geneid | 55218 |
---|---|
ensemblid | ENSG00000081177.19 |
hgncid | 20217 |
symbol | EXD2 |
name | exonuclease 3'-5' domain containing 2 |
refseq_nuc | NM_001193360.2 |
refseq_prot | NP_001180289.1 |
ensembl_nuc | ENST00000685843.1 |
ensembl_prot | ENSP00000510642.1 |
mane_status | MANE Select |
chr | chr14 |
start | 69191498 |
end | 69244018 |
strand | + |
ver | v1.2 |
region | chr14:69191498-69244018 |
region5000 | chr14:69186498-69249018 |
regionname0 | EXD2_chr14_69191498_69244018 |
regionname5000 | EXD2_chr14_69186498_69249018 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 621 | 168 | 67 | 38 | 22 | 8 | 32 | 18 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0002 | 1/0 | 621 | 64 | 25 | 16 | 9 | 5 | 8 | 7 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0003 | 0/0 | 621 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0004 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1866 | 101 | 53 | 21 | 5 | 5 | 17 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
c0002 | 1/0 | 1866 | 64 | 25 | 16 | 9 | 5 | 8 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
c0003 | 0/1 | 1866 | 59 | 9 | 15 | 17 | 3 | 14 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
c0004 | 0/0 | 1866 | 5 | 3 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
c0005 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
c0006 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
c0007 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
c0008 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
c0009 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3144 | 100 | 15 | 28 | 27 | 8 | 20 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0002 | 0/0 | 3144 | 50 | 15 | 16 | 1 | 3 | 15 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0003 | 0/0 | 3144 | 22 | 20 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0004 | 0/0 | 3144 | 16 | 12 | 3 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0005 | 0/0 | 3144 | 11 | 1 | 3 | 4 | 3 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0006 | 0/0 | 3144 | 10 | 10 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0007 | 0/0 | 3144 | 5 | 3 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0008 | 0/0 | 3144 | 3 | 3 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0009 | 0/0 | 3144 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0010 | 0/0 | 3144 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0011 | 0/0 | 3144 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0012 | 0/0 | 3142 | 2 | 0 | 0 | 0 | 0 | 2 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0013 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0014 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0015 | 0/0 | 3144 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0016 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0017 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0018 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0019 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0020 | 0/0 | 3144 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
t0021 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0003 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1866 | 101 | 53 | 21 | 5 | 5 | 17 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0003 | 0/1 | 1866 | 59 | 9 | 15 | 17 | 3 | 14 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0004 | 0/0 | 1866 | 5 | 3 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0007 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0008 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0009 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0002c0002 | 1/0 | 1866 | 64 | 25 | 16 | 9 | 5 | 8 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0003c0006 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0004c0005 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5009 | 48 | 15 | 16 | 1 | 2 | 14 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0003 | 0/0 | 5009 | 22 | 20 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0005 | 0/0 | 5009 | 11 | 1 | 3 | 4 | 3 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0006 | 0/0 | 5009 | 8 | 8 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0008 | 0/0 | 5009 | 3 | 3 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0010 | 0/0 | 5009 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0012 | 0/0 | 5007 | 2 | 0 | 0 | 0 | 0 | 2 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0014 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0015 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0016 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0017 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0001t0019 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0003t0001 | 0/1 | 5009 | 55 | 6 | 15 | 17 | 3 | 13 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0003t0006 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0003t0009 | 0/0 | 5009 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0003t0020 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0004t0007 | 0/0 | 5009 | 5 | 3 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0007t0006 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0008t0021 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0001c0009t0002 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0002c0002t0001 | 1/0 | 5009 | 44 | 9 | 13 | 9 | 5 | 7 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0002c0002t0004 | 0/0 | 5009 | 16 | 12 | 3 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0002c0002t0011 | 0/0 | 5009 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0002c0002t0013 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0002c0002t0018 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0003c0006t0002 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
a0004c0005t0001 | 0/0 | 5009 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | copy fasta | chr14 | 69186498 | 69249018 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0012g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0014g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0015g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0016g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0001t0019g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0003 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0009g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0003t0020g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0004t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0004t0007g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0004t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0004t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0004t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0007t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0008t0021g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0001c0009t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0001g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0002c0002t0018g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0003c0006t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
a0004c0005t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0078 | EUR | GBR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0200 | EUR | GBR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | GBR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0015 | EUR | GBR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0198 | EUR | FIN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0032 | EUR | FIN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0076 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0213 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0201 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0062 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0157 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0042 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01069 | hp1 | a0002 | c0002 | t0004 | g0182 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0197 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01081 | hp2 | a0001 | c0004 | t0007 | g0169 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01169 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01175 | hp1 | a0002 | c0002 | t0004 | g0178 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0072 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01192 | hp2 | a0002 | c0002 | t0004 | g0188 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0045 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0158 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01496 | hp1 | a0001 | c0004 | t0007 | g0170 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0155 | EUR | IBS | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0199 | EUR | IBS | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0156 | EUR | IBS | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0195 | EUR | IBS | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0049 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01943 | hp1 | a0001 | c0003 | t0001 | g0075 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0055 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | KHV | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02056 | hp2 | a0001 | c0003 | t0001 | g0036 | EAS | KHV | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02135 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | KHV | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | CDX | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | CDX | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02257 | hp1 | a0001 | c0001 | t0014 | g0100 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0051 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02258 | hp1 | a0002 | c0002 | t0004 | g0179 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0203 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02451 | hp2 | a0001 | c0004 | t0007 | g0168 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02572 | hp1 | a0001 | c0001 | t0016 | g0102 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02572 | hp2 | a0001 | c0001 | t0019 | g0147 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0034 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02615 | hp1 | a0002 | c0002 | t0004 | g0183 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02615 | hp2 | a0002 | c0002 | t0004 | g0181 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02622 | hp1 | a0001 | c0004 | t0007 | g0171 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0071 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0077 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02717 | hp1 | a0002 | c0002 | t0004 | g0174 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0033 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0104 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02895 | hp1 | a0001 | c0001 | t0010 | g0148 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02895 | hp2 | a0002 | c0002 | t0004 | g0175 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02896 | hp2 | a0002 | c0002 | t0011 | g0012 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02897 | hp1 | a0002 | c0002 | t0011 | g0013 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0149 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02922 | hp1 | a0001 | c0003 | t0006 | g0145 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0144 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0040 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03017 | hp2 | a0001 | c0009 | t0002 | g0087 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03041 | hp1 | a0002 | c0002 | t0004 | g0184 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03041 | hp2 | a0002 | c0002 | t0013 | g0205 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0066 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03225 | hp1 | a0001 | c0004 | t0007 | g0172 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03239 | hp2 | a0001 | c0001 | t0012 | g0166 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03453 | hp1 | a0001 | c0008 | t0021 | g0216 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03453 | hp2 | a0002 | c0002 | t0004 | g0176 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03486 | hp1 | a0001 | c0003 | t0009 | g0006 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03492 | hp1 | a0001 | c0003 | t0001 | g0043 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03516 | hp1 | a0002 | c0002 | t0018 | g0173 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0047 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03669 | hp1 | a0001 | c0001 | t0015 | g0117 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0208 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03688 | hp2 | a0001 | c0003 | t0020 | g0074 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0017 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0063 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0046 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0192 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04115 | hp1 | a0002 | c0002 | t0004 | g0187 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0004 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0027 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0167 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18522 | hp1 | a0002 | c0002 | t0004 | g0180 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18906 | hp1 | a0002 | c0002 | t0004 | g0185 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18940 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18949 | hp1 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18956 | hp1 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18956 | hp2 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18967 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18989 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA18989 | hp2 | a0004 | c0005 | t0001 | g0067 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19030 | hp1 | a0001 | c0007 | t0006 | g0103 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19043 | hp1 | a0002 | c0002 | t0004 | g0177 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19063 | hp2 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA19240 | hp2 | a0001 | c0001 | t0017 | g0163 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20129 | hp1 | a0001 | c0003 | t0009 | g0006 | AFR | ASW | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | ASW | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0194 | EUR | TSI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0048 | EUR | TSI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | TSI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20805 | hp2 | a0003 | c0006 | t0002 | g0088 | EUR | TSI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | GIH | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | GIH | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03471 | hp1 | a0002 | c0002 | t0004 | g0186 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | USA | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
HG06807 | hp2 | a0002 | c0002 | t0004 | g0189 | AFR | USA | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0222 | AFR | USA | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | USA | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0095 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0003 | REF | REF | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0223 | REF | REF | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69209744
|
G | A | 1 | a0004 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.274G>A | p.Glu92Lys | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/10 | 499/5009 | 274/1866 | 92/621 | chr14 | 69209744 | ||
chr14:69230572
|
G | A | 1 | a0003 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.691G>A | p.Asp231Asn | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/10 | 916/5009 | 691/1866 | 231/621 | chr14 | 69230572 | ||
chr14:69237836
|
G | T | 3 | a0001a0003a0004 | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
