|
T | G | 14 | a0001c0001t0007g0007a0001c0001t0007g0071a0001c0001t0007g0179others(11): Show | 16 | HG01081.hp1 HG01255.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.690+148A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626598 | ||||||
chr7:15626605
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.690+141G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626605 | ||||||
chr7:15626650
|
C | CAAGAATT others(321): Show |
1 | a0002c0002t0004g0324 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.690+95_690+96insTT others(326): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626650 | ||||||
chr7:15626650
|
C | CAAGAATT others(323): Show |
1 | a0002c0002t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.690+95_690+96insTT others(328): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626650 | ||||||
chr7:15626705
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.690+41C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 2/2 | chr7 | 15626705 | ||||||
chr7:15627019
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-101C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627019 | ||||||
chr7:15627124
|
T | C | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.518-206A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627124 | ||||||
chr7:15627126
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.518-208G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627126 | ||||||
chr7:15627153
|
T | A | 1 | a0001c0001t0014g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.518-235A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627153 | ||||||
chr7:15627243
|
T | C | 9 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-325A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627243 | ||||||
chr7:15627422
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.518-504C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627422 | ||||||
chr7:15627454
|
G | C | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-536C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627454 | ||||||
chr7:15627504
|
G | T | 2 | a0003c0003t0003g0119a0003c0003t0003g0154 | 2 | NA18977.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.518-586C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627504 | ||||||
chr7:15627512
|
A | G | 1 | a0003c0003t0003g0107 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.518-594T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627512 | ||||||
chr7:15627522
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 7 | HG00140.hp1 HG01099.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-604C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627522 | ||||||
chr7:15627546
|
A | T | 20 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-628T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627546 | ||||||
chr7:15627643
|
G | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-725C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627643 | ||||||
chr7:15627715
|
G | A | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-797C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627715 | ||||||
chr7:15627782
|
A | T | 1 | a0003c0003t0003g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.518-864T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627782 | ||||||
chr7:15627808
|
A | AACACACA others(5): Show |
93 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(90): Show | 96 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.518-902_518-891dup others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627808
|
A | AACACACA others(7): Show |
4 | a0001c0001t0001g0051a0001c0001t0001g0138a0001c0001t0021g0225others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-904_518-891dup others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627808
|
A | AACACACA others(9): Show |
12 | a0001c0001t0001g0059a0001c0001t0007g0007a0001c0001t0013g0021others(9): Show | 13 | HG00735.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.518-906_518-891dup others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627808
|
A | AACACACA others(11): Show |
19 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0088others(16): Show | 19 | HG00099.hp1 HG01081.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-908_518-891dup others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627808
|
A | AACACACA others(13): Show |
102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.518-891_518-890ins others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627808
|
A | AACACACA others(15): Show |
15 | a0001c0001t0001g0074a0001c0001t0001g0094a0001c0001t0001g0100others(12): Show | 16 | HG01243.hp1 HG01255.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.518-891_518-890ins others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627808
|
A | AACACACA others(17): Show |
9 | a0001c0001t0001g0043a0001c0001t0001g0095a0001c0001t0001g0162others(6): Show | 9 | HG01074.hp1 HG01081.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.518-891_518-890ins others(24): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627808
|
A | AACACACA others(19): Show |
3 | a0001c0001t0020g0229a0001c0001t0034g0217a0005c0011t0001g0211 | 3 | HG02145.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.518-891_518-890ins others(26): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627808
|
A | AACACACA others(21): Show |
2 | a0001c0001t0015g0017a0001c0001t0023g0002 | 3 | HG01884.hp2 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.518-891_518-890ins others(28): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627808
|
A | ACACACAC others(14): Show |
2 | a0001c0001t0001g0069a0002c0002t0004g0339 | 2 | HG01934.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.518-891_518-890ins others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627808 | ||||||
chr7:15627827
|
G | A | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-909C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627827 | ||||||
chr7:15627828
|
T | C | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-910A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627828 | ||||||
chr7:15627838
|
A | G | 3 | a0003c0003t0003g0105a0003c0003t0003g0128a0003c0003t0003g0164 | 3 | HG01928.hp1 HG02273.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.518-920T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627838 | ||||||
chr7:15627906
|
A | T | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.518-988T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15627906 | ||||||
chr7:15628070
|
G | T | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.518-1152C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628070 | ||||||
chr7:15628204
|
T | A | 1 | a0001c0001t0008g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.518-1286A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628204 | ||||||
chr7:15628254
|
T | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-1336A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628254 | ||||||
chr7:15628402
|
C | A | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.518-1484G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628402 | ||||||
chr7:15628445
|
C | G | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-1527G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628445 | ||||||
chr7:15628467
|
G | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-1549C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628467 | ||||||
chr7:15628468
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0160others(1): Show | 4 | HG02155.hp2 NA18959.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-1550C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628468 | ||||||
chr7:15628554
|
T | G | 2 | a0003c0003t0003g0119a0003c0003t0003g0154 | 2 | NA18977.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.518-1636A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628554 | ||||||
chr7:15628561
|
G | C | 8 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.518-1643C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628561 | ||||||
chr7:15628628
|
C | G | 20 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-1710G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628628 | ||||||
chr7:15628697
|
C | T | 2 | a0002c0002t0026g0243a0002c0002t0026g0250 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.518-1779G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628697 | ||||||
chr7:15628865
|
C | A | 1 | a0002c0002t0028g0026 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.518-1947G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628865 | ||||||
chr7:15628901
|
G | A | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-1983C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628901 | ||||||
chr7:15628957
|
A | G | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.518-2039T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628957 | ||||||
chr7:15628990
|
T | C | 1 | a0001c0001t0021g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.518-2072A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15628990 | ||||||
chr7:15629068
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.518-2150G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629068 | ||||||
chr7:15629092
|
T | C | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.518-2174A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629092 | ||||||
chr7:15629112
|
C | T | 20 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-2194G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629112 | ||||||
chr7:15629223
|
A | T | 1 | a0002c0002t0010g0310 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.518-2305T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629223 | ||||||
chr7:15629358
|
G | C | 150 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.518-2440C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629358 | ||||||
chr7:15629359
|
C | T | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.518-2441G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629359 | ||||||
chr7:15629375
|
A | G | 151 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.518-2457T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629375 | ||||||
chr7:15629394
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.518-2476A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629394 | ||||||
chr7:15629458
|
A | G | 4 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0163others(1): Show | 4 | HG00140.hp2 HG01934.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-2540T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629458 | ||||||
chr7:15629554
|
A | C | 4 | a0001c0001t0006g0056a0001c0001t0006g0060a0001c0001t0006g0061others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-2636T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629554 | ||||||
chr7:15629671
|
G | C | 22 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(19): Show | 23 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.518-2753C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629671 | ||||||
chr7:15629774
|
CCT | C | 12 | a0001c0001t0001g0187a0001c0001t0013g0021a0001c0001t0013g0022others(9): Show | 12 | HG01106.hp1 HG01261.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.518-2858_518-2857d others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629774 | ||||||
chr7:15629808
|
G | A | 2 | a0002c0002t0005g0262a0002c0002t0005g0274 | 2 | HG01099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.518-2890C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629808 | ||||||
chr7:15629847
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.518-2929A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629847 | ||||||
chr7:15629982
|
A | T | 1 | a0001c0001t0006g0153 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.518-3064T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15629982 | ||||||
chr7:15630031
|
C | G | 1 | a0003c0003t0003g0191 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.518-3113G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630031 | ||||||
chr7:15630033
|
A | G | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.518-3115T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630033 | ||||||
chr7:15630181
|
C | A | 55 | a0001c0001t0009g0233a0003c0003t0003g0001a0003c0003t0003g0049others(52): Show | 58 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-3263G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630181 | ||||||
chr7:15630277
|
C | T | 4 | a0001c0001t0008g0189a0001c0001t0021g0236a0001c0001t0021g0237others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-3359G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630277 | ||||||
chr7:15630487
|
C | G | 1 | a0001c0001t0023g0002 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.518-3569G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630487 | ||||||
chr7:15630638
|
T | A | 1 | a0002c0002t0010g0309 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.518-3720A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15630638 | ||||||
chr7:15631017
|
G | T | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.518-4099C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631017 | ||||||
chr7:15631020
|
T | A | 20 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-4102A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631020 | ||||||
chr7:15631082
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.518-4164A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631082 | ||||||
chr7:15631143
|
C | G | 21 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(18): Show | 22 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.518-4225G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631143 | ||||||
chr7:15631192
|
C | T | 2 | a0002c0002t0002g0290a0002c0002t0002g0292 | 2 | HG00673.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.518-4274G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631192 | ||||||
chr7:15631214
|
T | C | 4 | a0001c0001t0008g0189a0001c0001t0021g0236a0001c0001t0021g0237others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-4296A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631214 | ||||||
chr7:15631231
|
C | CA | 23 | a0001c0001t0001g0047a0001c0001t0001g0108a0001c0001t0018g0075others(20): Show | 23 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.518-4314dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631231 | ||||||
chr7:15631490
|
T | C | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.518-4572A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631490 | ||||||
chr7:15631677
|
C | G | 16 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(13): Show | 16 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.518-4759G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631677 | ||||||
chr7:15631700
|
C | T | 263 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.518-4782G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631700 | ||||||
chr7:15631846
|
A | C | 23 | a0001c0001t0015g0017a0001c0001t0018g0075a0001c0001t0018g0101others(20): Show | 24 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.518-4928T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631846 | ||||||
chr7:15631871
|
A | G | 1 | a0001c0001t0006g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.518-4953T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631871 | ||||||
chr7:15631906
|
A | ATG | 5 | a0001c0001t0006g0060a0001c0001t0006g0061a0001c0001t0009g0222others(2): Show | 5 | HG00639.hp2 HG00741.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-4990_518-4989d others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTG | 3 | a0001c0001t0006g0056a0001c0001t0037g0235a0002c0002t0022g0256 | 3 | HG01109.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.518-4992_518-4989d others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0007g0181a0001c0001t0014g0218 | 2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.518-4998_518-4989d others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(7): Show |
5 | a0001c0001t0007g0179a0001c0001t0007g0180a0001c0001t0007g0182others(2): Show | 5 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-5002_518-4989d others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(9): Show |
60 | a0001c0001t0001g0077a0001c0001t0001g0088a0001c0001t0001g0115others(57): Show | 65 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.518-5004_518-4989d others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(11): Show |
35 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.518-5006_518-4989d others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(13): Show |
34 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(31): Show | 36 | HG00140.hp1 HG00735.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.518-5008_518-4989d others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(15): Show |
63 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0062others(60): Show | 64 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.518-5010_518-4989d others(24): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(17): Show |
23 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0066others(20): Show | 24 | HG00280.hp2 HG01175.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.518-5012_518-4989d others(26): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(19): Show |
19 | a0001c0001t0001g0043a0001c0001t0001g0092a0001c0001t0001g0146others(16): Show | 19 | HG01123.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-5014_518-4989d others(28): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(21): Show |
13 | a0001c0001t0001g0054a0001c0001t0001g0091a0001c0001t0001g0113others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.518-4989_518-4988i others(30): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631906
|
A | ATGTGTGT others(23): Show |
4 | a0001c0001t0035g0214a0001c0010t0029g0027a0002c0002t0005g0274others(1): Show | 4 | HG01099.hp2 HG02559.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-4989_518-4988i others(32): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631906 | ||||||
chr7:15631932
|
G | GTGTGTGT others(14): Show |
1 | a0001c0001t0001g0059 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.518-5015_518-5014i others(23): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631932 | ||||||
chr7:15631932
|
G | GTGTGTGT others(18): Show |
1 | a0001c0001t0013g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.518-5015_518-5014i others(27): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631932 | ||||||
chr7:15631933
|
G | T | 24 | a0001c0001t0007g0007a0001c0001t0007g0071a0001c0001t0007g0179others(21): Show | 26 | HG01081.hp1 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.518-5015C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631933 | ||||||
chr7:15631982
|
T | C | 3 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218 | 3 | HG02486.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.518-5064A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15631982 | ||||||
chr7:15632056
|
A | C | 2 | a0002c0002t0002g0283a0002c0002t0002g0322 | 2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.518-5138T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632056 | ||||||
chr7:15632139
|
A | G | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.518-5221T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632139 | ||||||
chr7:15632234
|
G | A | 4 | a0001c0001t0006g0056a0001c0001t0006g0060a0001c0001t0006g0061others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-5316C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632234 | ||||||
chr7:15632403
|
T | C | 1 | a0002c0002t0005g0263 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.518-5485A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632403 | ||||||
chr7:15632490
|
A | C | 3 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218 | 3 | HG02486.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.518-5572T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632490 | ||||||
chr7:15632988
|
G | C | 1 | a0003c0003t0008g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.518-6070C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15632988 | ||||||
chr7:15633073
|
G | T | 1 | a0003c0003t0008g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.518-6155C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633073 | ||||||
