geneid | 161829 |
---|---|
ensemblid | ENSG00000178997.12 |
hgncid | 28507 |
symbol | EXD1 |
name | exonuclease 3'-5' domain containing 1 |
refseq_nuc | NM_001286441.2 |
refseq_prot | NP_001273370.1 |
ensembl_nuc | ENST00000458580.7 |
ensembl_prot | ENSP00000415056.2 |
mane_status | MANE Select |
chr | chr15 |
start | 41182728 |
end | 41230757 |
strand | - |
ver | v1.2 |
region | chr15:41182728-41230757 |
region5000 | chr15:41177728-41235757 |
regionname0 | EXD1_chr15_41182728_41230757 |
regionname5000 | EXD1_chr15_41177728_41235757 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 572 | 267 | 77 | 47 | 109 | 6 | 27 | 77 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002 | 1/0 | 572 | 42 | 16 | 11 | 3 | 4 | 7 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0003 | 0/0 | 572 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0004 | 0/0 | 572 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0005 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0006 | 0/0 | 572 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0007 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0008 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0009 | 0/0 | 572 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1719 | 133 | 51 | 14 | 51 | 3 | 14 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0002 | 0/1 | 1719 | 122 | 19 | 32 | 56 | 1 | 13 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0003 | 0/0 | 1719 | 32 | 9 | 9 | 3 | 4 | 7 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0004 | 0/0 | 1719 | 8 | 6 | 2 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0005 | 0/0 | 1719 | 6 | 6 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0006 | 0/0 | 1719 | 3 | 0 | 1 | 0 | 2 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0007 | 0/0 | 1719 | 3 | 0 | 0 | 3 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0008 | 0/0 | 1719 | 2 | 0 | 0 | 2 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0009 | 0/0 | 1719 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0010 | 0/0 | 1719 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0011 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0012 | 0/0 | 1719 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0013 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0014 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0015 | 1/0 | 1719 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0016 | 0/0 | 1719 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
c0017 | 0/0 | 1719 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1536 | 176 | 45 | 43 | 59 | 7 | 21 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0002 | 0/0 | 1537 | 65 | 17 | 10 | 24 | 2 | 12 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0003 | 0/0 | 1536 | 40 | 1 | 4 | 33 | 1 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0004 | 0/0 | 1536 | 22 | 21 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0005 | 0/0 | 1536 | 4 | 4 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0006 | 0/0 | 1536 | 2 | 2 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0007 | 1/0 | 1536 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0008 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0009 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0010 | 0/0 | 1536 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0011 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0012 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0013 | 0/0 | 1536 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0014 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
t0015 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1719 | 133 | 51 | 14 | 51 | 3 | 14 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0002 | 0/1 | 1719 | 122 | 19 | 32 | 56 | 1 | 13 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0005 | 0/0 | 1719 | 6 | 6 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0006 | 0/0 | 1719 | 3 | 0 | 1 | 0 | 2 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0008 | 0/0 | 1719 | 2 | 0 | 0 | 2 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0011 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0003 | 0/0 | 1719 | 32 | 9 | 9 | 3 | 4 | 7 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0004 | 0/0 | 1719 | 8 | 6 | 2 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0013 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0015 | 1/0 | 1719 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0003c0007 | 0/0 | 1719 | 3 | 0 | 0 | 3 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0004c0009 | 0/0 | 1719 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0005c0010 | 0/0 | 1719 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0006c0014 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0007c0016 | 0/0 | 1719 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0008c0012 | 0/0 | 1719 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0009c0017 | 0/0 | 1719 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3254 | 11 | 11 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0001t0002 | 0/0 | 3255 | 62 | 17 | 10 | 21 | 2 | 12 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0001t0003 | 0/0 | 3254 | 36 | 1 | 4 | 29 | 1 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0001t0004 | 0/0 | 3254 | 22 | 21 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0001t0009 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0001t0015 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0002t0001 | 0/1 | 3254 | 113 | 15 | 31 | 53 | 1 | 12 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0002t0002 | 0/0 | 3255 | 2 | 0 | 0 | 2 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0002t0006 | 0/0 | 3254 | 2 | 2 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0002t0008 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0002t0010 | 0/0 | 3254 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0002t0012 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0002t0013 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0002t0014 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0005t0001 | 0/0 | 3254 | 6 | 6 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0006t0001 | 0/0 | 3254 | 3 | 0 | 1 | 0 | 2 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0008t0001 | 0/0 | 3254 | 2 | 0 | 0 | 2 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0001c0011t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0003t0001 | 0/0 | 3254 | 27 | 4 | 9 | 3 | 4 | 7 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0003t0005 | 0/0 | 3254 | 4 | 4 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0003t0011 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0004t0001 | 0/0 | 3254 | 8 | 6 | 2 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0013t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0002c0015t0007 | 1/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0003c0007t0003 | 0/0 | 3254 | 3 | 0 | 0 | 3 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0004c0009t0001 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0005c0010t0002 | 0/0 | 3255 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0006c0014t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0007c0016t0001 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0008c0012t0003 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
a0009c0017t0001 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | copy fasta | chr15 | 41177728 | 41235757 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0009g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0001t0015g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0010g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0012g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0013g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0002t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0006t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0006t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0008t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0008t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0001c0011t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0003t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0013t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0002c0015t0007g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0003c0007t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0003c0007t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0003c0007t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0004c0009t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0005c0010t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0006c0014t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0007c0016t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0008c0012t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
a0009c0017t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | GBR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0114 | EUR | GBR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00323 | hp1 | a0002 | c0003 | t0001 | g0297 | EUR | FIN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00323 | hp2 | a0001 | c0006 | t0001 | g0266 | EUR | FIN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0283 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00639 | hp1 | a0002 | c0003 | t0001 | g0115 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00642 | hp1 | a0002 | c0003 | t0001 | g0095 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00642 | hp2 | a0002 | c0003 | t0001 | g0121 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | CHS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01070 | hp1 | a0002 | c0003 | t0001 | g0127 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01106 | hp1 | a0002 | c0003 | t0001 | g0124 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01109 | hp1 | a0002 | c0004 | t0001 | g0006 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0312 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01243 | hp1 | a0002 | c0004 | t0001 | g0001 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | PUR | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01255 | hp1 | a0001 | c0002 | t0010 | g0211 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0120 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0286 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01433 | hp2 | a0001 | c0006 | t0001 | g0230 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01515 | hp1 | a0002 | c0003 | t0001 | g0093 | EUR | IBS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0178 | EUR | IBS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01517 | hp1 | a0001 | c0006 | t0001 | g0249 | EUR | IBS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0278 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0309 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01975 | hp2 | a0002 | c0003 | t0001 | g0117 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02055 | hp1 | a0002 | c0003 | t0005 | g0101 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0236 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02145 | hp2 | a0002 | c0004 | t0001 | g0083 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CDX | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | CDX | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | CDX | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | CDX | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02258 | hp1 | a0002 | c0003 | t0005 | g0100 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02300 | hp1 | a0002 | c0003 | t0001 | g0125 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0252 | AMR | PEL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02451 | hp2 | a0001 | c0002 | t0012 | g0265 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | KHV | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0229 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02602 | hp1 | a0002 | c0003 | t0001 | g0105 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02615 | hp1 | a0001 | c0005 | t0001 | g0107 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0316 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0106 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0277 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0285 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02809 | hp1 | a0002 | c0003 | t0011 | g0109 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0270 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02922 | hp1 | a0002 | c0004 | t0001 | g0129 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02922 | hp2 | a0001 | c0005 | t0001 | g0096 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02965 | hp1 | a0002 | c0003 | t0001 | g0103 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02976 | hp1 | a0001 | c0002 | t0014 | g0094 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0191 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03098 | hp1 | a0002 | c0003 | t0001 | g0126 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03130 | hp2 | a0002 | c0003 | t0005 | g0102 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0271 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03195 | hp2 | a0002 | c0003 | t0001 | g0010 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03225 | hp1 | a0001 | c0005 | t0001 | g0098 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03453 | hp1 | a0002 | c0004 | t0001 | g0086 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03486 | hp1 | a0002 | c0003 | t0005 | g0099 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0116 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03492 | hp2 | a0002 | c0003 | t0001 | g0119 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03516 | hp1 | a0002 | c0013 | t0001 | g0032 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03540 | hp2 | a0006 | c0014 | t0001 | g0194 | AFR | GWD | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0292 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0313 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0240 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03831 | hp1 | a0002 | c0003 | t0001 | g0092 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0122 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0284 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04184 | hp1 | a0002 | c0003 | t0001 | g0110 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04204 | hp1 | a0002 | c0003 | t0001 | g0091 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04228 | hp1 | a0004 | c0009 | t0001 | g0195 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG04228 | hp2 | a0009 | c0017 | t0001 | g0108 | SAS | STU | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | CHB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | CHB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18906 | hp1 | a0002 | c0004 | t0001 | g0084 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18944 | hp2 | a0001 | c0008 | t0001 | g0300 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18956 | hp2 | a0001 | c0008 | t0001 | g0301 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18968 | hp1 | a0003 | c0007 | t0003 | g0078 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18971 | hp1 | a0003 | c0007 | t0003 | g0080 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18989 | hp2 | a0005 | c0010 | t0002 | g0090 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19005 | hp2 | a0001 | c0002 | t0008 | g0287 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19010 | hp1 | a0007 | c0016 | t0001 | g0243 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19011 | hp1 | a0008 | c0012 | t0003 | g0132 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19055 | hp1 | a0001 | c0001 | t0009 | g0188 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19060 | hp1 | a0002 | c0003 | t0001 | g0104 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19083 | hp2 | a0003 | c0007 | t0003 | g0079 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA19240 | hp2 | a0001 | c0002 | t0006 | g0004 | AFR | YRI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20129 | hp1 | a0002 | c0004 | t0001 | g0001 | AFR | ASW | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | ASW | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0227 | EUR | TSI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20805 | hp2 | a0002 | c0003 | t0001 | g0123 | EUR | TSI | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20905 | hp1 | a0001 | c0002 | t0013 | g0238 | SAS | GIH | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | GIH | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG01123 | hp2 | a0002 | c0003 | t0001 | g0118 | AMR | CLM | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02109 | hp1 | a0001 | c0002 | t0006 | g0003 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02486 | hp1 | a0002 | c0004 | t0001 | g0085 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG02559 | hp2 | a0001 | c0011 | t0001 | g0071 | AFR | ACB | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG03471 | hp2 | a0001 | c0005 | t0001 | g0097 | AFR | MSL | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | USA | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | USA | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | USA | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | USA | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | LWK | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0259 | REF | REF | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
homoSapiens_grch38 | hp1 | a0002 | c0015 | t0007 | g0267 | REF | REF | EXD1_chr15_41177728_41235757 | EXD1 | chr15 | 41177728 | 41235757 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41184011
|
T | C | 7 | a0001a0003a0004others(4): Show | 275 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
missense_variant | MODERATE | c.1639A>G | p.Thr547Ala | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1971/3254 | 1639/1719 | 547/572 | chr15 | 41184011 | ||
chr15:41184130
|
T | C | 1 | a0007 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.1520A>G | p.Gln507Arg | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1852/3254 | 1520/1719 | 507/572 | chr15 | 41184130 | ||
chr15:41184224
|
C | G | 1 | a0008 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.1426G>C | p.Gly476Arg | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1758/3254 | 1426/1719 | 476/572 | chr15 | 41184224 | ||
chr15:41184274
|
C | G | 1 | a0006 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1376G>C | p.Gly459Ala | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1708/3254 | 1376/1719 | 459/572 | chr15 | 41184274 | ||
chr15:41184535
|
C | T | 1 | a0005 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.1115G>A | p.Arg372His | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1447/3254 | 1115/1719 | 372/572 | chr15 | 41184535 | ||
chr15:41191561
|
T | C | 1 | a0009 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.745A>G | p.Met249Val | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/12 | 1077/3254 | 745/1719 | 249/572 | chr15 | 41191561 | ||
chr15:41195839
|
C | T | 1 | a0004 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.656G>A | p.Arg219His | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/12 | 988/3254 | 656/1719 | 219/572 | chr15 | 41195839 | ||
chr15:41215804
|
T | G | 1 | a0003 | 3 | NA18968.hp1 NA18971.hp1 NA19083.hp2 |
missense_variant | MODERATE | c.418A>C | p.Asn140His | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/12 | 750/3254 | 418/1719 | 140/572 | chr15 | 41215804 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41184267
|
G | A | 9 | a0001c0001a0001c0005a0002c0003others(6): Show | 186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
synonymous_variant | LOW | c.1383C>T | p.Thr461Thr | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 1715/3254 | 1383/1719 | 461/572 | chr15 | 41184267 | ||
chr15:41190033
|
T | C | 1 | a0001c0006 | 3 | HG00323.hp2 HG01433.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.960A>G | p.Ala320Ala | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/12 | 1292/3254 | 960/1719 | 320/572 | chr15 | 41190033 | ||
chr15:41191442
|
C | T | 1 | a0002c0004 | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.864G>A | p.Gln288Gln | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/12 | 1196/3254 | 864/1719 | 288/572 | chr15 | 41191442 | ||
chr15:41191484
|
A | G | 6 | a0001c0001a0001c0011a0002c0013others(3): Show | 140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
synonymous_variant | LOW | c.822T>C | p.Pro274Pro | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/12 | 1154/3254 | 822/1719 | 274/572 | chr15 | 41191484 | ||
chr15:41226495
|
G | A | 1 | a0001c0008 | 2 | NA18944.hp2 NA18956.hp2 |
