geneid | 11086 |
---|---|
ensemblid | ENSG00000168594.15 |
hgncid | 207 |
symbol | ADAM29 |
name | ADAM metallopeptidase domain 29 |
refseq_nuc | NM_014269.4 |
refseq_prot | NP_055084.3 |
ensembl_nuc | ENST00000359240.7 |
ensembl_prot | ENSP00000352177.3 |
mane_status | MANE Select |
chr | chr4 |
start | 174918358 |
end | 174978180 |
strand | + |
ver | v1.2 |
region | chr4:174918358-174978180 |
region5000 | chr4:174913358-174983180 |
regionname0 | ADAM29_chr4_174918358_174978180 |
regionname5000 | ADAM29_chr4_174913358_174983180 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 820 | 205 | 47 | 46 | 74 | 5 | 31 | 50 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0002 | 0/0 | 838 | 55 | 5 | 13 | 30 | 1 | 6 | 26 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0003 | 0/0 | 820 | 32 | 0 | 1 | 26 | 0 | 5 | 13 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004 | 0/0 | 820 | 26 | 22 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0005 | 0/0 | 820 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0006 | 0/0 | 820 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0007 | 0/0 | 820 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0008 | 0/0 | 820 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0009 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0010 | 0/0 | 820 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2463 | 197 | 39 | 46 | 74 | 5 | 31 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0002 | 0/0 | 2517 | 55 | 5 | 13 | 30 | 1 | 6 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0003 | 0/0 | 2463 | 32 | 0 | 1 | 26 | 0 | 5 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0004 | 0/0 | 2463 | 25 | 21 | 4 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0005 | 0/0 | 2517 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0006 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0007 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0008 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0009 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0010 | 0/0 | 2463 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0011 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0012 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0013 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0014 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0015 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0016 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
c0017 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 865 | 135 | 15 | 25 | 82 | 2 | 11 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0002 | 0/0 | 865 | 106 | 45 | 13 | 33 | 0 | 15 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0003 | 0/1 | 865 | 40 | 3 | 20 | 2 | 3 | 11 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0004 | 1/0 | 863 | 28 | 5 | 7 | 11 | 1 | 3 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0005 | 0/0 | 863 | 5 | 3 | 0 | 0 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0006 | 0/0 | 865 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0007 | 0/0 | 865 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0008 | 0/0 | 865 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0009 | 0/0 | 865 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0010 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0011 | 0/0 | 863 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0012 | 0/0 | 865 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0013 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0014 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
t0015 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
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 | 9 | 1 | 0 | 8 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0009 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2463 | 197 | 39 | 46 | 74 | 5 | 31 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0006 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0008 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0009 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0013 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0016 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0002c0002 | 0/0 | 2517 | 55 | 5 | 13 | 30 | 1 | 6 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0003c0003 | 0/0 | 2463 | 32 | 0 | 1 | 26 | 0 | 5 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004c0004 | 0/0 | 2463 | 25 | 21 | 4 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004c0015 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0005c0005 | 0/0 | 2517 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0005c0007 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0006c0010 | 0/0 | 2463 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0007c0012 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0008c0014 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0009c0017 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0010c0011 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3327 | 96 | 10 | 17 | 59 | 2 | 8 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0001t0002 | 0/0 | 3327 | 43 | 16 | 9 | 10 | 0 | 8 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0001t0003 | 0/1 | 3327 | 33 | 3 | 14 | 1 | 3 | 11 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0001t0004 | 1/0 | 3325 | 12 | 3 | 6 | 0 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0001t0005 | 0/0 | 3325 | 5 | 3 | 0 | 0 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0001t0006 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0001t0007 | 0/0 | 3327 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0001t0008 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0001t0015 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0006t0002 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0008t0002 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0009t0011 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0009t0013 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0013t0001 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0001c0016t0002 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0002c0002t0001 | 0/0 | 3381 | 28 | 2 | 7 | 17 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0002c0002t0002 | 0/0 | 3381 | 6 | 2 | 0 | 1 | 0 | 3 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0002c0002t0003 | 0/0 | 3381 | 5 | 0 | 4 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0002c0002t0004 | 0/0 | 3379 | 15 | 1 | 1 | 11 | 1 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0002c0002t0012 | 0/0 | 3381 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0003c0003t0001 | 0/0 | 3327 | 8 | 0 | 1 | 6 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0003c0003t0002 | 0/0 | 3327 | 24 | 0 | 0 | 20 | 0 | 4 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004c0004t0001 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004c0004t0002 | 0/0 | 3327 | 19 | 15 | 4 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004c0004t0004 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004c0004t0006 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004c0004t0009 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004c0004t0010 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0004c0015t0002 | 0/0 | 3381 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0005c0005t0002 | 0/0 | 3381 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0005c0007t0002 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0006c0010t0003 | 0/0 | 3327 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0007c0012t0014 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0008c0014t0001 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0009c0017t0002 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
a0010c0011t0002 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | copy fasta | chr4 | 174913358 | 174983180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0009 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0015g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0006t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0006t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0008t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0008t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0009t0011g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0009t0013g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0013t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0016t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0012g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0009g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0015t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0005t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0005t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0007t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0007t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0006c0010t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0006c0010t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0007c0012t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0008c0014t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0009c0017t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0010c0011t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | FIN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0066 | EUR | FIN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00408 | hp2 | a0003 | c0003 | t0002 | g0261 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00423 | hp2 | a0003 | c0003 | t0001 | g0120 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00438 | hp2 | a0003 | c0003 | t0002 | g0023 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00544 | hp1 | a0002 | c0002 | t0004 | g0081 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00558 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0132 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00621 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00639 | hp1 | a0004 | c0004 | t0002 | g0267 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00639 | hp2 | a0006 | c0010 | t0003 | g0051 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00642 | hp2 | a0002 | c0002 | t0012 | g0049 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00735 | hp2 | a0002 | c0002 | t0003 | g0042 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00741 | hp1 | a0004 | c0004 | t0002 | g0269 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0168 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01106 | hp1 | a0002 | c0002 | t0003 | g0070 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01109 | hp1 | a0004 | c0004 | t0002 | g0027 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0197 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01256 | hp2 | a0002 | c0002 | t0003 | g0072 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0094 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0076 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01433 | hp1 | a0004 | c0004 | t0002 | g0273 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0030 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01891 | hp1 | a0001 | c0008 | t0002 | g0098 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0090 