chr7:15633187
|
G | A | 1 | a0003c0003t0003g0049 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.518-6269C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633187 | ||||||
chr7:15633282
|
C | T | 55 | a0001c0001t0009g0233a0003c0003t0003g0001a0003c0003t0003g0049others(52): Show | 58 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-6364G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633282 | ||||||
chr7:15633312
|
C | G | 3 | a0001c0001t0019g0117a0001c0001t0019g0118a0001c0010t0029g0027 | 3 | HG01074.hp1 HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.518-6394G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633312 | ||||||
chr7:15633332
|
C | G | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-6414G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633332 | ||||||
chr7:15633420
|
A | G | 3 | a0002c0002t0002g0275a0002c0002t0002g0276a0002c0002t0002g0278 | 3 | HG01255.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.518-6502T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633420 | ||||||
chr7:15633453
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.518-6535G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633453 | ||||||
chr7:15633559
|
C | G | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.518-6641G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633559 | ||||||
chr7:15633642
|
G | A | 20 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(17): Show | 20 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-6724C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633642 | ||||||
chr7:15633696
|
C | T | 67 | a0001c0001t0007g0007a0001c0001t0007g0071a0001c0001t0007g0179others(64): Show | 71 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.518-6778G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633696 | ||||||
chr7:15633741
|
T | C | 1 | a0002c0002t0004g0333 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.518-6823A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15633741 | ||||||
chr7:15634022
|
G | A | 56 | a0001c0001t0009g0233a0003c0003t0003g0001a0003c0003t0003g0049others(53): Show | 59 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.518-7104C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634022 | ||||||
chr7:15634240
|
A | G | 1 | a0001c0001t0037g0235 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.518-7322T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634240 | ||||||
chr7:15634314
|
G | C | 16 | a0001c0001t0006g0056a0001c0001t0006g0060a0001c0001t0006g0061others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.518-7396C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634314 | ||||||
chr7:15634371
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.518-7453T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634371 | ||||||
chr7:15634546
|
G | T | 1 | a0001c0001t0001g0048 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.518-7628C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634546 | ||||||
chr7:15634610
|
A | G | 21 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(18): Show | 21 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.518-7692T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634610 | ||||||
chr7:15634748
|
C | T | 8 | a0001c0001t0001g0044a0001c0001t0012g0003a0001c0001t0012g0031others(5): Show | 9 | HG01109.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-7830G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634748 | ||||||
chr7:15634756
|
C | G | 4 | a0001c0001t0001g0043a0001c0001t0019g0117a0001c0001t0019g0118others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-7838G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634756 | ||||||
chr7:15634789
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0139 | 4 | HG01192.hp1 HG01256.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-7871A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15634789 | ||||||
chr7:15635033
|
A | G | 4 | a0001c0001t0001g0043a0001c0001t0019g0117a0001c0001t0019g0118others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-8115T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635033 | ||||||
chr7:15635049
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.518-8131T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635049 | ||||||
chr7:15635084
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0077others(17): Show | 21 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.518-8166A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635084 | ||||||
chr7:15635132
|
C | T | 1 | a0001c0001t0006g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.518-8214G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635132 | ||||||
chr7:15635205
|
G | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(173): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.518-8287C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635205 | ||||||
chr7:15635362
|
G | T | 14 | a0001c0001t0006g0176a0001c0001t0018g0075a0001c0001t0018g0102others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.518-8444C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635362 | ||||||
chr7:15635407
|
T | C | 1 | a0002c0002t0004g0328 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.518-8489A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635407 | ||||||
chr7:15635672
|
T | A | 18 | a0001c0001t0001g0184a0001c0001t0007g0007a0001c0001t0007g0071others(15): Show | 19 | HG01081.hp1 HG01255.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-8754A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635672 | ||||||
chr7:15635673
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.518-8755T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635673 | ||||||
chr7:15635713
|
T | TA | 30 | a0001c0001t0006g0176a0001c0001t0009g0230a0001c0001t0009g0231others(27): Show | 31 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.518-8796dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635713 | ||||||
chr7:15635924
|
A | C | 4 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-9006T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635924 | ||||||
chr7:15635944
|
G | A | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(264): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.518-9026C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635944 | ||||||
chr7:15635968
|
A | T | 1 | a0002c0002t0002g0265 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.518-9050T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15635968 | ||||||
chr7:15636010
|
G | A | 270 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(267): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.518-9092C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636010 | ||||||
chr7:15636117
|
T | G | 9 | a0001c0001t0001g0184a0001c0001t0007g0071a0001c0001t0009g0233others(6): Show | 9 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-9199A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636117 | ||||||
chr7:15636285
|
C | A | 2 | a0002c0002t0026g0250a0003c0003t0038g0234 | 2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.518-9367G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636285 | ||||||
chr7:15636394
|
G | A | 200 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.518-9476C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636394 | ||||||
chr7:15636417
|
A | C | 2 | a0001c0001t0018g0177a0001c0001t0023g0002 | 3 | HG01884.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.518-9499T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636417 | ||||||
chr7:15636579
|
T | G | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-9661A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636579 | ||||||
chr7:15636648
|
A | G | 1 | a0001c0001t0007g0179 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.518-9730T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636648 | ||||||
chr7:15636789
|
A | G | 9 | a0001c0001t0001g0184a0001c0001t0007g0071a0001c0001t0009g0233others(6): Show | 9 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-9871T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15636789 | ||||||
chr7:15637074
|
A | C | 2 | a0001c0001t0014g0220a0001c0001t0020g0229 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.518-10156T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637074 | ||||||
chr7:15637318
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-10400G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637318 | ||||||
chr7:15637370
|
C | T | 13 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(10): Show | 14 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.518-10452G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637370 | ||||||
chr7:15637386
|
T | C | 9 | a0001c0001t0001g0184a0001c0001t0007g0071a0001c0001t0009g0233others(6): Show | 9 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-10468A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637386 | ||||||
chr7:15637400
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.518-10482G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637400 | ||||||
chr7:15637520
|
ACACACAC others(5): Show |
A | 2 | a0001c0001t0001g0089a0001c0001t0013g0024 | 2 | HG00621.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.518-10614_518-1060 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637520 | ||||||
chr7:15637534
|
A | G | 1 | a0002c0002t0005g0273 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.518-10616T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637534 | ||||||
chr7:15637554
|
A | G | 1 | a0003c0003t0027g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-10636T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637554 | ||||||
chr7:15637610
|
T | C | 1 | a0003c0003t0017g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.518-10692A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637610 | ||||||
chr7:15637678
|
A | C | 3 | a0002c0002t0010g0307a0002c0002t0010g0309a0002c0002t0010g0310 | 3 | HG00323.hp2 HG01358.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.518-10760T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637678 | ||||||
chr7:15637709
|
T | C | 2 | a0002c0002t0004g0246a0002c0002t0010g0247 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-10791A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637709 | ||||||
chr7:15637814
|
T | G | 2 | a0001c0001t0008g0041a0001c0001t0008g0042 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.518-10896A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637814 | ||||||
chr7:15637929
|
C | G | 1 | a0010c0006t0001g0035 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.518-11011G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15637929 | ||||||
chr7:15638037
|
T | A | 1 | a0002c0002t0002g0305 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.518-11119A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638037 | ||||||
chr7:15638125
|
T | C | 6 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.518-11207A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638125 | ||||||
chr7:15638145
|
C | A | 7 | a0001c0001t0001g0184a0001c0001t0009g0233a0002c0002t0002g0248others(4): Show | 7 | HG02647.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-11227G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638145 | ||||||
chr7:15638309
|
C | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0138 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.518-11391G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638309 | ||||||
chr7:15638373
|
C | T | 1 | a0001c0001t0009g0222 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.518-11455G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638373 | ||||||
chr7:15638391
|
C | T | 2 | a0003c0003t0003g0157a0003c0003t0003g0201 | 2 | NA18948.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.518-11473G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638391 | ||||||
chr7:15638494
|
ATCT | A | 6 | a0001c0001t0001g0184a0002c0002t0002g0248a0002c0002t0004g0244others(3): Show | 6 | HG02647.hp1 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-11579_518-1157 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638494 | ||||||
chr7:15638526
|
A | G | 3 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079 | 3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-11608T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638526 | ||||||
chr7:15638543
|
G | A | 11 | a0001c0001t0001g0043a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 12 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.518-11625C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638543 | ||||||
chr7:15638753
|
T | C | 1 | a0001c0001t0016g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.518-11835A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638753 | ||||||
chr7:15638771
|
G | C | 2 | a0002c0002t0002g0275a0002c0002t0002g0276 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.518-11853C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638771 | ||||||
chr7:15638804
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.518-11886G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638804 | ||||||
chr7:15638870
|
C | T | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0043others(112): Show | 119 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.518-11952G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638870 | ||||||
chr7:15638981
|
C | A | 4 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0181others(1): Show | 5 | HG02630.hp2 HG02717.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-12063G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638981 | ||||||
chr7:15638982
|
C | T | 1 | a0001c0001t0014g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.518-12064G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638982 | ||||||
chr7:15638999
|
G | A | 291 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(288): Show | 300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.518-12081C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15638999 | ||||||
chr7:15639130
|
C | A | 1 | a0001c0001t0014g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.518-12212G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639130 | ||||||
chr7:15639141
|
AT | A | 4 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-12224delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639141 | ||||||
chr7:15639188
|
T | C | 1 | a0001c0001t0013g0020 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.518-12270A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639188 | ||||||
chr7:15639289
|
T | C | 3 | a0001c0001t0001g0187a0001c0001t0015g0012a0001c0001t0015g0013 | 3 | HG02809.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.518-12371A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639289 | ||||||
chr7:15639502
|
T | C | 3 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079 | 3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-12584A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639502 | ||||||
chr7:15639578
|
CT | C | 6 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-12661delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639578 | ||||||
chr7:15639672
|
T | C | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-12754A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639672 | ||||||
chr7:15639871
|
T | C | 1 | a0002c0002t0026g0250 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.518-12953A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639871 | ||||||
chr7:15639921
|
T | A | 1 | a0002c0002t0010g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.518-13003A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639921 | ||||||
chr7:15639986
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0138 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.518-13068C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15639986 | ||||||
chr7:15640108
|
T | G | 3 | a0002c0002t0004g0254a0002c0002t0004g0255a0002c0002t0040g0252 | 3 | HG01109.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.518-13190A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640108 | ||||||
chr7:15640252
|
G | T | 1 | a0002c0002t0002g0322 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.518-13334C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640252 | ||||||
chr7:15640254
|
T | G | 1 | a0002c0002t0002g0322 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.518-13336A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640254 | ||||||
chr7:15640254
|
T | TTG | 28 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0044others(25): Show | 29 | HG00099.hp1 HG01106.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.518-13338_518-1333 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640254 | ||||||
chr7:15640254
|
T | TTGTG | 3 | a0001c0001t0001g0162a0001c0001t0015g0019a0002c0002t0010g0307 | 3 | HG00323.hp2 HG02015.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.518-13340_518-1333 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640254 | ||||||
chr7:15640370
|
T | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0138others(2): Show | 5 | HG01256.hp2 HG01258.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-13452A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640370 | ||||||
chr7:15640447
|
C | T | 70 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0187others(67): Show | 73 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.518-13529G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640447 | ||||||
chr7:15640478
|
G | A | 7 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0002g0248others(4): Show | 7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-13560C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640478 | ||||||
chr7:15640483
|
A | G | 1 | a0001c0001t0018g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.518-13565T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640483 | ||||||
chr7:15640515
|
T | C | 7 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(4): Show | 8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.518-13597A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640515 | ||||||
chr7:15640642
|
G | A | 1 | a0003c0003t0003g0191 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.518-13724C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640642 | ||||||
chr7:15640825
|
A | G | 7 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0002g0248others(4): Show | 7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-13907T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640825 | ||||||
chr7:15640833
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.518-13915T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640833 | ||||||
chr7:15640842
|
T | C | 4 | a0002c0002t0002g0305a0002c0002t0002g0306a0002c0002t0002g0331others(1): Show | 4 | HG01361.hp1 HG01928.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-13924A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640842 | ||||||
chr7:15640849
|
C | A | 1 | a0011c0005t0001g0034 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.518-13931G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15640849 | ||||||
chr7:15641230
|
C | A | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.518-14312G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641230 | ||||||
chr7:15641230
|
C | T | 2 | a0001c0001t0019g0117a0001c0001t0019g0118 | 2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.518-14312G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641230 | ||||||
chr7:15641344
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-14426G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641344 | ||||||
chr7:15641361
|
T | TTTTG | 3 | a0001c0001t0001g0122a0003c0003t0003g0190a0008c0007t0003g0037 | 3 | NA18942.hp1 NA18954.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.518-14447_518-1444 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641361 | ||||||
chr7:15641361
|
TTTTG | T | 12 | a0002c0002t0002g0275a0002c0002t0002g0276a0002c0002t0004g0333others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.518-14447_518-1444 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641361 | ||||||
chr7:15641579