synonymous_variant | LOW | c.81C>T | p.Phe27Phe | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/12 | 413/3254 | 81/1719 | 27/572 | chr15 | 41226495 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41183051
|
C | G | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | 316 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*880G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 880 | chr15 | 41183051 | |||||
chr15:41183053
|
A | C | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*878T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 878 | chr15 | 41183053 | |||||
chr15:41183158
|
C | T | 3 | a0001c0001t0003a0003c0007t0003a0008c0012t0003 | 40 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*773G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 773 | chr15 | 41183158 | |||||
chr15:41183167
|
G | A | 1 | a0001c0002t0010 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 764 | chr15 | 41183167 | |||||
chr15:41183273
|
G | C | 4 | a0001c0001t0003a0001c0001t0004a0003c0007t0003others(1): Show | 62 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*658C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 658 | chr15 | 41183273 | |||||
chr15:41183332
|
T | G | 1 | a0002c0003t0011 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*599A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 599 | chr15 | 41183332 | |||||
chr15:41183460
|
T | TA | 3 | a0001c0001t0002a0001c0002t0002a0005c0010t0002 | 65 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*470dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 470 | chr15 | 41183460 | |||||
chr15:41183521
|
T | C | 1 | a0001c0002t0012 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*410A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 410 | chr15 | 41183521 | |||||
chr15:41183635
|
A | T | 1 | a0001c0002t0008 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 296 | chr15 | 41183635 | |||||
chr15:41183758
|
T | G | 1 | a0002c0003t0005 | 4 | HG02055.hp1 HG02258.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*173A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 173 | chr15 | 41183758 | |||||
chr15:41183819
|
T | C | 1 | a0001c0002t0013 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 112 | chr15 | 41183819 | |||||
chr15:41183903
|
T | C | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*28A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 12/12 | 28 | chr15 | 41183903 | |||||
chr15:41226581
|
T | C | 1 | a0001c0002t0014 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/12 | 6 | chr15 | 41226581 | |||||
chr15:41230653
|
C | A | 1 | a0001c0001t0015 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-228G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/12 | 4078 | chr15 | 41230653 | |||||
chr15:41230741
|
A | T | 1 | a0001c0002t0006 | 2 | HG02109.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-316T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/12 | 4166 | chr15 | 41230741 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41184658
|
C | CT | 142 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(139): Show | 143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1057-66dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184658 | ||||||
chr15:41184658
|
C | CTT | 130 | a0001c0001t0002g0183a0001c0001t0003g0031a0001c0002t0001g0041others(127): Show | 130 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1057-67_1057-66dup others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184658 | ||||||
chr15:41184677
|
T | C | 269 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(266): Show | 270 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.1057-84A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184677 | ||||||
chr15:41184678
|
G | A | 3 | a0001c0001t0002g0133a0001c0001t0002g0166a0001c0001t0002g0181 | 3 | HG01884.hp1 HG02055.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1057-85C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184678 | ||||||
chr15:41184718
|
G | A | 1 | a0002c0004t0001g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1057-125C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184718 | ||||||
chr15:41184816
|
A | G | 274 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(271): Show | 275 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.1057-223T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184816 | ||||||
chr15:41184846
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1057-253G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184846 | ||||||
chr15:41184889
|
C | G | 1 | a0001c0001t0002g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1057-296G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184889 | ||||||
chr15:41184935
|
C | T | 130 | a0001c0002t0001g0041a0001c0002t0001g0111a0001c0002t0001g0112others(127): Show | 130 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1057-342G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184935 | ||||||
chr15:41184945
|
A | C | 269 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(266): Show | 270 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.1057-352T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184945 | ||||||
chr15:41184952
|
G | A | 1 | a0001c0001t0003g0042 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1057-359C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41184952 | ||||||
chr15:41185009
|
A | T | 2 | a0001c0001t0002g0166a0001c0001t0002g0181 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1057-416T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185009 | ||||||
chr15:41185095
|
C | A | 1 | a0001c0001t0004g0012 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1057-502G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185095 | ||||||
chr15:41185107
|
G | T | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1057-514C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185107 | ||||||
chr15:41185143
|
T | C | 2 | a0002c0003t0001g0115a0002c0003t0001g0120 | 2 | HG00639.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1057-550A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185143 | ||||||
chr15:41185263
|
A | AT | 306 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.1057-671dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185263 | ||||||
chr15:41185336
|
T | TTTTTG | 60 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(57): Show | 61 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1057-748_1057-744d others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185336 | ||||||
chr15:41185357
|
A | T | 306 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.1057-764T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185357 | ||||||
chr15:41185361
|
T | G | 1 | a0001c0001t0003g0060 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1057-768A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185361 | ||||||
chr15:41185570
|
G | C | 1 | a0001c0001t0003g0037 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1057-977C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185570 | ||||||
chr15:41185615
|
G | A | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-1022C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185615 | ||||||
chr15:41185616
|
C | T | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-1023G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185616 | ||||||
chr15:41185628
|
G | A | 1 | a0001c0002t0001g0313 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1057-1035C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185628 | ||||||
chr15:41185845
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0167 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1057-1252C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41185845 | ||||||
chr15:41186150
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1057-1557C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186150 | ||||||
chr15:41186240
|
G | A | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 139 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.1057-1647C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186240 | ||||||
chr15:41186403
|
T | C | 268 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(265): Show | 269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1057-1810A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186403 | ||||||
chr15:41186470
|
C | CA | 70 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(67): Show | 71 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.1057-1878dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | ||||||
chr15:41186470
|
C | CAA | 11 | a0001c0001t0002g0149a0001c0001t0002g0151a0001c0001t0002g0165others(8): Show | 12 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1057-1879_1057-187 others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | ||||||
chr15:41186470
|
C | CAAAAAAA others(4): Show |
6 | a0001c0002t0001g0206a0001c0002t0001g0270a0001c0002t0001g0271others(3): Show | 6 | HG01891.hp2 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-1888_1057-187 others(15): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | ||||||
chr15:41186470
|
C | CAAAAAAA others(5): Show |
79 | a0001c0002t0001g0041a0001c0002t0001g0111a0001c0002t0001g0191others(76): Show | 79 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1057-1889_1057-187 others(16): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | ||||||
chr15:41186470
|
C | CAAAAAAA others(6): Show |
40 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0128others(37): Show | 40 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1057-1890_1057-187 others(17): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | ||||||
chr15:41186470
|
C | CAAAAAAA others(7): Show |
3 | a0001c0002t0001g0239a0001c0002t0001g0261a0001c0002t0008g0287 | 3 | HG01109.hp2 HG02148.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1057-1891_1057-187 others(18): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | ||||||
chr15:41186470
|
C | CAAAAAAA others(8): Show |
1 | a0001c0002t0001g0212 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1057-1892_1057-187 others(19): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | ||||||
chr15:41186470
|
C | CAAAAAAA others(9): Show |
1 | a0001c0002t0001g0259 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1057-1893_1057-187 others(20): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | ||||||
chr15:41186470
|
C | CAAAAAAA others(10): Show |
1 | a0001c0002t0001g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1057-1894_1057-187 others(21): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186470 | ||||||
chr15:41186511
|
G | T | 5 | a0001c0005t0001g0007a0001c0005t0001g0008a0001c0005t0001g0096others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057-1918C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186511 | ||||||
chr15:41186878
|
G | A | 2 | a0001c0001t0003g0040a0001c0001t0003g0061 | 2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1057-2285C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186878 | ||||||
chr15:41186889
|
T | C | 6 | a0001c0001t0002g0138a0001c0001t0002g0144a0001c0001t0002g0145others(3): Show | 6 | HG01496.hp2 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-2296A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186889 | ||||||
chr15:41186890
|
TTTTC | T | 6 | a0001c0001t0002g0138a0001c0001t0002g0144a0001c0001t0002g0145others(3): Show | 6 | HG01496.hp2 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-2301_1057-229 others(8): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186890 | ||||||
chr15:41186894
|
C | CT | 51 | a0001c0001t0002g0089a0001c0001t0002g0130a0001c0001t0002g0131others(48): Show | 51 | HG00408.hp1 HG01167.hp2 HG01169.hp2 others(48): Show |
intron_variant | MODIFIER | c.1057-2302dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186894 | ||||||
chr15:41186894
|
C | T | 1 | a0001c0001t0009g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1057-2301G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186894 | ||||||
chr15:41186988
|
G | A | 5 | a0001c0005t0001g0007a0001c0005t0001g0008a0001c0005t0001g0096others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057-2395C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41186988 | ||||||
chr15:41187020
|
C | G | 184 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1057-2427G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187020 | ||||||
chr15:41187027
|
G | A | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-2434C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187027 | ||||||
chr15:41187385
|
C | T | 1 | a0001c0002t0008g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1056+2552G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187385 | ||||||
chr15:41187782
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1056+2155C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187782 | ||||||
chr15:41187857
|
A | C | 1 | a0001c0002t0001g0219 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1056+2080T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187857 | ||||||
chr15:41187965
|
G | C | 5 | a0001c0005t0001g0007a0001c0005t0001g0008a0001c0005t0001g0096others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056+1972C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187965 | ||||||
chr15:41187971
|
C | T | 29 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1056+1966G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41187971 | ||||||
chr15:41188010
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0167 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1056+1927G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188010 | ||||||
chr15:41188013
|
C | T | 266 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(263): Show | 267 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.1056+1924G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188013 | ||||||
chr15:41188015
|
CA | C | 21 | a0001c0001t0002g0089a0001c0001t0002g0130a0001c0001t0002g0133others(18): Show | 21 | HG01175.hp1 HG01358.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1056+1921delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188015 | ||||||
chr15:41188015
|
CAA | C | 171 | a0001c0001t0002g0002a0001c0001t0002g0131a0001c0001t0002g0134others(168): Show | 172 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.1056+1920_1056+192 others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188015 | ||||||
chr15:41188015
|
CAAA | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG01515.hp1 HG01943.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1056+1919_1056+192 others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188015 | ||||||
chr15:41188015
|
CAAAA | C | 92 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1056+1918_1056+192 others(8): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188015 | ||||||
chr15:41188079
|
G | T | 3 | a0001c0002t0012g0265a0001c0002t0014g0094a0006c0014t0001g0194 | 3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1056+1858C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188079 | ||||||
chr15:41188194
|
A | C | 315 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(312): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.1056+1743T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188194 | ||||||
chr15:41188217
|
C | T | 1 | a0006c0014t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1056+1720G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188217 | ||||||
chr15:41188265
|
C | T | 2 | a0002c0004t0001g0085a0002c0004t0001g0086 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1056+1672G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188265 | ||||||
chr15:41188342
|
C | G | 1 | a0002c0003t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1056+1595G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188342 | ||||||
chr15:41188350
|
C | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1056+1587G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188350 | ||||||
chr15:41188462
|
G | A | 7 | a0002c0004t0001g0001a0002c0004t0001g0006a0002c0004t0001g0083others(4): Show | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1056+1475C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188462 | ||||||
chr15:41188496
|
G | A | 121 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1056+1441C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188496 | ||||||
chr15:41188551
|
C | T | 28 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0103others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1056+1386G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188551 | ||||||
chr15:41188600
|
C | T | 64 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(61): Show | 64 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1056+1337G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188600 | ||||||
chr15:41188625
|
T | G | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1056+1312A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188625 | ||||||
chr15:41188644
|
G | A | 5 | a0001c0001t0004g0029a0001c0001t0004g0045a0001c0001t0004g0055others(2): Show | 5 | HG02257.hp1 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1056+1293C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188644 | ||||||
chr15:41188682
|
G | A | 1 | a0002c0004t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1056+1255C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188682 | ||||||
chr15:41188698
|
C | G | 1 | a0001c0002t0001g0292 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1056+1239G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188698 | ||||||
chr15:41188782
|
C | T | 1 | a0002c0003t0001g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1056+1155G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188782 | ||||||
chr15:41188803
|
CT | C | 168 | a0001c0001t0001g0018a0001c0001t0002g0002a0001c0001t0002g0089others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1056+1133delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188803 | ||||||
chr15:41188803
|
CTT | C | 9 | a0001c0001t0003g0034a0001c0002t0001g0041a0001c0002t0001g0196others(6): Show | 9 | HG01070.hp1 HG01192.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1056+1132_1056+113 others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188803 | ||||||
chr15:41188910
|
C | G | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1056+1027G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188910 | ||||||
chr15:41188930
|
G | C | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+1007C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188930 | ||||||
chr15:41188990
|
G | T | 7 | a0002c0003t0001g0114a0002c0003t0001g0115a0002c0003t0001g0120others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1056+947C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41188990 | ||||||
chr15:41189056
|
A | G | 130 | a0001c0002t0001g0041a0001c0002t0001g0111a0001c0002t0001g0112others(127): Show | 130 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1056+881T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189056 | ||||||
chr15:41189222
|
A | T | 135 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0143others(132): Show | 135 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1056+715T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189222 | ||||||
chr15:41189241
|
G | A | 1 | a0002c0003t0001g0120 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1056+696C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189241 | ||||||
chr15:41189326
|
C | T | 1 | a0001c0002t0001g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1056+611G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189326 | ||||||
chr15:41189408
|
A | G | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1056+529T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189408 | ||||||
chr15:41189478
|
A | G | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+459T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189478 | ||||||
chr15:41189550
|
T | C | 4 | a0001c0001t0002g0138a0001c0001t0002g0145a0001c0001t0002g0155others(1): Show | 4 | HG01891.hp1 HG03041.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+387A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189550 | ||||||
chr15:41189713
|
T | C | 1 | a0007c0016t0001g0243 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1056+224A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189713 | ||||||
chr15:41189732
|
TAGAC | T | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1056+201_1056+204d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189732 | ||||||
chr15:41189807
|
C | T | 1 | a0001c0002t0001g0274 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1056+130G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189807 | ||||||
chr15:41189815
|
A | G | 139 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1056+122T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 11/11 | chr15 | 41189815 | ||||||
chr15:41190187
|