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01975 | hp2 | a0003 | c0003 | t0001 | g0222 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01981 | hp1 | a0006 | c0010 | t0003 | g0058 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0079 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0159 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02040 | hp1 | a0002 | c0002 | t0004 | g0093 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02056 | hp1 | a0003 | c0003 | t0002 | g0250 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02071 | hp2 | a0002 | c0002 | t0004 | g0096 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02074 | hp1 | a0010 | c0011 | t0002 | g0259 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02074 | hp2 | a0003 | c0003 | t0001 | g0171 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02129 | hp1 | a0003 | c0003 | t0002 | g0167 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02135 | hp1 | a0003 | c0003 | t0002 | g0239 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02155 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | CDX | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02155 | hp2 | a0003 | c0003 | t0001 | g0192 | EAS | CDX | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02258 | hp2 | a0004 | c0004 | t0009 | g0240 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02273 | hp2 | a0002 | c0002 | t0003 | g0065 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02451 | hp1 | a0004 | c0004 | t0002 | g0271 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02572 | hp1 | a0004 | c0004 | t0002 | g0034 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02602 | hp1 | a0003 | c0003 | t0002 | g0004 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02615 | hp1 | a0004 | c0004 | t0002 | g0242 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02622 | hp1 | a0001 | c0008 | t0002 | g0097 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02630 | hp1 | a0001 | c0013 | t0001 | g0198 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02630 | hp2 | a0005 | c0007 | t0002 | g0234 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02647 | hp2 | a0004 | c0004 | t0002 | g0026 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02723 | hp2 | a0004 | c0004 | t0009 | g0241 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02809 | hp1 | a0005 | c0007 | t0002 | g0230 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02818 | hp1 | a0001 | c0016 | t0002 | g0037 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02818 | hp2 | a0008 | c0014 | t0001 | g0175 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02886 | hp1 | a0005 | c0005 | t0002 | g0235 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02886 | hp2 | a0004 | c0004 | t0010 | g0179 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02895 | hp1 | a0005 | c0005 | t0002 | g0022 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02895 | hp2 | a0004 | c0004 | t0002 | g0276 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02897 | hp1 | a0005 | c0005 | t0002 | g0022 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02922 | hp1 | a0001 | c0009 | t0013 | g0039 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03041 | hp2 | a0004 | c0004 | t0002 | g0272 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03098 | hp1 | a0001 | c0009 | t0011 | g0095 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03098 | hp2 | a0004 | c0004 | t0006 | g0050 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0099 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03139 | hp1 | a0004 | c0004 | t0002 | g0178 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03209 | hp2 | a0004 | c0004 | t0001 | g0184 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03225 | hp2 | a0001 | c0006 | t0002 | g0032 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0266 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0180 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03453 | hp2 | a0004 | c0004 | t0004 | g0074 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0237 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03516 | hp1 | a0004 | c0004 | t0002 | g0025 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03654 | hp1 | a0002 | c0002 | t0004 | g0077 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03704 | hp1 | a0003 | c0003 | t0002 | g0236 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0262 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0109 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0067 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03927 | hp2 | a0003 | c0003 | t0002 | g0281 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0125 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0130 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | STU | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04199 | hp2 | a0003 | c0003 | t0002 | g0248 | SAS | STU | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0091 | SAS | STU | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | STU | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18522 | hp1 | a0004 | c0004 | t0002 | g0025 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0100 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18612 | hp1 | a0003 | c0003 | t0002 | g0119 | EAS | CHB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18906 | hp2 | a0004 | c0004 | t0002 | g0027 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18942 | hp2 | a0003 | c0003 | t0002 | g0257 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18944 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18945 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18949 | hp2 | a0002 | c0002 | t0004 | g0084 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18950 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18957 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18971 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18972 | hp2 | a0001 | c0001 | t0015 | g0153 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18973 | hp2 | a0009 | c0017 | t0002 | g0282 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0187 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18981 | hp1 | a0003 | c0003 | t0002 | g0265 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18981 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18982 | hp1 | a0002 | c0002 | t0004 | g0089 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18984 | hp1 | a0003 | c0003 | t0001 | g0170 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18984 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18986 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18989 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18992 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19010 | hp1 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0181 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19043 | hp2 | a0005 | c0005 | t0002 | g0231 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19065 | hp2 | a0003 | c0003 | t0002 | g0263 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19074 | hp1 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19080 | hp1 | a0002 | c0002 | t0004 | g0080 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19080 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19083 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19090 | hp1 | a0001 | c0001 | t0007 | g0104 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19091 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19240 | hp1 | a0002 | c0002 | t0004 | g0075 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19240 | hp2 | a0004 | c0015 | t0002 | g0229 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20129 | hp1 | a0004 | c0004 | t0002 | g0228 | AFR | ASW | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20129 | hp2 | a0004 | c0004 | t0002 | g0274 | AFR | ASW | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20752 | hp1 | a0002 | c0002 | t0004 | g0086 | EUR | TSI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0044 | EUR | TSI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | GIH | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01123 | hp1 | a0002 | c0002 | t0004 | g0083 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02109 | hp1 | a0004 | c0004 | t0002 | g0275 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02486 | hp1 | a0004 | c0004 | t0002 | g0268 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02559 | hp1 | a0004 | c0004 | t0002 | g0026 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG06807 | hp1 | a0007 | c0012 | t0014 | g0031 | AFR | USA | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | USA | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20300 | hp2 | a0001 | c0006 | t0002 | g0033 | AFR | USA | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0009 | REF | REF | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0087 | REF | REF | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:174976088
|
G | C | 1 | a0010 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.563G>C | p.Ser188Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 1233/3325 | 563/2463 | 188/820 | chr4 | 174976088 | ||
chr4:174977404
|
C | T | 3 | a0003a0009a0010 | 34 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(31): Show |
missense_variant | MODERATE | c.1879C>T | p.Pro627Ser | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2549/3325 | 1879/2463 | 627/820 | chr4 | 174977404 | ||
chr4:174977693
|
G | A | 1 | a0007 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.2168G>A | p.Arg723His | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2838/3325 | 2168/2463 | 723/820 | chr4 | 174977693 | ||
chr4:174977749
|
C | T | 1 | a0009 | 1 | NA18973.hp2 | stop_gained | HIGH | c.2224C>T | p.Gln742* | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2894/3325 | 2224/2463 | 742/820 | chr4 | 174977749 | ||
chr4:174977783
|
A | G | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2258A>G | p.Gln753Arg | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2928/3325 | 2258/2463 | 753/820 | chr4 | 174977783 | ||
chr4:174977816
|
C | T | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2291C>T | p.Thr764Ile | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2961/3325 | 2291/2463 | 764/820 | chr4 | 174977816 | ||
chr4:174977832
|
A | T | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2307A>T | p.Gln769His | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2977/3325 | 2307/2463 | 769/820 | chr4 | 174977832 | ||
chr4:174977837
|
G | A | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2312G>A | p.Arg771Gln | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2982/3325 | 2312/2463 | 771/820 | chr4 | 174977837 | ||
chr4:174977839
|
G | T | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2314G>T | p.Val772Leu | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2984/3325 | 2314/2463 | 772/820 | chr4 | 174977839 | ||
chr4:174977843
|
T | C | 2 | a0006a0008 | 3 | HG00639.hp2 HG01981.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.2318T>C | p.Met773Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2988/3325 | 2318/2463 | 773/820 | chr4 | 174977843 | ||
chr4:174977850
|