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0015g0012a0001c0001t0015g0013 | 3 | HG02809.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.518-14661C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641579 | ||||||
chr7:15641787
|
A | G | 1 | a0003c0003t0003g0152 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.518-14869T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641787 | ||||||
chr7:15641806
|
T | A | 2 | a0001c0001t0018g0101a0002c0002t0005g0258 | 2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.518-14888A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641806 | ||||||
chr7:15641889
|
G | A | 2 | a0002c0002t0022g0303a0002c0002t0022g0320 | 2 | HG00741.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.518-14971C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641889 | ||||||
chr7:15641976
|
T | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0077others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.518-15058A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15641976 | ||||||
chr7:15642090
|
T | C | 1 | a0001c0001t0014g0220 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.518-15172A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642090 | ||||||
chr7:15642110
|
C | T | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-15192G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642110 | ||||||
chr7:15642165
|
T | A | 1 | a0003c0003t0003g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.518-15247A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642165 | ||||||
chr7:15642244
|
G | A | 1 | a0007c0008t0007g0178 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.518-15326C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642244 | ||||||
chr7:15642279
|
C | T | 1 | a0002c0002t0026g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.518-15361G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642279 | ||||||
chr7:15642387
|
T | C | 1 | a0003c0003t0027g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-15469A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642387 | ||||||
chr7:15642413
|
G | C | 2 | a0002c0002t0004g0246a0002c0002t0010g0247 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-15495C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642413 | ||||||
chr7:15642544
|
C | T | 5 | a0004c0004t0011g0311a0004c0004t0011g0312a0004c0004t0011g0313others(2): Show | 5 | HG00558.hp1 HG00741.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-15626G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642544 | ||||||
chr7:15642546
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0132 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.518-15628T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642546 | ||||||
chr7:15642652
|
C | A | 2 | a0002c0002t0002g0275a0002c0002t0002g0276 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.518-15734G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642652 | ||||||
chr7:15642974
|
T | C | 2 | a0002c0002t0002g0326a0002c0002t0002g0327 | 2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.518-16056A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642974 | ||||||
chr7:15642982
|
G | A | 7 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0002g0248others(4): Show | 7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-16064C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15642982 | ||||||
chr7:15643044
|
A | G | 1 | a0003c0003t0003g0076 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.518-16126T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643044 | ||||||
chr7:15643193
|
C | G | 7 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0002g0248others(4): Show | 7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-16275G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643193 | ||||||
chr7:15643264
|
T | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0044others(71): Show | 76 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.518-16346A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643264 | ||||||
chr7:15643273
|
G | T | 206 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.518-16355C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643273 | ||||||
chr7:15643343
|
C | T | 4 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032others(1): Show | 5 | HG01123.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-16425G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643343 | ||||||
chr7:15643493
|
G | T | 2 | a0001c0001t0016g0014a0001c0001t0016g0015 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.518-16575C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643493 | ||||||
chr7:15643505
|
T | C | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.518-16587A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643505 | ||||||
chr7:15643508
|
G | A | 1 | a0010c0006t0001g0035 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.518-16590C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643508 | ||||||
chr7:15643619
|
G | C | 2 | a0002c0002t0004g0241a0002c0002t0004g0242 | 2 | HG01515.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.518-16701C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643619 | ||||||
chr7:15643667
|
G | T | 4 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-16749C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643667 | ||||||
chr7:15643751
|
A | C | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-16833T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15643751 | ||||||
chr7:15644212
|
A | C | 1 | a0004c0004t0011g0313 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.518-17294T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644212 | ||||||
chr7:15644273
|
C | T | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-17355G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644273 | ||||||
chr7:15644426
|
A | G | 15 | a0001c0001t0018g0075a0001c0001t0018g0101a0001c0001t0018g0102others(12): Show | 16 | HG00738.hp1 HG01069.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.518-17508T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644426 | ||||||
chr7:15644444
|
C | T | 2 | a0001c0001t0016g0014a0001c0001t0016g0015 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.518-17526G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644444 | ||||||
chr7:15644460
|
C | G | 1 | a0002c0002t0010g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.518-17542G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644460 | ||||||
chr7:15644626
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.518-17708A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644626 | ||||||
chr7:15644821
|
A | G | 35 | a0001c0001t0006g0176a0001c0001t0009g0230a0001c0001t0009g0231others(32): Show | 36 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.518-17903T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644821 | ||||||
chr7:15644898
|
C | T | 3 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079 | 3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-17980G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15644898 | ||||||
chr7:15645417
|
T | C | 1 | a0001c0001t0009g0222 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.518-18499A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645417 | ||||||
chr7:15645457
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | NA18983.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.518-18539C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645457 | ||||||
chr7:15645506
|
T | C | 1 | a0002c0002t0022g0303 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.518-18588A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645506 | ||||||
chr7:15645558
|
A | G | 4 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-18640T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645558 | ||||||
chr7:15645618
|
T | TA | 3 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0167 | 4 | HG02559.hp1 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-18701dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645618 | ||||||
chr7:15645725
|
A | G | 7 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0002g0248others(4): Show | 7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-18807T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645725 | ||||||
chr7:15645734
|
T | C | 1 | a0002c0002t0002g0265 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.518-18816A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645734 | ||||||
chr7:15645756
|
C | A | 4 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-18838G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645756 | ||||||
chr7:15645833
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.518-18915A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645833 | ||||||
chr7:15645946
|
G | A | 7 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(4): Show | 8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.518-19028C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645946 | ||||||
chr7:15645963
|
A | G | 1 | a0009c0012t0005g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.518-19045T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645963 | ||||||
chr7:15645982
|
C | T | 5 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0002g0248others(2): Show | 5 | HG01081.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-19064G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15645982 | ||||||
chr7:15646002
|
G | A | 30 | a0001c0001t0006g0176a0001c0001t0009g0230a0001c0001t0009g0231others(27): Show | 30 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.518-19084C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646002 | ||||||
chr7:15646075
|
T | A | 1 | a0003c0003t0003g0106 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.518-19157A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646075 | ||||||
chr7:15646126
|
A | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0077others(12): Show | 16 | HG00099.hp1 HG00323.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.518-19208T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646126 | ||||||
chr7:15646146
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-19228A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646146 | ||||||
chr7:15646370
|
T | A | 1 | a0003c0003t0027g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-19452A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646370 | ||||||
chr7:15646394
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.518-19476T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646394 | ||||||
chr7:15646452
|
T | G | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.518-19534A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646452 | ||||||
chr7:15646548
|
G | C | 279 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.518-19630C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646548 | ||||||
chr7:15646892
|
G | T | 3 | a0001c0001t0014g0220a0001c0001t0020g0229a0001c0010t0029g0027 | 3 | HG02280.hp2 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.518-19974C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646892 | ||||||
chr7:15646956
|
A | G | 7 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0002g0248others(4): Show | 7 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-20038T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15646956 | ||||||
chr7:15647283
|
G | C | 34 | a0001c0001t0006g0176a0001c0001t0009g0230a0001c0001t0009g0231others(31): Show | 35 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.518-20365C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15647283 | ||||||
chr7:15647417
|
C | G | 2 | a0002c0002t0004g0246a0002c0002t0010g0247 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-20499G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15647417 | ||||||
chr7:15647813
|
C | G | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-20895G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15647813 | ||||||
chr7:15647872
|
A | C | 1 | a0002c0002t0004g0239 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.518-20954T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15647872 | ||||||
chr7:15648375
|
T | C | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(84): Show | 89 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.518-21457A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648375 | ||||||
chr7:15648387
|
G | A | 1 | a0001c0001t0006g0153 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.518-21469C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648387 | ||||||
chr7:15648656
|
G | A | 4 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-21738C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648656 | ||||||
chr7:15648843
|
T | C | 1 | a0001c0001t0019g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.518-21925A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648843 | ||||||
chr7:15648855
|
T | C | 1 | a0002c0002t0002g0325 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.518-21937A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648855 | ||||||
chr7:15648887
|
A | G | 2 | a0002c0002t0004g0244a0002c0002t0026g0243 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.518-21969T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15648887 | ||||||
chr7:15649222
|
A | C | 254 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(251): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.518-22304T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649222 | ||||||
chr7:15649323
|
A | C | 1 | a0001c0001t0035g0214 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.518-22405T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649323 | ||||||
chr7:15649350
|
T | A | 3 | a0001c0001t0007g0071a0002c0002t0004g0246a0002c0002t0010g0247 | 3 | HG01081.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-22432A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649350 | ||||||
chr7:15649354
|
C | T | 4 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0246others(1): Show | 4 | HG01081.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-22436G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649354 | ||||||
chr7:15649399
|
G | A | 1 | a0001c0001t0021g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.518-22481C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649399 | ||||||
chr7:15649414
|
T | C | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-22496A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649414 | ||||||
chr7:15649454
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.518-22536T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649454 | ||||||
chr7:15649472
|
GT | G | 7 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(4): Show | 8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.518-22555delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649472 | ||||||
chr7:15649579
|
T | C | 2 | a0003c0003t0003g0096a0003c0003t0003g0098 | 2 | NA18995.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.518-22661A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649579 | ||||||
chr7:15649712
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.518-22794C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649712 | ||||||
chr7:15649735
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.518-22817T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649735 | ||||||
chr7:15649921
|
A | T | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-23003T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15649921 | ||||||
chr7:15650144
|
A | G | 1 | a0002c0002t0005g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.518-23226T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650144 | ||||||
chr7:15650488
|
G | C | 2 | a0001c0001t0001g0044a0001c0001t0006g0056 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.518-23570C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650488 | ||||||
chr7:15650507
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.518-23589T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650507 | ||||||
chr7:15650586
|
T | A | 3 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079 | 3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-23668A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650586 | ||||||
chr7:15650605
|
T | G | 2 | a0001c0001t0001g0074a0006c0009t0001g0078 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.518-23687A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650605 | ||||||
chr7:15650615
|
A | C | 1 | a0001c0001t0015g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.518-23697T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650615 | ||||||
chr7:15650714
|
A | G | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-23796T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650714 | ||||||
chr7:15650731
|
T | A | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.518-23813A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15650731 | ||||||
chr7:15651046
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.518-24128C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651046 | ||||||
chr7:15651177
|
G | C | 1 | a0002c0002t0002g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.518-24259C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651177 | ||||||
chr7:15651287
|
A | G | 2 | a0002c0002t0004g0244a0002c0002t0026g0243 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.518-24369T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651287 | ||||||
chr7:15651306
|
T | A | 1 | a0003c0003t0003g0200 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.518-24388A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651306 | ||||||
chr7:15651644
|
C | T | 1 | a0003c0003t0003g0156 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.518-24726G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651644 | ||||||
chr7:15651775
|
AG | A | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-24858delC | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651775 | ||||||
chr7:15651793
|
C | T | 4 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0246others(1): Show | 4 | HG01081.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-24875G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651793 | ||||||
chr7:15651954
|
G | A | 3 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079 | 3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-25036C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651954 | ||||||
chr7:15651975
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.518-25057A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651975 | ||||||
chr7:15651982
|
C | G | 3 | a0002c0002t0002g0325a0002c0002t0002g0326a0002c0002t0002g0327 | 3 | HG03017.hp2 HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.518-25064G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15651982 | ||||||
chr7:15652044
|
G | C | 1 | a0001c0001t0007g0182 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.518-25126C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652044 | ||||||
chr7:15652182
|
G | A | 3 | a0001c0001t0014g0220a0001c0001t0020g0229a0001c0010t0029g0027 | 3 | HG02280.hp2 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.518-25264C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652182 | ||||||
chr7:15652259
|
C | G | 1 | a0002c0002t0005g0266 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.518-25341G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652259 | ||||||
chr7:15652294
|
G | A | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-25376C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652294 | ||||||
chr7:15652421
|
T | C | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-25503A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652421 | ||||||
chr7:15652468
|
A | G | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(65): Show | 70 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.518-25550T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652468 | ||||||
chr7:15652525
|
A | G | 38 | a0001c0001t0006g0176a0001c0001t0009g0230a0001c0001t0009g0231others(35): Show | 39 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.518-25607T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652525 | ||||||
chr7:15652687
|
T | G | 3 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079 | 3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-25769A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652687 | ||||||