G | A | 1 | a0001c0002t0001g0197 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.865-59C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190187 | ||||||
chr15:41190267
|
C | T | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-139G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190267 | ||||||
chr15:41190367
|
A | T | 2 | a0001c0001t0003g0034a0001c0001t0003g0052 | 2 | NA18957.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.865-239T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190367 | ||||||
chr15:41190586
|
C | A | 13 | a0001c0002t0001g0232a0001c0002t0001g0234a0001c0002t0001g0239others(10): Show | 13 | HG01109.hp2 HG01123.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.865-458G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190586 | ||||||
chr15:41190602
|
T | C | 269 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(266): Show | 270 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.865-474A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190602 | ||||||
chr15:41190618
|
C | T | 1 | a0002c0003t0001g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.865-490G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190618 | ||||||
chr15:41190819
|
G | A | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.864+623C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190819 | ||||||
chr15:41190833
|
A | C | 1 | a0001c0005t0001g0097 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.864+609T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190833 | ||||||
chr15:41190898
|
GTTTA | G | 303 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.864+540_864+543del others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190898 | ||||||
chr15:41190906
|
A | G | 29 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.864+536T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41190906 | ||||||
chr15:41191002
|
C | T | 1 | a0001c0002t0001g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.864+440G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191002 | ||||||
chr15:41191053
|
G | A | 1 | a0001c0002t0001g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.864+389C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191053 | ||||||
chr15:41191336
|
A | G | 1 | a0002c0003t0001g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.864+106T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191336 | ||||||
chr15:41191425
|
A | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.864+17T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191425 | ||||||
chr15:41191433
|
T | TA | 307 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(304): Show | 308 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(305): Show |
splice_region_variant&intron_variant | LOW | c.864+8dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191433 | ||||||
chr15:41191438
|
C | T | 315 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(312): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
splice_region_variant&intron_variant | LOW | c.864+4G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 10/11 | chr15 | 41191438 | ||||||
chr15:41191803
|
G | A | 6 | a0001c0002t0001g0213a0001c0002t0001g0224a0001c0002t0001g0315others(3): Show | 6 | HG00609.hp2 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-218C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41191803 | ||||||
chr15:41191816
|
G | A | 1 | a0001c0001t0004g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.721-231C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41191816 | ||||||
chr15:41192070
|
T | C | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-485A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192070 | ||||||
chr15:41192089
|
C | A | 182 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.721-504G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192089 | ||||||
chr15:41192116
|
C | T | 28 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0136others(25): Show | 28 | HG00408.hp1 HG01496.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.721-531G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192116 | ||||||
chr15:41192130
|
C | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-545G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192130 | ||||||
chr15:41192248
|
C | A | 1 | a0001c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.721-663G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192248 | ||||||
chr15:41192479
|
T | C | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-894A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192479 | ||||||
chr15:41192506
|
A | C | 1 | a0001c0001t0002g0169 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.721-921T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192506 | ||||||
chr15:41192592
|
GCAT | G | 9 | a0001c0002t0001g0203a0001c0002t0001g0204a0001c0002t0001g0209others(6): Show | 9 | HG01109.hp2 HG01243.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.721-1010_721-1008d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | ||||||
chr15:41192592
|
GCATT | G | 33 | a0001c0002t0001g0196a0001c0002t0001g0198a0001c0002t0001g0199others(30): Show | 33 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.721-1011_721-1008d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | ||||||
chr15:41192592
|
GCATTT | G | 71 | a0001c0002t0001g0041a0001c0002t0001g0111a0001c0002t0001g0112others(68): Show | 71 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.721-1012_721-1008d others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | ||||||
chr15:41192592
|
GCATTTT | G | 6 | a0001c0002t0001g0205a0001c0002t0001g0282a0001c0002t0001g0284others(3): Show | 6 | HG00673.hp2 HG03098.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-1013_721-1008d others(8): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | ||||||
chr15:41192592
|
GCATTTTT others(15): Show |
G | 1 | a0001c0001t0002g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.721-1029_721-1008d others(24): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192592 | ||||||
chr15:41192593
|
C | T | 7 | a0001c0002t0001g0212a0001c0002t0001g0242a0001c0002t0001g0244others(4): Show | 7 | HG00558.hp2 HG02523.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.721-1008G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192593 | ||||||
chr15:41192594
|
A | ATTTT | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0020others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-1013_721-1010d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | ||||||
chr15:41192594
|
AT | A | 19 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0052others(16): Show | 20 | HG01106.hp1 HG01123.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1010delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | ||||||
chr15:41192594
|
ATT | A | 40 | a0001c0001t0003g0034a0001c0001t0003g0042a0001c0001t0003g0043others(37): Show | 40 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.721-1011_721-1010d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | ||||||
chr15:41192594
|
ATTT | A | 19 | a0001c0001t0003g0026a0001c0001t0003g0033a0001c0001t0003g0035others(16): Show | 19 | HG00099.hp1 HG00558.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.721-1012_721-1010d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | ||||||
chr15:41192594
|
ATTTTTTT others(3): Show |
A | 1 | a0002c0004t0001g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.721-1019_721-1010d others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | ||||||
chr15:41192594
|
ATTTTTTT others(6): Show |
A | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-1022_721-1010d others(15): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | ||||||
chr15:41192594
|
ATTTTTTT others(14): Show |
A | 2 | a0001c0001t0002g0089a0001c0001t0002g0180 | 2 | HG02027.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.721-1030_721-1010d others(23): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | ||||||
chr15:41192594
|
ATTTTTTT others(15): Show |
A | 60 | a0001c0001t0002g0002a0001c0001t0002g0130a0001c0001t0002g0133others(57): Show | 61 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.721-1031_721-1010d others(24): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | ||||||
chr15:41192594
|
ATTTTTTT others(16): Show |
A | 2 | a0001c0005t0001g0007a0001c0005t0001g0008 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.721-1032_721-1010d others(25): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192594 | ||||||
chr15:41192596
|
T | A | 2 | a0001c0002t0001g0208a0001c0002t0001g0269 | 2 | HG03239.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.721-1011A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192596 | ||||||
chr15:41192597
|
T | A | 9 | a0001c0002t0001g0203a0001c0002t0001g0204a0001c0002t0001g0209others(6): Show | 9 | HG01109.hp2 HG01243.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.721-1012A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192597 | ||||||
chr15:41192598
|
T | A | 33 | a0001c0002t0001g0196a0001c0002t0001g0198a0001c0002t0001g0199others(30): Show | 33 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.721-1013A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192598 | ||||||
chr15:41192599
|
T | A | 71 | a0001c0002t0001g0041a0001c0002t0001g0111a0001c0002t0001g0112others(68): Show | 71 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.721-1014A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192599 | ||||||
chr15:41192600
|
T | A | 6 | a0001c0002t0001g0205a0001c0002t0001g0282a0001c0002t0001g0284others(3): Show | 6 | HG00673.hp2 HG03098.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-1015A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192600 | ||||||
chr15:41192606
|
T | G | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.721-1021A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192606 | ||||||
chr15:41192611
|
T | G | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.721-1026A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192611 | ||||||
chr15:41192616
|
T | A | 1 | a0001c0001t0002g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.721-1031A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192616 | ||||||
chr15:41192689
|
A | G | 2 | a0001c0001t0002g0162a0001c0001t0002g0167 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.721-1104T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192689 | ||||||
chr15:41192737
|
C | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-1152G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192737 | ||||||
chr15:41192790
|
AT | A | 156 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(153): Show | 157 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.721-1206delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192790 | ||||||
chr15:41192790
|
ATT | A | 104 | a0001c0001t0002g0150a0001c0001t0002g0166a0001c0001t0002g0171others(101): Show | 104 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.721-1207_721-1206d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192790 | ||||||
chr15:41192842
|
C | A | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-1257G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192842 | ||||||
chr15:41192952
|
A | G | 18 | a0001c0002t0001g0232a0001c0002t0001g0234a0001c0002t0001g0239others(15): Show | 18 | HG00609.hp1 HG01109.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-1367T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41192952 | ||||||
chr15:41193011
|
C | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.721-1426G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193011 | ||||||
chr15:41193028
|
T | A | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.721-1443A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193028 | ||||||
chr15:41193423
|
A | G | 4 | a0002c0003t0005g0099a0002c0003t0005g0100a0002c0003t0005g0101others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-1838T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193423 | ||||||
chr15:41193499
|
G | A | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.721-1914C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193499 | ||||||
chr15:41193745
|
C | CA | 139 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(136): Show | 140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.720+2029dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193745 | ||||||
chr15:41193999
|
A | AT | 59 | a0001c0002t0001g0112a0001c0002t0001g0128a0001c0002t0001g0198others(56): Show | 59 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.720+1775dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193999 | ||||||
chr15:41193999
|
AT | A | 71 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(68): Show | 71 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.720+1775delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193999 | ||||||
chr15:41193999
|
ATT | A | 52 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(49): Show | 53 | HG00408.hp1 HG01081.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.720+1774_720+1775d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41193999 | ||||||
chr15:41194046
|
C | G | 2 | a0001c0001t0003g0057a0001c0001t0003g0058 | 2 | HG02027.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.720+1729G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194046 | ||||||
chr15:41194059
|
T | C | 133 | a0001c0002t0001g0041a0001c0002t0001g0111a0001c0002t0001g0112others(130): Show | 133 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.720+1716A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194059 | ||||||
chr15:41194081
|
A | G | 274 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(271): Show | 275 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.720+1694T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194081 | ||||||
chr15:41194195
|
T | C | 139 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.720+1580A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194195 | ||||||
chr15:41194226
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.720+1549A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194226 | ||||||
chr15:41194241
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0002g0181 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.720+1534C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194241 | ||||||
chr15:41194306
|
G | A | 29 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.720+1469C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194306 | ||||||
chr15:41194319
|
G | A | 1 | a0001c0002t0001g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.720+1456C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194319 | ||||||
chr15:41194334
|
A | C | 1 | a0002c0003t0001g0092 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.720+1441T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194334 | ||||||
chr15:41194452
|
G | C | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+1323C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194452 | ||||||
chr15:41194573
|
A | C | 7 | a0002c0004t0001g0001a0002c0004t0001g0006a0002c0004t0001g0083others(4): Show | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+1202T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194573 | ||||||
chr15:41194709
|
A | G | 2 | a0001c0002t0001g0207a0001c0002t0001g0209 | 2 | HG01081.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.720+1066T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194709 | ||||||
chr15:41194781
|
A | G | 139 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.720+994T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194781 | ||||||
chr15:41194792
|
G | A | 6 | a0001c0002t0001g0250a0001c0002t0001g0251a0001c0002t0001g0252others(3): Show | 6 | HG00323.hp2 HG00738.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+983C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41194792 | ||||||
chr15:41195231
|
TAAC | T | 29 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.720+541_720+543del others(3): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195231 | ||||||
chr15:41195285
|
C | T | 4 | a0001c0001t0002g0141a0001c0001t0002g0150a0001c0001t0002g0151others(1): Show | 4 | NA18939.hp1 NA18956.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+490G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195285 | ||||||
chr15:41195318
|
C | T | 1 | a0001c0001t0003g0054 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.720+457G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195318 | ||||||
chr15:41195348
|
T | C | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.720+427A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195348 | ||||||
chr15:41195584
|
G | A | 2 | a0001c0001t0003g0038a0001c0001t0003g0048 | 2 | NA18945.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.720+191C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195584 | ||||||
chr15:41195663
|
C | CA | 174 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.720+111dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195663 | ||||||
chr15:41195663
|
CA | C | 8 | a0001c0002t0001g0227a0001c0002t0001g0237a0001c0002t0001g0240others(5): Show | 8 | HG02451.hp2 HG02922.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+111delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195663 | ||||||
chr15:41195697
|
C | T | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+78G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195697 | ||||||
chr15:41195736
|
G | C | 29 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.720+39C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 9/11 | chr15 | 41195736 | ||||||
chr15:41196119
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.535-82G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196119 | ||||||
chr15:41196120
|
G | A | 1 | a0006c0014t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.535-83C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196120 | ||||||
chr15:41196207
|
C | T | 139 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.535-170G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196207 | ||||||
chr15:41196312
|
A | AT | 59 | a0001c0001t0003g0044a0001c0001t0004g0012a0001c0001t0004g0029others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.535-276dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196312 | ||||||
chr15:41196312
|
A | ATT | 58 | a0001c0001t0001g0018a0001c0001t0003g0011a0001c0001t0003g0026others(55): Show | 58 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.535-277_535-276dup others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196312 | ||||||
chr15:41196312
|
A | ATTT | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG02027.hp1 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.535-278_535-276dup others(3): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196312 | ||||||
chr15:41196312
|
ATTTTT | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(59): Show | 63 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.535-280_535-276del others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196312 | ||||||
chr15:41196628
|
A | G | 1 | a0001c0001t0003g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.535-591T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196628 | ||||||
chr15:41196753
|
C | G | 315 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(312): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.535-716G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196753 | ||||||
chr15:41196940
|
C | T | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-903G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41196940 | ||||||
chr15:41197105
|
G | A | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-1068C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197105 | ||||||
chr15:41197293
|
T | C | 1 | a0001c0001t0003g0050 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.535-1256A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197293 | ||||||
chr15:41197368
|
A | G | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-1331T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197368 | ||||||
chr15:41197376
|
T | C | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-1339A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197376 | ||||||
chr15:41197388
|
C | T | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-1351G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197388 | ||||||
chr15:41197657
|
T | A | 1 | a0001c0002t0001g0222 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.535-1620A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197657 | ||||||
chr15:41197707
|
A | G | 315 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(312): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.535-1670T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197707 | ||||||
chr15:41197796