missense_variant | MODERATE | c.1554G>T | p.Gln518His | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/10 | 1779/5009 | 1554/1866 | 518/621 | chr14 | 69237836 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69228866
|
C | T | 1 | a0001c0009 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.384C>T | p.Ser128Ser | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/10 | 609/5009 | 384/1866 | 128/621 | chr14 | 69228866 | ||
chr14:69230505
|
G | A | 1 | a0001c0004 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
synonymous_variant | LOW | c.624G>A | p.Lys208Lys | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/10 | 849/5009 | 624/1866 | 208/621 | chr14 | 69230505 | ||
chr14:69236441
|
A | G | 2 | a0001c0003a0004c0005 | 60 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(57): Show |
synonymous_variant | LOW | c.1191A>G | p.Leu397Leu | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/10 | 1416/5009 | 1191/1866 | 397/621 | chr14 | 69236441 | ||
chr14:69237617
|
C | T | 1 | a0001c0008 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1335C>T | p.Ile445Ile | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/10 | 1560/5009 | 1335/1866 | 445/621 | chr14 | 69237617 | ||
chr14:69241046
|
C | T | 1 | a0001c0007 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1812C>T | p.Asn604Asn | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2037/5009 | 1812/1866 | 604/621 | chr14 | 69241046 | ||
chr14:69241070
|
C | T | 1 | a0001c0004 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
synonymous_variant | LOW | c.1836C>T | p.Phe612Phe | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2061/5009 | 1836/1866 | 612/621 | chr14 | 69241070 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69191572
|
G | A | 1 | a0001c0003t0009 | 2 | HG03486.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-151G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/10 | 17899 | chr14 | 69191572 | |||||
chr14:69203941
|
C | T | 1 | a0001c0008t0021 | 1 | HG03453.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/10 | chr14 | 69203941 | ||||||
chr14:69203955
|
C | G | 1 | a0001c0004t0007 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-93C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/10 | 5516 | chr14 | 69203955 | |||||
chr14:69241346
|
G | A | 1 | a0002c0002t0013 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 246 | chr14 | 69241346 | |||||
chr14:69241486
|
CAG | C | 1 | a0001c0001t0012 | 2 | HG03239.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*387_*388delAG | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 387 | chr14 | 69241486 | |||||
chr14:69241524
|
G | A | 7 | a0001c0001t0002a0001c0001t0010a0001c0001t0014others(4): Show | 55 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*424G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 424 | chr14 | 69241524 | |||||
chr14:69241526
|
A | C | 1 | a0001c0001t0016 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*426A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 426 | chr14 | 69241526 | |||||
chr14:69241661
|
T | C | 1 | a0001c0008t0021 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 561 | chr14 | 69241661 | |||||
chr14:69241750
|
T | C | 1 | a0001c0001t0010 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*650T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 650 | chr14 | 69241750 | |||||
chr14:69242047
|
G | C | 1 | a0001c0001t0017 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*947G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 947 | chr14 | 69242047 | |||||
chr14:69242392
|
T | G | 1 | a0002c0002t0018 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1292 | chr14 | 69242392 | |||||
chr14:69242499
|
G | A | 1 | a0001c0001t0012 | 2 | HG03239.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1399G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1399 | chr14 | 69242499 | |||||
chr14:69242656
|
G | A | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(16): Show | 112 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1556G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1556 | chr14 | 69242656 | |||||
chr14:69242699
|
C | T | 1 | a0002c0002t0004 | 16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1599C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1599 | chr14 | 69242699 | |||||
chr14:69242918
|
T | G | 1 | a0001c0001t0019 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1818T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1818 | chr14 | 69242918 | |||||
chr14:69243212
|
C | T | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(7): Show | 81 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2112C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2112 | chr14 | 69243212 | |||||
chr14:69243249
|
C | T | 1 | a0001c0004t0007 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2149C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2149 | chr14 | 69243249 | |||||
chr14:69243445
|
G | A | 1 | a0001c0004t0007 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2345G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2345 | chr14 | 69243445 | |||||
chr14:69243468
|
C | G | 1 | a0001c0001t0015 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2368C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2368 | chr14 | 69243468 | |||||
chr14:69243470
|
C | T | 1 | a0001c0001t0008 | 3 | HG02818.hp2 HG02965.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2370C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2370 | chr14 | 69243470 | |||||
chr14:69243540
|
C | G | 3 | a0001c0001t0005a0001c0001t0017a0002c0002t0011 | 14 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2440C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2440 | chr14 | 69243540 | |||||
chr14:69243691
|
A | G | 1 | a0001c0003t0020 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2591A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2591 | chr14 | 69243691 | |||||
chr14:69243990
|
G | A | 1 | a0001c0001t0014 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2890G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2890 | chr14 | 69243990 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69191678
|
G | A | 1 | a0002c0002t0001g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-132+87G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69191678 | ||||||
chr14:69191723
|
C | A | 222 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(219): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-132+132C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69191723 | ||||||
chr14:69191810
|
T | C | 2 | a0002c0002t0011g0012a0002c0002t0011g0013 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-132+219T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69191810 | ||||||
chr14:69191983
|
C | T | 5 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220others(2): Show | 5 | HG02145.hp1 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-132+392C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69191983 | ||||||
chr14:69192016
|
T | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+425T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192016 | ||||||
chr14:69192052
|
C | T | 3 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163 | 3 | HG01074.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-132+461C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192052 | ||||||
chr14:69192295
|
A | G | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-132+704A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192295 | ||||||
chr14:69192317
|
C | T | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+726C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192317 | ||||||
chr14:69192503
|
CAG | C | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+914_-132+915d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69192503 | |||||
chr14:69192509
|
T | A | 4 | a0001c0003t0001g0014a0001c0003t0001g0015a0001c0003t0001g0016others(1): Show | 4 | HG00140.hp2 HG00639.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-132+918T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192509 | ||||||
chr14:69192647
|
T | G | 8 | a0001c0001t0012g0166a0001c0001t0012g0167a0001c0004t0007g0168others(5): Show | 8 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-132+1056T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192647 | ||||||
chr14:69192834
|
G | C | 1 | a0001c0001t0003g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-132+1243G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192834 | ||||||
chr14:69192902
|
G | A | 14 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(11): Show | 14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-132+1311G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192902 | ||||||
chr14:69192942
|
G | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+1351G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192942 | ||||||
chr14:69193029
|
G | A | 1 | a0001c0001t0005g0032 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-132+1438G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193029 | ||||||
chr14:69193040
|
A | C | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+1449A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193040 | ||||||
chr14:69193050
|
T | TTC | 54 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(51): Show | 60 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.-132+1469_-132+147 others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69193050 | |||||
chr14:69193060
|
C | CT | 29 | a0001c0001t0002g0151a0001c0001t0005g0152a0001c0001t0005g0153others(26): Show | 29 | HG00738.hp1 HG01074.hp2 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.-132+1485dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69193060 | |||||
chr14:69193060
|
C | CTT | 5 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220others(2): Show | 5 | HG02145.hp1 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-132+1484_-132+148 others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69193060 | |||||
chr14:69193061
|
T | TC | 2 | a0001c0001t0005g0032a0001c0003t0001g0033 | 2 | HG00280.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-132+1470_-132+147 others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193061 | ||||||
chr14:69193118
|
G | A | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+1527G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193118 | ||||||
chr14:69193128
|
A | G | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+1537A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193128 | ||||||
chr14:69193245
|
G | C | 1 | a0001c0001t0003g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-132+1654G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193245 | ||||||
chr14:69193259
|
G | A | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-132+1668G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193259 | ||||||
chr14:69193275
|
T | C | 1 | a0001c0003t0001g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-132+1684T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193275 | ||||||
chr14:69193279
|
A | G | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+1688A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193279 | ||||||
chr14:69193328
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-132+1737G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193328 | ||||||
chr14:69193339
|
G | A | 1 | a0001c0001t0017g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-132+1748G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193339 | ||||||
chr14:69193825
|
TA | T | 8 | a0001c0001t0012g0166a0001c0001t0012g0167a0001c0004t0007g0168others(5): Show | 8 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-132+2237delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69193825 | |||||
chr14:69193863
|
A | G | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+2272A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193863 | ||||||
chr14:69194142
|
CT | C | 161 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(158): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-132+2565delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69194142 | |||||
chr14:69194345
|
T | C | 174 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(171): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.-132+2754T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194345 | ||||||
chr14:69194417
|
T | C | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+2826T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194417 | ||||||
chr14:69194496
|
CT | C | 46 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0080others(43): Show | 49 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-132+2913delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69194496 | |||||
chr14:69194948
|
G | T | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-132+3357G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194948 | ||||||
chr14:69194954
|
T | C | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+3363T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194954 | ||||||
chr14:69194990
|
G | A | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+3399G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194990 | ||||||
chr14:69195092
|
C | T | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+3501C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195092 | ||||||
chr14:69195204
|
G | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+3613G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195204 | ||||||
chr14:69195216
|
C | CA | 16 | a0002c0002t0004g0174a0002c0002t0004g0175a0002c0002t0004g0176others(13): Show | 16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-132+3641dupA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69195216 | |||||
chr14:69195229
|
AAAAG | A | 164 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(161): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-132+3640_-132+364 others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69195229 | |||||
chr14:69195356
|
C | T | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+3765C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195356 | ||||||
chr14:69195388
|
A | G | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+3797A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195388 | ||||||
chr14:69195400
|
C | T | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+3809C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195400 | ||||||
chr14:69195443
|
C | T | 1 | a0001c0001t0006g0222 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-132+3852C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195443 | ||||||
chr14:69195491
|
G | C | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+3900G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195491 | ||||||
chr14:69195608
|
G | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+4017G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195608 | ||||||
chr14:69195893
|
A | G | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+4302A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195893 | ||||||
chr14:69196250
|
A | T | 1 | a0001c0003t0001g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-132+4659A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196250 | ||||||
chr14:69196375
|
C | T | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-132+4784C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196375 | ||||||
chr14:69196584
|
T | C | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-132+4993T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196584 | ||||||
chr14:69196622
|
CT | C | 118 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0080others(115): Show | 122 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.-132+5048delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69196622 | |||||
chr14:69196622
|
CTT | C | 52 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(49): Show | 57 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-132+5047_-132+504 others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69196622 | |||||