chr7:15652711
|
A | G | 1 | a0002c0002t0022g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.518-25793T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652711 | ||||||
chr7:15652716
|
G | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 7 | HG00140.hp1 HG01099.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-25798C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652716 | ||||||
chr7:15652752
|
T | G | 5 | a0001c0001t0007g0071a0002c0002t0004g0244a0002c0002t0004g0246others(2): Show | 5 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-25834A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652752 | ||||||
chr7:15652775
|
G | A | 5 | a0001c0001t0007g0071a0002c0002t0004g0244a0002c0002t0004g0246others(2): Show | 5 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-25857C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652775 | ||||||
chr7:15652830
|
G | C | 5 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0087others(2): Show | 5 | HG01243.hp2 HG01258.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-25912C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652830 | ||||||
chr7:15652903
|
A | G | 5 | a0003c0003t0003g0104a0003c0003t0003g0105a0003c0003t0003g0107others(2): Show | 5 | NA18948.hp2 NA18949.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-25985T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15652903 | ||||||
chr7:15653096
|
C | T | 6 | a0001c0001t0013g0021a0001c0001t0013g0022a0001c0001t0013g0023others(3): Show | 6 | HG01255.hp2 HG01261.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-26178G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653096 | ||||||
chr7:15653190
|
T | C | 3 | a0001c0001t0009g0223a0002c0002t0004g0245a0002c0002t0010g0249 | 3 | HG02486.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.518-26272A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653190 | ||||||
chr7:15653267
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.518-26349C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653267 | ||||||
chr7:15653365
|
A | C | 1 | a0001c0001t0007g0182 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.518-26447T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653365 | ||||||
chr7:15653374
|
G | A | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-26456C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653374 | ||||||
chr7:15653473
|
G | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.518-26555C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653473 | ||||||
chr7:15653750
|
T | G | 1 | a0002c0002t0004g0296 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.518-26832A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653750 | ||||||
chr7:15653788
|
C | T | 1 | a0003c0003t0003g0191 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.518-26870G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653788 | ||||||
chr7:15653797
|
T | C | 2 | a0001c0001t0020g0227a0001c0001t0020g0228 | 2 | HG02717.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.518-26879A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653797 | ||||||
chr7:15653851
|
A | G | 1 | a0001c0001t0018g0075 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.518-26933T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653851 | ||||||
chr7:15653986
|
A | T | 2 | a0002c0002t0004g0246a0002c0002t0010g0247 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-27068T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15653986 | ||||||
chr7:15654074
|
T | C | 1 | a0002c0002t0002g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.518-27156A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654074 | ||||||
chr7:15654154
|
G | A | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-27236C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654154 | ||||||
chr7:15654281
|
A | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.518-27363T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654281 | ||||||
chr7:15654377
|
T | C | 1 | a0001c0001t0019g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.518-27459A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654377 | ||||||
chr7:15654468
|
G | A | 3 | a0001c0001t0007g0071a0002c0002t0004g0246a0002c0002t0010g0247 | 3 | HG01081.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.518-27550C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654468 | ||||||
chr7:15654490
|
G | T | 1 | a0001c0001t0015g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.518-27572C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654490 | ||||||
chr7:15654518
|
T | C | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-27600A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654518 | ||||||
chr7:15654640
|
G | A | 1 | a0003c0003t0027g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-27722C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654640 | ||||||
chr7:15654950
|
A | T | 1 | a0003c0003t0003g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.518-28032T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654950 | ||||||
chr7:15654958
|
A | T | 6 | a0002c0002t0005g0262a0002c0002t0005g0263a0002c0002t0005g0264others(3): Show | 6 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.518-28040T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15654958 | ||||||
chr7:15655009
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518-28091G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655009 | ||||||
chr7:15655020
|
T | A | 5 | a0001c0001t0001g0114a0001c0001t0014g0215a0001c0001t0014g0216others(2): Show | 5 | HG01243.hp1 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-28102A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655020 | ||||||
chr7:15655090
|
A | C | 1 | a0003c0003t0003g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.518-28172T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655090 | ||||||
chr7:15655130
|
G | C | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.518-28212C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655130 | ||||||
chr7:15655168
|
G | A | 18 | a0001c0001t0001g0043a0001c0001t0001g0188a0001c0001t0008g0039others(15): Show | 19 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-28250C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655168 | ||||||
chr7:15655212
|
T | G | 279 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.518-28294A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655212 | ||||||
chr7:15655355
|
T | C | 6 | a0001c0001t0013g0021a0001c0001t0013g0022a0001c0001t0013g0023others(3): Show | 6 | HG01255.hp2 HG01261.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-28437A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655355 | ||||||
chr7:15655397
|
C | G | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-28479G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655397 | ||||||
chr7:15655454
|
C | T | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-28536G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655454 | ||||||
chr7:15655524
|
C | G | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.518-28606G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655524 | ||||||
chr7:15655657
|
G | A | 1 | a0001c0001t0012g0029 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.518-28739C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655657 | ||||||
chr7:15655793
|
A | G | 279 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.518-28875T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655793 | ||||||
chr7:15655837
|
A | G | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0044others(84): Show | 89 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.518-28919T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655837 | ||||||
chr7:15655924
|
T | A | 2 | a0002c0002t0026g0250a0003c0003t0038g0234 | 2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.518-29006A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15655924 | ||||||
chr7:15656064
|
C | T | 3 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079 | 3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.518-29146G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656064 | ||||||
chr7:15656097
|
A | C | 1 | a0004c0004t0011g0277 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.518-29179T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656097 | ||||||
chr7:15656099
|
C | A | 2 | a0001c0001t0019g0117a0001c0001t0019g0118 | 2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.518-29181G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656099 | ||||||
chr7:15656291
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.518-29373C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656291 | ||||||
chr7:15656339
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.518-29421A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656339 | ||||||
chr7:15656370
|
T | G | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-29452A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656370 | ||||||
chr7:15656387
|
G | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(75): Show | 79 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.518-29469C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656387 | ||||||
chr7:15656437
|
C | CT | 8 | a0001c0001t0007g0071a0001c0001t0009g0233a0001c0001t0023g0002others(5): Show | 9 | HG01081.hp1 HG01884.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+29448dupA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656437 | ||||||
chr7:15656526
|
T | C | 279 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.517+29360A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656526 | ||||||
chr7:15656612
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.517+29274A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656612 | ||||||
chr7:15656717
|
A | C | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.517+29169T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656717 | ||||||
chr7:15656800
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.517+29086A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656800 | ||||||
chr7:15656823
|
T | C | 2 | a0003c0003t0003g0057a0003c0003t0003g0159 | 2 | HG02071.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.517+29063A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656823 | ||||||
chr7:15656934
|
T | C | 1 | a0001c0001t0006g0136 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.517+28952A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656934 | ||||||
chr7:15656980
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.517+28906C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15656980 | ||||||
chr7:15657051
|
T | C | 279 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.517+28835A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657051 | ||||||
chr7:15657070
|
G | A | 2 | a0002c0002t0004g0246a0002c0002t0010g0247 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.517+28816C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657070 | ||||||
chr7:15657359
|
T | C | 1 | a0003c0003t0038g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.517+28527A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657359 | ||||||
chr7:15657417
|
T | A | 1 | a0001c0001t0007g0007 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.517+28469A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657417 | ||||||
chr7:15657444
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.517+28442A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657444 | ||||||
chr7:15657451
|
T | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0053others(6): Show | 10 | HG00140.hp1 HG00280.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+28435A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657451 | ||||||
chr7:15657953
|
G | A | 1 | a0003c0003t0003g0207 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.517+27933C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15657953 | ||||||
chr7:15658021
|
C | A | 15 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0006g0056others(12): Show | 16 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.517+27865G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658021 | ||||||
chr7:15658086
|
G | A | 2 | a0002c0002t0004g0244a0002c0002t0026g0243 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+27800C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658086 | ||||||
chr7:15658311
|
A | T | 1 | a0002c0002t0002g0327 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.517+27575T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658311 | ||||||
chr7:15658334
|
G | A | 2 | a0002c0002t0026g0250a0003c0003t0038g0234 | 2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.517+27552C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658334 | ||||||
chr7:15658382
|
G | A | 1 | a0001c0001t0015g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.517+27504C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658382 | ||||||
chr7:15658465
|
C | A | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.517+27421G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658465 | ||||||
chr7:15658553
|
C | T | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(187): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.517+27333G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658553 | ||||||
chr7:15658604
|
G | A | 6 | a0001c0001t0007g0071a0001c0001t0009g0233a0002c0002t0004g0244others(3): Show | 6 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+27282C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658604 | ||||||
chr7:15658620
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.517+27266G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658620 | ||||||
chr7:15658659
|
T | G | 2 | a0002c0002t0004g0244a0002c0002t0026g0243 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+27227A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658659 | ||||||
chr7:15658701
|
G | A | 38 | a0001c0001t0006g0176a0001c0001t0009g0230a0001c0001t0009g0231others(35): Show | 39 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.517+27185C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658701 | ||||||
chr7:15658822
|
C | T | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+27064G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15658822 | ||||||
chr7:15659157
|
G | A | 1 | a0001c0001t0021g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.517+26729C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659157 | ||||||
chr7:15659190
|
G | C | 253 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(250): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.517+26696C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659190 | ||||||
chr7:15659382
|
T | A | 60 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(57): Show | 61 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.517+26504A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659382 | ||||||
chr7:15659396
|
G | A | 5 | a0001c0001t0007g0071a0002c0002t0004g0244a0002c0002t0004g0246others(2): Show | 5 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+26490C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659396 | ||||||
chr7:15659401
|
T | G | 1 | a0002c0002t0022g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.517+26485A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659401 | ||||||
chr7:15659411
|
G | A | 78 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(75): Show | 79 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.517+26475C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659411 | ||||||
chr7:15659690
|
G | A | 2 | a0001c0001t0014g0220a0001c0001t0020g0229 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.517+26196C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659690 | ||||||
chr7:15659758
|
C | CA | 65 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0043others(62): Show | 68 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.517+26127dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659758 | ||||||
chr7:15659758
|
CA | C | 9 | a0001c0001t0001g0045a0001c0001t0006g0056a0001c0001t0016g0016others(6): Show | 9 | HG00558.hp1 HG00738.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+26127delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659758 | ||||||
chr7:15659758
|
CAAAAA | C | 11 | a0001c0001t0006g0176a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 12 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.517+26123_517+2612 others(9): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15659758 | ||||||
chr7:15660007
|
A | G | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+25879T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660007 | ||||||
chr7:15660025
|
A | G | 5 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0007g0071others(2): Show | 5 | HG01081.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+25861T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660025 | ||||||
chr7:15660045
|
G | A | 2 | a0002c0002t0004g0246a0002c0002t0010g0247 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.517+25841C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660045 | ||||||
chr7:15660113
|
A | G | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+25773T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660113 | ||||||
chr7:15660191
|
C | A | 263 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.517+25695G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660191 | ||||||
chr7:15660274
|
G | A | 1 | a0002c0002t0004g0257 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.517+25612C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660274 | ||||||
chr7:15660406
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.517+25480A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660406 | ||||||
chr7:15660565
|
C | T | 1 | a0001c0001t0018g0177 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.517+25321G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660565 | ||||||
chr7:15660649
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.517+25237A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660649 | ||||||
chr7:15660691
|
C | T | 1 | a0001c0001t0016g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517+25195G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660691 | ||||||
chr7:15660816
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0006g0056 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.517+25070C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660816 | ||||||
chr7:15660935
|
C | G | 1 | a0001c0001t0007g0182 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.517+24951G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15660935 | ||||||
chr7:15661000
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0012g0030a0002c0002t0004g0296 | 3 | NA18944.hp1 NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.517+24886C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661000 | ||||||
chr7:15661005
|
T | G | 1 | a0008c0007t0003g0037 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.517+24881A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661005 | ||||||
chr7:15661012
|
C | CA | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.517+24873dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | ||||||
chr7:15661012
|
C | CAA | 40 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0077others(37): Show | 40 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.517+24872_517+2487 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | ||||||
chr7:15661012
|
C | CAAA | 12 | a0001c0001t0001g0114a0001c0001t0001g0187a0001c0001t0012g0030others(9): Show | 12 | HG00609.hp1 HG01243.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.517+24871_517+2487 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | ||||||
chr7:15661012
|
CA | C | 35 | a0001c0001t0001g0043a0001c0001t0001g0184a0001c0001t0001g0188others(32): Show | 36 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.517+24873delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | ||||||
chr7:15661012
|
CAA | C | 6 | a0001c0001t0007g0007a0001c0001t0007g0183a0001c0001t0014g0215others(3): Show | 7 | HG02145.hp2 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+24872_517+2487 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | ||||||
chr7:15661012