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.535-1759A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197796 | ||||||
chr15:41197814
|
T | C | 141 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(138): Show | 142 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.535-1777A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197814 | ||||||
chr15:41197835
|
A | C | 1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.535-1798T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197835 | ||||||
chr15:41197836
|
G | T | 1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.535-1799C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197836 | ||||||
chr15:41197837
|
G | C | 65 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(62): Show | 65 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.535-1800C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197837 | ||||||
chr15:41197837
|
G | GGTTAAGC others(294): Show |
1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.535-1801_535-1800i others(303): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41197837 | ||||||
chr15:41198101
|
G | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0134a0001c0001t0002g0135others(30): Show | 34 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.535-2064C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198101 | ||||||
chr15:41198256
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.535-2219C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198256 | ||||||
chr15:41198291
|
C | T | 1 | a0001c0002t0001g0309 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.535-2254G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198291 | ||||||
chr15:41198335
|
G | A | 1 | a0001c0001t0004g0069 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.535-2298C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198335 | ||||||
chr15:41198344
|
G | A | 1 | a0001c0002t0001g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.535-2307C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198344 | ||||||
chr15:41198376
|
A | G | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-2339T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198376 | ||||||
chr15:41198473
|
C | G | 139 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 140 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.535-2436G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198473 | ||||||
chr15:41198490
|
A | T | 4 | a0001c0001t0003g0040a0001c0001t0003g0043a0001c0001t0003g0053others(1): Show | 4 | HG00544.hp1 HG00558.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-2453T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198490 | ||||||
chr15:41198491
|
A | T | 4 | a0001c0001t0003g0040a0001c0001t0003g0043a0001c0001t0003g0053others(1): Show | 4 | HG00544.hp1 HG00558.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-2454T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198491 | ||||||
chr15:41198637
|
C | T | 78 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 78 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.535-2600G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198637 | ||||||
chr15:41198657
|
C | G | 1 | a0001c0002t0008g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.535-2620G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198657 | ||||||
chr15:41198700
|
T | TA | 142 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(139): Show | 143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.535-2664dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198700 | ||||||
chr15:41198706
|
A | C | 1 | a0002c0004t0001g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.535-2669T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198706 | ||||||
chr15:41198708
|
A | T | 3 | a0001c0002t0001g0269a0001c0002t0001g0290a0001c0005t0001g0096 | 3 | HG02922.hp2 HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.535-2671T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198708 | ||||||
chr15:41198708
|
AT | A | 6 | a0001c0002t0001g0228a0002c0003t0001g0009a0002c0003t0001g0091others(3): Show | 6 | HG01070.hp2 HG01515.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-2672delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198708 | ||||||
chr15:41198709
|
T | A | 96 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.535-2672A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198709 | ||||||
chr15:41198710
|
T | A | 8 | a0001c0001t0004g0072a0001c0002t0014g0094a0002c0003t0001g0009others(5): Show | 8 | HG01515.hp1 HG02074.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.535-2673A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198710 | ||||||
chr15:41198782
|
T | C | 182 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.535-2745A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198782 | ||||||
chr15:41198829
|
T | C | 181 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.535-2792A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198829 | ||||||
chr15:41198862
|
C | T | 2 | a0001c0005t0001g0007a0001c0005t0001g0008 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.535-2825G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198862 | ||||||
chr15:41198879
|
G | T | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-2842C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41198879 | ||||||
chr15:41199248
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.535-3211C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199248 | ||||||
chr15:41199267
|
A | G | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-3230T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199267 | ||||||
chr15:41199334
|
C | A | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.535-3297G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199334 | ||||||
chr15:41199412
|
T | G | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-3375A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199412 | ||||||
chr15:41199458
|
A | G | 186 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.535-3421T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199458 | ||||||
chr15:41199595
|
ATATATAT | A | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.535-3565_535-3559d others(9): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199595 | ||||||
chr15:41199705
|
A | ATC | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.535-3670_535-3669d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199705 | ||||||
chr15:41199711
|
T | C | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-3674A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199711 | ||||||
chr15:41199728
|
A | ATC | 129 | a0001c0002t0001g0041a0001c0002t0001g0111a0001c0002t0001g0112others(126): Show | 129 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.535-3692_535-3691i others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199728 | ||||||
chr15:41199730
|
G | C | 276 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(273): Show | 277 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.535-3693C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199730 | ||||||
chr15:41199732
|
T | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-3695A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199732 | ||||||
chr15:41199737
|
ATG | A | 64 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(61): Show | 65 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.535-3702_535-3701d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199737 | ||||||
chr15:41199739
|
GTC | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-3704_535-3703d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199739 | ||||||
chr15:41199740
|
T | A | 201 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(198): Show | 201 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.535-3703A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199740 | ||||||
chr15:41199741
|
C | T | 201 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(198): Show | 201 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.535-3704G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199741 | ||||||
chr15:41199746
|
A | C | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3709T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199746 | ||||||
chr15:41199748
|
T | C | 201 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(198): Show | 201 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.535-3711A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199748 | ||||||
chr15:41199748
|
T | G | 64 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(61): Show | 65 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.535-3711A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199748 | ||||||
chr15:41199753
|
A | G | 2 | a0001c0002t0001g0203a0001c0002t0001g0204 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.535-3716T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199753 | ||||||
chr15:41199755
|
G | A | 64 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(61): Show | 65 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.535-3718C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199755 | ||||||
chr15:41199755
|
G | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-3718C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199755 | ||||||
chr15:41199757
|
T | TATATAAT others(74): Show |
1 | a0001c0002t0001g0259 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(83): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATAAT others(72): Show |
3 | a0001c0001t0003g0011a0001c0001t0003g0051a0001c0001t0003g0088 | 3 | NA18984.hp1 NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.535-3721_535-3720i others(81): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATAAT others(74): Show |
1 | a0001c0002t0001g0242 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.535-3721_535-3720i others(83): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATAAT others(37): Show |
2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3721_535-3720i others(46): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATAAT others(51): Show |
62 | a0001c0001t0003g0026a0001c0001t0003g0030a0001c0001t0003g0031others(59): Show | 62 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(60): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATAAT others(51): Show |
4 | a0001c0002t0001g0311a0001c0005t0001g0096a0001c0005t0001g0097others(1): Show | 4 | HG02922.hp2 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(60): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATAAT others(74): Show |
110 | a0001c0002t0001g0041a0001c0002t0001g0111a0001c0002t0001g0112others(107): Show | 110 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(83): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATAAT others(97): Show |
1 | a0001c0002t0001g0222 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(106): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATAAT others(97): Show |
14 | a0001c0002t0001g0208a0001c0002t0001g0224a0001c0002t0001g0233others(11): Show | 14 | HG00408.hp2 HG00544.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(106): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATAAT others(120): Show |
1 | a0001c0002t0001g0241 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(129): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATATC others(113): Show |
1 | a0001c0002t0001g0296 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.535-3721_535-3720i others(122): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATCAT others(44): Show |
1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(53): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATCAT others(42): Show |
61 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(58): Show | 62 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(51): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATCAT others(37): Show |
2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.535-3721_535-3720i others(46): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATGAT others(90): Show |
9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.535-3721_535-3720i others(99): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATGAT others(92): Show |
1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.535-3721_535-3720i others(101): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATGAT others(106): Show |
1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(115): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199757
|
T | TATATTAT others(97): Show |
1 | a0001c0002t0001g0292 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.535-3721_535-3720i others(106): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199757 | ||||||
chr15:41199759
|
C | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3722G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199759 | ||||||
chr15:41199764
|
A | G | 5 | a0001c0002t0001g0226a0001c0002t0001g0240a0001c0002t0001g0274others(2): Show | 5 | HG00639.hp2 HG02109.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.535-3727T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199764 | ||||||
chr15:41199766
|
G | C | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3729C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199766 | ||||||
chr15:41199768
|
T | C | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3731A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199768 | ||||||
chr15:41199777
|
C | G | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0189 | 3 | NA19005.hp1 NA19080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.535-3740G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199777 | ||||||
chr15:41199785
|
A | C | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-3748T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199785 | ||||||
chr15:41199811
|
T | A | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3774A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199811 | ||||||
chr15:41199812
|
C | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3775G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199812 | ||||||
chr15:41199820
|
G | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3783C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199820 | ||||||
chr15:41199822
|
T | TATA | 306 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.535-3788_535-3786d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199822 | ||||||
chr15:41199839
|
T | C | 2 | a0002c0003t0001g0010a0002c0003t0001g0095 | 2 | HG00642.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.535-3802A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199839 | ||||||
chr15:41199865
|
C | A | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3828G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199865 | ||||||
chr15:41199867
|
G | A | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-3830C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199867 | ||||||
chr15:41199897
|
A | G | 11 | a0001c0001t0002g0144a0001c0001t0002g0170a0001c0001t0002g0179others(8): Show | 11 | HG00609.hp1 HG02027.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-3860T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41199897 | ||||||
chr15:41200048
|
C | T | 9 | a0001c0002t0014g0094a0002c0004t0001g0001a0002c0004t0001g0006others(6): Show | 10 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-4011G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200048 | ||||||
chr15:41200085
|
G | T | 186 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.535-4048C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200085 | ||||||
chr15:41200092
|
G | A | 28 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.535-4055C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200092 | ||||||
chr15:41200137
|
G | A | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-4100C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200137 | ||||||
chr15:41200186
|
A | C | 1 | a0001c0002t0001g0272 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.535-4149T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200186 | ||||||
chr15:41200459
|
G | A | 1 | a0001c0001t0004g0045 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.535-4422C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200459 | ||||||
chr15:41200771
|
T | C | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.535-4734A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200771 | ||||||
chr15:41200815
|
T | C | 304 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.535-4778A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200815 | ||||||
chr15:41200879
|
A | AT | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 83 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.535-4843dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200879 | ||||||
chr15:41200943
|
G | A | 3 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310 | 3 | HG01943.hp1 HG01952.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.535-4906C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200943 | ||||||
chr15:41200945
|
C | A | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.535-4908G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41200945 | ||||||
chr15:41201116
|
T | G | 4 | a0001c0001t0003g0040a0001c0001t0003g0043a0001c0001t0003g0053others(1): Show | 4 | HG00544.hp1 HG00558.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-5079A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201116 | ||||||
chr15:41201162
|
C | T | 1 | a0001c0002t0002g0283 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.535-5125G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201162 | ||||||
chr15:41201259
|
C | G | 1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.535-5222G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201259 | ||||||
chr15:41201485
|
AT | A | 56 | a0001c0001t0002g0141a0001c0001t0002g0168a0001c0001t0002g0175others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.535-5449delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201485 | ||||||
chr15:41201485
|
ATT | A | 233 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 233 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.535-5450_535-5449d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201485 | ||||||
chr15:41201485
|
ATTT | A | 14 | a0001c0001t0002g0002a0001c0001t0002g0157a0001c0001t0002g0174others(11): Show | 15 | HG01081.hp1 HG01106.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.535-5451_535-5449d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201485 | ||||||
chr15:41201521
|
G | A | 64 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(61): Show | 64 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.535-5484C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201521 | ||||||
chr15:41201590
|
A | T | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-5553T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201590 | ||||||
chr15:41201909
|
T | C | 1 | a0002c0004t0001g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.535-5872A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41201909 | ||||||
chr15:41202066
|
G | A | 1 | a0005c0010t0002g0090 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.535-6029C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202066 | ||||||
chr15:41202088
|
C | G | 1 | a0001c0002t0001g0273 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.535-6051G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202088 | ||||||
chr15:41202148
|
T | TTA | 6 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(3): Show | 6 | HG00642.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.535-6113_535-6112d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202148 | ||||||
chr15:41202148
|
TTA | T | 129 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(126): Show | 130 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.535-6113_535-6112d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202148 | ||||||
chr15:41202153
|
T | C | 1 | a0001c0001t0002g0189 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.535-6116A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202153 | ||||||
chr15:41202155
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(59): Show | 63 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.535-6118A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202155 | ||||||
chr15:41202164
|
A | AT | 6 | a0001c0002t0001g0193a0001c0002t0001g0280a0001c0002t0001g0309others(3): Show | 6 | HG00597.hp2 HG01943.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-6128dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202164 | ||||||
chr15:41202164
|
A | T | 10 | a0001c0002t0001g0207a0001c0002t0001g0214a0001c0002t0001g0270others(7): Show | 10 | HG00639.hp2 HG01081.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-6127T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202164 | ||||||
chr15:41202166
|