T | TCAGAGTC others(47): Show |
1 | a0002 | 55 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(52): Show |
disruptive_inframe_insertion | MODERATE | c.2345_2398dupTGCCTT others(48): Show |
p.Met782_Val799dup | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3069/3325 | 2399/2463 | 800/820 | INFO_REALIGN_3_PRIME | chr4 | 174977850 | |
chr4:174977870
|
T | C | 1 | a0004 | 26 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
missense_variant | MODERATE | c.2345T>C | p.Met782Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3015/3325 | 2345/2463 | 782/820 | chr4 | 174977870 | ||
chr4:174977937
|
G | GCAACCTC others(47): Show |
1 | a0005 | 4 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
stop_gained&conservative_inframe_insertion | HIGH | c.2436_2437insGGTCAA others(48): Show |
p.Gln812_Ser813insGl others(52): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3107/3325 | 2437/2463 | 813/820 | INFO_REALIGN_3_PRIME | chr4 | 174977937 | |
chr4:174977962
|
A | G | 1 | a0005 | 2 | HG02630.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.2437A>G | p.Ser813Gly | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3107/3325 | 2437/2463 | 813/820 | chr4 | 174977962 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:174976095
|
T | C | 4 | a0001c0006a0005c0005a0005c0007others(1): Show | 9 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(6): Show |
synonymous_variant | LOW | c.570T>C | p.Tyr190Tyr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 1240/3325 | 570/2463 | 190/820 | chr4 | 174976095 | ||
chr4:174976359
|
G | A | 1 | a0001c0013 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.834G>A | p.Thr278Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 1504/3325 | 834/2463 | 278/820 | chr4 | 174976359 | ||
chr4:174977559
|
T | C | 1 | a0001c0008 | 2 | HG01891.hp1 HG02622.hp1 |
synonymous_variant | LOW | c.2034T>C | p.Tyr678Tyr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2704/3325 | 2034/2463 | 678/820 | chr4 | 174977559 | ||
chr4:174977763
|
G | A | 1 | a0001c0009 | 2 | HG02922.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.2238G>A | p.Thr746Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2908/3325 | 2238/2463 | 746/820 | chr4 | 174977763 | ||
chr4:174977796
|
C | T | 1 | a0006c0010 | 2 | HG00639.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.2271C>T | p.Ser757Ser | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2941/3325 | 2271/2463 | 757/820 | chr4 | 174977796 | ||
chr4:174977817
|
A | G | 1 | a0006c0010 | 2 | HG00639.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.2292A>G | p.Thr764Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2962/3325 | 2292/2463 | 764/820 | chr4 | 174977817 | ||
chr4:174977820
|
C | T | 1 | a0006c0010 | 2 | HG00639.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.2295C>T | p.Pro765Pro | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2965/3325 | 2295/2463 | 765/820 | chr4 | 174977820 | ||
chr4:174977850
|
T | C | 1 | a0006c0010 | 2 | HG00639.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.2325T>C | p.Ser775Ser | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2995/3325 | 2325/2463 | 775/820 | chr4 | 174977850 | ||
chr4:174977877
|
C | A | 1 | a0001c0016 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.2352C>A | p.Ser784Ser | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3022/3325 | 2352/2463 | 784/820 | chr4 | 174977877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:174918369
|
T | C | 1 | a0004c0004t0010 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-659T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/5 | 57157 | chr4 | 174918369 | |||||
chr4:174918404
|
A | G | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(23): Show | 257 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-624A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/5 | chr4 | 174918404 | ||||||
chr4:174918460
|
G | A | 1 | a0001c0001t0008 | 2 | HG03130.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-568G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/5 | 57066 | chr4 | 174918460 | |||||
chr4:174920749
|
G | T | 4 | a0001c0001t0003a0002c0002t0003a0002c0002t0012others(1): Show | 41 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(38): Show |
5_prime_UTR_variant | MODIFIER | c.-494G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/5 | 54777 | chr4 | 174920749 | |||||
chr4:174931001
|
A | ATG | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | 296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
5_prime_UTR_variant | MODIFIER | c.-434_-433insGT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/5 | 44523 | INFO_REALIGN_3_PRIME | chr4 | 174931001 | ||||
chr4:174931004
|
C | T | 9 | a0001c0001t0001a0001c0001t0007a0001c0001t0015others(6): Show | 140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
5_prime_UTR_variant | MODIFIER | c.-432C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/5 | 44522 | chr4 | 174931004 | |||||
chr4:174931027
|
G | A | 1 | a0004c0004t0009 | 2 | HG02258.hp2 HG02723.hp2 |
5_prime_UTR_variant | MODIFIER | c.-409G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/5 | 44499 | chr4 | 174931027 | |||||
chr4:174975361
|
G | A | 1 | a0001c0001t0007 | 3 | HG00609.hp1 NA19010.hp1 NA19090.hp1 |
5_prime_UTR_variant | MODIFIER | c.-165G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 165 | chr4 | 174975361 | |||||
chr4:174975456
|
A | T | 1 | a0001c0009t0011 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 70 | chr4 | 174975456 | |||||
chr4:174977937
|
G | GCAACCTC others(47): Show |
1 | a0004c0015t0002 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.2461_*51dupTAGAGCC others(47): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 52 | INFO_REALIGN_3_PRIME | chr4 | 174977937 | ||||
chr4:174978016
|
A | G | 1 | a0007c0012t0014 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 28 | chr4 | 174978016 | |||||
chr4:174978094
|
C | T | 1 | a0001c0001t0015 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*106C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 106 | chr4 | 174978094 | |||||
chr4:174978122
|
C | T | 2 | a0001c0009t0011a0001c0009t0013 | 2 | HG02922.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*134C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 134 | chr4 | 174978122 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:174918574
|
C | T | 70 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(67): Show | 88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-557+103C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918574 | ||||||
chr4:174918576
|
G | A | 81 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(78): Show | 99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-557+105G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918576 | ||||||
chr4:174918585
|
G | T | 138 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(135): Show | 150 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-557+114G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918585 | ||||||
chr4:174918741
|
T | C | 7 | a0001c0001t0002g0035a0001c0006t0002g0032a0001c0006t0002g0033others(4): Show | 7 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-557+270T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918741 | ||||||
chr4:174918747
|
T | TA | 12 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0040others(9): Show | 14 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-557+284dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 174918747 | |||||
chr4:174918812
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-557+341A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918812 | ||||||
chr4:174918895
|
T | C | 5 | a0001c0006t0002g0032a0001c0006t0002g0033a0002c0002t0002g0029others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-557+424T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918895 | ||||||
chr4:174918952
|
A | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(221): Show | 257 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.-557+481A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918952 | ||||||
chr4:174919271
|
A | G | 1 | a0001c0001t0002g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-557+800A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919271 | ||||||
chr4:174919586
|
T | C | 9 | a0001c0001t0002g0232a0001c0001t0002g0233a0004c0004t0002g0228others(6): Show | 10 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-556-1101T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919586 | ||||||
chr4:174919633
|
C | G | 1 | a0001c0009t0013g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-556-1054C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919633 | ||||||
chr4:174919741
|
T | C | 1 | a0003c0003t0002g0236 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-556-946T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919741 | ||||||
chr4:174919751
|
G | A | 264 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(261): Show | 303 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.-556-936G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919751 | ||||||
chr4:174919752
|
T | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(58): Show | 78 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-556-935T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919752 | ||||||
chr4:174920007
|
T | A | 1 | a0002c0002t0001g0101 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-556-680T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920007 | ||||||
chr4:174920033
|
T | C | 8 | a0001c0001t0003g0008a0001c0001t0003g0040a0001c0001t0003g0041others(5): Show | 9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-556-654T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920033 | ||||||
chr4:174920083
|
G | A | 7 | a0001c0001t0002g0035a0001c0006t0002g0032a0001c0006t0002g0033others(4): Show | 7 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-556-604G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920083 | ||||||
chr4:174920113
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-556-574A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920113 | ||||||
chr4:174920150
|
C | G | 3 | a0001c0001t0004g0011a0001c0001t0006g0073a0004c0004t0004g0074 | 4 | HG03041.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-556-537C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920150 | ||||||
chr4:174920164
|
C | T | 1 | a0001c0006t0002g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-556-523C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920164 | ||||||
chr4:174920185
|
A | T | 1 | a0002c0002t0004g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-556-502A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920185 | ||||||
chr4:174920498
|
C | T | 1 | a0001c0001t0003g0005 | 3 | HG01106.hp2 HG01123.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-556-189C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920498 | ||||||
chr4:174920550
|
G | T | 1 | a0001c0001t0002g0284 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-556-137G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920550 | ||||||
chr4:174920962
|
A | G | 15 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0214others(12): Show | 18 | HG00323.hp2 HG01192.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-451+170A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174920962 | ||||||