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0087others(1): Show | 4 | HG01258.hp2 HG01433.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+24864_517+2487 others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661012 | ||||||
chr7:15661041
|
A | G | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+24845T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661041 | ||||||
chr7:15661042
|
G | A | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+24844C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661042 | ||||||
chr7:15661242
|
C | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.517+24644G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661242 | ||||||
chr7:15661347
|
G | A | 1 | a0010c0006t0001g0035 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.517+24539C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661347 | ||||||
chr7:15661437
|
C | T | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+24449G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661437 | ||||||
chr7:15661467
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+24419G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661467 | ||||||
chr7:15661511
|
C | A | 1 | a0002c0002t0002g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+24375G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661511 | ||||||
chr7:15661569
|
A | C | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+24317T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661569 | ||||||
chr7:15661728
|
A | G | 1 | a0001c0001t0006g0153 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.517+24158T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661728 | ||||||
chr7:15661835
|
A | G | 1 | a0003c0003t0003g0209 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.517+24051T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661835 | ||||||
chr7:15661889
|
C | T | 1 | a0002c0002t0005g0263 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.517+23997G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15661889 | ||||||
chr7:15662202
|
C | A | 1 | a0001c0001t0013g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.517+23684G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662202 | ||||||
chr7:15662251
|
A | T | 1 | a0001c0001t0007g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.517+23635T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662251 | ||||||
chr7:15662377
|
G | A | 13 | a0001c0001t0001g0043a0001c0001t0006g0176a0001c0001t0008g0039others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.517+23509C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662377 | ||||||
chr7:15662383
|
A | T | 15 | a0001c0001t0001g0043a0001c0001t0006g0176a0001c0001t0008g0039others(12): Show | 16 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.517+23503T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662383 | ||||||
chr7:15662393
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+23493A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662393 | ||||||
chr7:15662410
|
C | A | 2 | a0002c0002t0002g0306a0002c0002t0004g0296 | 2 | HG02148.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.517+23476G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662410 | ||||||
chr7:15662416
|
A | G | 1 | a0003c0003t0003g0076 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.517+23470T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662416 | ||||||
chr7:15662467
|
T | G | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+23419A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662467 | ||||||
chr7:15662479
|
G | A | 1 | a0002c0002t0002g0265 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.517+23407C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662479 | ||||||
chr7:15662514
|
A | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0052others(87): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.517+23372T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662514 | ||||||
chr7:15662653
|
A | C | 1 | a0002c0002t0002g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+23233T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662653 | ||||||
chr7:15662709
|
T | C | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+23177A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662709 | ||||||
chr7:15662816
|
C | T | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+23070G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662816 | ||||||
chr7:15662985
|
C | T | 1 | a0004c0004t0011g0313 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.517+22901G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15662985 | ||||||
chr7:15663005
|
G | C | 61 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 62 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.517+22881C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663005 | ||||||
chr7:15663008
|
T | C | 2 | a0001c0001t0014g0220a0001c0001t0020g0229 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.517+22878A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663008 | ||||||
chr7:15663098
|
C | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0052others(86): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.517+22788G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663098 | ||||||
chr7:15663276
|
A | G | 1 | a0002c0002t0002g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+22610T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663276 | ||||||
chr7:15663332
|
A | C | 2 | a0002c0002t0004g0245a0002c0002t0010g0249 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.517+22554T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663332 | ||||||
chr7:15663335
|
CT | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0132a0001c0001t0014g0220others(4): Show | 7 | HG01069.hp2 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+22550delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663335 | ||||||
chr7:15663415
|
C | A | 78 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(75): Show | 79 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.517+22471G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663415 | ||||||
chr7:15663442
|
C | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0052others(84): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.517+22444G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663442 | ||||||
chr7:15663507
|
AT | A | 256 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.517+22378delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663507 | ||||||
chr7:15663583
|
C | G | 1 | a0002c0002t0026g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517+22303G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663583 | ||||||
chr7:15663685
|
T | G | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+22201A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663685 | ||||||
chr7:15663756
|
C | G | 1 | a0001c0001t0001g0109 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517+22130G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663756 | ||||||
chr7:15663814
|
G | A | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+22072C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663814 | ||||||
chr7:15663937
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.517+21949T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663937 | ||||||
chr7:15663942
|
G | A | 1 | a0001c0001t0006g0153 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.517+21944C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663942 | ||||||
chr7:15663944
|
C | T | 2 | a0002c0002t0004g0244a0002c0002t0026g0243 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+21942G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663944 | ||||||
chr7:15663952
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0015g0012a0001c0001t0015g0013others(1): Show | 4 | HG02809.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+21934A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663952 | ||||||
chr7:15663971
|
T | G | 4 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+21915A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663971 | ||||||
chr7:15663982
|
A | G | 4 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+21904T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663982 | ||||||
chr7:15663994
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+21892C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15663994 | ||||||
chr7:15664190
|
G | A | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+21696C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664190 | ||||||
chr7:15664284
|
T | G | 2 | a0002c0002t0004g0244a0002c0002t0026g0243 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+21602A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664284 | ||||||
chr7:15664305
|
A | G | 1 | a0001c0001t0015g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.517+21581T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664305 | ||||||
chr7:15664316
|
C | A | 9 | a0002c0002t0002g0011a0002c0002t0002g0283a0002c0002t0002g0293others(6): Show | 10 | HG00099.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+21570G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664316 | ||||||
chr7:15664344
|
A | T | 1 | a0002c0002t0010g0310 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.517+21542T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664344 | ||||||
chr7:15664432
|
C | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.517+21454G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664432 | ||||||
chr7:15664693
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.517+21193G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15664693 | ||||||
chr7:15665008
|
G | A | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+20878C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665008 | ||||||
chr7:15665041
|
T | TCA | 53 | a0001c0001t0001g0077a0001c0001t0001g0147a0001c0001t0001g0165others(50): Show | 54 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.517+20843_517+2084 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
T | TCACA | 25 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0122others(22): Show | 25 | HG00639.hp1 HG01243.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.517+20841_517+2084 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
T | TCACACA | 12 | a0001c0001t0001g0044a0001c0001t0001g0142a0001c0001t0001g0162others(9): Show | 12 | HG02015.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.517+20839_517+2084 others(10): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
T | TCACACAC others(1): Show |
6 | a0001c0001t0001g0043a0001c0001t0008g0039a0001c0001t0008g0040others(3): Show | 6 | HG01074.hp1 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.517+20837_517+2084 others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
T | TCACACAC others(3): Show |
2 | a0001c0001t0008g0041a0001c0001t0008g0042 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.517+20835_517+2084 others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
TCA | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0054others(14): Show | 18 | HG01081.hp1 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+20843_517+2084 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
TCACA | T | 9 | a0001c0001t0007g0183a0001c0001t0012g0003a0001c0001t0012g0031others(6): Show | 10 | HG01099.hp2 HG02132.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+20841_517+2084 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
TCACACA | T | 6 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(3): Show | 7 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+20839_517+2084 others(10): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
TCACACAC others(1): Show |
T | 6 | a0001c0001t0012g0030a0002c0002t0002g0248a0002c0002t0004g0238others(3): Show | 6 | HG01928.hp1 HG02071.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+20837_517+2084 others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
TCACACAC others(3): Show |
T | 59 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(56): Show | 60 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.517+20835_517+2084 others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.517+20833_517+2084 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665041
|
TCACACAC others(7): Show |
T | 4 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+20831_517+2084 others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665041 | ||||||
chr7:15665140
|
C | T | 2 | a0001c0001t0016g0014a0001c0001t0016g0015 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.517+20746G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665140 | ||||||
chr7:15665230
|
G | T | 284 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(281): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.517+20656C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665230 | ||||||
chr7:15665280
|
T | G | 1 | a0001c0001t0006g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.517+20606A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665280 | ||||||
chr7:15665289
|
G | GA | 36 | a0001c0001t0009g0230a0001c0001t0009g0231a0001c0001t0009g0232others(33): Show | 37 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.517+20596dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665289 | ||||||
chr7:15665302
|
C | G | 1 | a0001c0001t0013g0021 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.517+20584G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665302 | ||||||
chr7:15665376
|
T | A | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+20510A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665376 | ||||||
chr7:15665580
|
T | C | 1 | a0002c0002t0002g0336 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.517+20306A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665580 | ||||||
chr7:15665624
|
G | C | 5 | a0001c0001t0007g0071a0002c0002t0004g0244a0002c0002t0004g0246others(2): Show | 5 | HG01081.hp1 HG02647.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+20262C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665624 | ||||||
chr7:15665742
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.517+20144A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665742 | ||||||
chr7:15665917
|
T | G | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19969A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665917 | ||||||
chr7:15665918
|
C | CATATATG others(31): Show |
1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19967_517+1996 others(42): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665918 | ||||||
chr7:15665919
|
C | A | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19967G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665919 | ||||||
chr7:15665920
|
C | T | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19966G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665920 | ||||||
chr7:15665985
|
G | C | 3 | a0002c0002t0002g0009a0002c0002t0002g0265a0002c0002t0002g0330 | 4 | HG00738.hp1 HG01069.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+19901C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15665985 | ||||||
chr7:15666154
|
T | A | 1 | a0002c0002t0010g0249 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.517+19732A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666154 | ||||||
chr7:15666233
|
A | G | 3 | a0002c0002t0004g0254a0002c0002t0004g0255a0002c0002t0040g0252 | 3 | HG01109.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.517+19653T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666233 | ||||||
chr7:15666284
|
A | G | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19602T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666284 | ||||||
chr7:15666478
|
C | G | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+19408G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666478 | ||||||
chr7:15666503
|
C | G | 1 | a0001c0001t0007g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.517+19383G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666503 | ||||||
chr7:15666590
|
A | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0108 | 2 | NA18963.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.517+19296T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666590 | ||||||
chr7:15666611
|
G | T | 4 | a0001c0001t0006g0058a0001c0001t0006g0080a0001c0001t0032g0079others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+19275C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666611 | ||||||
chr7:15666620
|
T | C | 1 | a0003c0003t0027g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.517+19266A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666620 | ||||||
chr7:15666657
|
C | G | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0044others(212): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.517+19229G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666657 | ||||||
chr7:15666694
|
G | GT | 4 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0097others(1): Show | 5 | HG00408.hp1 HG02056.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+19191dupA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666694 | ||||||
chr7:15666751
|
C | CA | 16 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0008g0072others(13): Show | 17 | HG01175.hp2 HG01433.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.517+19134dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | ||||||
chr7:15666751
|
C | CAA | 7 | a0002c0002t0002g0286a0002c0002t0002g0318a0002c0002t0002g0325others(4): Show | 7 | HG02683.hp1 HG03017.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+19133_517+1913 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | ||||||
chr7:15666751
|
C | CAAA | 7 | a0001c0001t0001g0166a0001c0001t0014g0221a0002c0002t0002g0330others(4): Show | 7 | HG01074.hp2 HG01123.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+19132_517+1913 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | ||||||
chr7:15666751
|
CA | C | 12 | a0001c0001t0008g0040a0001c0001t0018g0075a0001c0001t0018g0101others(9): Show | 13 | HG00738.hp1 HG01069.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.517+19134delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | ||||||
chr7:15666751
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0012g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.517+19123_517+1913 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | ||||||
chr7:15666751
|
CAAAAAAA others(7): Show |
C | 4 | a0003c0003t0003g0049a0003c0003t0003g0103a0003c0003t0003g0119others(1): Show | 4 | NA18977.hp1 NA18977.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+19121_517+1913 others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666751 | ||||||
chr7:15666765
|
AAAAAAAA others(9): Show |
A | 1 | a0002c0002t0002g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+19105_517+1912 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666765 | ||||||
chr7:15666766
|
AAAAAAAA others(8): Show |
A | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+19105_517+1911 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666766 | ||||||
chr7:15666767
|
AAAAAAAA others(9): Show |
A | 2 | a0003c0003t0003g0159a0003c0003t0003g0194 | 2 | NA19001.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.517+19103_517+1911 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666767 | ||||||
chr7:15666767
|
AAAAAAAA others(11): Show |
A | 3 | a0001c0001t0001g0044a0001c0001t0006g0056a0001c0001t0009g0226 | 3 | HG00639.hp1 HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.517+19101_517+1911 others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666767 | ||||||
chr7:15666768
|
AAAAAAAA others(8): Show |
A | 4 | a0001c0001t0006g0060a0001c0001t0006g0061a0001c0001t0006g0173others(1): Show | 4 | HG02015.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+19103_517+1911 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666768 | ||||||
chr7:15666768
|
AAAAAAAA others(10): Show |
A | 10 | a0001c0001t0009g0224a0001c0001t0013g0021a0001c0001t0013g0022others(7): Show | 10 | HG00609.hp1 HG01255.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+19101_517+1911 others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666768 | ||||||
chr7:15666769