A | AT | 26 | a0001c0002t0001g0041a0001c0002t0001g0128a0001c0002t0001g0196others(23): Show | 26 | HG00609.hp2 HG00673.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.535-6130dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202166 | ||||||
chr15:41202166
|
A | T | 135 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(132): Show | 136 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.535-6129T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202166 | ||||||
chr15:41202166
|
AT | A | 4 | a0001c0001t0002g0189a0001c0005t0001g0096a0001c0005t0001g0097others(1): Show | 4 | HG02922.hp2 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-6130delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202166 | ||||||
chr15:41202166
|
ATT | A | 12 | a0001c0001t0003g0033a0001c0001t0003g0039a0001c0001t0003g0042others(9): Show | 12 | HG01928.hp2 HG01975.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.535-6131_535-6130d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202166 | ||||||
chr15:41202168
|
T | A | 24 | a0001c0002t0001g0203a0001c0002t0001g0204a0002c0003t0001g0010others(21): Show | 24 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.535-6131A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202168 | ||||||
chr15:41202170
|
T | A | 3 | a0002c0003t0001g0103a0002c0003t0001g0117a0002c0003t0001g0126 | 3 | HG01975.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.535-6133A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202170 | ||||||
chr15:41202174
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.535-6137A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202174 | ||||||
chr15:41202185
|
T | A | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.535-6148A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202185 | ||||||
chr15:41202445
|
A | G | 1 | a0001c0002t0012g0265 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.535-6408T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202445 | ||||||
chr15:41202466
|
C | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-6429G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202466 | ||||||
chr15:41202475
|
C | CAT | 3 | a0001c0005t0001g0096a0001c0005t0001g0097a0001c0005t0001g0098 | 3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.535-6440_535-6439d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202475 | ||||||
chr15:41202566
|
T | C | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.535-6529A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202566 | ||||||
chr15:41202682
|
G | A | 3 | a0002c0003t0001g0114a0002c0003t0001g0124a0002c0003t0001g0127 | 3 | HG00099.hp2 HG01070.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.535-6645C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202682 | ||||||
chr15:41202713
|
C | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-6676G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202713 | ||||||
chr15:41202772
|
G | A | 16 | a0001c0001t0003g0011a0001c0001t0003g0030a0001c0001t0003g0031others(13): Show | 16 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.534+6729C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202772 | ||||||
chr15:41202825
|
C | T | 28 | a0001c0001t0002g0089a0001c0001t0002g0130a0001c0001t0002g0131others(25): Show | 28 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.534+6676G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202825 | ||||||
chr15:41202917
|
C | CA | 22 | a0001c0001t0002g0089a0001c0001t0002g0130a0001c0001t0002g0173others(19): Show | 22 | HG00673.hp2 HG01243.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.534+6583dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202917 | ||||||
chr15:41202917
|
CA | C | 9 | a0001c0001t0002g0163a0001c0001t0003g0034a0001c0002t0001g0193others(6): Show | 9 | HG00597.hp2 HG00609.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.534+6583delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202917 | ||||||
chr15:41202917
|
CAA | C | 32 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(29): Show | 33 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.534+6582_534+6583d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202917 | ||||||
chr15:41202918
|
A | T | 4 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0153others(1): Show | 4 | HG02040.hp1 NA18942.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+6583T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41202918 | ||||||
chr15:41203206
|
A | G | 308 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.534+6295T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203206 | ||||||
chr15:41203262
|
C | T | 29 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.534+6239G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203262 | ||||||
chr15:41203333
|
C | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.534+6168G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203333 | ||||||
chr15:41203542
|
A | G | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.534+5959T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203542 | ||||||
chr15:41203734
|
T | A | 40 | a0001c0005t0001g0107a0002c0003t0001g0009a0002c0003t0001g0010others(37): Show | 41 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.534+5767A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203734 | ||||||
chr15:41203825
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0167 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.534+5676C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203825 | ||||||
chr15:41203871
|
C | T | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.534+5630G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203871 | ||||||
chr15:41203876
|
C | T | 1 | a0001c0001t0004g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.534+5625G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203876 | ||||||
chr15:41203916
|
C | CA | 49 | a0001c0002t0001g0041a0001c0002t0001g0111a0001c0002t0001g0112others(46): Show | 49 | HG00323.hp2 HG00597.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.534+5584dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAA | 7 | a0001c0002t0001g0281a0001c0002t0001g0292a0002c0003t0001g0010others(4): Show | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+5583_534+5584d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAAA | 16 | a0001c0001t0003g0040a0001c0001t0003g0061a0001c0005t0001g0107others(13): Show | 16 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.534+5582_534+5584d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAAAA | 42 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(39): Show | 42 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.534+5581_534+5584d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAAAAA | 46 | a0001c0001t0002g0002a0001c0001t0002g0134a0001c0001t0002g0138others(43): Show | 47 | HG00673.hp1 HG01081.hp1 HG01257.hp2 others(44): Show |
intron_variant | MODIFIER | c.534+5580_534+5584d others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAAAAAA | 18 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0143others(15): Show | 18 | HG00408.hp1 HG01106.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+5579_534+5584d others(8): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(7): Show | 10 | HG01169.hp2 HG01433.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.534+5577_534+5584d others(10): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAAAAAAA others(2): Show |
18 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(15): Show | 18 | HG01175.hp2 HG02027.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+5576_534+5584d others(11): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(4): Show | 7 | HG01884.hp1 HG02071.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+5575_534+5584d others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0002g0168a0001c0001t0002g0181 | 2 | HG02055.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.534+5574_534+5584d others(13): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0014g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.534+5572_534+5584d others(15): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203916
|
CAAAAAAA others(5): Show |
C | 3 | a0002c0003t0001g0114a0002c0003t0001g0124a0002c0003t0001g0127 | 3 | HG00099.hp2 HG01070.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.534+5573_534+5584d others(14): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203916 | ||||||
chr15:41203973
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.534+5528G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41203973 | ||||||
chr15:41204068
|
C | A | 308 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.534+5433G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204068 | ||||||
chr15:41204141
|
G | A | 1 | a0001c0002t0012g0265 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.534+5360C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204141 | ||||||
chr15:41204226
|
C | T | 11 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(8): Show | 12 | HG01109.hp1 HG01243.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.534+5275G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204226 | ||||||
chr15:41204237
|
G | GACTCTGT others(6): Show |
1 | a0001c0001t0003g0075 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.534+5251_534+5263d others(15): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204237 | ||||||
chr15:41204247
|
C | CA | 33 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 33 | HG00642.hp1 HG00642.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.534+5253dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204247 | ||||||
chr15:41204247
|
C | CAAAAAAA others(294): Show |
1 | a0001c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.534+5253_534+5254i others(303): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204247 | ||||||
chr15:41204247
|
CA | C | 68 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0131others(65): Show | 69 | HG00408.hp1 HG00639.hp1 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.534+5253delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204247 | ||||||
chr15:41204320
|
G | A | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.534+5181C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204320 | ||||||
chr15:41204380
|
G | C | 1 | a0001c0002t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.534+5121C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204380 | ||||||
chr15:41204466
|
G | A | 21 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0136others(18): Show | 21 | HG00408.hp1 HG02040.hp1 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.534+5035C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204466 | ||||||
chr15:41204515
|
C | T | 54 | a0001c0002t0001g0113a0001c0002t0001g0191a0001c0002t0001g0192others(51): Show | 54 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.534+4986G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204515 | ||||||
chr15:41204530
|
A | G | 275 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(272): Show | 276 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.534+4971T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204530 | ||||||
chr15:41204759
|
C | CAT | 5 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(2): Show | 5 | HG01106.hp1 HG01515.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+4740_534+4741d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204759 | ||||||
chr15:41204797
|
G | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.534+4704C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204797 | ||||||
chr15:41204882
|
C | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.534+4619G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41204882 | ||||||
chr15:41205032
|
T | C | 1 | a0001c0002t0001g0262 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.534+4469A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205032 | ||||||
chr15:41205212
|
C | T | 3 | a0001c0002t0001g0193a0001c0002t0001g0219a0001c0002t0001g0220 | 3 | HG00597.hp2 HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.534+4289G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205212 | ||||||
chr15:41205229
|
T | C | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 141 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.534+4272A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205229 | ||||||
chr15:41205332
|
C | A | 142 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(139): Show | 143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.534+4169G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205332 | ||||||
chr15:41205387
|
G | A | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.534+4114C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205387 | ||||||
chr15:41205392
|
A | C | 1 | a0002c0003t0001g0009 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.534+4109T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205392 | ||||||
chr15:41205436
|
CTGTA | C | 142 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(139): Show | 143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.534+4061_534+4064d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205436 | ||||||
chr15:41205467
|
T | G | 1 | a0001c0002t0001g0269 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.534+4034A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205467 | ||||||
chr15:41205548
|
T | C | 2 | a0001c0002t0006g0003a0001c0002t0006g0004 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.534+3953A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205548 | ||||||
chr15:41205605
|
C | G | 142 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(139): Show | 143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.534+3896G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205605 | ||||||
chr15:41205702
|
GGAAGGAG others(9): Show |
G | 76 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(73): Show | 76 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.534+3783_534+3798d others(18): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205702 | ||||||
chr15:41205710
|
GGAAGGAG others(1): Show |
G | 64 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(61): Show | 65 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.534+3783_534+3790d others(10): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205710 | ||||||
chr15:41205718
|
A | G | 47 | a0001c0002t0014g0094a0001c0005t0001g0007a0001c0005t0001g0008others(44): Show | 48 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.534+3783T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205718 | ||||||
chr15:41205721
|
A | G | 7 | a0002c0004t0001g0001a0002c0004t0001g0006a0002c0004t0001g0083others(4): Show | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+3780T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205721 | ||||||
chr15:41205805
|
G | A | 1 | a0001c0002t0014g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.534+3696C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205805 | ||||||
chr15:41205853
|
G | T | 142 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(139): Show | 143 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.534+3648C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205853 | ||||||
chr15:41205879
|
C | CT | 18 | a0001c0001t0002g0141a0001c0001t0002g0150a0001c0001t0002g0151others(15): Show | 18 | HG00099.hp1 HG00673.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.534+3621dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205879 | ||||||
chr15:41205956
|
T | C | 2 | a0001c0001t0004g0069a0001c0001t0004g0070 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.534+3545A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205956 | ||||||
chr15:41205980
|
A | G | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.534+3521T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41205980 | ||||||
chr15:41206175
|
ACAGGAAA others(90): Show |
A | 1 | a0001c0002t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.534+3229_534+3325d others(99): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206175 | ||||||
chr15:41206261
|
G | C | 1 | a0001c0002t0001g0235 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.534+3240C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206261 | ||||||
chr15:41206474
|
GA | G | 7 | a0001c0001t0003g0074a0001c0002t0001g0212a0001c0002t0001g0227others(4): Show | 7 | HG00639.hp2 HG00738.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+3026delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206474 | ||||||
chr15:41206474
|
GAA | G | 62 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(59): Show | 62 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.534+3025_534+3026d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206474 | ||||||
chr15:41206474
|
GAAA | G | 77 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(74): Show | 78 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.534+3024_534+3026d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206474 | ||||||
chr15:41206618
|
C | CT | 119 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0128others(116): Show | 119 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.534+2882dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206618 | ||||||
chr15:41206618
|
C | CTT | 12 | a0001c0002t0001g0111a0001c0002t0001g0200a0001c0002t0001g0222others(9): Show | 12 | HG01175.hp1 HG02074.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.534+2881_534+2882d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206618 | ||||||
chr15:41206618
|
CTT | C | 6 | a0001c0001t0002g0153a0001c0001t0002g0181a0001c0001t0015g0316others(3): Show | 6 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+2881_534+2882d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206618 | ||||||
chr15:41206618
|
CTTT | C | 134 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(131): Show | 135 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.534+2880_534+2882d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206618 | ||||||
chr15:41206691
|
G | A | 1 | a0001c0002t0001g0295 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.534+2810C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206691 | ||||||
chr15:41206754
|
T | C | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.534+2747A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206754 | ||||||
chr15:41206756
|
G | A | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.534+2745C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206756 | ||||||
chr15:41206771
|
G | A | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.534+2730C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206771 | ||||||
chr15:41206870
|
G | T | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2631C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206870 | ||||||
chr15:41206890
|
G | T | 1 | a0001c0001t0003g0043 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.534+2611C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206890 | ||||||
chr15:41206929
|
CT | C | 39 | a0001c0002t0001g0113a0001c0002t0001g0214a0001c0002t0001g0244others(36): Show | 39 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.534+2571delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206929 | ||||||
chr15:41206929
|
CTT | C | 125 | a0001c0001t0001g0022a0001c0001t0002g0089a0001c0001t0002g0133others(122): Show | 125 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.534+2570_534+2571d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206929 | ||||||
chr15:41206929
|
CTTT | C | 131 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(128): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.534+2569_534+2571d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206929 | ||||||
chr15:41206929
|
CTTTT | C | 11 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0143others(8): Show | 11 | HG00099.hp1 HG01167.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+2568_534+2571d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206929 | ||||||
chr15:41206954
|
T | A | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2547A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206954 | ||||||
chr15:41206966
|
C | T | 52 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(49): Show | 52 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.534+2535G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206966 | ||||||
chr15:41206969
|
C | G | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2532G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206969 | ||||||
chr15:41206994
|
G | T | 5 | a0002c0004t0001g0001a0002c0004t0001g0006a0002c0004t0001g0083others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+2507C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41206994 | ||||||
chr15:41207082
|
A | C | 1 | a0001c0002t0001g0292 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.534+2419T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207082 | ||||||