chr4:174921011
|
A | G | 3 | a0001c0001t0002g0283a0001c0001t0008g0099a0001c0001t0008g0100 | 3 | HG01070.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-451+219A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921011 | ||||||
chr4:174921079
|
A | G | 148 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(145): Show | 163 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-451+287A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921079 | ||||||
chr4:174921343
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-451+551C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921343 | ||||||
chr4:174921344
|
G | A | 74 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(71): Show | 92 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-451+552G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921344 | ||||||
chr4:174921429
|
T | G | 222 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(219): Show | 255 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-451+637T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921429 | ||||||
chr4:174921478
|
C | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02132.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-451+686C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921478 | ||||||
chr4:174921504
|
A | G | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+712A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921504 | ||||||
chr4:174921580
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-451+788G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921580 | ||||||
chr4:174921635
|
A | G | 222 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(219): Show | 255 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-451+843A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921635 | ||||||
chr4:174921828
|
G | A | 74 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(71): Show | 92 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-451+1036G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921828 | ||||||
chr4:174921832
|
G | A | 2 | a0001c0001t0002g0238a0002c0002t0002g0237 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-451+1040G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921832 | ||||||
chr4:174921891
|
G | A | 5 | a0001c0001t0002g0003a0001c0001t0002g0238a0001c0008t0002g0097others(2): Show | 8 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-451+1099G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921891 | ||||||
chr4:174922016
|
A | G | 1 | a0009c0017t0002g0282 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-451+1224A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922016 | ||||||
chr4:174922077
|
A | G | 3 | a0001c0001t0004g0011a0001c0001t0006g0073a0004c0004t0004g0074 | 4 | HG03041.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-451+1285A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922077 | ||||||
chr4:174922174
|
C | T | 5 | a0001c0006t0002g0032a0001c0006t0002g0033a0002c0002t0002g0029others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-451+1382C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922174 | ||||||
chr4:174922223
|
AT | A | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+1432delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922223 | ||||||
chr4:174922226
|
C | A | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+1434C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922226 | ||||||
chr4:174922277
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-451+1485A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922277 | ||||||
chr4:174922306
|
G | A | 2 | a0001c0001t0002g0035a0004c0004t0002g0034 | 2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-451+1514G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922306 | ||||||
chr4:174922455
|
C | G | 1 | a0003c0003t0002g0281 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-451+1663C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922455 | ||||||
chr4:174922729
|
TA | T | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+1943delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174922729 | |||||
chr4:174922744
|
C | T | 2 | a0001c0001t0002g0035a0004c0004t0002g0034 | 2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-451+1952C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922744 | ||||||
chr4:174922778
|
T | C | 1 | a0003c0003t0002g0239 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-451+1986T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922778 | ||||||
chr4:174923009
|
G | A | 9 | a0001c0001t0002g0232a0001c0001t0002g0233a0004c0004t0002g0228others(6): Show | 10 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-451+2217G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923009 | ||||||
chr4:174923065
|
TA | T | 81 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(78): Show | 99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+2274delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923065 | ||||||
chr4:174923119
|
G | A | 81 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(78): Show | 99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+2327G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923119 | ||||||
chr4:174923156
|
G | A | 263 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(260): Show | 302 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.-451+2364G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923156 | ||||||
chr4:174923205
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-451+2413C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923205 | ||||||
chr4:174923214
|
A | G | 2 | a0001c0001t0002g0280a0001c0001t0002g0285 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-451+2422A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923214 | ||||||
chr4:174923245
|
C | G | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+2453C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923245 | ||||||
chr4:174923306
|
C | T | 1 | a0001c0009t0011g0095 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-451+2514C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923306 | ||||||
chr4:174923350
|
T | C | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+2558T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923350 | ||||||
chr4:174923380
|
T | G | 81 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(78): Show | 99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+2588T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923380 | ||||||
chr4:174923434
|
G | C | 81 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(78): Show | 99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+2642G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923434 | ||||||
chr4:174923519
|
T | TGATA | 8 | a0001c0001t0002g0232a0004c0004t0002g0026a0004c0004t0002g0272others(5): Show | 9 | HG01433.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-451+2727_-451+272 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923519 | ||||||
chr4:174923519
|
T | TGATATA | 8 | a0001c0001t0002g0233a0001c0009t0013g0039a0004c0004t0002g0027others(5): Show | 10 | HG01109.hp1 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-451+2727_-451+272 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923519 | ||||||
chr4:174923519
|
TTATATGT others(1): Show |
T | 6 | a0001c0001t0002g0264a0002c0002t0002g0262a0002c0002t0002g0266others(3): Show | 6 | HG02559.hp2 HG03239.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-451+2733_-451+274 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923519 | |||||
chr4:174923519
|
TTATATGT others(3): Show |
T | 34 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(31): Show | 47 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-451+2733_-451+274 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923519 | |||||
chr4:174923519
|
TTATATGT others(9): Show |
T | 4 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0016t0002g0037others(1): Show | 4 | HG02615.hp1 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-451+2733_-451+274 others(20): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923519 | |||||
chr4:174923519
|
TTATATGT others(17): Show |
T | 3 | a0001c0006t0002g0033a0004c0004t0009g0240a0004c0004t0009g0241 | 3 | HG02258.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-451+2733_-451+275 others(28): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923519 | |||||
chr4:174923520
|
T | G | 9 | a0001c0001t0002g0270a0001c0001t0002g0285a0004c0004t0002g0025others(6): Show | 10 | HG00639.hp1 HG00741.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-451+2728T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923520 | ||||||
chr4:174923523
|
ATG | A | 4 | a0002c0002t0002g0029a0002c0002t0002g0030a0004c0004t0002g0228others(1): Show | 4 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-451+2733_-451+273 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923523 | |||||
chr4:174923525
|
G | A | 28 | a0001c0001t0002g0035a0001c0001t0002g0232a0001c0001t0002g0233others(25): Show | 32 | HG00741.hp1 HG01109.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.-451+2733G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923525 | ||||||
chr4:174923525
|
G | GTGTA | 9 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(6): Show | 12 | HG00609.hp2 HG00673.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
G | GTGTATA | 47 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(44): Show | 53 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
G | GTGTATAT others(1): Show |
26 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0152others(23): Show | 26 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
G | GTGTATAT others(3): Show |
17 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(14): Show | 17 | HG00408.hp1 HG00438.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
G | GTGTATAT others(5): Show |
28 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0021others(25): Show | 33 | HG00323.hp2 HG01168.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(16): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
G | GTGTATAT others(7): Show |
8 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(5): Show | 9 | HG00558.hp2 HG01261.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(18): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
G | GTGTATAT others(13): Show |
1 | a0002c0002t0001g0206 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-451+2734_-451+273 others(24): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
G | GTGTGTGT others(3): Show |
1 | a0002c0002t0001g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-451+2734_-451+273 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
GTA | G | 7 | a0001c0001t0004g0078a0001c0001t0004g0079a0001c0001t0006g0082others(4): Show | 7 | HG00544.hp1 HG01168.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-451+2768_-451+276 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
GTATA | G | 4 | a0001c0001t0003g0071a0001c0001t0004g0076a0002c0002t0003g0072others(1): Show | 4 | HG01256.hp2 HG01361.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-451+2766_-451+276 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