chr14:69196647
|
A | G | 1 | a0001c0001t0003g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-132+5056A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196647 | ||||||
chr14:69196689
|
T | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0081a0001c0001t0002g0082 | 4 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-132+5098T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196689 | ||||||
chr14:69196726
|
C | T | 1 | a0001c0001t0006g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-132+5135C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196726 | ||||||
chr14:69196762
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-132+5171T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196762 | ||||||
chr14:69196786
|
C | T | 2 | a0001c0001t0010g0148a0001c0001t0010g0149 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-132+5195C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196786 | ||||||
chr14:69196792
|
AT | A | 108 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0080others(105): Show | 111 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.-132+5215delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69196792 | |||||
chr14:69196833
|
G | A | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(4): Show | 7 | HG00741.hp2 HG01255.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-132+5242G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196833 | ||||||
chr14:69196883
|
G | C | 1 | a0002c0002t0004g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-132+5292G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196883 | ||||||
chr14:69197051
|
C | T | 8 | a0002c0002t0004g0182a0002c0002t0004g0183a0002c0002t0004g0184others(5): Show | 8 | HG01069.hp1 HG01192.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-132+5460C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197051 | ||||||
chr14:69197176
|
G | T | 1 | a0002c0002t0001g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-132+5585G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197176 | ||||||
chr14:69197412
|
T | C | 177 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(174): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-132+5821T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197412 | ||||||
chr14:69197421
|
C | CT | 9 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0121others(6): Show | 9 | HG01081.hp2 HG01496.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-132+5840dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69197421 | |||||
chr14:69197676
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0081a0001c0001t0002g0082 | 4 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-132+6085G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197676 | ||||||
chr14:69197781
|
CT | C | 218 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(215): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-131-6132delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69197781 | |||||
chr14:69197839
|
T | A | 1 | a0002c0002t0001g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-131-6078T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197839 | ||||||
chr14:69197913
|
A | T | 56 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(53): Show | 62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-131-6004A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197913 | ||||||
chr14:69198137
|
T | C | 2 | a0001c0001t0006g0190a0001c0001t0006g0217 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-131-5780T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198137 | ||||||
chr14:69198418
|
C | T | 56 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(53): Show | 62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-131-5499C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198418 | ||||||
chr14:69198435
|
C | T | 1 | a0002c0002t0004g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-131-5482C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198435 | ||||||
chr14:69198525
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-5392T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198525 | ||||||
chr14:69198529
|
C | T | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-131-5388C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198529 | ||||||
chr14:69198698
|
A | C | 1 | a0002c0002t0001g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-131-5219A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198698 | ||||||
chr14:69198762
|
C | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-5155C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198762 | ||||||
chr14:69199115
|
A | G | 163 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(160): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-131-4802A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199115 | ||||||
chr14:69199128
|
C | T | 56 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(53): Show | 62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-131-4789C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199128 | ||||||
chr14:69199163
|
G | A | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-131-4754G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199163 | ||||||
chr14:69199192
|
C | T | 2 | a0001c0001t0006g0190a0001c0001t0006g0217 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-131-4725C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199192 | ||||||
chr14:69199208
|
C | A | 21 | a0001c0001t0005g0032a0001c0001t0005g0152a0001c0001t0005g0153others(18): Show | 21 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-131-4709C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199208 | ||||||
chr14:69199358
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4559T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199358 | ||||||
chr14:69199490
|
T | G | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-131-4427T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199490 | ||||||
chr14:69199545
|
G | A | 1 | a0002c0002t0004g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-131-4372G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199545 | ||||||
chr14:69199599
|
A | AT | 23 | a0001c0001t0002g0001a0001c0001t0002g0083a0001c0001t0002g0084others(20): Show | 25 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-131-4305dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69199599 | |||||
chr14:69199599
|
AT | A | 16 | a0001c0001t0005g0032a0001c0001t0005g0152a0001c0001t0005g0153others(13): Show | 16 | HG00280.hp2 HG00738.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-131-4305delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69199599 | |||||
chr14:69199698
|
A | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4219A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199698 | ||||||
chr14:69199754
|
A | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4163A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199754 | ||||||
chr14:69199775
|
A | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4142A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199775 | ||||||
chr14:69199808
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-131-4109G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199808 | ||||||
chr14:69199854
|
A | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4063A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199854 | ||||||
chr14:69199889
|
A | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4028A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199889 | ||||||
chr14:69199955
|
A | G | 160 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(157): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.-131-3962A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199955 | ||||||
chr14:69200025
|
G | A | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-131-3892G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200025 | ||||||
chr14:69200135
|
A | G | 163 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(160): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-131-3782A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200135 | ||||||
chr14:69200149
|
G | A | 1 | a0002c0002t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-131-3768G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200149 | ||||||
chr14:69200157
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-3760G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200157 | ||||||
chr14:69200385
|
G | A | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-131-3532G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200385 | ||||||
chr14:69200405
|
A | C | 1 | a0001c0003t0020g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-131-3512A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200405 | ||||||
chr14:69200493
|
C | T | 1 | a0002c0002t0004g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-131-3424C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200493 | ||||||
chr14:69200709
|
CA | C | 175 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(172): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-131-3197delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69200709 | |||||
chr14:69200799
|
C | T | 2 | a0001c0001t0006g0190a0001c0001t0006g0217 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-131-3118C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200799 | ||||||
chr14:69200904
|
T | C | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131-3013T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200904 | ||||||
chr14:69201132
|
G | A | 56 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(53): Show | 62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-131-2785G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201132 | ||||||
chr14:69201147
|
G | A | 2 | a0001c0001t0006g0190a0001c0001t0006g0217 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-131-2770G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201147 | ||||||
chr14:69201276
|
C | T | 1 | a0001c0003t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-131-2641C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201276 | ||||||
chr14:69201344
|
A | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-2573A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201344 | ||||||
chr14:69201405
|
T | A | 1 | a0002c0002t0001g0191 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-131-2512T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201405 | ||||||
chr14:69201672
|
G | GT | 12 | a0001c0001t0002g0070a0001c0001t0002g0118a0001c0001t0003g0141others(9): Show | 12 | HG00741.hp1 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-131-2217dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | |||||
chr14:69201672
|
G | GTT | 5 | a0001c0001t0008g0104a0001c0001t0008g0143a0001c0001t0008g0144others(2): Show | 5 | HG02615.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-131-2218_-131-221 others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | |||||
chr14:69201672
|
G | GTTTTTTG others(10): Show |
3 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170 | 3 | HG01081.hp2 HG01496.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-131-2239_-131-223 others(21): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | |||||
chr14:69201672
|
G | GTTTTTTG others(11): Show |
2 | a0001c0004t0007g0171a0001c0004t0007g0172 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-131-2239_-131-223 others(22): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | |||||
chr14:69201672
|
GT | G | 121 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0080others(118): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.-131-2217delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | |||||
chr14:69201672
|
GTTTTTTT others(6): Show |
G | 2 | a0002c0002t0001g0028a0002c0002t0001g0029 | 2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-131-2229_-131-221 others(17): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | |||||
chr14:69201672
|
GTTTTTTT others(7): Show |
G | 12 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(9): Show | 12 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-131-2230_-131-221 others(18): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | |||||
chr14:69201672
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0002g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-131-2231_-131-221 others(19): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | |||||
chr14:69201680
|
T | G | 1 | a0001c0001t0006g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-131-2237T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201680 | ||||||
chr14:69201681
|
T | G | 4 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-131-2236T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201681 | ||||||
chr14:69201684
|
T | G | 2 | a0001c0001t0002g0123a0001c0003t0001g0037 | 2 | HG01192.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.-131-2233T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201684 | ||||||
chr14:69201742
|
G | C | 2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-131-2175G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201742 | ||||||
chr14:69202043
|
C | T | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131-1874C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202043 | ||||||
chr14:69202070
|
C | T | 17 | a0001c0001t0003g0018a0001c0001t0003g0079a0001c0001t0003g0124others(14): Show | 17 | HG01243.hp1 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-131-1847C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202070 | ||||||
chr14:69202071
|
G | T | 1 | a0001c0001t0019g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-131-1846G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202071 | ||||||
chr14:69202126
|
A | G | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-131-1791A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202126 | ||||||
chr14:69202270
|
G | T | 1 | a0001c0001t0002g0112 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-131-1647G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202270 | ||||||
chr14:69202275
|
G | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-1642G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202275 | ||||||
chr14:69202471
|
C | T | 193 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(190): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.-131-1446C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202471 | ||||||
chr14:69202496
|
G | A | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-131-1421G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202496 | ||||||
chr14:69202592
|
T | C | 1 | a0001c0003t0001g0038 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-131-1325T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202592 | ||||||
chr14:69202690
|
C | G | 163 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(160): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-131-1227C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202690 | ||||||
chr14:69202877
|
T | C | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131-1040T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202877 | ||||||
chr14:69202919
|
T | C | 16 | a0002c0002t0004g0174a0002c0002t0004g0175a0002c0002t0004g0176others(13): Show | 16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-131-998T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202919 | ||||||
chr14:69202946
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-131-971T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202946 | ||||||
chr14:69203157
|
C | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-760C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203157 | ||||||
chr14:69203229
|
GT | G | 6 | a0001c0001t0005g0152a0001c0001t0005g0153a0001c0001t0005g0159others(3): Show | 6 | NA18940.hp2 NA18956.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-131-682delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69203229 | |||||
chr14:69203239
|