chr15:41207097
|
C | T | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2404G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207097 | ||||||
chr15:41207102
|
G | T | 1 | a0001c0002t0001g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.534+2399C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207102 | ||||||
chr15:41207110
|
G | A | 1 | a0001c0002t0010g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.534+2391C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207110 | ||||||
chr15:41207151
|
G | A | 65 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(62): Show | 65 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.534+2350C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207151 | ||||||
chr15:41207358
|
A | T | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2143T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207358 | ||||||
chr15:41207455
|
T | G | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+2046A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207455 | ||||||
chr15:41207529
|
C | G | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1972G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207529 | ||||||
chr15:41207536
|
T | C | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+1965A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207536 | ||||||
chr15:41207550
|
A | T | 29 | a0001c0002t0001g0128a0001c0002t0001g0193a0001c0002t0001g0196others(26): Show | 29 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.534+1951T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207550 | ||||||
chr15:41207605
|
T | C | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+1896A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41207605 | ||||||
chr15:41208002
|
C | G | 3 | a0001c0005t0001g0096a0001c0005t0001g0097a0001c0005t0001g0098 | 3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.534+1499G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208002 | ||||||
chr15:41208010
|
C | CA | 7 | a0001c0001t0001g0022a0001c0002t0001g0315a0001c0005t0001g0096others(4): Show | 7 | HG02109.hp2 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+1490dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208010 | ||||||
chr15:41208010
|
CA | C | 67 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(64): Show | 68 | HG00408.hp1 HG01070.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.534+1490delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208010 | ||||||
chr15:41208032
|
G | A | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+1469C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208032 | ||||||
chr15:41208056
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.534+1445A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208056 | ||||||
chr15:41208083
|
C | G | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1418G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208083 | ||||||
chr15:41208145
|
G | T | 3 | a0001c0005t0001g0096a0001c0005t0001g0097a0001c0005t0001g0098 | 3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.534+1356C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208145 | ||||||
chr15:41208163
|
G | T | 28 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.534+1338C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208163 | ||||||
chr15:41208351
|
T | G | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.534+1150A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208351 | ||||||
chr15:41208369
|
G | A | 5 | a0002c0004t0001g0001a0002c0004t0001g0006a0002c0004t0001g0083others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+1132C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | ||||||
chr15:41208369
|
G | GA | 8 | a0001c0002t0001g0204a0001c0002t0001g0263a0001c0002t0001g0302others(5): Show | 8 | HG01515.hp1 HG02074.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+1131dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | ||||||
chr15:41208369
|
GA | G | 9 | a0001c0002t0001g0205a0001c0002t0001g0228a0001c0002t0001g0240others(6): Show | 9 | HG01070.hp2 HG01943.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.534+1131delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | ||||||
chr15:41208369
|
GAAA | G | 133 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 134 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.534+1129_534+1131d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | ||||||
chr15:41208369
|
GAAAA | G | 6 | a0001c0001t0002g0174a0001c0001t0002g0184a0001c0001t0003g0026others(3): Show | 6 | HG00099.hp1 HG01081.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+1128_534+1131d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208369 | ||||||
chr15:41208442
|
A | G | 65 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(62): Show | 65 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.534+1059T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208442 | ||||||
chr15:41208621
|
G | A | 187 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.534+880C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208621 | ||||||
chr15:41208727
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.534+774C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208727 | ||||||
chr15:41208809
|
A | G | 1 | a0001c0001t0003g0042 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.534+692T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208809 | ||||||
chr15:41208987
|
T | TA | 151 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 153 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.534+513dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41208987 | ||||||
chr15:41209192
|
A | G | 209 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.534+309T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41209192 | ||||||
chr15:41209285
|
T | C | 156 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(153): Show | 158 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.534+216A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41209285 | ||||||
chr15:41209323
|
G | A | 1 | a0001c0001t0003g0035 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.534+178C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 7/11 | chr15 | 41209323 | ||||||
chr15:41209778
|
C | CT | 230 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(227): Show | 231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.448-192dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41209778 | ||||||
chr15:41209870
|
T | C | 1 | a0001c0002t0001g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.448-283A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41209870 | ||||||
chr15:41209946
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.448-359A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41209946 | ||||||
chr15:41210150
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-563T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210150 | ||||||
chr15:41210180
|
G | T | 11 | a0001c0001t0004g0005a0001c0001t0004g0063a0001c0001t0004g0064others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.448-593C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210180 | ||||||
chr15:41210183
|
G | C | 1 | a0001c0008t0001g0300 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.448-596C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210183 | ||||||
chr15:41210377
|
C | T | 1 | a0001c0002t0001g0041 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.448-790G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210377 | ||||||
chr15:41210393
|
C | T | 4 | a0001c0001t0002g0141a0001c0001t0002g0150a0001c0001t0002g0151others(1): Show | 4 | NA18939.hp1 NA18956.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-806G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210393 | ||||||
chr15:41210417
|
C | T | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.448-830G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210417 | ||||||
chr15:41210662
|
T | TA | 69 | a0001c0001t0002g0136a0001c0001t0002g0173a0001c0001t0003g0011others(66): Show | 69 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.448-1076dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210662 | ||||||
chr15:41210662
|
T | TAA | 18 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(15): Show | 19 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.448-1077_448-1076d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210662 | ||||||
chr15:41210693
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.448-1106C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210693 | ||||||
chr15:41210828
|
T | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1241A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210828 | ||||||
chr15:41210830
|
C | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1243G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210830 | ||||||
chr15:41210932
|
G | A | 2 | a0001c0002t0001g0203a0001c0002t0001g0204 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.448-1345C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41210932 | ||||||
chr15:41211000
|
A | C | 18 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0001g0110others(15): Show | 18 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.448-1413T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211000 | ||||||
chr15:41211038
|
C | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1451G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211038 | ||||||
chr15:41211100
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.448-1513G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211100 | ||||||
chr15:41211397
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1810G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211397 | ||||||
chr15:41211469
|
T | A | 1 | a0001c0002t0001g0305 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.448-1882A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211469 | ||||||
chr15:41211484
|
T | A | 5 | a0002c0004t0001g0001a0002c0004t0001g0006a0002c0004t0001g0083others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-1897A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211484 | ||||||
chr15:41211489
|
A | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1902T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211489 | ||||||
chr15:41211508
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-1921T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211508 | ||||||
chr15:41211532
|
C | T | 170 | a0001c0001t0002g0089a0001c0001t0002g0130a0001c0001t0002g0131others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.448-1945G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211532 | ||||||
chr15:41211608
|
A | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2021T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211608 | ||||||
chr15:41211620
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2033G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211620 | ||||||
chr15:41211704
|
A | G | 2 | a0001c0002t0001g0201a0001c0002t0001g0229 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.448-2117T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211704 | ||||||
chr15:41211795
|
T | TAAAAAAA others(1): Show |
9 | a0001c0001t0001g0027a0001c0001t0003g0011a0001c0001t0003g0026others(6): Show | 9 | HG00099.hp1 HG00558.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-2216_448-2209d others(10): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211795 | ||||||
chr15:41211795
|
T | TAAAAAAA others(2): Show |
70 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(67): Show | 71 | HG00544.hp1 HG00673.hp1 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.448-2217_448-2209d others(11): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211795 | ||||||
chr15:41211795
|
T | TAAAAAAA others(3): Show |
5 | a0001c0001t0003g0087a0001c0001t0004g0065a0001c0011t0001g0071others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-2218_448-2209d others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211795 | ||||||
chr15:41211795
|
TA | T | 30 | a0001c0001t0002g0131a0001c0001t0002g0134a0001c0001t0002g0138others(27): Show | 30 | HG00099.hp2 HG01070.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.448-2209delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41211795 | ||||||
chr15:41212032
|
CA | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2446delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212032 | ||||||
chr15:41212041
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2454T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212041 | ||||||
chr15:41212246
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.448-2659C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212246 | ||||||
chr15:41212265
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.448-2678G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212265 | ||||||
chr15:41212277
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0018others(6): Show | 9 | HG02109.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-2690C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212277 | ||||||
chr15:41212387
|
A | G | 1 | a0001c0002t0001g0314 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.448-2800T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212387 | ||||||
chr15:41212454
|
C | CA | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.448-2868dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212454 | ||||||
chr15:41212535
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.448-2948C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212535 | ||||||
chr15:41212704
|
G | A | 1 | a0001c0002t0001g0111 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.447+3071C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41212704 | ||||||
chr15:41213047
|
A | T | 1 | a0001c0002t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.447+2728T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213047 | ||||||
chr15:41213049
|
T | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.447+2726A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213049 | ||||||
chr15:41213211
|
A | AT | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2563dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213211 | ||||||
chr15:41213457
|
G | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2318C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213457 | ||||||
chr15:41213501
|
T | TTTTTGTT others(3): Show |
1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.447+2264_447+2273d others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | ||||||
chr15:41213501
|
T | TTTTTGTT others(8): Show |
13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | HG02109.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.447+2259_447+2273d others(17): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | ||||||
chr15:41213501
|
T | TTTTTGTT others(13): Show |
13 | a0001c0001t0001g0023a0001c0001t0003g0081a0001c0001t0004g0012others(10): Show | 13 | HG00673.hp1 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.447+2254_447+2273d others(22): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | ||||||
chr15:41213501
|
T | TTTTTGTT others(18): Show |
55 | a0001c0001t0003g0011a0001c0001t0003g0030a0001c0001t0003g0031others(52): Show | 56 | HG00544.hp1 HG00558.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.447+2249_447+2273d others(27): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | ||||||
chr15:41213501
|
T | TTTTTGTT others(23): Show |
2 | a0001c0001t0003g0026a0001c0001t0004g0028 | 2 | HG00099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.447+2273_447+2274i others(32): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213501 | ||||||
chr15:41213540
|
C | CA | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2234dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213540 | ||||||
chr15:41213584
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2191G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213584 | ||||||
chr15:41213603
|
C | T | 65 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0030others(62): Show | 65 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.447+2172G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213603 | ||||||
chr15:41213629
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+2146T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213629 | ||||||
chr15:41213697
|
C | T | 1 | a0001c0002t0010g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.447+2078G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213697 | ||||||
chr15:41213839
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1936G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213839 | ||||||
chr15:41213851
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1924T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213851 | ||||||
chr15:41213937
|
A | G | 7 | a0002c0004t0001g0001a0002c0004t0001g0006a0002c0004t0001g0083others(4): Show | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.447+1838T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41213937 | ||||||
chr15:41214036
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1739T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214036 | ||||||
chr15:41214098
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1677A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214098 | ||||||
chr15:41214143
|
G | C | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.447+1632C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214143 | ||||||
chr15:41214276
|
G | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1499C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214276 | ||||||
chr15:41214288
|
A | G | 1 | a0001c0002t0001g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.447+1487T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214288 | ||||||
chr15:41214311
|
G | A | 2 | a0001c0005t0001g0007a0001c0005t0001g0008 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.447+1464C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214311 | ||||||
chr15:41214421
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+1354C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214421 | ||||||
chr15:41214428
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.447+1347C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214428 | ||||||
chr15:41214475
|
C | T | 1 | a0001c0002t0002g0283 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.447+1300G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214475 | ||||||
chr15:41214512
|
CA | C | 87 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(84): Show | 88 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.447+1262delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214512 | ||||||
chr15:41214598
|
C | G | 10 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(7): Show | 10 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.447+1177G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214598 | ||||||
chr15:41214665
|
G | A | 1 | a0001c0002t0001g0269 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.447+1110C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214665 | ||||||
chr15:41214689
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.447+1086T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214689 | ||||||
chr15:41214904
|
C | T | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.447+871G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214904 | ||||||
chr15:41214938
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+837C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214938 | ||||||
chr15:41214992
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+783C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41214992 | ||||||
chr15:41215025
|
G | A | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.447+750C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215025 | ||||||
chr15:41215113
|
C | T | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.447+662G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215113 | ||||||
chr15:41215270
|
C | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+505G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215270 | ||||||
chr15:41215271
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+504C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215271 | ||||||
chr15:41215452
|
C | T | 3 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092 | 3 | HG02074.hp2 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.447+323G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215452 | ||||||
chr15:41215457
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.447+318G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215457 | ||||||
chr15:41215461
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+314A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215461 | ||||||