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0012g0003a0001c0001t0012g0032 | 3 | HG02818.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.517+19105_517+1911 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666769 | ||||||
chr7:15666769
|
AAAAAAAA others(7): Show |
A | 11 | a0001c0001t0001g0054a0001c0001t0001g0146a0001c0001t0021g0225others(8): Show | 11 | HG01891.hp2 HG03540.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.517+19103_517+1911 others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666769 | ||||||
chr7:15666769
|
AAAAAAAA others(9): Show |
A | 60 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(57): Show | 64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.517+19101_517+1911 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666769 | ||||||
chr7:15666769
|
AAAAAAAA others(11): Show |
A | 4 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | HG01167.hp1 HG02602.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+19099_517+1911 others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666769 | ||||||
chr7:15666770
|
AAAAAAAA others(8): Show |
A | 10 | a0001c0001t0001g0047a0001c0001t0001g0125a0001c0001t0001g0127others(7): Show | 10 | HG01884.hp1 HG04115.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+19101_517+1911 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666770 | ||||||
chr7:15666770
|
AAAAAAAA others(10): Show |
A | 49 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(46): Show | 50 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.517+19099_517+1911 others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666770 | ||||||
chr7:15666771
|
AAAAAAAA others(9): Show |
A | 4 | a0001c0001t0001g0069a0001c0001t0001g0170a0001c0001t0012g0029others(1): Show | 4 | HG00323.hp1 HG03239.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+19099_517+1911 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666771 | ||||||
chr7:15666771
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.517+19097_517+1911 others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666771 | ||||||
chr7:15666772
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0109 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517+19099_517+1911 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666772 | ||||||
chr7:15666772
|
AAAAAAAA others(10): Show |
A | 4 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0114others(1): Show | 4 | HG01243.hp1 HG02056.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+19097_517+1911 others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666772 | ||||||
chr7:15666773
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.517+19097_517+1911 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666773 | ||||||
chr7:15666774
|
AAAAAAAT others(4): Show |
A | 1 | a0003c0003t0003g0144 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.517+19101_517+1911 others(15): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666774 | ||||||
chr7:15666777
|
A | T | 8 | a0001c0001t0007g0180a0001c0001t0018g0075a0001c0001t0018g0102others(5): Show | 9 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+19109T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666777 | ||||||
chr7:15666779
|
A | AAAAAAAA others(6): Show |
1 | a0002c0002t0026g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517+19106_517+1910 others(17): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | ||||||
chr7:15666779
|
A | AAAAAAAA others(8): Show |
1 | a0002c0002t0004g0244 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.517+19106_517+1910 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | ||||||
chr7:15666779
|
A | AT | 4 | a0002c0002t0010g0251a0004c0004t0011g0312a0004c0004t0011g0313others(1): Show | 4 | HG00558.hp1 HG00741.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+19106_517+1910 others(5): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | ||||||
chr7:15666779
|
A | ATATATAT | 3 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0034g0217 | 3 | HG02145.hp2 HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.517+19106_517+1910 others(11): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | ||||||
chr7:15666779
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0014g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.517+19106_517+1910 others(15): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | ||||||
chr7:15666779
|
A | T | 25 | a0001c0001t0001g0188a0001c0001t0007g0007a0001c0001t0007g0179others(22): Show | 27 | HG00738.hp1 HG01069.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.517+19107T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | ||||||
chr7:15666779
|
AATAT | A | 7 | a0001c0001t0001g0038a0001c0001t0006g0176a0001c0001t0008g0041others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+19103_517+1910 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666779 | ||||||
chr7:15666780
|
AT | A | 12 | a0001c0001t0001g0193a0001c0001t0006g0081a0001c0001t0009g0231others(9): Show | 12 | HG01361.hp1 HG01928.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.517+19105delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666780 | ||||||
chr7:15666780
|
ATAT | A | 8 | a0001c0001t0001g0006a0001c0001t0006g0058a0001c0001t0006g0080others(5): Show | 9 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+19103_517+1910 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666780 | ||||||
chr7:15666781
|
T | A | 57 | a0001c0001t0001g0077a0001c0001t0001g0162a0001c0001t0001g0166others(54): Show | 59 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.517+19105A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666781 | ||||||
chr7:15666783
|
T | A | 18 | a0001c0001t0001g0167a0001c0001t0006g0081a0001c0001t0006g0153others(15): Show | 19 | HG00621.hp1 HG02647.hp2 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.517+19103A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666783 | ||||||
chr7:15666785
|
T | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0167others(4): Show | 8 | HG02559.hp1 HG02818.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.517+19101A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666785 | ||||||
chr7:15666787
|
T | A | 2 | a0001c0001t0006g0176a0001c0001t0018g0177 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.517+19099A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666787 | ||||||
chr7:15666962
|
A | T | 1 | a0001c0001t0014g0220 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.517+18924T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15666962 | ||||||
chr7:15667010
|
G | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(79): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.517+18876C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667010 | ||||||
chr7:15667135
|
C | A | 1 | a0001c0001t0001g0146 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.517+18751G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667135 | ||||||
chr7:15667142
|
T | G | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+18744A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667142 | ||||||
chr7:15667145
|
G | T | 1 | a0002c0002t0002g0278 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.517+18741C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667145 | ||||||
chr7:15667242
|
G | A | 35 | a0001c0001t0009g0230a0001c0001t0009g0231a0001c0001t0009g0232others(32): Show | 36 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.517+18644C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667242 | ||||||
chr7:15667289
|
C | CAAAAAA | 70 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(67): Show | 74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.517+18591_517+1859 others(10): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA | 15 | a0001c0001t0001g0127a0001c0001t0001g0133a0001c0001t0001g0147others(12): Show | 15 | HG01346.hp2 HG01934.hp2 HG03098.hp1 others(12): Show |
intron_variant | MODIFIER | c.517+18590_517+1859 others(11): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(1): Show |
5 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(2): Show | 6 | HG01255.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.517+18589_517+1859 others(12): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0038a0001c0001t0006g0056a0001c0001t0007g0071others(4): Show | 8 | HG01081.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+18588_517+1859 others(13): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(3): Show |
18 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0077others(15): Show | 19 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.517+18587_517+1859 others(14): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(4): Show |
19 | a0001c0001t0001g0044a0001c0001t0001g0168a0001c0001t0001g0169others(16): Show | 19 | HG01106.hp2 HG01169.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.517+18586_517+1859 others(15): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(5): Show |
11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG01109.hp1 HG01361.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+18585_517+1859 others(16): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0008g0189a0001c0001t0021g0236a0002c0002t0004g0239others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+18584_517+1859 others(17): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(7): Show |
22 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0001t0001g0066others(19): Show | 23 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.517+18583_517+1859 others(18): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(8): Show |
46 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(43): Show | 48 | HG00323.hp1 HG00621.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.517+18582_517+1859 others(19): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(9): Show |
30 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0062others(27): Show | 30 | HG00741.hp1 HG01071.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.517+18581_517+1859 others(20): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(10): Show |
7 | a0001c0001t0001g0100a0001c0001t0001g0113a0001c0001t0012g0030others(4): Show | 7 | HG00673.hp1 HG02273.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+18580_517+1859 others(21): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(11): Show |
5 | a0001c0001t0018g0101a0002c0002t0005g0269a0003c0003t0003g0128others(2): Show | 5 | HG01123.hp1 HG01928.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+18579_517+1859 others(22): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(13): Show |
2 | a0003c0003t0003g0190a0003c0003t0008g0112 | 2 | HG02055.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.517+18577_517+1859 others(24): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.517+18576_517+1859 others(25): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667289
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.517+18575_517+1859 others(26): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667289 | ||||||
chr7:15667303
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0006g0176a0001c0001t0018g0177 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.517+18582_517+1858 others(15): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667303 | ||||||
chr7:15667349
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+18537G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667349 | ||||||
chr7:15667490
|
T | G | 1 | a0001c0001t0012g0030 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517+18396A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667490 | ||||||
chr7:15667505
|
C | T | 3 | a0001c0001t0009g0223a0002c0002t0004g0245a0002c0002t0010g0249 | 3 | HG02486.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.517+18381G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667505 | ||||||
chr7:15667506
|
G | A | 1 | a0001c0001t0016g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.517+18380C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667506 | ||||||
chr7:15667820
|
G | A | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(206): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.517+18066C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667820 | ||||||
chr7:15667881
|
T | C | 1 | a0001c0001t0021g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.517+18005A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15667881 | ||||||
chr7:15668025
|
G | A | 1 | a0002c0002t0002g0329 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.517+17861C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668025 | ||||||
chr7:15668217
|
C | T | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+17669G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668217 | ||||||
chr7:15668426
|
T | C | 2 | a0001c0001t0006g0176a0001c0001t0018g0177 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.517+17460A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668426 | ||||||
chr7:15668548
|
C | T | 33 | a0001c0001t0009g0230a0001c0001t0009g0231a0001c0001t0009g0232others(30): Show | 34 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.517+17338G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668548 | ||||||
chr7:15668638
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.517+17248G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668638 | ||||||
chr7:15668639
|
G | T | 1 | a0002c0002t0002g0297 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.517+17247C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668639 | ||||||
chr7:15668677
|
T | A | 9 | a0002c0002t0002g0271a0002c0002t0002g0280a0002c0002t0002g0281others(6): Show | 9 | NA18940.hp2 NA18950.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+17209A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668677 | ||||||
chr7:15668856
|
T | C | 2 | a0001c0001t0020g0229a0001c0001t0021g0225 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.517+17030A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15668856 | ||||||
chr7:15669025
|
A | C | 15 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.517+16861T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669025 | ||||||
chr7:15669228
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.517+16658A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669228 | ||||||
chr7:15669343
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.517+16543A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669343 | ||||||
chr7:15669360
|
A | C | 35 | a0001c0001t0009g0230a0001c0001t0009g0231a0001c0001t0009g0232others(32): Show | 36 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.517+16526T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669360 | ||||||
chr7:15669879
|
T | C | 1 | a0003c0003t0003g0119 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.517+16007A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15669879 | ||||||
chr7:15670147
|
A | G | 1 | a0007c0008t0007g0178 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517+15739T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670147 | ||||||
chr7:15670162
|
T | G | 2 | a0001c0001t0001g0074a0006c0009t0001g0078 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.517+15724A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670162 | ||||||
chr7:15670234
|
G | A | 3 | a0001c0001t0018g0102a0002c0002t0005g0272a0002c0002t0005g0273 | 3 | NA18944.hp2 NA18990.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.517+15652C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670234 | ||||||
chr7:15670314
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.517+15572T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670314 | ||||||
chr7:15670429
|
G | A | 1 | a0002c0002t0002g0288 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.517+15457C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670429 | ||||||
chr7:15670483
|
T | G | 1 | a0002c0002t0004g0238 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.517+15403A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670483 | ||||||
chr7:15670488
|
C | T | 1 | a0004c0004t0011g0311 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.517+15398G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670488 | ||||||
chr7:15670599
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.517+15287G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670599 | ||||||
chr7:15670600
|
G | A | 2 | a0001c0001t0019g0117a0001c0001t0019g0118 | 2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.517+15286C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670600 | ||||||
chr7:15670633
|
T | A | 3 | a0001c0001t0007g0071a0002c0002t0004g0246a0002c0002t0010g0247 | 3 | HG01081.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.517+15253A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670633 | ||||||
chr7:15670635
|
T | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0077others(16): Show | 20 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.517+15251A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670635 | ||||||
chr7:15670831
|
G | A | 1 | a0002c0002t0004g0244 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.517+15055C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670831 | ||||||
chr7:15670936
|
A | G | 1 | a0001c0001t0014g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.517+14950T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15670936 | ||||||
chr7:15671123
|
A | G | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+14763T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671123 | ||||||
chr7:15671227
|
A | G | 1 | a0006c0009t0001g0078 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.517+14659T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671227 | ||||||
chr7:15671310
|
A | G | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+14576T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671310 | ||||||
chr7:15671399
|
A | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | NA18983.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.517+14487T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671399 | ||||||
chr7:15671403
|
T | C | 1 | a0002c0002t0002g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+14483A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671403 | ||||||
chr7:15671495
|
A | G | 1 | a0001c0001t0021g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.517+14391T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671495 | ||||||
chr7:15671529
|
T | C | 7 | a0001c0001t0007g0007a0001c0001t0007g0179a0001c0001t0007g0180others(4): Show | 8 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+14357A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671529 | ||||||
chr7:15671792
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0043others(26): Show | 31 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.517+14094G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671792 | ||||||
chr7:15671851
|
G | A | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+14035C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671851 | ||||||
chr7:15671924
|
C | G | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+13962G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671924 | ||||||
chr7:15671960
|
G | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(86): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.517+13926C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671960 | ||||||
chr7:15671984
|
G | A | 1 | a0001c0001t0009g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+13902C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671984 | ||||||
chr7:15671987
|
G | A | 2 | a0002c0002t0005g0272a0002c0002t0005g0273 | 2 | NA18944.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.517+13899C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15671987 | ||||||
chr7:15672087
|
C | T | 2 | a0002c0002t0004g0259a0002c0002t0004g0260 | 2 | NA19007.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.517+13799G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672087 | ||||||
chr7:15672283
|
T | C | 1 | a0002c0002t0002g0301 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.517+13603A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672283 | ||||||
chr7:15672363
|
A | T | 10 | a0001c0001t0001g0044a0001c0001t0006g0056a0001c0001t0006g0176others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+13523T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672363 | ||||||
chr7:15672467