A | AT | 58 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(55): Show | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.-131-663dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69203239 | |||||
chr14:69203239
|
AT | A | 10 | a0001c0001t0002g0105a0001c0001t0010g0148a0001c0001t0010g0149others(7): Show | 10 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-131-663delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69203239 | |||||
chr14:69203367
|
T | C | 1 | a0001c0003t0001g0039 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-131-550T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203367 | ||||||
chr14:69203402
|
C | G | 14 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(11): Show | 14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-131-515C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203402 | ||||||
chr14:69203517
|
C | A | 1 | a0001c0001t0002g0092 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-131-400C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203517 | ||||||
chr14:69203595
|
A | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-322A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203595 | ||||||
chr14:69203652
|
G | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-265G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203652 | ||||||
chr14:69203738
|
T | C | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131-179T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203738 | ||||||
chr14:69204031
|
G | A | 1 | a0001c0001t0006g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-48+31G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204031 | ||||||
chr14:69204219
|
A | G | 152 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(149): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-48+219A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204219 | ||||||
chr14:69204279
|
G | A | 1 | a0002c0002t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-48+279G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204279 | ||||||
chr14:69204312
|
A | G | 1 | a0001c0004t0007g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-48+312A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204312 | ||||||
chr14:69204392
|
T | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+392T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204392 | ||||||
chr14:69204509
|
G | A | 1 | a0001c0001t0005g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-48+509G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204509 | ||||||
chr14:69204547
|
A | G | 8 | a0002c0002t0004g0182a0002c0002t0004g0183a0002c0002t0004g0184others(5): Show | 8 | HG01069.hp1 HG01192.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+547A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204547 | ||||||
chr14:69204626
|
A | T | 1 | a0002c0002t0004g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-48+626A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204626 | ||||||
chr14:69204669
|
G | A | 5 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0008g0104others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+669G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204669 | ||||||
chr14:69204681
|
T | TACTGACT others(8): Show |
1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-48+682_-48+683ins others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69204681 | |||||
chr14:69204683
|
A | G | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-48+683A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204683 | ||||||
chr14:69204740
|
G | T | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-48+740G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204740 | ||||||
chr14:69205032
|
T | C | 177 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(174): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-48+1032T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205032 | ||||||
chr14:69205053
|
C | T | 1 | a0001c0003t0001g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-48+1053C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205053 | ||||||
chr14:69205129
|
T | G | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-48+1129T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205129 | ||||||
chr14:69205215
|
T | C | 4 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1215T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205215 | ||||||
chr14:69205486
|
A | T | 1 | a0003c0006t0002g0088 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-48+1486A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205486 | ||||||
chr14:69205629
|
C | T | 14 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(11): Show | 14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48+1629C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205629 | ||||||
chr14:69205794
|
A | G | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-48+1794A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205794 | ||||||
chr14:69205834
|
A | T | 1 | a0001c0001t0019g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-48+1834A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205834 | ||||||
chr14:69205992
|
C | T | 4 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1992C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205992 | ||||||
chr14:69206110
|
G | A | 1 | a0001c0001t0005g0153 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+2110G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206110 | ||||||
chr14:69206151
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2151G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206151 | ||||||
chr14:69206211
|
G | T | 1 | a0001c0001t0005g0160 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-48+2211G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206211 | ||||||
chr14:69206422
|
G | C | 1 | a0001c0001t0012g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-48+2422G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206422 | ||||||
chr14:69206455
|
C | CCTTTTTT others(1): Show |
6 | a0001c0001t0003g0124a0001c0001t0003g0125a0001c0001t0003g0141others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(10): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | ||||||
chr14:69206455
|
C | CCTTTTTT others(2): Show |
9 | a0001c0001t0002g0123a0001c0001t0003g0079a0001c0001t0003g0126others(6): Show | 9 | HG01192.hp1 HG01433.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(11): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | ||||||
chr14:69206455
|
C | CCTTTTTT others(3): Show |
5 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0135others(2): Show | 5 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | ||||||
chr14:69206455
|
C | CCTTTTTT others(4): Show |
8 | a0001c0001t0002g0089a0001c0001t0002g0098a0001c0001t0002g0151others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(13): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | ||||||
chr14:69206455
|
C | CCTTTTTT others(5): Show |
10 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0096others(7): Show | 10 | HG00280.hp2 HG00738.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(14): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | ||||||
chr14:69206455
|
C | CCTTTTTT others(6): Show |
9 | a0001c0001t0002g0080a0001c0001t0002g0097a0001c0001t0002g0120others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | ||||||
chr14:69206455
|
C | CCTTTTTT others(7): Show |
7 | a0001c0001t0002g0091a0001c0001t0002g0101a0001c0001t0003g0139others(4): Show | 7 | HG01361.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(16): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | ||||||
chr14:69206455
|
C | CCTTTTTT others(10): Show |
2 | a0001c0001t0005g0165a0002c0002t0001g0162 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(19): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | ||||||
chr14:69206455
|
C | CCTTTTTT others(11): Show |
2 | a0001c0001t0005g0164a0001c0001t0016g0102 | 2 | HG01074.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(20): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | ||||||
chr14:69206455
|
C | CT | 12 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(9): Show | 12 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+2486dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | |||||
chr14:69206455
|
CTT | C | 5 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0001t0002g0114others(2): Show | 5 | HG00741.hp2 HG01346.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2485_-48+2486d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | |||||
chr14:69206455
|
CTTT | C | 18 | a0001c0001t0002g0001a0001c0001t0002g0084a0001c0001t0002g0085others(15): Show | 20 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-48+2484_-48+2486d others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | |||||
chr14:69206455
|
CTTTT | C | 9 | a0001c0001t0002g0105a0001c0001t0006g0218a0001c0001t0006g0219others(6): Show | 9 | HG02145.hp1 HG02922.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+2483_-48+2486d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | |||||
chr14:69206455
|
CTTTTTTT | C | 16 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(13): Show | 16 | HG01081.hp2 HG01361.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+2480_-48+2486d others(9): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | |||||
chr14:69206455
|
CTTTTTTT others(3): Show |
C | 51 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(48): Show | 57 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.-48+2477_-48+2486d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | |||||
chr14:69206455
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0003t0001g0033a0001c0003t0001g0040 | 2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-48+2476_-48+2486d others(13): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | |||||
chr14:69206455
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0002g0008a0001c0001t0002g0081a0001c0001t0002g0082 | 4 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+2474_-48+2486d others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | |||||
chr14:69206455
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-48+2472_-48+2486d others(17): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | |||||
chr14:69206456
|
T | C | 5 | a0001c0001t0002g0094a0001c0001t0003g0138a0001c0001t0010g0148others(2): Show | 5 | HG00140.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+2456T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206456 | ||||||
chr14:69206458
|
T | C | 5 | a0001c0001t0002g0083a0001c0001t0002g0086a0001c0001t0002g0114others(2): Show | 5 | HG00741.hp2 HG01346.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2458T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206458 | ||||||
chr14:69206459
|
T | C | 16 | a0001c0001t0002g0001a0001c0001t0002g0084a0001c0001t0002g0085others(13): Show | 18 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-48+2459T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206459 | ||||||
chr14:69206460
|
T | C | 9 | a0001c0001t0002g0105a0001c0001t0006g0218a0001c0001t0006g0219others(6): Show | 9 | HG02145.hp1 HG02922.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+2460T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206460 | ||||||
chr14:69206465
|
T | C | 3 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0069 | 3 | HG01981.hp1 NA18940.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-48+2465T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206465 | ||||||
chr14:69206466
|
T | C | 51 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(48): Show | 57 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.-48+2466T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206466 | ||||||
chr14:69206467
|
T | C | 2 | a0001c0003t0001g0033a0001c0003t0001g0040 | 2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-48+2467T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206467 | ||||||
chr14:69206469
|
T | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0081a0001c0001t0002g0082 | 4 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+2469T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206469 | ||||||
chr14:69206574
|
G | A | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-48+2574G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206574 | ||||||
chr14:69206643
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2643G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206643 | ||||||
chr14:69206790
|
A | G | 1 | a0001c0001t0005g0159 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-47-2634A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206790 | ||||||
chr14:69206964
|
C | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-2460C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206964 | ||||||
chr14:69207114
|
A | G | 1 | a0001c0003t0009g0006 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-47-2310A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207114 | ||||||
chr14:69207233
|
C | A | 2 | a0001c0003t0001g0041a0001c0003t0001g0069 | 2 | NA18940.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-47-2191C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207233 | ||||||
chr14:69207339
|
C | T | 14 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(11): Show | 14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-2085C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207339 | ||||||
chr14:69207473
|
G | A | 22 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0121others(19): Show | 22 | HG01192.hp1 HG01243.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47-1951G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207473 | ||||||
chr14:69207615
|
T | C | 1 | a0002c0002t0004g0182 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-47-1809T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207615 | ||||||
chr14:69207635
|
G | A | 56 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(53): Show | 62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-47-1789G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207635 | ||||||
chr14:69207893
|
C | CT | 34 | a0001c0001t0002g0008a0001c0001t0002g0080a0001c0001t0002g0081others(31): Show | 35 | HG00140.hp1 HG00733.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47-1516dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69207893 | |||||
chr14:69207972
|
G | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-1452G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207972 | ||||||
chr14:69208193
|
TGGCCA | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-1225_-47-1221d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69208193 | |||||
chr14:69208210
|
A | AT | 166 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-47-1196dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69208210 | |||||
chr14:69208210
|
A | ATT | 10 | a0001c0001t0002g0097a0001c0001t0002g0118a0001c0003t0001g0041others(7): Show | 10 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47-1197_-47-1196d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69208210 | |||||
chr14:69208233
|
C | T | 4 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0150others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1191C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208233 | ||||||
chr14:69208296
|
C | T | 4 | a0001c0003t0001g0014a0001c0003t0001g0015a0001c0003t0001g0016others(1): Show | 4 | HG00140.hp2 HG00639.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-1128C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208296 | ||||||
chr14:69208356
|
G | A | 11 | a0001c0001t0005g0032a0001c0001t0005g0152a0001c0001t0005g0153others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-1068G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208356 | ||||||
chr14:69208450
|
T | A | 2 | a0002c0002t0001g0192a0002c0002t0001g0201 | 2 | HG00735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-47-974T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208450 | ||||||
chr14:69208463
|
G | A | 1 | a0001c0003t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-47-961G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208463 | ||||||
chr14:69208517
|