chr15:41215579
|
G | A | 6 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(3): Show | 6 | HG00642.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+196C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215579 | ||||||
chr15:41215667
|
T | C | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.447+108A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215667 | ||||||
chr15:41215685
|
C | CA | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.447+89dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215685 | ||||||
chr15:41215685
|
C | CAA | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.447+88_447+89dupTT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 6/11 | chr15 | 41215685 | ||||||
chr15:41215839
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
splice_region_variant&intron_variant | LOW | c.389-6T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41215839 | ||||||
chr15:41215972
|
G | C | 10 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(7): Show | 10 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.389-139C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41215972 | ||||||
chr15:41216012
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.389-179G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216012 | ||||||
chr15:41216056
|
T | C | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.389-223A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216056 | ||||||
chr15:41216230
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.389-397T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216230 | ||||||
chr15:41216304
|
T | TA | 72 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(69): Show | 73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.388+363dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216304 | ||||||
chr15:41216304
|
TA | T | 9 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143others(6): Show | 9 | HG01167.hp2 HG01515.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+363delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216304 | ||||||
chr15:41216319
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.388+349C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216319 | ||||||
chr15:41216321
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.388+347C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216321 | ||||||
chr15:41216435
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.388+233A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216435 | ||||||
chr15:41216466
|
T | C | 13 | a0001c0001t0004g0005a0001c0001t0004g0012a0001c0001t0004g0063others(10): Show | 13 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.388+202A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216466 | ||||||
chr15:41216587
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.388+81G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 5/11 | chr15 | 41216587 | ||||||
chr15:41216966
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.260+131G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 4/11 | chr15 | 41216966 | ||||||
chr15:41217042
|
A | G | 1 | a0001c0002t0001g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.260+55T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 4/11 | chr15 | 41217042 | ||||||
chr15:41217072
|
A | G | 3 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092 | 3 | HG02074.hp2 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.260+25T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 4/11 | chr15 | 41217072 | ||||||
chr15:41217090
|
T | A | 185 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
splice_region_variant&intron_variant | LOW | c.260+7A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 4/11 | chr15 | 41217090 | ||||||
chr15:41217214
|
C | T | 1 | a0001c0002t0001g0232 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.203-60G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217214 | ||||||
chr15:41217529
|
C | CT | 70 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(67): Show | 71 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.203-376dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217529 | ||||||
chr15:41217529
|
C | CTT | 7 | a0001c0001t0001g0027a0001c0001t0002g0140a0001c0001t0002g0182others(4): Show | 7 | HG02071.hp2 HG02293.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.203-377_203-376dup others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217529 | ||||||
chr15:41217529
|
C | CTTT | 71 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(68): Show | 71 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.203-378_203-376dup others(3): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217529 | ||||||
chr15:41217529
|
C | CTTTT | 9 | a0001c0001t0003g0087a0001c0001t0004g0077a0002c0004t0001g0001others(6): Show | 10 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.203-379_203-376dup others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217529 | ||||||
chr15:41217597
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.203-443G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217597 | ||||||
chr15:41217641
|
C | G | 1 | a0001c0006t0001g0230 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.203-487G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217641 | ||||||
chr15:41217684
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-530G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217684 | ||||||
chr15:41217748
|
C | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-594G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217748 | ||||||
chr15:41217748
|
C | G | 2 | a0001c0005t0001g0007a0001c0005t0001g0008 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.203-594G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217748 | ||||||
chr15:41217828
|
C | G | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.203-674G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41217828 | ||||||
chr15:41218078
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-924C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218078 | ||||||
chr15:41218142
|
C | T | 2 | a0001c0002t0001g0203a0001c0002t0001g0204 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.203-988G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218142 | ||||||
chr15:41218162
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-1008A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218162 | ||||||
chr15:41218197
|
C | T | 1 | a0001c0002t0001g0305 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.203-1043G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218197 | ||||||
chr15:41218259
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-1105A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218259 | ||||||
chr15:41218296
|
A | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-1142T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218296 | ||||||
chr15:41218451
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.203-1297G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218451 | ||||||
chr15:41218460
|
C | T | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.203-1306G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218460 | ||||||
chr15:41218486
|
C | CA | 64 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0131others(61): Show | 65 | HG00408.hp1 HG00609.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.203-1333dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218486 | ||||||
chr15:41218486
|
C | CAAA | 6 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0004g0005others(3): Show | 6 | HG02293.hp1 HG02896.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-1335_203-1333d others(5): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218486 | ||||||
chr15:41218486
|
C | CAAAA | 72 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(69): Show | 73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.203-1336_203-1333d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218486 | ||||||
chr15:41218486
|
CA | C | 12 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0227others(9): Show | 12 | HG01070.hp2 HG01884.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.203-1333delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218486 | ||||||
chr15:41218518
|
G | T | 1 | a0001c0002t0001g0315 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.202+1312C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218518 | ||||||
chr15:41218545
|
G | C | 1 | a0002c0003t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.202+1285C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218545 | ||||||
chr15:41218561
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+1269T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218561 | ||||||
chr15:41218684
|
C | T | 3 | a0001c0002t0001g0304a0001c0002t0001g0305a0001c0002t0001g0306 | 3 | NA18966.hp2 NA18986.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.202+1146G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218684 | ||||||
chr15:41218891
|
G | A | 1 | a0009c0017t0001g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.202+939C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218891 | ||||||
chr15:41218894
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+936A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218894 | ||||||
chr15:41218961
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+869A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41218961 | ||||||
chr15:41219061
|
C | T | 3 | a0001c0002t0001g0193a0001c0002t0001g0219a0001c0002t0001g0220 | 3 | HG00597.hp2 HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.202+769G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219061 | ||||||
chr15:41219084
|
T | C | 1 | a0001c0001t0003g0074 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.202+746A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219084 | ||||||
chr15:41219138
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+692A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219138 | ||||||
chr15:41219151
|
C | A | 1 | a0001c0002t0001g0111 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.202+679G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219151 | ||||||
chr15:41219187
|
A | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.202+643T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219187 | ||||||
chr15:41219293
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.202+537T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219293 | ||||||
chr15:41219385
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.202+445C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219385 | ||||||
chr15:41219607
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+223C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219607 | ||||||
chr15:41219718
|
A | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.202+112T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219718 | ||||||
chr15:41219751
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 85 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.202+79T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219751 | ||||||
chr15:41219762
|
A | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.202+68T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219762 | ||||||
chr15:41219819
|
G | C | 1 | a0001c0002t0001g0279 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.202+11C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 3/11 | chr15 | 41219819 | ||||||
chr15:41220101
|
A | C | 1 | a0001c0002t0001g0192 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.134-203T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220101 | ||||||
chr15:41220187
|
T | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-289A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220187 | ||||||
chr15:41220237
|
C | A | 65 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(62): Show | 66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.134-339G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220237 | ||||||
chr15:41220302
|
G | A | 3 | a0001c0005t0001g0096a0001c0005t0001g0097a0001c0005t0001g0098 | 3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.134-404C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220302 | ||||||
chr15:41220339
|
C | T | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-441G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220339 | ||||||
chr15:41220375
|
A | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-477T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220375 | ||||||
chr15:41220393
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.134-495G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220393 | ||||||
chr15:41220427
|
C | T | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-529G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220427 | ||||||
chr15:41220474
|
T | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-576A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220474 | ||||||
chr15:41220510
|
A | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-612T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220510 | ||||||
chr15:41220773
|
T | C | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.134-875A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220773 | ||||||
chr15:41220861
|
T | C | 3 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0001g0276 | 3 | HG00639.hp2 HG00738.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.134-963A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41220861 | ||||||
chr15:41221059
|
T | C | 185 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.134-1161A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221059 | ||||||
chr15:41221105
|
A | C | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.134-1207T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221105 | ||||||
chr15:41221129
|
A | T | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1231T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221129 | ||||||
chr15:41221154
|
T | C | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1256A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221154 | ||||||
chr15:41221323
|
G | C | 1 | a0001c0002t0001g0305 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.134-1425C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221323 | ||||||
chr15:41221330
|
G | A | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1432C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221330 | ||||||
chr15:41221419
|
G | A | 2 | a0001c0001t0015g0316a0002c0003t0001g0127 | 2 | HG01070.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.134-1521C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221419 | ||||||
chr15:41221443
|
C | CT | 29 | a0001c0002t0001g0193a0001c0002t0001g0196a0001c0002t0001g0197others(26): Show | 29 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-1546dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221443 | ||||||
chr15:41221443
|
CT | C | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1546delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221443 | ||||||
chr15:41221454
|
G | A | 2 | a0001c0002t0001g0277a0001c0002t0001g0292 | 2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.134-1556C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221454 | ||||||
chr15:41221494
|
G | A | 1 | a0001c0001t0015g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.134-1596C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221494 | ||||||
chr15:41221822
|
G | C | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1924C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221822 | ||||||
chr15:41221826
|
A | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1928T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221826 | ||||||
chr15:41221883
|
T | C | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-1985A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221883 | ||||||
chr15:41221935
|
AC | A | 65 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(62): Show | 66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.134-2038delG | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221935 | ||||||
chr15:41221938
|
A | T | 65 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(62): Show | 66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.134-2040T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221938 | ||||||
chr15:41221960
|
C | T | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2062G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41221960 | ||||||
chr15:41222072
|
A | C | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.134-2174T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222072 | ||||||
chr15:41222100
|
G | A | 29 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.134-2202C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222100 | ||||||
chr15:41222136
|
C | T | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2238G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222136 | ||||||
chr15:41222208
|
A | C | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.134-2310T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222208 | ||||||
chr15:41222208
|
A | T | 2 | a0001c0005t0001g0007a0001c0005t0001g0008 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.134-2310T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222208 | ||||||
chr15:41222226
|
T | C | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2328A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222226 | ||||||
chr15:41222273
|
G | C | 1 | a0001c0002t0001g0314 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.134-2375C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222273 | ||||||
chr15:41222300
|
C | A | 4 | a0001c0002t0001g0278a0001c0002t0001g0279a0001c0002t0001g0293others(1): Show | 4 | HG01257.hp1 HG01346.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-2402G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222300 | ||||||
chr15:41222501
|
A | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2603T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222501 | ||||||
chr15:41222535
|
A | G | 182 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.134-2637T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222535 | ||||||
chr15:41222576
|
T | A | 1 | a0002c0003t0011g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.134-2678A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222576 | ||||||
chr15:41222600
|
A | G | 4 | a0002c0003t0005g0099a0002c0003t0005g0100a0002c0003t0005g0101others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-2702T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222600 | ||||||
chr15:41222638
|
A | AT | 11 | a0001c0001t0002g0089a0001c0001t0002g0137a0001c0002t0001g0212others(8): Show | 11 | HG00609.hp2 HG02027.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-2741dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222638 | ||||||
chr15:41222638
|
AT | A | 35 | a0001c0005t0001g0096a0001c0005t0001g0097a0001c0005t0001g0098others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.134-2741delA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222638 | ||||||
chr15:41222638
|
ATTTT | A | 72 | a0001c0001t0001g0027a0001c0001t0003g0011a0001c0001t0003g0026others(69): Show | 73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.134-2744_134-2741d others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222638 | ||||||
chr15:41222638
|
ATTTTT | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-2745_134-2741d others(7): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222638 | ||||||
chr15:41222643
|
T | A | 1 | a0001c0001t0004g0076 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.134-2745A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222643 | ||||||
chr15:41222665
|
G | A | 3 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092 | 3 | HG02074.hp2 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.134-2767C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222665 | ||||||
chr15:41222678
|
G | C | 182 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.134-2780C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222678 | ||||||
chr15:41222712
|
A | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2814T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222712 | ||||||
chr15:41222763
|
C | T | 1 | a0001c0002t0010g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.134-2865G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222763 | ||||||
chr15:41222773
|
A | T | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2875T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222773 | ||||||
chr15:41222774
|
T | TA | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-2877dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222774 | ||||||
chr15:41222934
|