GTATATA | G | 10 | a0001c0001t0003g0010a0001c0001t0003g0064a0001c0001t0003g0066others(7): Show | 12 | HG00323.hp1 HG01106.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-451+2764_-451+276 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
GTATATAT others(1): Show |
G | 25 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(22): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-451+2762_-451+276 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
GTATATAT others(3): Show |
G | 3 | a0001c0001t0003g0040a0001c0001t0006g0073a0004c0004t0006g0050 | 3 | HG01433.hp2 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-451+2760_-451+276 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923525
|
GTATATAT others(15): Show |
G | 1 | a0001c0001t0001g0105 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-451+2748_-451+276 others(26): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | |||||
chr4:174923526
|
T | G | 1 | a0001c0001t0002g0028 | 2 | HG00735.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-451+2734T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923526 | ||||||
chr4:174923528
|
T | G | 6 | a0001c0001t0002g0264a0002c0002t0002g0262a0002c0002t0002g0266others(3): Show | 6 | HG02559.hp2 HG03239.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-451+2736T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923528 | ||||||
chr4:174923530
|
T | G | 33 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(30): Show | 46 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-451+2738T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923530 | ||||||
chr4:174923533
|
A | G | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+2741A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923533 | ||||||
chr4:174923536
|
T | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0016t0002g0037others(1): Show | 4 | HG02615.hp1 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-451+2744T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923536 | ||||||
chr4:174923544
|
T | G | 2 | a0004c0004t0009g0240a0004c0004t0009g0241 | 2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-451+2752T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923544 | ||||||
chr4:174923549
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-451+2757A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923549 | ||||||
chr4:174923560
|
T | G | 221 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(218): Show | 254 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-451+2768T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923560 | ||||||
chr4:174923602
|
A | C | 2 | a0001c0001t0002g0035a0004c0004t0002g0034 | 2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-451+2810A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923602 | ||||||
chr4:174923602
|
A | G | 1 | a0004c0004t0001g0184 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-451+2810A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923602 | ||||||
chr4:174923721
|
A | G | 40 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(37): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-451+2929A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923721 | ||||||
chr4:174923812
|
C | A | 2 | a0001c0001t0008g0099a0001c0001t0008g0100 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-451+3020C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923812 | ||||||
chr4:174923865
|
A | C | 5 | a0001c0006t0002g0032a0001c0006t0002g0033a0002c0002t0002g0029others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-451+3073A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923865 | ||||||
chr4:174923876
|
C | G | 3 | a0002c0002t0001g0017a0002c0002t0001g0200a0002c0002t0001g0205 | 4 | NA18947.hp2 NA18962.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-451+3084C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923876 | ||||||
chr4:174923909
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 10 | NA18939.hp2 NA18945.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.-451+3117C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923909 | ||||||
chr4:174923980
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-451+3188T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923980 | ||||||
chr4:174924114
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-451+3322T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924114 | ||||||
chr4:174924283
|
T | C | 2 | a0001c0001t0008g0099a0001c0001t0008g0100 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-451+3491T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924283 | ||||||
chr4:174924440
|
C | T | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+3648C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924440 | ||||||
chr4:174924596
|
G | A | 1 | a0002c0002t0004g0083 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-451+3804G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924596 | ||||||
chr4:174924718
|
C | T | 70 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(67): Show | 88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-451+3926C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924718 | ||||||
chr4:174924841
|
G | A | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+4049G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924841 | ||||||
chr4:174924959
|
G | A | 81 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(78): Show | 99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+4167G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924959 | ||||||
chr4:174925169
|
A | G | 76 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(73): Show | 94 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-451+4377A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925169 | ||||||
chr4:174925176
|
G | A | 2 | a0001c0001t0008g0099a0001c0001t0008g0100 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-451+4384G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925176 | ||||||
chr4:174925204
|
C | T | 1 | a0004c0004t0002g0275 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-451+4412C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925204 | ||||||
chr4:174925275
|
C | A | 70 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(67): Show | 88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-451+4483C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925275 | ||||||
chr4:174925327
|
A | G | 1 | a0001c0009t0013g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-451+4535A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925327 | ||||||
chr4:174925349
|
ACT | A | 36 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(33): Show | 41 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-451+4560_-451+456 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174925349 | |||||
chr4:174925367
|
AT | A | 153 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(150): Show | 169 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.-451+4585delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174925367 | |||||
chr4:174925390
|
A | G | 2 | a0001c0001t0002g0035a0004c0004t0002g0034 | 2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-451+4598A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925390 | ||||||
chr4:174925405
|
A | G | 1 | a0001c0006t0002g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-451+4613A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925405 | ||||||
chr4:174925456
|
T | A | 1 | a0002c0002t0004g0084 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-451+4664T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925456 | ||||||
chr4:174925485
|
T | C | 1 | a0004c0015t0002g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-451+4693T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925485 | ||||||
chr4:174925498
|
A | G | 1 | a0002c0002t0002g0266 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-451+4706A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925498 | ||||||
chr4:174925539
|
C | A | 1 | a0001c0001t0004g0085 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-451+4747C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925539 | ||||||
chr4:174925590
|
C | T | 1 | a0003c0003t0002g0261 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-451+4798C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925590 | ||||||
chr4:174925682
|
CAGG | C | 5 | a0001c0006t0002g0032a0001c0006t0002g0033a0002c0002t0002g0029others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-451+4893_-451+489 others(7): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174925682 | |||||
chr4:174925685
|
G | A | 4 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0009t0013g0039others(1): Show | 4 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-451+4893G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925685 | ||||||
chr4:174925763
|
G | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0110a0001c0001t0001g0141others(6): Show | 11 | HG00423.hp1 HG00673.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.-451+4971G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925763 | ||||||
chr4:174925825
|
G | A | 138 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(135): Show | 150 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-451+5033G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925825 | ||||||
chr4:174925993
|
A | T | 74 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(71): Show | 92 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-450-4993A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925993 | ||||||
chr4:174926033
|
A | G | 2 | a0001c0001t0008g0099a0001c0001t0008g0100 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-450-4953A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926033 | ||||||
chr4:174926037
|
A | T | 2 | a0001c0001t0006g0082a0001c0009t0011g0095 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-450-4949A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926037 | ||||||
chr4:174926252
|
C | T | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-450-4734C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926252 | ||||||
chr4:174926263
|
C | T | 3 | a0001c0001t0004g0011a0001c0001t0006g0073a0004c0004t0004g0074 | 4 | HG03041.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-450-4723C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926263 | ||||||
chr4:174926265
|
C | T | 9 | a0001c0001t0002g0232a0001c0001t0002g0233a0004c0004t0002g0228others(6): Show | 10 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-450-4721C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926265 | ||||||
chr4:174926270
|
A | G | 4 | a0004c0004t0002g0026a0004c0004t0002g0242a0004c0004t0002g0274others(1): Show | 5 | HG02109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-450-4716A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926270 | ||||||
chr4:174926285
|
C | A | 42 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(39): Show | 48 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-450-4701C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926285 | ||||||
chr4:174926313
|
A | G | 2 | a0001c0001t0002g0035a0004c0004t0002g0034 | 2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-450-4673A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926313 | ||||||