C | G | 1 | a0002c0002t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-47-907C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208517 | ||||||
chr14:69208559
|
C | G | 3 | a0001c0001t0002g0109a0001c0001t0002g0110a0001c0001t0002g0111 | 3 | HG02486.hp1 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-47-865C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208559 | ||||||
chr14:69208651
|
A | G | 10 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0008g0104others(7): Show | 10 | HG01081.hp2 HG01496.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-773A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208651 | ||||||
chr14:69208696
|
C | T | 1 | a0001c0003t0001g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-47-728C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208696 | ||||||
chr14:69208800
|
C | G | 1 | a0001c0001t0006g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-624C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208800 | ||||||
chr14:69208805
|
G | C | 177 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(174): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-47-619G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208805 | ||||||
chr14:69208891
|
C | T | 4 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-533C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208891 | ||||||
chr14:69209366
|
T | G | 11 | a0001c0001t0005g0032a0001c0001t0005g0152a0001c0001t0005g0153others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-58T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69209366 | ||||||
chr14:69209824
|
TA | T | 43 | a0001c0001t0002g0123a0001c0001t0003g0018a0001c0001t0003g0079others(40): Show | 43 | HG01081.hp2 HG01192.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.333+39delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69209824 | |||||
chr14:69209874
|
C | T | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG00642.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.333+71C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69209874 | ||||||
chr14:69209893
|
G | A | 1 | a0002c0002t0001g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.333+90G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69209893 | ||||||
chr14:69210246
|
C | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+443C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69210246 | ||||||
chr14:69210263
|
C | T | 14 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(11): Show | 14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+460C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69210263 | ||||||
chr14:69210535
|
C | T | 2 | a0001c0003t0001g0068a0001c0003t0001g0076 | 2 | HG00639.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.333+732C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69210535 | ||||||
chr14:69210598
|
G | C | 222 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(219): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.333+795G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69210598 | ||||||
chr14:69211794
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.333+1991C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211794 | ||||||
chr14:69211815
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+2012G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211815 | ||||||
chr14:69211880
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.333+2077G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211880 | ||||||
chr14:69211927
|
A | G | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.333+2124A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211927 | ||||||
chr14:69211949
|
A | C | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.333+2146A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211949 | ||||||
chr14:69212268
|
T | C | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.333+2465T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212268 | ||||||
chr14:69212293
|
C | G | 1 | a0002c0002t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.333+2490C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212293 | ||||||
chr14:69212295
|
T | G | 1 | a0002c0002t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.333+2492T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212295 | ||||||
chr14:69212329
|
A | T | 1 | a0001c0001t0012g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.333+2526A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212329 | ||||||
chr14:69212333
|
C | T | 1 | a0001c0001t0014g0100 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.333+2530C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212333 | ||||||
chr14:69212678
|
A | C | 1 | a0002c0002t0001g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.333+2875A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212678 | ||||||
chr14:69212687
|
C | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+2884C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212687 | ||||||
chr14:69212689
|
A | G | 1 | a0001c0001t0005g0032 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.333+2886A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212689 | ||||||
chr14:69212699
|
AT | A | 64 | a0001c0001t0002g0091a0001c0001t0002g0107a0001c0001t0002g0111others(61): Show | 64 | HG01069.hp1 HG01175.hp2 HG01192.hp1 others(61): Show |
intron_variant | MODIFIER | c.333+2922delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69212699 | |||||
chr14:69212699
|
ATT | A | 117 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(114): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.333+2921_333+2922d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69212699 | |||||
chr14:69212699
|
ATTTT | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+2919_333+2922d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69212699 | |||||
chr14:69212739
|
A | T | 12 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(9): Show | 12 | HG01361.hp2 HG02056.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.333+2936A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212739 | ||||||
chr14:69212750
|
C | A | 2 | a0001c0003t0001g0004a0001c0003t0001g0042 | 3 | HG00738.hp2 HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.333+2947C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212750 | ||||||
chr14:69212910
|
G | A | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.333+3107G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212910 | ||||||
chr14:69212920
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+3117G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212920 | ||||||
chr14:69212958
|
G | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0085a0001c0001t0002g0093others(7): Show | 12 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.333+3155G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212958 | ||||||
chr14:69213054
|
G | A | 18 | a0001c0001t0002g0123a0001c0001t0003g0018a0001c0001t0003g0079others(15): Show | 18 | HG01192.hp1 HG01243.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.333+3251G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213054 | ||||||
chr14:69213070
|
A | G | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.333+3267A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213070 | ||||||
chr14:69213084
|
C | CT | 65 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(62): Show | 71 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.333+3297dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213084 | |||||
chr14:69213312
|
C | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+3509C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213312 | ||||||
chr14:69213373
|
CT | C | 20 | a0002c0002t0001g0193a0002c0002t0001g0202a0002c0002t0001g0203others(17): Show | 20 | HG01069.hp1 HG01069.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.333+3595delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213373 | |||||
chr14:69213373
|
CTTTT | C | 6 | a0001c0001t0003g0142a0001c0001t0005g0159a0001c0003t0001g0004others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+3592_333+3595d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213373 | |||||
chr14:69213373
|
CTTTTT | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(130): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.333+3591_333+3595d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213373 | |||||
chr14:69213373
|
CTTTTTT | C | 34 | a0001c0001t0002g0089a0001c0001t0002g0105a0001c0001t0003g0018others(31): Show | 34 | HG01243.hp1 HG01361.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.333+3590_333+3595d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213373 | |||||
chr14:69213379
|
T | C | 5 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220others(2): Show | 5 | HG02145.hp1 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+3576T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213379 | ||||||
chr14:69213537
|
A | AT | 14 | a0002c0002t0004g0174a0002c0002t0004g0175a0002c0002t0004g0176others(11): Show | 14 | HG01069.hp1 HG01192.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+3754dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | |||||
chr14:69213537
|
A | ATTTT | 25 | a0001c0001t0002g0001a0001c0001t0002g0083a0001c0001t0002g0084others(22): Show | 27 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.333+3751_333+3754d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | |||||
chr14:69213537
|
A | ATTTTT | 49 | a0001c0001t0002g0085a0001c0001t0002g0089a0001c0001t0002g0090others(46): Show | 49 | HG00280.hp2 HG01074.hp2 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.333+3750_333+3754d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | |||||
chr14:69213537
|
A | ATTTTTT | 33 | a0001c0001t0002g0080a0001c0001t0002g0094a0001c0001t0002g0096others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.333+3749_333+3754d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | |||||
chr14:69213537
|
A | ATTTTTTT | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.333+3748_333+3754d others(9): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | |||||
chr14:69213537
|
A | ATTTTTTT others(1): Show |
9 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0039others(6): Show | 11 | HG01981.hp1 HG02135.hp2 HG04184.hp1 others(8): Show |
intron_variant | MODIFIER | c.333+3747_333+3754d others(10): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | |||||
chr14:69213537
|
ATT | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0081a0001c0001t0002g0082others(2): Show | 6 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+3753_333+3754d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | |||||
chr14:69213724
|
T | C | 193 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(190): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.333+3921T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213724 | ||||||
chr14:69213808
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4005T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213808 | ||||||
chr14:69213922
|
CA | C | 222 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(219): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.333+4120delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213922 | ||||||
chr14:69214037
|
ATT | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4237_333+4238d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69214037 | |||||
chr14:69214781
|
T | G | 5 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0150others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4978T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69214781 | ||||||
chr14:69214986
|
T | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5183T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69214986 | ||||||
chr14:69215001
|
T | G | 200 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(197): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.333+5198T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215001 | ||||||
chr14:69215134
|
A | G | 2 | a0001c0001t0006g0190a0001c0001t0006g0217 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.333+5331A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215134 | ||||||
chr14:69215142
|
G | T | 1 | a0001c0001t0002g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.333+5339G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215142 | ||||||
chr14:69215162
|
C | T | 2 | a0001c0001t0006g0190a0001c0001t0006g0217 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.333+5359C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215162 | ||||||
chr14:69215243
|
G | A | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.333+5440G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215243 | ||||||
chr14:69215279
|
G | T | 1 | a0001c0001t0002g0090 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.333+5476G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215279 | ||||||
chr14:69215285
|
A | G | 2 | a0001c0003t0001g0048a0001c0003t0001g0049 | 2 | HG01934.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.333+5482A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215285 | ||||||
chr14:69215294
|
ATATATGT others(3): Show |
A | 4 | a0001c0003t0001g0046a0001c0003t0001g0047a0001c0003t0006g0145others(1): Show | 4 | HG02922.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+5493_333+5502d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215294 | |||||
chr14:69215294
|
ATATATGT others(5): Show |
A | 53 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(50): Show | 59 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.333+5493_333+5504d others(14): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215294 | |||||
chr14:69215298
|
A | ATG | 52 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0081others(49): Show | 55 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.333+5529_333+5530d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | |||||
chr14:69215298
|
A | ATGTG | 13 | a0001c0001t0002g0080a0001c0001t0002g0094a0001c0001t0002g0096others(10): Show | 13 | HG00140.hp1 HG02109.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.333+5527_333+5530d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | |||||
chr14:69215298
|
A | ATGTGTG | 20 | a0001c0001t0002g0092a0001c0001t0002g0123a0001c0001t0003g0018others(17): Show | 20 | HG01074.hp2 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.333+5525_333+5530d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | |||||
chr14:69215298
|
A | ATGTGTGT others(1): Show |
20 | a0001c0001t0003g0124a0001c0001t0003g0127a0001c0001t0003g0128others(17): Show | 20 | HG01361.hp2 HG01891.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.333+5523_333+5530d others(10): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | |||||
chr14:69215298
|
A | ATGTGTGT others(3): Show |
10 | a0001c0001t0003g0129a0001c0001t0003g0139a0001c0001t0003g0150others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+5521_333+5530d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | |||||
chr14:69215298
|
A | ATGTGTGT others(5): Show |
1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.333+5519_333+5530d others(14): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | |||||
chr14:69215298
|
A | G | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.333+5495A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215298 | ||||||
chr14:69215298
|
ATG | A | 2 | a0002c0002t0001g0031a0002c0002t0001g0194 | 2 | HG02055.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.333+5529_333+5530d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | |||||
chr14:69215298
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0006g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.333+5521_333+5530d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | |||||
chr14:69215332
|
G | A | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.333+5529G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215332 | ||||||
chr14:69215334
|
A | G | 1 | a0002c0002t0001g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.333+5531A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215334 | ||||||