C | CA | 27 | a0001c0002t0001g0112a0001c0002t0001g0193a0001c0002t0001g0200others(24): Show | 27 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.134-3037dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222934 | ||||||
chr15:41222934
|
CA | C | 45 | a0001c0001t0015g0316a0001c0002t0001g0201a0001c0002t0001g0202others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.134-3037delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222934 | ||||||
chr15:41222934
|
CAAAAAAA others(1): Show |
C | 134 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0002g0002others(131): Show | 136 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.134-3044_134-3037d others(10): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222934 | ||||||
chr15:41222934
|
CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG02109.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-3045_134-3037d others(11): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41222934 | ||||||
chr15:41223005
|
C | T | 1 | a0002c0004t0001g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.134-3107G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223005 | ||||||
chr15:41223016
|
T | G | 66 | a0001c0001t0001g0027a0001c0001t0003g0011a0001c0001t0003g0026others(63): Show | 66 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.134-3118A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223016 | ||||||
chr15:41223391
|
G | C | 29 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.133+3052C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223391 | ||||||
chr15:41223738
|
G | A | 1 | a0001c0002t0001g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.133+2705C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223738 | ||||||
chr15:41223761
|
A | G | 1 | a0001c0002t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133+2682T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223761 | ||||||
chr15:41223789
|
C | T | 5 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198others(2): Show | 5 | HG01192.hp1 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+2654G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223789 | ||||||
chr15:41223807
|
G | A | 1 | a0001c0002t0001g0294 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.133+2636C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223807 | ||||||
chr15:41223822
|
A | G | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+2621T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223822 | ||||||
chr15:41223932
|
C | T | 65 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(62): Show | 66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.133+2511G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223932 | ||||||
chr15:41223999
|
T | C | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+2444A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41223999 | ||||||
chr15:41224083
|
G | T | 1 | a0001c0001t0002g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133+2360C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224083 | ||||||
chr15:41224092
|
A | C | 1 | a0004c0009t0001g0195 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.133+2351T>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224092 | ||||||
chr15:41224230
|
G | A | 65 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(62): Show | 66 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.133+2213C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224230 | ||||||
chr15:41224280
|
T | C | 3 | a0003c0007t0003g0078a0003c0007t0003g0079a0003c0007t0003g0080 | 3 | NA18968.hp1 NA18971.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.133+2163A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224280 | ||||||
chr15:41224362
|
C | T | 4 | a0002c0003t0005g0099a0002c0003t0005g0100a0002c0003t0005g0101others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+2081G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224362 | ||||||
chr15:41224415
|
T | C | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+2028A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224415 | ||||||
chr15:41224473
|
C | G | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1970G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224473 | ||||||
chr15:41224487
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+1956T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224487 | ||||||
chr15:41224625
|
C | T | 29 | a0001c0005t0001g0107a0002c0003t0001g0010a0002c0003t0001g0095others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.133+1818G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224625 | ||||||
chr15:41224650
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.133+1793C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224650 | ||||||
chr15:41224674
|
C | T | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1769G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224674 | ||||||
chr15:41224782
|
C | T | 1 | a0002c0003t0001g0127 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.133+1661G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224782 | ||||||
chr15:41224899
|
G | C | 1 | a0001c0002t0001g0192 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.133+1544C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224899 | ||||||
chr15:41224967
|
T | TA | 149 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(146): Show | 151 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.133+1475dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41224967 | ||||||
chr15:41225093
|
A | G | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1350T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225093 | ||||||
chr15:41225288
|
T | C | 1 | a0001c0001t0003g0081 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.133+1155A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225288 | ||||||
chr15:41225303
|
G | A | 1 | a0001c0002t0001g0296 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.133+1140C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225303 | ||||||
chr15:41225320
|
C | T | 3 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0136 | 3 | NA18942.hp2 NA18967.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.133+1123G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225320 | ||||||
chr15:41225334
|
C | T | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1109G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225334 | ||||||
chr15:41225348
|
G | GCCAAGGT others(41): Show |
1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.133+1047_133+1094d others(50): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225348 | ||||||
chr15:41225429
|
A | G | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+1014T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225429 | ||||||
chr15:41225483
|
G | C | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+960C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225483 | ||||||
chr15:41225587
|
G | GA | 14 | a0002c0003t0001g0114a0002c0003t0001g0115a0002c0003t0001g0116others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.133+855dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225587 | ||||||
chr15:41225587
|
GA | G | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.133+855delT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225587 | ||||||
chr15:41225587
|
GAA | G | 5 | a0002c0004t0001g0001a0002c0004t0001g0006a0002c0004t0001g0083others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+854_133+855del others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225587 | ||||||
chr15:41225706
|
G | A | 1 | a0002c0003t0001g0093 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.133+737C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225706 | ||||||
chr15:41225749
|
A | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+694T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225749 | ||||||
chr15:41225774
|
G | C | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.133+669C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225774 | ||||||
chr15:41225822
|
A | G | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+621T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225822 | ||||||
chr15:41225901
|
CAAAACAA others(4): Show |
C | 72 | a0001c0001t0001g0027a0001c0001t0003g0011a0001c0001t0003g0026others(69): Show | 73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.133+531_133+541del others(11): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225901 | ||||||
chr15:41225911
|
C | CA | 5 | a0001c0002t0001g0193a0001c0002t0001g0298a0001c0002t0001g0299others(2): Show | 5 | HG00597.hp2 HG03098.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+531dupT | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225911 | ||||||
chr15:41225919
|
AC | A | 76 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(73): Show | 77 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.133+523delG | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225919 | ||||||
chr15:41225920
|
C | A | 72 | a0001c0001t0001g0027a0001c0001t0003g0011a0001c0001t0003g0026others(69): Show | 73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.133+523G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225920 | ||||||
chr15:41225974
|
T | C | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+469A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225974 | ||||||
chr15:41225975
|
C | T | 63 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0002g0130others(60): Show | 64 | HG00408.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.133+468G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41225975 | ||||||
chr15:41226019
|
A | G | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+424T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226019 | ||||||
chr15:41226024
|
A | G | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.133+419T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226024 | ||||||
chr15:41226045
|
G | C | 1 | a0002c0003t0001g0127 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.133+398C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226045 | ||||||
chr15:41226079
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.133+364A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226079 | ||||||
chr15:41226177
|
G | A | 2 | a0001c0005t0001g0007a0001c0005t0001g0008 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.133+266C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226177 | ||||||
chr15:41226184
|
A | G | 142 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(139): Show | 144 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.133+259T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 2/11 | chr15 | 41226184 | ||||||
chr15:41226720
|
T | G | 1 | a0001c0001t0003g0082 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-53-92A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41226720 | ||||||
chr15:41226734
|
T | C | 2 | a0001c0002t0001g0302a0001c0002t0001g0303 | 2 | NA18971.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-53-106A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41226734 | ||||||
chr15:41226991
|
G | T | 3 | a0001c0005t0001g0096a0001c0005t0001g0097a0001c0005t0001g0098 | 3 | HG02922.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-53-363C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41226991 | ||||||
chr15:41227115
|
T | G | 7 | a0002c0004t0001g0001a0002c0004t0001g0006a0002c0004t0001g0083others(4): Show | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53-487A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227115 | ||||||
chr15:41227182
|
C | A | 9 | a0001c0002t0001g0128a0001c0002t0001g0304a0001c0002t0001g0305others(6): Show | 9 | HG01943.hp1 HG01952.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-554G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227182 | ||||||
chr15:41227427
|
T | C | 1 | a0001c0002t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-53-799A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227427 | ||||||
chr15:41227498
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-53-870A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227498 | ||||||
chr15:41227539
|
T | C | 152 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(149): Show | 154 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.-53-911A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227539 | ||||||
chr15:41227619
|
G | A | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-991C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227619 | ||||||
chr15:41227635
|
G | C | 1 | a0001c0001t0003g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-53-1007C>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227635 | ||||||
chr15:41227675
|
CAA | C | 143 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 145 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.-53-1049_-53-1048d others(4): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227675 | ||||||
chr15:41227861
|
C | T | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1233G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227861 | ||||||
chr15:41227862
|
C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1234G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227862 | ||||||
chr15:41227866
|
A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1238T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227866 | ||||||
chr15:41227868
|
G | T | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1240C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227868 | ||||||
chr15:41227871
|
GAAACCCC others(22): Show |
G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1272_-53-1244d others(31): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227871 | ||||||
chr15:41227878
|
C | T | 1 | a0002c0003t0001g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-53-1250G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227878 | ||||||
chr15:41227902
|
T | TTGTGGGG others(3): Show |
1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1275_-53-1274i others(12): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227902 | ||||||
chr15:41227903
|
A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1275T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227903 | ||||||
chr15:41227905
|
C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1277G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227905 | ||||||
chr15:41227906
|
C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1278G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227906 | ||||||
chr15:41227907
|
A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1279T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227907 | ||||||
chr15:41227909
|
C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1281G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227909 | ||||||
chr15:41227910
|
T | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1282A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227910 | ||||||
chr15:41227913
|
A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1285T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227913 | ||||||
chr15:41227916
|
G | T | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1288C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227916 | ||||||
chr15:41227917
|
A | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1289T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227917 | ||||||
chr15:41227918
|
C | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-53-1290G>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227918 | ||||||
chr15:41227975
|
A | G | 2 | a0001c0002t0014g0094a0006c0014t0001g0194 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-53-1347T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41227975 | ||||||
chr15:41228116
|
T | G | 1 | a0001c0002t0001g0313 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-53-1488A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228116 | ||||||
chr15:41228125
|
A | T | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-1497T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228125 | ||||||
chr15:41228221
|
C | T | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-1593G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228221 | ||||||
chr15:41228317
|
T | C | 1 | a0001c0002t0001g0314 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53-1689A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228317 | ||||||
chr15:41228334
|
G | A | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-1706C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228334 | ||||||
chr15:41228450
|
G | T | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-1822C>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228450 | ||||||
chr15:41228609
|
C | A | 4 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0189others(1): Show | 4 | NA19005.hp1 NA19055.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+1870G>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228609 | ||||||
chr15:41228637
|
G | A | 72 | a0001c0001t0001g0027a0001c0001t0003g0011a0001c0001t0003g0026others(69): Show | 73 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-54+1842C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228637 | ||||||
chr15:41228732
|
C | T | 4 | a0002c0003t0001g0009a0002c0003t0001g0091a0002c0003t0001g0092others(1): Show | 4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+1747G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228732 | ||||||
chr15:41228754
|
A | G | 1 | a0001c0002t0001g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-54+1725T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228754 | ||||||
chr15:41228787
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-54+1692G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228787 | ||||||
chr15:41228830
|
A | G | 1 | a0001c0001t0004g0012 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-54+1649T>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41228830 | ||||||
chr15:41229139
|
C | T | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+1340G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229139 | ||||||
chr15:41229206
|
G | A | 1 | a0002c0004t0001g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-54+1273C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229206 | ||||||
chr15:41229218
|
C | T | 1 | a0001c0002t0001g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-54+1261G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229218 | ||||||
chr15:41229284
|
CCTAGACA others(21): Show |
C | 1 | a0001c0001t0002g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-54+1167_-54+1194d others(30): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229284 | ||||||
chr15:41229295
|
T | A | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-54+1184A>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229295 | ||||||
chr15:41229384
|
A | T | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-54+1095T>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229384 | ||||||
chr15:41229391
|
T | G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-54+1088A>C | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229391 | ||||||
chr15:41229407
|
GGAGGTTG others(19): Show |
G | 1 | a0001c0001t0003g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-54+1046_-54+1071d others(28): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229407 | ||||||
chr15:41229539
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-54+940G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229539 | ||||||
chr15:41229636
|
C | T | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+843G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229636 | ||||||
chr15:41229769
|
A | AAACAAC | 83 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-54+704_-54+709dup others(6): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229769 | ||||||
chr15:41229787
|
C | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-54+692G>A | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229787 | ||||||
chr15:41229921
|
G | A | 1 | a0002c0004t0001g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-54+558C>T | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41229921 | ||||||
chr15:41230082
|
C | CT | 121 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.-54+396dupA | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41230082 | ||||||
chr15:41230082
|
C | CTT | 6 | a0001c0001t0004g0005a0001c0005t0001g0007a0001c0005t0001g0008others(3): Show | 6 | HG01109.hp1 HG02074.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+395_-54+396dup others(2): Show |
EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41230082 | ||||||
chr15:41230091
|
T | C | 1 | a0001c0002t0001g0315 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-54+388A>G | EXD1 | ENSG00000178997.12 | transcript | ENST00000458580.7 | protein_coding | 1/11 | chr15 | 41230091 |