chr4:174926376
|
T | C | 70 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(67): Show | 88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-450-4610T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926376 | ||||||
chr4:174926409
|
T | C | 2 | a0001c0001t0001g0112a0002c0002t0001g0113 | 2 | NA18962.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-450-4577T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926409 | ||||||
chr4:174926417
|
T | G | 1 | a0004c0004t0006g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-450-4569T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926417 | ||||||
chr4:174926541
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0148 | 3 | NA18945.hp1 NA18947.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-450-4445A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926541 | ||||||
chr4:174926600
|
T | C | 261 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(258): Show | 297 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.-450-4386T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926600 | ||||||
chr4:174926639
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-450-4347G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926639 | ||||||
chr4:174926721
|
C | CA | 17 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0219others(14): Show | 18 | HG01074.hp1 HG01934.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.-450-4248dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174926721 | |||||
chr4:174926721
|
C | CAA | 6 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0009t0013g0039others(3): Show | 6 | HG02451.hp1 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-450-4249_-450-424 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174926721 | |||||
chr4:174926721
|
C | CAAA | 58 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(55): Show | 75 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-450-4250_-450-424 others(7): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174926721 | |||||
chr4:174926721
|
CA | C | 9 | a0001c0001t0001g0169a0001c0006t0002g0032a0001c0006t0002g0033others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-450-4248delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174926721 | |||||
chr4:174926758
|
A | G | 40 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(37): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-450-4228A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926758 | ||||||
chr4:174926833
|
G | T | 1 | a0001c0001t0006g0082 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-450-4153G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926833 | ||||||
chr4:174926977
|
C | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0169 | 2 | NA18942.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-450-4009C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926977 | ||||||
chr4:174927217
|
A | C | 76 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(73): Show | 94 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-450-3769A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927217 | ||||||
chr4:174927391
|
A | G | 42 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(39): Show | 48 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-450-3595A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927391 | ||||||
chr4:174927432
|
A | C | 143 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(140): Show | 155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-450-3554A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927432 | ||||||
chr4:174927654
|
C | A | 3 | a0001c0001t0004g0011a0001c0001t0006g0073a0004c0004t0004g0074 | 4 | HG03041.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-450-3332C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927654 | ||||||
chr4:174927684
|
G | C | 1 | a0001c0009t0013g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-450-3302G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927684 | ||||||
chr4:174927887
|
T | C | 1 | a0006c0010t0003g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-450-3099T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927887 | ||||||
chr4:174927936
|
T | C | 1 | a0002c0002t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-450-3050T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927936 | ||||||
chr4:174927992
|
C | T | 2 | a0001c0001t0002g0035a0004c0004t0002g0034 | 2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-450-2994C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927992 | ||||||
chr4:174928138
|
A | G | 1 | a0001c0001t0006g0082 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-450-2848A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928138 | ||||||
chr4:174928195
|
A | G | 264 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(261): Show | 303 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.-450-2791A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928195 | ||||||
chr4:174928292
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-450-2694G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928292 | ||||||
chr4:174928292
|
G | T | 40 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0009others(37): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-450-2694G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928292 | ||||||
chr4:174928296
|
G | C | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-450-2690G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928296 | ||||||
chr4:174928365
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-450-2621G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928365 | ||||||
chr4:174928569
|
T | TAAAAAAA others(1): Show |
20 | a0001c0001t0001g0021a0001c0001t0001g0140a0001c0001t0001g0147others(17): Show | 21 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-450-2412_-450-240 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174928569 | |||||
chr4:174928569
|
T | TAAAAAAA others(2): Show |
163 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(160): Show | 183 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.-450-2413_-450-240 others(13): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174928569 | |||||
chr4:174928569
|
T | TAAAAAAA others(3): Show |
5 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0008g0099others(2): Show | 5 | HG00621.hp1 HG03130.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-450-2414_-450-240 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174928569 | |||||
chr4:174928569
|
T | TTAAAA | 14 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(11): Show | 16 | HG00735.hp1 HG01243.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.-450-2417_-450-241 others(9): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928569 | ||||||
chr4:174928569
|
T | TTAAAAA | 62 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(59): Show | 78 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-450-2417_-450-241 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928569 | ||||||
chr4:174928747
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-450-2239A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928747 | ||||||
chr4:174928767
|
G | T | 1 | a0001c0001t0003g0062 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-450-2219G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928767 | ||||||
chr4:174928820
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0009t0013g0039others(1): Show | 4 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-450-2166A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928820 | ||||||
chr4:174928833
|
T | A | 76 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(73): Show | 94 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-450-2153T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928833 | ||||||
chr4:174928931
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-450-2055G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928931 | ||||||
chr4:174929035
|
A | C | 2 | a0001c0001t0005g0278a0001c0001t0005g0279 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-450-1951A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929035 | ||||||
chr4:174929081
|
G | A | 1 | a0001c0001t0006g0082 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-450-1905G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929081 | ||||||
chr4:174929332
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-450-1654G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929332 | ||||||
chr4:174929454
|
T | G | 73 | a0001c0001t0001g0117a0001c0001t0002g0001a0001c0001t0002g0007others(70): Show | 91 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-450-1532T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929454 | ||||||
chr4:174929455
|
T | C | 2 | a0004c0015t0002g0229a0007c0012t0014g0031 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-450-1531T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929455 | ||||||
chr4:174929647
|
GT | G | 39 | a0001c0001t0001g0102a0001c0001t0001g0149a0001c0001t0001g0156others(36): Show | 41 | HG00280.hp1 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.-450-1334delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174929647 | |||||
chr4:174929723
|
T | C | 2 | a0001c0001t0003g0052a0001c0001t0003g0053 | 2 | HG01099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-450-1263T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929723 | ||||||
chr4:174929755
|
CT | C | 219 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(216): Show | 255 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.-450-1217delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174929755 | |||||
chr4:174929859
|
C | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0038 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-450-1127C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929859 | ||||||
chr4:174929868
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-450-1118T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929868 | ||||||
chr4:174929902
|
G | A | 2 | a0002c0002t0002g0262a0002c0002t0002g0266 | 2 | HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-450-1084G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929902 | ||||||
chr4:174929975
|
C | A | 103 | a0001c0001t0001g0102a0001c0001t0001g0149a0001c0001t0001g0156others(100): Show | 122 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-450-1011C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929975 | ||||||
chr4:174929984
|
A | T | 1 | a0001c0001t0002g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-450-1002A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929984 | ||||||
chr4:174929991
|
T | C | 103 | a0001c0001t0001g0102a0001c0001t0001g0149a0001c0001t0001g0156others(100): Show | 122 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-450-995T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929991 | ||||||
chr4:174930051
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-450-935C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930051 | ||||||
chr4:174930073
|
C | T | 2 | a0002c0002t0003g0070a0002c0002t0003g0072 | 2 | HG01106.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-450-913C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930073 | ||||||