chr14:69215340
|
C | CAAT | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5539_333+5541d others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215340 | |||||
chr14:69215360
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5557G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215360 | ||||||
chr14:69215366
|
C | T | 14 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(11): Show | 14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+5563C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215366 | ||||||
chr14:69215409
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5606G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215409 | ||||||
chr14:69215411
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5608G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215411 | ||||||
chr14:69215443
|
G | T | 3 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163 | 3 | HG01074.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.333+5640G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215443 | ||||||
chr14:69215505
|
A | G | 16 | a0002c0002t0004g0174a0002c0002t0004g0175a0002c0002t0004g0176others(13): Show | 16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.333+5702A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215505 | ||||||
chr14:69215761
|
A | T | 200 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(197): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.333+5958A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215761 | ||||||
chr14:69215787
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.333+5984G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215787 | ||||||
chr14:69215819
|
C | CT | 27 | a0001c0001t0002g0123a0001c0001t0003g0018a0001c0001t0003g0079others(24): Show | 27 | HG00140.hp2 HG00639.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.333+6028dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215819 | |||||
chr14:69215819
|
C | CTT | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+6027_333+6028d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215819 | |||||
chr14:69215865
|
T | A | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.333+6062T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215865 | ||||||
chr14:69215895
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.333+6092G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215895 | ||||||
chr14:69216070
|
T | C | 24 | a0001c0001t0002g0008a0001c0001t0002g0080a0001c0001t0002g0081others(21): Show | 25 | HG00140.hp1 HG00733.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.333+6267T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216070 | ||||||
chr14:69216073
|
C | T | 2 | a0001c0001t0006g0219a0001c0001t0006g0220 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.333+6270C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216073 | ||||||
chr14:69216251
|
C | T | 5 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0008g0104others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+6448C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216251 | ||||||
chr14:69216305
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+6502T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216305 | ||||||
chr14:69216359
|
T | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+6556T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216359 | ||||||
chr14:69216607
|
C | T | 7 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0098others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+6804C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216607 | ||||||
chr14:69216739
|
A | G | 177 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(174): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.333+6936A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216739 | ||||||
chr14:69216946
|
A | G | 14 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(11): Show | 14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+7143A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216946 | ||||||
chr14:69217315
|
G | C | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.333+7512G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217315 | ||||||
chr14:69217411
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.333+7608G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217411 | ||||||
chr14:69217542
|
C | CT | 5 | a0001c0001t0003g0125a0001c0001t0005g0164a0001c0001t0005g0165others(2): Show | 5 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+7749dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69217542 | |||||
chr14:69217552
|
T | A | 5 | a0001c0003t0001g0007a0001c0003t0001g0068a0001c0003t0001g0075others(2): Show | 6 | HG00639.hp1 HG01071.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+7749T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217552 | ||||||
chr14:69217645
|
T | C | 1 | a0002c0002t0001g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.333+7842T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217645 | ||||||
chr14:69217714
|
A | G | 2 | a0002c0002t0004g0187a0002c0002t0004g0188 | 2 | HG01192.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.333+7911A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217714 | ||||||
chr14:69218220
|
C | T | 1 | a0002c0002t0001g0214 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.333+8417C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218220 | ||||||
chr14:69218221
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+8418G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218221 | ||||||
chr14:69218305
|
A | G | 4 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+8502A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218305 | ||||||
chr14:69218378
|
A | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+8575A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218378 | ||||||
chr14:69218536
|
G | A | 2 | a0001c0001t0003g0138a0001c0001t0003g0139 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.333+8733G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218536 | ||||||
chr14:69218556
|
T | A | 1 | a0001c0001t0002g0085 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.333+8753T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218556 | ||||||
chr14:69218593
|
G | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+8790G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218593 | ||||||
chr14:69218774
|
C | A | 2 | a0001c0004t0007g0169a0001c0004t0007g0170 | 2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.333+8971C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218774 | ||||||
chr14:69219270
|
A | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+9467A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219270 | ||||||
chr14:69219399
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.334-9417G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219399 | ||||||
chr14:69219417
|
T | C | 1 | a0001c0001t0006g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.334-9399T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219417 | ||||||
chr14:69219459
|
G | A | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.334-9357G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219459 | ||||||
chr14:69219551
|
T | C | 2 | a0001c0001t0006g0190a0001c0001t0006g0217 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.334-9265T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219551 | ||||||
chr14:69219802
|
G | A | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.334-9014G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219802 | ||||||
chr14:69219845
|
G | A | 1 | a0002c0002t0004g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.334-8971G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219845 | ||||||
chr14:69219878
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-8938G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219878 | ||||||
chr14:69220030
|
T | A | 2 | a0001c0001t0002g0085a0001c0001t0002g0108 | 2 | HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.334-8786T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220030 | ||||||
chr14:69220244
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-8572T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220244 | ||||||
chr14:69220253
|
G | GT | 14 | a0001c0001t0002g0085a0002c0002t0001g0010a0002c0002t0001g0162others(11): Show | 15 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.334-8528dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTT | 11 | a0001c0001t0002g0093a0001c0001t0002g0105a0001c0001t0002g0106others(8): Show | 11 | HG00642.hp2 HG00735.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.334-8529_334-8528d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTT | 15 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0081others(12): Show | 18 | HG00733.hp2 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-8530_334-8528d others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTT | 11 | a0001c0001t0002g0086a0001c0001t0002g0091a0001c0001t0002g0094others(8): Show | 11 | HG00140.hp1 HG01074.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.334-8531_334-8528d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTTT | 11 | a0001c0001t0002g0080a0001c0001t0002g0084a0001c0001t0002g0092others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.334-8532_334-8528d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTTTT | 5 | a0001c0001t0002g0083a0001c0001t0002g0101a0001c0001t0002g0122others(2): Show | 5 | HG00741.hp2 HG01346.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-8533_334-8528d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTTTTG others(4): Show |
1 | a0001c0001t0005g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.334-8557_334-8556i others(13): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTTTTG others(5): Show |
3 | a0001c0001t0005g0155a0001c0001t0005g0156a0001c0001t0005g0158 | 3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.334-8557_334-8556i others(14): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTTTTG others(6): Show |
4 | a0001c0001t0005g0032a0001c0001t0005g0159a0001c0001t0005g0160others(1): Show | 4 | HG00280.hp2 NA18940.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-8557_334-8556i others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTTTTG others(7): Show |
1 | a0001c0003t0001g0161 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.334-8557_334-8556i others(16): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTTTTG others(11): Show |
2 | a0001c0001t0005g0152a0001c0001t0005g0153 | 2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.334-8557_334-8556i others(20): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTTTTT others(15): Show |
1 | a0001c0001t0003g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.334-8549_334-8528d others(24): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
G | GTTTTTTT others(16): Show |
1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-8550_334-8528d others(25): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
GTTTT | G | 10 | a0001c0001t0003g0018a0001c0001t0003g0079a0001c0001t0003g0126others(7): Show | 10 | HG01243.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.334-8531_334-8528d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
GTTTTT | G | 9 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-8532_334-8528d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
GTTTTTT | G | 21 | a0001c0001t0002g0070a0001c0001t0003g0141a0001c0001t0003g0150others(18): Show | 23 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.334-8533_334-8528d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
GTTTTTTT | G | 39 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(36): Show | 43 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.334-8534_334-8528d others(9): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
GTTTTTTT others(2): Show |
G | 6 | a0002c0002t0001g0011a0002c0002t0001g0021a0002c0002t0001g0022others(3): Show | 6 | HG01361.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-8536_334-8528d others(11): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
GTTTTTTT others(3): Show |
G | 8 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0023others(5): Show | 8 | HG02056.hp1 HG02155.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-8537_334-8528d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
GTTTTTTT others(6): Show |
G | 3 | a0001c0001t0006g0190a0002c0002t0001g0206a0002c0002t0001g0207 | 3 | HG01106.hp2 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.334-8540_334-8528d others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0003g0125a0001c0001t0006g0217a0001c0001t0016g0102 | 3 | HG02572.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.334-8541_334-8528d others(16): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220253
|
GTTTTTTT others(8): Show |
G | 2 | a0002c0002t0001g0212a0002c0002t0004g0189 | 2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.334-8542_334-8528d others(17): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | |||||
chr14:69220258
|
T | C | 1 | a0001c0004t0007g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.334-8558T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220258 | ||||||
chr14:69220259
|
T | C | 4 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(1): Show | 4 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-8557T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220259 | ||||||
chr14:69220302
|
G | A | 1 | a0002c0002t0001g0208 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.334-8514G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220302 | ||||||
chr14:69220357
|
A | G | 177 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(174): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.334-8459A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220357 | ||||||
chr14:69220363
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334-8453C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220363 | ||||||
chr14:69220419
|
C | T | 1 | a0001c0003t0020g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.334-8397C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220419 | ||||||
chr14:69220431
|
C | T | 1 | a0002c0002t0004g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.334-8385C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220431 | ||||||
chr14:69220557
|
A | AT | 14 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086others(11): Show | 14 | HG00741.hp2 HG01346.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.334-8243dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220557 | |||||
chr14:69220557
|
AT | A | 6 | a0001c0001t0003g0129a0001c0001t0010g0149a0001c0003t0001g0056others(3): Show | 6 | HG01943.hp1 HG02258.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-8243delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220557 | |||||
chr14:69220574
|
A | T | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.334-8242A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220574 | ||||||
chr14:69220652
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-8164T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220652 | ||||||
chr14:69220714
|
C | G | 1 | a0002c0002t0001g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.334-8102C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220714 | ||||||
chr14:69220783
|
C | T | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-8033C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220783 | ||||||
chr14:69221048
|
T | C | 1 | a0001c0001t0005g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.334-7768T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221048 | ||||||
chr14:69221135
|
C | T | 1 | a0001c0003t0001g0061 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.334-7681C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221135 | ||||||
chr14:69221169
|
G | A | 1 | a0001c0003t0001g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.334-7647G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221169 | ||||||
chr14:69221204
|