|
A | T | 2 | a0001c0001t0015g0017a0003c0003t0038g0234 | 2 | HG02109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.517+13419T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672467 | ||||||
chr7:15672629
|
A | G | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+13257T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672629 | ||||||
chr7:15672689
|
A | G | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+13197T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672689 | ||||||
chr7:15672771
|
A | C | 9 | a0001c0001t0006g0176a0001c0001t0007g0007a0001c0001t0007g0179others(6): Show | 10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+13115T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672771 | ||||||
chr7:15672797
|
C | T | 4 | a0002c0002t0002g0305a0002c0002t0002g0306a0002c0002t0002g0331others(1): Show | 4 | HG01361.hp1 HG01928.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+13089G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672797 | ||||||
chr7:15672854
|
C | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(75): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.517+13032G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672854 | ||||||
chr7:15672870
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+13016G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672870 | ||||||
chr7:15672871
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+13015T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672871 | ||||||
chr7:15672879
|
G | A | 1 | a0001c0001t0034g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.517+13007C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672879 | ||||||
chr7:15672892
|
G | GA | 9 | a0001c0001t0006g0176a0001c0001t0007g0007a0001c0001t0007g0179others(6): Show | 10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+12993dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672892 | ||||||
chr7:15672892
|
GAAAAA | G | 89 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(86): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.517+12989_517+1299 others(9): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672892 | ||||||
chr7:15672928
|
C | T | 15 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032others(12): Show | 17 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.517+12958G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672928 | ||||||
chr7:15672947
|
C | G | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+12939G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15672947 | ||||||
chr7:15673054
|
C | T | 1 | a0003c0003t0003g0076 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.517+12832G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673054 | ||||||
chr7:15673201
|
G | A | 1 | a0001c0001t0018g0075 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.517+12685C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673201 | ||||||
chr7:15673227
|
C | T | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.517+12659G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673227 | ||||||
chr7:15673319
|
T | C | 1 | a0003c0003t0003g0174 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.517+12567A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673319 | ||||||
chr7:15673329
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.517+12557A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673329 | ||||||
chr7:15673344
|
G | A | 1 | a0004c0004t0011g0240 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.517+12542C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673344 | ||||||
chr7:15673414
|
G | A | 24 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0009g0233others(21): Show | 26 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.517+12472C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673414 | ||||||
chr7:15673439
|
G | A | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(264): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.517+12447C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673439 | ||||||
chr7:15673480
|
G | C | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.517+12406C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673480 | ||||||
chr7:15673522
|
C | G | 2 | a0002c0002t0004g0245a0002c0002t0010g0249 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.517+12364G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673522 | ||||||
chr7:15673556
|
AT | A | 17 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032others(14): Show | 19 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.517+12329delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673556 | ||||||
chr7:15673597
|
C | CA | 128 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0045others(125): Show | 131 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.517+12288dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | ||||||
chr7:15673597
|
C | CAA | 27 | a0001c0001t0001g0048a0001c0001t0001g0108a0001c0001t0001g0109others(24): Show | 27 | HG00639.hp1 HG01074.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.517+12287_517+1228 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | ||||||
chr7:15673597
|
CA | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(88): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.517+12288delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | ||||||
chr7:15673597
|
CAA | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0165others(23): Show | 27 | HG00408.hp2 HG01081.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.517+12287_517+1228 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | ||||||
chr7:15673597
|
CAAA | C | 27 | a0001c0001t0001g0187a0001c0001t0009g0233a0001c0001t0014g0221others(24): Show | 27 | HG00673.hp1 HG00735.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.517+12286_517+1228 others(7): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | ||||||
chr7:15673597
|
CAAAA | C | 11 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032others(8): Show | 12 | HG01109.hp1 HG02630.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.517+12285_517+1228 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | ||||||
chr7:15673597
|
CAAAAA | C | 6 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(3): Show | 7 | HG00738.hp1 HG01069.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+12284_517+1228 others(9): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673597 | ||||||
chr7:15673658
|
C | T | 1 | a0002c0002t0004g0333 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.517+12228G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673658 | ||||||
chr7:15673659
|
G | A | 1 | a0002c0002t0002g0332 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.517+12227C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673659 | ||||||
chr7:15673672
|
C | G | 1 | a0002c0002t0026g0250 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517+12214G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673672 | ||||||
chr7:15673679
|
G | T | 9 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(6): Show | 10 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+12207C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673679 | ||||||
chr7:15673703
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0006g0068 | 2 | HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.517+12183A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673703 | ||||||
chr7:15673755
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.517+12131G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673755 | ||||||
chr7:15673931
|
A | T | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+11955T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673931 | ||||||
chr7:15673976
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.517+11910G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673976 | ||||||
chr7:15673992
|
T | A | 2 | a0002c0002t0025g0334a0002c0002t0025g0335 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.517+11894A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15673992 | ||||||
chr7:15674200
|
T | C | 9 | a0001c0001t0006g0176a0001c0001t0007g0007a0001c0001t0007g0179others(6): Show | 10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+11686A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674200 | ||||||
chr7:15674242
|
A | G | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+11644T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674242 | ||||||
chr7:15674309
|
T | C | 171 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(168): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.517+11577A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674309 | ||||||
chr7:15674384
|
G | A | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.517+11502C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674384 | ||||||
chr7:15674394
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517+11492A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674394 | ||||||
chr7:15674470
|
G | A | 3 | a0001c0001t0016g0014a0001c0001t0016g0015a0001c0001t0016g0016 | 3 | HG01891.hp1 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.517+11416C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674470 | ||||||
chr7:15674476
|
T | A | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+11410A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674476 | ||||||
chr7:15674554
|
T | TTG | 107 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.517+11331_517+1133 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674554 | ||||||
chr7:15674554
|
T | TTGTG | 8 | a0001c0001t0001g0162a0002c0002t0002g0275a0002c0002t0002g0276others(5): Show | 8 | HG00408.hp2 HG01099.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+11331_517+1133 others(8): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674554 | ||||||
chr7:15674554
|
TTC | T | 6 | a0001c0001t0001g0187a0001c0001t0012g0003a0001c0001t0012g0031others(3): Show | 7 | HG02273.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+11330_517+1133 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674554 | ||||||
chr7:15674554
|
TTCTGTG | T | 21 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0009g0233others(18): Show | 22 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.517+11326_517+1133 others(10): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674554 | ||||||
chr7:15674556
|
C | CTG | 27 | a0001c0001t0001g0062a0001c0001t0008g0072a0002c0002t0002g0010others(24): Show | 28 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.517+11328_517+1132 others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674556 | ||||||
chr7:15674556
|
C | G | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(137): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.517+11330G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674556 | ||||||
chr7:15674559
|
T | C | 1 | a0001c0001t0008g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.517+11327A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674559 | ||||||
chr7:15674793
|
T | A | 3 | a0002c0002t0004g0333a0002c0002t0025g0334a0002c0002t0025g0335 | 3 | HG01106.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.517+11093A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674793 | ||||||
chr7:15674900
|
A | T | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+10986T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674900 | ||||||
chr7:15674989
|
GT | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(178): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.517+10896delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15674989 | ||||||
chr7:15675112
|
C | A | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.517+10774G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675112 | ||||||
chr7:15675431
|
T | C | 268 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(265): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.517+10455A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675431 | ||||||
chr7:15675455
|
T | C | 10 | a0001c0001t0001g0184a0001c0001t0006g0176a0001c0001t0007g0007others(7): Show | 11 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+10431A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675455 | ||||||
chr7:15675516
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.517+10370A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675516 | ||||||
chr7:15675520
|
G | C | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+10366C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675520 | ||||||
chr7:15675618
|
G | T | 4 | a0001c0001t0014g0220a0001c0001t0019g0117a0001c0001t0019g0118others(1): Show | 4 | HG01074.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+10268C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675618 | ||||||
chr7:15675639
|
G | C | 8 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0009g0233others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+10247C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675639 | ||||||
chr7:15675776
|
G | C | 1 | a0004c0004t0011g0277 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.517+10110C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15675776 | ||||||
chr7:15676016
|
A | G | 16 | a0001c0001t0006g0153a0003c0003t0003g0057a0003c0003t0003g0123others(13): Show | 16 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.517+9870T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676016 | ||||||
chr7:15676094
|
A | G | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(169): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.517+9792T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676094 | ||||||
chr7:15676248
|
A | G | 6 | a0002c0002t0002g0010a0002c0002t0002g0284a0002c0002t0002g0285others(3): Show | 7 | NA18942.hp2 NA18954.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+9638T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676248 | ||||||
chr7:15676569
|
C | T | 33 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0009g0222others(30): Show | 35 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.517+9317G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676569 | ||||||
chr7:15676570
|
T | C | 1 | a0001c0001t0020g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.517+9316A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676570 | ||||||
chr7:15676596
|
C | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(89): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.517+9290G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676596 | ||||||
chr7:15676698
|
G | A | 1 | a0002c0002t0002g0336 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.517+9188C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676698 | ||||||
chr7:15676700
|
G | C | 8 | a0002c0002t0002g0009a0002c0002t0002g0253a0002c0002t0004g0254others(5): Show | 9 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+9186C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676700 | ||||||
chr7:15676782
|
C | T | 1 | a0001c0010t0029g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.517+9104G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676782 | ||||||
chr7:15676808
|
A | C | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+9078T>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676808 | ||||||
chr7:15676836
|
C | T | 1 | a0001c0001t0035g0214 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.517+9050G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676836 | ||||||
chr7:15676839
|
C | A | 9 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(6): Show | 10 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+9047G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676839 | ||||||
chr7:15676857
|
C | CA | 21 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0009g0222others(18): Show | 22 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.517+9028dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15676857 | ||||||
chr7:15677086
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.517+8800G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677086 | ||||||
chr7:15677182
|
A | G | 1 | a0005c0011t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+8704T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677182 | ||||||
chr7:15677184
|
G | T | 9 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(6): Show | 10 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+8702C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677184 | ||||||
chr7:15677227
|
A | G | 1 | a0003c0003t0003g0191 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.517+8659T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677227 | ||||||
chr7:15677348
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(34): Show | 38 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.517+8538T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677348 | ||||||
chr7:15677429
|
T | C | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+8457A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677429 | ||||||
chr7:15677499
|
G | A | 9 | a0001c0001t0001g0187a0001c0001t0013g0021a0001c0001t0013g0022others(6): Show | 9 | HG01255.hp2 HG01261.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+8387C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677499 | ||||||
chr7:15677505
|
T | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0008g0111others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+8381A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677505 | ||||||
chr7:15677633
|
G | A | 1 | a0002c0002t0002g0337 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.517+8253C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677633 | ||||||
chr7:15677863
|
T | A | 1 | a0001c0001t0014g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.517+8023A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15677863 | ||||||
chr7:15678306
|
A | G | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+7580T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678306 | ||||||
chr7:15678374
|
CTGT | C | 9 | a0001c0001t0006g0176a0001c0001t0007g0007a0001c0001t0007g0179others(6): Show | 10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+7509_517+7511d others(5): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678374 | ||||||
chr7:15678413
|
C | T | 1 | a0001c0001t0007g0179 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517+7473G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678413 | ||||||
chr7:15678529
|
C | T | 1 | a0002c0002t0002g0283 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.517+7357G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678529 | ||||||
chr7:15678828
|
T | C | 1 | a0009c0012t0005g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.517+7058A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678828 | ||||||
chr7:15678859
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.517+7027G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678859 | ||||||
chr7:15678879
|
CG | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0003c0003t0008g0112 | 3 | HG01243.hp1 HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.517+7006delC | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678879 | ||||||
chr7:15678887
|
A | G | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+6999T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678887 | ||||||
chr7:15678906
|
C | T | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.517+6980G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678906 | ||||||
chr7:15678957
|
A | T | 1 | a0003c0003t0003g0190 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.517+6929T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678957 | ||||||
chr7:15678982
|
A | G | 1 | a0003c0003t0003g0119 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.517+6904T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15678982 | ||||||
chr7:15679000
|
T | A | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6886A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679000 | ||||||
chr7:15679071
|
A | G | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+6815T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679071 | ||||||
chr7:15679118
|
A | G | 1 | a0002c0002t0004g0339 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.517+6768T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679118 | ||||||