chr4:174930369
|
T | G | 67 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(64): Show | 84 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-450-617T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930369 | ||||||
chr4:174930658
|
G | A | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-450-328G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930658 | ||||||
chr4:174930803
|
A | G | 1 | a0001c0001t0002g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-450-183A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930803 | ||||||
chr4:174930828
|
T | C | 258 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(255): Show | 296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-450-158T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930828 | ||||||
chr4:174931291
|
A | T | 2 | a0001c0001t0002g0284a0003c0003t0002g0257 | 2 | NA18942.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-262+117A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931291 | ||||||
chr4:174931337
|
A | G | 9 | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0006t0002g0032others(6): Show | 12 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-262+163A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931337 | ||||||
chr4:174931470
|
T | C | 1 | a0007c0012t0014g0031 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-262+296T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931470 | ||||||
chr4:174931541
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-262+367T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931541 | ||||||
chr4:174931749
|
T | C | 68 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(65): Show | 85 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-262+575T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931749 | ||||||
chr4:174931778
|
G | T | 67 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(64): Show | 84 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-262+604G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931778 | ||||||
chr4:174931785
|
C | G | 8 | a0001c0001t0002g0232a0001c0001t0006g0082a0004c0004t0002g0228others(5): Show | 9 | HG02109.hp2 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-262+611C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931785 | ||||||
chr4:174931816
|
T | TCA | 15 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0214others(12): Show | 18 | HG00323.hp2 HG01192.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-262+661_-262+662d others(4): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174931816 | |||||
chr4:174931816
|
T | TCACA | 74 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(71): Show | 81 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-262+659_-262+662d others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174931816 | |||||
chr4:174931816
|
T | TCACACA | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0227 | 3 | HG00642.hp1 NA19060.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-262+657_-262+662d others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174931816 | |||||
chr4:174931816
|
TCA | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(65): Show | 85 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-262+661_-262+662d others(4): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174931816 | |||||
chr4:174931874
|
A | G | 1 | a0004c0004t0002g0242 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-262+700A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931874 | ||||||
chr4:174931881
|
T | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(65): Show | 85 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-262+707T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931881 | ||||||
chr4:174931934
|
A | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0016t0002g0037 | 3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-262+760A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931934 | ||||||
chr4:174932163
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-262+989C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932163 | ||||||
chr4:174932253
|
T | C | 258 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(255): Show | 296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-262+1079T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932253 | ||||||
chr4:174932297
|
G | GA | 67 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(64): Show | 83 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-262+1132dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174932297 | |||||
chr4:174932308
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 6 | HG00423.hp1 HG00621.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-262+1134G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932308 | ||||||
chr4:174932336
|
T | C | 8 | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0006t0002g0032others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-262+1162T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932336 | ||||||
chr4:174932364
|
G | A | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 201 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-262+1190G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932364 | ||||||
chr4:174932379
|
A | T | 1 | a0001c0001t0001g0196 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-262+1205A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932379 | ||||||
chr4:174932384
|
A | G | 127 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(124): Show | 139 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-262+1210A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932384 | ||||||
chr4:174932621
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-262+1447G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932621 | ||||||
chr4:174932872
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(88): Show | 101 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-262+1698G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932872 | ||||||
chr4:174932916
|
A | C | 1 | a0002c0002t0002g0262 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-262+1742A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932916 | ||||||
chr4:174932966
|
C | T | 2 | a0001c0008t0002g0097a0001c0008t0002g0098 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-262+1792C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932966 | ||||||
chr4:174933028
|
A | G | 3 | a0001c0001t0002g0233a0005c0007t0002g0230a0005c0007t0002g0234 | 3 | HG02630.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-262+1854A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933028 | ||||||
chr4:174933270
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-262+2096A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933270 | ||||||
chr4:174933318
|
C | T | 67 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(64): Show | 84 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-262+2144C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933318 | ||||||
chr4:174933347
|
C | T | 63 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(60): Show | 80 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-262+2173C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933347 | ||||||
chr4:174933362
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-262+2188T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933362 | ||||||
chr4:174933477
|
TA | T | 7 | a0001c0001t0002g0232a0001c0001t0006g0082a0002c0002t0004g0081others(4): Show | 8 | HG00544.hp1 HG02109.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-262+2313delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174933477 | |||||
chr4:174933511
|
G | C | 3 | a0001c0001t0002g0233a0005c0007t0002g0230a0005c0007t0002g0234 | 3 | HG02630.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-262+2337G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933511 | ||||||
chr4:174933515
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-262+2341G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933515 | ||||||
chr4:174933531
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-262+2357A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933531 | ||||||
chr4:174934002
|
T | G | 128 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(125): Show | 140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.-262+2828T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934002 | ||||||
chr4:174934158
|
T | C | 2 | a0001c0001t0002g0277a0001c0001t0002g0283 | 2 | HG01070.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-261-2775T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934158 | ||||||
chr4:174934183
|
C | T | 249 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(246): Show | 286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-261-2750C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934183 | ||||||
chr4:174934258
|
A | G | 63 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(60): Show | 80 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-261-2675A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934258 | ||||||
chr4:174934301
|
T | A | 2 | a0001c0001t0002g0003a0004c0004t0006g0050 | 5 | HG02258.hp1 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261-2632T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934301 | ||||||
chr4:174934365
|
T | C | 1 | a0001c0001t0003g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-261-2568T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934365 | ||||||
chr4:174934421
|
T | C | 249 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(246): Show | 286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-261-2512T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934421 | ||||||
chr4:174934429
|
T | G | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-261-2504T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934429 | ||||||
chr4:174934551
|
G | A | 3 | a0001c0001t0004g0011a0001c0001t0005g0181a0004c0004t0004g0074 | 4 | HG03130.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261-2382G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934551 | ||||||
chr4:174934642
|
A | G | 9 | a0001c0001t0002g0232a0001c0001t0006g0082a0004c0004t0002g0034others(6): Show | 10 | HG02109.hp2 HG02572.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261-2291A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934642 | ||||||
chr4:174934966
|
T | C | 146 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(143): Show | 161 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-261-1967T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934966 | ||||||
chr4:174935062
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-261-1871T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935062 | ||||||
chr4:174935154
|
G | T | 249 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(246): Show | 286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-261-1779G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935154 | ||||||
chr4:174935160
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0111others(2): Show | 7 | NA18939.hp2 NA18945.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261-1773C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935160 | ||||||
chr4:174935188
|