T | C | 1 | a0001c0001t0002g0092 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.334-7612T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221204 | ||||||
chr14:69221230
|
C | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-7586C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221230 | ||||||
chr14:69221329
|
C | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-7487C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221329 | ||||||
chr14:69221425
|
A | T | 1 | a0001c0001t0012g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.334-7391A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221425 | ||||||
chr14:69221490
|
T | C | 177 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(174): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.334-7326T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221490 | ||||||
chr14:69221521
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.334-7295A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221521 | ||||||
chr14:69221539
|
A | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-7277A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221539 | ||||||
chr14:69221658
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.334-7158C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221658 | ||||||
chr14:69221709
|
A | G | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.334-7107A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221709 | ||||||
chr14:69221724
|
T | A | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.334-7092T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221724 | ||||||
chr14:69221754
|
C | T | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-7062C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221754 | ||||||
chr14:69221760
|
C | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-7056C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221760 | ||||||
chr14:69221909
|
T | TA | 45 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0003g0018others(42): Show | 46 | HG00738.hp1 HG00738.hp2 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.334-6878dupA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | |||||
chr14:69221909
|
T | TAA | 54 | a0001c0001t0002g0008a0001c0001t0002g0080a0001c0001t0002g0081others(51): Show | 60 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.334-6879_334-6878d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | |||||
chr14:69221909
|
T | TAAA | 18 | a0001c0001t0002g0059a0001c0001t0002g0082a0001c0001t0002g0085others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-6880_334-6878d others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | |||||
chr14:69221909
|
T | TAAAA | 12 | a0001c0001t0002g0001a0001c0001t0002g0035a0001c0001t0002g0058others(9): Show | 14 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.334-6881_334-6878d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | |||||
chr14:69221909
|
TA | T | 30 | a0001c0001t0006g0217a0002c0002t0001g0009a0002c0002t0001g0191others(27): Show | 31 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.334-6878delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | |||||
chr14:69221909
|
TAAAA | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-6881_334-6878d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | |||||
chr14:69221909
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0002g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.334-6890_334-6878d others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | |||||
chr14:69221959
|
G | T | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-6857G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221959 | ||||||
chr14:69221960
|
C | T | 2 | a0002c0002t0001g0199a0002c0002t0001g0211 | 2 | HG01081.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.334-6856C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221960 | ||||||
chr14:69222086
|
CA | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-6715delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69222086 | |||||
chr14:69222207
|
T | G | 22 | a0001c0001t0002g0001a0001c0001t0002g0083a0001c0001t0002g0084others(19): Show | 24 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.334-6609T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222207 | ||||||
chr14:69222325
|
G | T | 177 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(174): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.334-6491G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222325 | ||||||
chr14:69222630
|
A | G | 16 | a0002c0002t0004g0174a0002c0002t0004g0175a0002c0002t0004g0176others(13): Show | 16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.334-6186A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222630 | ||||||
chr14:69222702
|
C | CT | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.334-6106dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69222702 | |||||
chr14:69222708
|
T | G | 1 | a0001c0001t0002g0112 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.334-6108T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222708 | ||||||
chr14:69222760
|
G | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-6056G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222760 | ||||||
chr14:69223295
|
C | CT | 4 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-5520dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69223295 | |||||
chr14:69223771
|
AT | A | 12 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(9): Show | 12 | HG01361.hp2 HG02056.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.334-5043delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69223771 | |||||
chr14:69223850
|
C | T | 1 | a0002c0002t0001g0194 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.334-4966C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69223850 | ||||||
chr14:69224512
|
G | C | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.334-4304G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224512 | ||||||
chr14:69224623
|
AT | A | 4 | a0002c0002t0001g0009a0002c0002t0001g0196a0002c0002t0001g0199others(1): Show | 5 | HG01081.hp1 HG01496.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-4185delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69224623 | |||||
chr14:69224632
|
A | T | 1 | a0001c0001t0002g0058 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.334-4184A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224632 | ||||||
chr14:69224848
|
G | A | 2 | a0001c0001t0006g0190a0001c0001t0006g0217 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.334-3968G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224848 | ||||||
chr14:69224944
|
A | C | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.334-3872A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224944 | ||||||
chr14:69224969
|
G | A | 1 | a0001c0003t0001g0065 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.334-3847G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224969 | ||||||
chr14:69224973
|
C | T | 1 | a0001c0001t0005g0164 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.334-3843C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224973 | ||||||
chr14:69225002
|
C | T | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-3814C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225002 | ||||||
chr14:69225478
|
A | G | 1 | a0001c0001t0006g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-3338A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225478 | ||||||
chr14:69225484
|
C | T | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-3332C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225484 | ||||||
chr14:69225513
|
T | A | 1 | a0002c0002t0001g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.334-3303T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225513 | ||||||
chr14:69225582
|
A | G | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.334-3234A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225582 | ||||||
chr14:69225837
|
A | G | 1 | a0001c0001t0006g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-2979A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225837 | ||||||
chr14:69225848
|
A | G | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0150others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-2968A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225848 | ||||||
chr14:69225977
|
A | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2839A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225977 | ||||||
chr14:69226101
|
A | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2715A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226101 | ||||||
chr14:69226237
|
C | G | 3 | a0001c0001t0006g0095a0001c0001t0006g0190a0001c0001t0006g0217 | 3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.334-2579C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226237 | ||||||
chr14:69226238
|
C | T | 1 | a0002c0002t0001g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.334-2578C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226238 | ||||||
chr14:69226386
|
T | C | 1 | a0001c0003t0001g0054 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.334-2430T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226386 | ||||||
chr14:69226402
|
G | A | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.334-2414G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226402 | ||||||
chr14:69226750
|
A | T | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-2066A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226750 | ||||||
chr14:69226773
|
GT | G | 163 | a0001c0001t0002g0001a0001c0001t0002g0058a0001c0001t0002g0059others(160): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.334-2024delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69226773 | |||||
chr14:69226880
|
G | A | 1 | a0002c0002t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-1936G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226880 | ||||||
chr14:69226923
|
T | C | 1 | a0001c0009t0002g0087 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.334-1893T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226923 | ||||||
chr14:69227002
|
T | C | 1 | a0001c0001t0006g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-1814T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227002 | ||||||
chr14:69227108
|
C | T | 1 | a0002c0002t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-1708C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227108 | ||||||
chr14:69227145
|
C | T | 5 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0150others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-1671C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227145 | ||||||
chr14:69227602
|
C | T | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.334-1214C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227602 | ||||||
chr14:69227646
|
G | A | 4 | a0001c0003t0001g0056a0001c0003t0001g0060a0001c0003t0001g0066others(1): Show | 4 | HG02630.hp1 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-1170G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227646 | ||||||
chr14:69227656
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-1160T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227656 | ||||||
chr14:69227829
|
A | G | 172 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(169): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.334-987A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227829 | ||||||
chr14:69227927
|
A | AT | 96 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0080others(93): Show | 99 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.334-880dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69227927 | |||||
chr14:69227979
|
C | G | 14 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(11): Show | 14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-837C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227979 | ||||||
chr14:69228185
|
CT | C | 97 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(94): Show | 103 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.334-608delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69228185 | |||||
chr14:69228185
|
CTT | C | 51 | a0001c0001t0002g0082a0001c0001t0002g0090a0001c0001t0002g0094others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.334-609_334-608del others(2): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69228185 | |||||
chr14:69228185
|
CTTT | C | 39 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0080others(36): Show | 42 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.334-610_334-608del others(3): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69228185 | |||||
chr14:69228230
|
C | T | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-586C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228230 | ||||||
chr14:69228290
|
C | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-526C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228290 | ||||||
chr14:69228440
|
C | G | 2 | a0001c0003t0001g0041a0001c0003t0001g0069 | 2 | NA18940.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.334-376C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228440 | ||||||
chr14:69228488
|
A | G | 179 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(176): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.334-328A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228488 | ||||||
chr14:69228551
|
C | T | 14 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(11): Show | 14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-265C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228551 | ||||||
chr14:69228593
|
C | A | 1 | a0001c0001t0006g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.334-223C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228593 | ||||||
chr14:69228630
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-186T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228630 | ||||||
chr14:69228674
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.334-142C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228674 | ||||||
chr14:69229075
|
G | A | 155 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(152): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
splice_region_variant&intron_variant | LOW | c.590+3G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229075 | ||||||
chr14:69229109
|
C | T | 1 | a0001c0003t0001g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.590+37C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229109 | ||||||
chr14:69229228
|
C | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.590+156C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229228 | ||||||
chr14:69229455
|
T | C | 56 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(53): Show | 62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.590+383T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229455 | ||||||
chr14:69229552
|
C | A | 16 | a0002c0002t0004g0174a0002c0002t0004g0175a0002c0002t0004g0176others(13): Show | 16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.590+480C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229552 | ||||||
chr14:69229619
|
C | G | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.590+547C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229619 | ||||||
chr14:69230212
|
C | T | 3 | a0001c0001t0008g0104a0001c0001t0008g0143a0001c0001t0008g0144 | 3 | HG02818.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.591-260C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230212 | ||||||
chr14:69230353
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.591-119G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230353 | ||||||
chr14:69230437
|
C | T | 1 | a0001c0001t0019g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591-35C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230437 | ||||||
chr14:69230457
|
C | G | 1 | a0001c0007t0006g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.591-15C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230457 | ||||||
chr14:69230468
|
T | C | 1 | a0001c0003t0001g0072 | 1 | HG01175.hp2 | splice_region_variant&intron_variant | LOW | c.591-4T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230468 | ||||||