chr7:15679191
|
G | A | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6695C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679191 | ||||||
chr7:15679197
|
G | A | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+6689C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679197 | ||||||
chr7:15679402
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+6484A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679402 | ||||||
chr7:15679440
|
T | A | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6446A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679440 | ||||||
chr7:15679494
|
A | G | 3 | a0001c0001t0001g0187a0001c0001t0009g0233a0003c0003t0038g0234 | 3 | HG02896.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517+6392T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679494 | ||||||
chr7:15679562
|
G | A | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6324C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679562 | ||||||
chr7:15679575
|
T | C | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6311A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679575 | ||||||
chr7:15679721
|
A | G | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.517+6165T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679721 | ||||||
chr7:15679746
|
T | C | 2 | a0002c0002t0004g0245a0002c0002t0010g0249 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.517+6140A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679746 | ||||||
chr7:15679782
|
A | G | 29 | a0001c0001t0009g0222a0001c0001t0009g0223a0001c0001t0009g0224others(26): Show | 30 | HG00639.hp1 HG00639.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.517+6104T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679782 | ||||||
chr7:15679840
|
T | C | 16 | a0001c0001t0009g0223a0001c0001t0009g0224a0001c0001t0009g0226others(13): Show | 16 | HG00639.hp1 HG01255.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.517+6046A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679840 | ||||||
chr7:15679965
|
G | C | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+5921C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15679965 | ||||||
chr7:15680011
|
A | T | 186 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(183): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.517+5875T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680011 | ||||||
chr7:15680135
|
C | G | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+5751G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680135 | ||||||
chr7:15680161
|
A | G | 1 | a0001c0001t0006g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.517+5725T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680161 | ||||||
chr7:15680162
|
C | T | 1 | a0003c0003t0003g0123 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.517+5724G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680162 | ||||||
chr7:15680216
|
A | T | 10 | a0001c0001t0001g0184a0001c0001t0006g0176a0001c0001t0007g0007others(7): Show | 11 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+5670T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680216 | ||||||
chr7:15680251
|
C | A | 2 | a0001c0001t0009g0233a0003c0003t0038g0234 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517+5635G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680251 | ||||||
chr7:15680406
|
C | T | 13 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(10): Show | 14 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.517+5480G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680406 | ||||||
chr7:15680465
|
A | G | 2 | a0001c0001t0001g0184a0002c0002t0005g0258 | 2 | HG02129.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.517+5421T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680465 | ||||||
chr7:15680470
|
T | C | 16 | a0001c0001t0009g0223a0001c0001t0009g0224a0001c0001t0009g0226others(13): Show | 16 | HG00639.hp1 HG01255.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.517+5416A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680470 | ||||||
chr7:15680514
|
C | T | 1 | a0003c0003t0027g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.517+5372G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680514 | ||||||
chr7:15680552
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.517+5334G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680552 | ||||||
chr7:15680727
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+5159C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680727 | ||||||
chr7:15680729
|
A | G | 13 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(10): Show | 14 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.517+5157T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680729 | ||||||
chr7:15680749
|
T | C | 9 | a0001c0001t0006g0176a0001c0001t0007g0007a0001c0001t0007g0179others(6): Show | 10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+5137A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680749 | ||||||
chr7:15680845
|
T | C | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+5041A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680845 | ||||||
chr7:15680903
|
T | C | 13 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(10): Show | 14 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.517+4983A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15680903 | ||||||
chr7:15681017
|
A | G | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+4869T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681017 | ||||||
chr7:15681019
|
C | CA | 34 | a0001c0001t0001g0187a0001c0001t0009g0222a0001c0001t0009g0223others(31): Show | 35 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.517+4866dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681019 | ||||||
chr7:15681088
|
G | A | 1 | a0003c0003t0003g0164 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.517+4798C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681088 | ||||||
chr7:15681112
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.517+4774A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681112 | ||||||
chr7:15681152
|
T | C | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+4734A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681152 | ||||||
chr7:15681272
|
T | C | 92 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0050others(89): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.517+4614A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681272 | ||||||
chr7:15681369
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.517+4517C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681369 | ||||||
chr7:15681380
|
A | G | 1 | a0002c0002t0004g0245 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.517+4506T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681380 | ||||||
chr7:15681465
|
ATTTC | A | 13 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(10): Show | 14 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.517+4417_517+4420d others(6): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681465 | ||||||
chr7:15681477
|
C | CA | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+4408dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681477 | ||||||
chr7:15681477
|
CA | C | 15 | a0001c0001t0001g0069a0001c0001t0006g0068a0002c0002t0002g0009others(12): Show | 16 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.517+4408delT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681477 | ||||||
chr7:15681486
|
AT | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0165a0001c0001t0001g0166others(6): Show | 10 | HG01081.hp2 HG01106.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+4399delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681486 | ||||||
chr7:15681514
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0033g0213 | 3 | HG01496.hp2 HG01978.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.517+4372G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681514 | ||||||
chr7:15681553
|
C | T | 261 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(258): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.517+4333G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681553 | ||||||
chr7:15681651
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+4235C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681651 | ||||||
chr7:15681653
|
C | G | 9 | a0001c0001t0006g0176a0001c0001t0007g0007a0001c0001t0007g0179others(6): Show | 10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+4233G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681653 | ||||||
chr7:15681761
|
T | C | 1 | a0002c0002t0002g0338 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.517+4125A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681761 | ||||||
chr7:15681841
|
G | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0050others(116): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.517+4045C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681841 | ||||||
chr7:15681916
|
C | T | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+3970G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15681916 | ||||||
chr7:15682131
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.517+3755C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682131 | ||||||
chr7:15682134
|
GT | G | 5 | a0001c0001t0001g0038a0001c0001t0008g0039a0001c0001t0008g0040others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+3751delA | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682134 | ||||||
chr7:15682276
|
C | G | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG01071.hp2 HG01167.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+3610G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682276 | ||||||
chr7:15682301
|
T | C | 32 | a0001c0001t0001g0187a0001c0001t0009g0222a0001c0001t0009g0223others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.517+3585A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682301 | ||||||
chr7:15682430
|
T | C | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+3456A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682430 | ||||||
chr7:15682533
|
C | T | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.517+3353G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682533 | ||||||
chr7:15682534
|
G | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0050others(85): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.517+3352C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682534 | ||||||
chr7:15682624
|
C | T | 50 | a0001c0001t0001g0187a0001c0001t0009g0222a0001c0001t0009g0223others(47): Show | 52 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.517+3262G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682624 | ||||||
chr7:15682681
|
C | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0050others(181): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.517+3205G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682681 | ||||||
chr7:15682711
|
T | G | 2 | a0001c0001t0008g0041a0001c0001t0008g0042 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.517+3175A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682711 | ||||||
chr7:15682813
|
G | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0050others(86): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.517+3073C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682813 | ||||||
chr7:15682824
|
T | G | 1 | a0001c0001t0008g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517+3062A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682824 | ||||||
chr7:15682842
|
C | T | 1 | a0001c0001t0006g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.517+3044G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682842 | ||||||
chr7:15682879
|
C | T | 2 | a0001c0001t0009g0233a0003c0003t0038g0234 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517+3007G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682879 | ||||||
chr7:15682941
|
A | G | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+2945T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15682941 | ||||||
chr7:15683042
|
T | C | 3 | a0001c0001t0009g0230a0001c0001t0009g0231a0001c0001t0009g0232 | 3 | HG03139.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.517+2844A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683042 | ||||||
chr7:15683049
|
G | T | 2 | a0001c0001t0014g0220a0001c0001t0036g0219 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.517+2837C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683049 | ||||||
chr7:15683074
|
G | A | 1 | a0001c0001t0016g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517+2812C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683074 | ||||||
chr7:15683098
|
G | C | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+2788C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683098 | ||||||
chr7:15683211
|
G | A | 99 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0043others(96): Show | 101 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.517+2675C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683211 | ||||||
chr7:15683255
|
G | A | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+2631C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683255 | ||||||
chr7:15683263
|
A | G | 9 | a0001c0001t0006g0176a0001c0001t0007g0007a0001c0001t0007g0179others(6): Show | 10 | HG01255.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+2623T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683263 | ||||||
chr7:15683305
|
A | T | 4 | a0002c0002t0002g0280a0002c0002t0002g0281a0002c0002t0002g0282others(1): Show | 4 | NA18940.hp2 NA18955.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+2581T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683305 | ||||||
chr7:15683525
|
A | G | 3 | a0001c0001t0006g0176a0001c0001t0018g0177a0007c0008t0007g0178 | 3 | HG02818.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.517+2361T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683525 | ||||||
chr7:15683727
|
C | T | 178 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0050others(175): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.517+2159G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683727 | ||||||
chr7:15683763
|
C | A | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.517+2123G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683763 | ||||||
chr7:15683782
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.517+2104C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683782 | ||||||
chr7:15683806
|
T | G | 1 | a0001c0001t0001g0121 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.517+2080A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683806 | ||||||
chr7:15683885
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+2001T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683885 | ||||||
chr7:15683974
|
T | A | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+1912A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683974 | ||||||
chr7:15683980
|
G | A | 1 | a0001c0001t0016g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517+1906C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683980 | ||||||
chr7:15683994
|
G | C | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+1892C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15683994 | ||||||
chr7:15684018
|
T | A | 2 | a0001c0001t0001g0187a0001c0001t0006g0173 | 2 | HG02976.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.517+1868A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684018 | ||||||
chr7:15684019
|
A | T | 1 | a0002c0002t0022g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.517+1867T>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684019 | ||||||
chr7:15684026
|
T | A | 2 | a0001c0001t0009g0233a0003c0003t0038g0234 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517+1860A>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684026 | ||||||
chr7:15684105
|
T | C | 2 | a0001c0001t0001g0175a0003c0003t0003g0174 | 2 | HG02074.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.517+1781A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684105 | ||||||
chr7:15684119
|
C | T | 5 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+1767G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684119 | ||||||
chr7:15684128
|
C | T | 117 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0050others(114): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.517+1758G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684128 | ||||||
chr7:15684370
|
C | A | 13 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(10): Show | 14 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.517+1516G>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684370 | ||||||
chr7:15684383
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+1503T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684383 | ||||||
chr7:15684390
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+1496C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684390 | ||||||
chr7:15684493
|
C | T | 1 | a0003c0003t0003g0049 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.517+1393G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684493 | ||||||
chr7:15684532
|
G | C | 180 | a0001c0001t0001g0006a0001c0001t0001g0122a0001c0001t0001g0124others(177): Show | 188 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.517+1354C>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684532 | ||||||
chr7:15684584
|
T | G | 49 | a0001c0001t0001g0187a0001c0001t0009g0222a0001c0001t0009g0223others(46): Show | 51 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.517+1302A>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684584 | ||||||
chr7:15684704
|
G | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | NA18939.hp2 NA18957.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+1182C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684704 | ||||||
chr7:15684914
|
T | C | 8 | a0002c0002t0002g0009a0002c0002t0002g0253a0002c0002t0004g0254others(5): Show | 9 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+972A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684914 | ||||||
chr7:15684923
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517+963G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15684923 | ||||||
chr7:15685058
|
TCTAA | T | 17 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(14): Show | 18 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.517+824_517+827del others(4): Show |
MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685058 | ||||||
chr7:15685281
|
T | C | 3 | a0001c0001t0012g0003a0001c0001t0012g0031a0001c0001t0012g0032 | 4 | HG02630.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+605A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685281 | ||||||
chr7:15685353
|
T | TA | 46 | a0001c0001t0001g0188a0001c0001t0008g0189a0001c0001t0021g0236others(43): Show | 47 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.517+532dupT | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685353 | ||||||
chr7:15685404
|
T | C | 24 | a0001c0001t0001g0193a0001c0001t0024g0196a0003c0003t0003g0001others(21): Show | 27 | HG00558.hp2 NA18940.hp1 NA18941.hp1 others(24): Show |
intron_variant | MODIFIER | c.517+482A>G | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685404 | ||||||
chr7:15685479
|
C | G | 43 | a0002c0002t0002g0009a0002c0002t0002g0248a0002c0002t0002g0253others(40): Show | 44 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.517+407G>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685479 | ||||||
chr7:15685501
|
G | A | 1 | a0001c0001t0015g0019 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.517+385C>T | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685501 | ||||||
chr7:15685517
|
G | T | 5 | a0001c0001t0014g0215a0001c0001t0014g0216a0001c0001t0014g0218others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+369C>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685517 | ||||||
chr7:15685531
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.517+355G>A | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685531 | ||||||
chr7:15685661
|
A | G | 10 | a0001c0001t0001g0038a0001c0001t0008g0039a0001c0001t0008g0040others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.517+225T>C | MEOX2 | ENSG00000106511.6 | transcript | ENST00000262041.6 | protein_coding | 1/2 | chr7 | 15685661 |