chr14:69230736
|
C | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0080others(93): Show | 99 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.717+138C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69230736 | ||||||
chr14:69230847
|
G | A | 177 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(174): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.717+249G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69230847 | ||||||
chr14:69230883
|
A | G | 3 | a0001c0001t0002g0083a0001c0009t0002g0087a0003c0006t0002g0088 | 3 | HG00741.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.717+285A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69230883 | ||||||
chr14:69231023
|
G | C | 1 | a0001c0004t0007g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.717+425G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231023 | ||||||
chr14:69231124
|
A | AT | 24 | a0001c0001t0003g0018a0001c0001t0003g0079a0001c0001t0003g0124others(21): Show | 24 | HG01243.hp1 HG01433.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.717+534dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231124 | |||||
chr14:69231134
|
T | C | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.717+536T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231134 | ||||||
chr14:69231160
|
A | T | 1 | a0001c0001t0002g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+562A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231160 | ||||||
chr14:69231164
|
T | C | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.717+566T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231164 | ||||||
chr14:69231236
|
C | T | 1 | a0001c0003t0001g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.717+638C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231236 | ||||||
chr14:69231260
|
C | A | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.717+662C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231260 | ||||||
chr14:69231372
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+774G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231372 | ||||||
chr14:69231414
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+816G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231414 | ||||||
chr14:69231501
|
C | G | 2 | a0002c0002t0001g0022a0002c0002t0001g0027 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.717+903C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231501 | ||||||
chr14:69231510
|
A | G | 4 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+912A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231510 | ||||||
chr14:69231619
|
G | C | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.717+1021G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231619 | ||||||
chr14:69231721
|
G | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+1123G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231721 | ||||||
chr14:69231820
|
CCT | C | 57 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0002g0058others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.717+1225_717+1226d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231820 | |||||
chr14:69231909
|
T | TA | 34 | a0001c0001t0005g0152a0001c0001t0005g0153a0001c0001t0005g0155others(31): Show | 34 | HG00735.hp2 HG00738.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.717+1338dupA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | |||||
chr14:69231909
|
T | TAA | 7 | a0001c0001t0005g0032a0001c0001t0005g0158a0001c0001t0005g0159others(4): Show | 7 | HG00280.hp2 HG01361.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1337_717+1338d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | |||||
chr14:69231909
|
TA | T | 74 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0080others(71): Show | 77 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.717+1338delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | |||||
chr14:69231909
|
TAA | T | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0150others(3): Show | 6 | HG01074.hp2 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+1337_717+1338d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | |||||
chr14:69231909
|
TAAAAAA | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+1333_717+1338d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | |||||
chr14:69231975
|
C | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+1377C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231975 | ||||||
chr14:69232293
|
T | A | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.717+1695T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232293 | ||||||
chr14:69232429
|
T | C | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.717+1831T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232429 | ||||||
chr14:69232456
|
C | T | 3 | a0001c0004t0007g0168a0001c0004t0007g0171a0001c0004t0007g0172 | 3 | HG02451.hp2 HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.717+1858C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232456 | ||||||
chr14:69232511
|
A | C | 1 | a0002c0002t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.717+1913A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232511 | ||||||
chr14:69232806
|
A | G | 2 | a0001c0001t0006g0095a0001c0001t0006g0217 | 2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1894A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232806 | ||||||
chr14:69232842
|
T | C | 52 | a0001c0003t0001g0002a0001c0003t0001g0003a0001c0003t0001g0004others(49): Show | 58 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.718-1858T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232842 | ||||||
chr14:69233062
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-1638T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233062 | ||||||
chr14:69233063
|
G | C | 1 | a0001c0001t0019g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.718-1637G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233063 | ||||||
chr14:69233153
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-1547G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233153 | ||||||
chr14:69233392
|
A | T | 1 | a0001c0001t0002g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.718-1308A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233392 | ||||||
chr14:69233412
|
A | T | 3 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163 | 3 | HG01074.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.718-1288A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233412 | ||||||
chr14:69233431
|
T | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-1269T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233431 | ||||||
chr14:69233513
|
G | A | 1 | a0001c0001t0003g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.718-1187G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233513 | ||||||
chr14:69233564
|
C | T | 3 | a0001c0001t0006g0095a0001c0001t0006g0190a0001c0001t0006g0217 | 3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1136C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233564 | ||||||
chr14:69233688
|
G | C | 1 | a0001c0003t0001g0065 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.718-1012G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233688 | ||||||
chr14:69233857
|
C | T | 52 | a0001c0003t0001g0002a0001c0003t0001g0003a0001c0003t0001g0004others(49): Show | 58 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.718-843C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233857 | ||||||
chr14:69233912
|
G | A | 2 | a0002c0002t0001g0022a0002c0002t0001g0027 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.718-788G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233912 | ||||||
chr14:69233963
|
C | T | 1 | a0001c0001t0015g0117 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.718-737C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233963 | ||||||
chr14:69234052
|
C | G | 1 | a0002c0002t0004g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.718-648C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69234052 | ||||||
chr14:69234082
|
T | A | 5 | a0001c0001t0002g0001a0001c0001t0002g0105a0001c0001t0002g0112others(2): Show | 7 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-618T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69234082 | ||||||
chr14:69234204
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-496T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69234204 | ||||||
chr14:69235097
|
T | C | 1 | a0001c0008t0021g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1049+66T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235097 | ||||||
chr14:69235146
|
C | A | 162 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(159): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1049+115C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235146 | ||||||
chr14:69235233
|
T | G | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1049+202T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235233 | ||||||
chr14:69235380
|
G | T | 11 | a0001c0001t0005g0032a0001c0001t0005g0152a0001c0001t0005g0153others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1049+349G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235380 | ||||||
chr14:69235611
|
T | C | 53 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(50): Show | 56 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1050-435T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235611 | ||||||
chr14:69235623
|
T | C | 1 | a0001c0001t0014g0100 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1050-423T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235623 | ||||||
chr14:69235777
|
G | T | 3 | a0001c0001t0005g0164a0001c0001t0005g0165a0001c0001t0017g0163 | 3 | HG01074.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1050-269G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235777 | ||||||
chr14:69235875
|
G | A | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1050-171G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235875 | ||||||
chr14:69236700
|
C | T | 1 | a0002c0002t0001g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1292+158C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69236700 | ||||||
chr14:69236871
|
G | C | 170 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(167): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1292+329G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69236871 | ||||||
chr14:69236961
|
C | T | 2 | a0002c0002t0001g0209a0002c0002t0001g0210 | 2 | HG00642.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1292+419C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69236961 | ||||||
chr14:69237024
|
T | C | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1292+482T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237024 | ||||||
chr14:69237039
|
C | A | 1 | a0004c0005t0001g0067 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1292+497C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237039 | ||||||
chr14:69237042
|
T | C | 1 | a0001c0003t0001g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1292+500T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237042 | ||||||
chr14:69237232
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1293-343G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237232 | ||||||
chr14:69237294
|
C | G | 1 | a0002c0002t0001g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1293-281C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237294 | ||||||
chr14:69237314
|
A | T | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1293-261A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237314 | ||||||
chr14:69237335
|
A | G | 200 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(197): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1293-240A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237335 | ||||||
chr14:69237442
|
T | C | 1 | a0002c0002t0001g0196 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1293-133T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237442 | ||||||
chr14:69237945
|
G | A | 11 | a0001c0001t0005g0032a0001c0001t0005g0152a0001c0001t0005g0153others(8): Show | 11 | HG00280.hp2 HG00738.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1649+14G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69237945 | ||||||
chr14:69237950
|
G | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649+19G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69237950 | ||||||
chr14:69238305
|
C | T | 2 | a0002c0002t0001g0030a0002c0002t0001g0031 | 2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1649+374C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69238305 | ||||||
chr14:69238424
|
A | G | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1649+493A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69238424 | ||||||
chr14:69238599
|
G | GT | 34 | a0001c0001t0002g0084a0001c0001t0005g0153a0001c0001t0005g0159others(31): Show | 34 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.1649+685dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 69238599 | |||||
chr14:69238599
|
GTT | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649+684_1649+685d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 69238599 | |||||
chr14:69238688
|
G | A | 1 | a0001c0003t0001g0041 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1649+757G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69238688 | ||||||
chr14:69238757
|
C | G | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649+826C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69238757 | ||||||
chr14:69239232
|
G | C | 2 | a0001c0001t0006g0095a0001c0001t0006g0217 | 2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1649+1301G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239232 | ||||||
chr14:69239242
|
G | A | 5 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0150others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649+1311G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239242 | ||||||
chr14:69239254
|
G | T | 2 | a0001c0001t0006g0095a0001c0001t0006g0217 | 2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1649+1323G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239254 | ||||||
chr14:69239401
|
T | A | 1 | a0001c0003t0001g0036 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1649+1470T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239401 | ||||||
chr14:69239459
|
C | T | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-1425C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239459 | ||||||
chr14:69239679
|
T | G | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1650-1205T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239679 | ||||||
chr14:69239686
|
C | A | 5 | a0001c0001t0002g0001a0001c0001t0002g0105a0001c0001t0002g0112others(2): Show | 7 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650-1198C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239686 | ||||||
chr14:69239808
|
G | A | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1650-1076G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239808 | ||||||
chr14:69239858
|
T | C | 5 | a0001c0004t0007g0168a0001c0004t0007g0169a0001c0004t0007g0170others(2): Show | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-1026T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239858 | ||||||
chr14:69240047
|
G | A | 2 | a0001c0001t0012g0166a0001c0001t0012g0167 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1650-837G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69240047 | ||||||
chr14:69240355
|
C | T | 1 | a0001c0003t0001g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1650-529C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69240355 | ||||||
chr14:69240638
|
G | A | 15 | a0002c0002t0001g0011a0002c0002t0001g0019a0002c0002t0001g0020others(12): Show | 15 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.1650-246G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69240638 | ||||||
chr14:69240870
|
T | C | 2 | a0002c0002t0001g0023a0002c0002t0001g0025 | 2 | NA19002.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1650-14T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69240870 |