C | T | 1 | a0004c0004t0002g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-261-1745C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935188 | ||||||
chr4:174935309
|
G | T | 248 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(245): Show | 285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-261-1624G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935309 | ||||||
chr4:174935442
|
T | C | 63 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(60): Show | 80 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-261-1491T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935442 | ||||||
chr4:174935463
|
A | C | 1 | a0004c0004t0006g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-261-1470A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935463 | ||||||
chr4:174935491
|
A | G | 250 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(247): Show | 287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-261-1442A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935491 | ||||||
chr4:174935492
|
T | C | 6 | a0001c0001t0002g0232a0001c0001t0006g0082a0004c0004t0002g0228others(3): Show | 7 | HG02109.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261-1441T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935492 | ||||||
chr4:174935531
|
G | A | 3 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0016t0002g0037 | 3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-261-1402G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935531 | ||||||
chr4:174935755
|
T | C | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-261-1178T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935755 | ||||||
chr4:174935851
|
T | G | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-261-1082T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935851 | ||||||
chr4:174936124
|
A | G | 2 | a0002c0002t0003g0070a0002c0002t0003g0072 | 2 | HG01106.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-261-809A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936124 | ||||||
chr4:174936249
|
A | C | 42 | a0001c0001t0002g0035a0001c0001t0002g0193a0001c0001t0002g0233others(39): Show | 47 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-261-684A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936249 | ||||||
chr4:174936256
|
C | T | 248 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(245): Show | 285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-261-677C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936256 | ||||||
chr4:174936297
|
T | C | 9 | a0001c0001t0002g0232a0001c0001t0006g0082a0004c0004t0002g0034others(6): Show | 10 | HG02109.hp2 HG02572.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261-636T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936297 | ||||||
chr4:174936417
|
C | T | 1 | a0001c0006t0002g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-261-516C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936417 | ||||||
chr4:174936591
|
A | G | 2 | a0001c0001t0008g0099a0001c0001t0008g0100 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-261-342A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936591 | ||||||
chr4:174936603
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-261-330T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936603 | ||||||
chr4:174936760
|
C | A | 4 | a0004c0004t0002g0228a0005c0005t0002g0022a0005c0005t0002g0231others(1): Show | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261-173C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936760 | ||||||
chr4:174936846
|
A | T | 36 | a0001c0001t0002g0193a0001c0001t0003g0005a0001c0001t0003g0008others(33): Show | 41 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-261-87A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936846 | ||||||
chr4:174936878
|
G | A | 248 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(245): Show | 285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-261-55G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936878 | ||||||
chr4:174937046
|
A | T | 1 | a0001c0001t0001g0166 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-181+33A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937046 | ||||||
chr4:174937098
|
C | T | 1 | a0002c0002t0001g0113 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-181+85C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937098 | ||||||
chr4:174937264
|
G | A | 2 | a0004c0015t0002g0229a0007c0012t0014g0031 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-181+251G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937264 | ||||||
chr4:174937269
|
C | G | 2 | a0005c0007t0002g0230a0005c0007t0002g0234 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-181+256C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937269 | ||||||
chr4:174937373
|
A | G | 1 | a0002c0002t0004g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-181+360A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937373 | ||||||
chr4:174937377
|
T | C | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+364T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937377 | ||||||
chr4:174937405
|
C | G | 2 | a0001c0001t0008g0099a0001c0001t0008g0100 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-181+392C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937405 | ||||||
chr4:174937531
|
A | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(88): Show | 101 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-181+518A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937531 | ||||||
chr4:174937552
|
A | G | 1 | a0002c0002t0012g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-181+539A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937552 | ||||||
chr4:174937645
|
C | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(61): Show | 81 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-181+632C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937645 | ||||||
chr4:174937757
|
G | C | 251 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(248): Show | 288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-181+744G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937757 | ||||||
chr4:174937837
|
A | T | 1 | a0001c0001t0003g0045 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-181+824A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937837 | ||||||
chr4:174937995
|
G | A | 249 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(246): Show | 286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-181+982G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937995 | ||||||
chr4:174938186
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0140 | 2 | NA19000.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-181+1173A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938186 | ||||||
chr4:174938222
|
A | C | 1 | a0001c0001t0001g0139 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-181+1209A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938222 | ||||||
chr4:174938231
|
C | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(61): Show | 81 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-181+1218C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938231 | ||||||
chr4:174938275
|
T | C | 8 | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0006t0002g0032others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+1262T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938275 | ||||||
chr4:174938461
|
A | G | 46 | a0001c0001t0001g0102a0001c0001t0001g0149a0001c0001t0001g0156others(43): Show | 51 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.-181+1448A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938461 | ||||||
chr4:174938509
|
G | A | 8 | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0006t0002g0032others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+1496G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938509 | ||||||
chr4:174938553
|
GTTTCATA others(9): Show |
G | 4 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0009t0013g0039others(1): Show | 4 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+1552_-181+156 others(20): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174938553 | |||||
chr4:174938572
|
T | C | 64 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(61): Show | 81 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-181+1559T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938572 | ||||||
chr4:174938871
|
C | T | 2 | a0002c0002t0001g0174a0002c0002t0001g0183 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-181+1858C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938871 | ||||||
chr4:174939056
|
A | C | 259 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(256): Show | 297 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.-181+2043A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939056 | ||||||
chr4:174939097
|
T | TA | 3 | a0001c0001t0006g0073a0001c0001t0008g0099a0001c0001t0008g0100 | 3 | HG03041.hp1 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-181+2085dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174939097 | |||||
chr4:174939145
|
A | G | 3 | a0001c0001t0006g0073a0001c0001t0008g0099a0001c0001t0008g0100 | 3 | HG03041.hp1 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-181+2132A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939145 | ||||||
chr4:174939173
|
T | G | 3 | a0001c0001t0004g0011a0001c0001t0005g0181a0004c0004t0004g0074 | 4 | HG03130.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+2160T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939173 | ||||||
chr4:174939177
|
A | G | 1 | a0001c0001t0002g0256 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-181+2164A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939177 | ||||||
chr4:174939269
|
A | G | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-181+2256A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939269 | ||||||
chr4:174939311
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-181+2298A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939311 | ||||||
chr4:174939405
|
G | A | 2 | a0004c0015t0002g0229a0007c0012t0014g0031 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-181+2392G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939405 | ||||||
chr4:174939412
|
C | A | 38 | a0001c0001t0002g0035a0001c0001t0002g0193a0001c0001t0003g0005others(35): Show | 43 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.-181+2399C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939412 | ||||||
chr4:174939746
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0285a0004c0004t0002g0267 | 3 | HG00639.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-181+2733A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939746 | ||||||
chr4:174939893
|
A | C | 6 | a0001c0001t0004g0011a0001c0001t0005g0181a0001c0008t0002g0097others(3): Show | 7 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-181+2880A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939893 | ||||||
chr4:174939910
|
A | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(221): Show | 258 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.-181+2897A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939910 | ||||||
chr4:174940020
|
C | G | 126 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(123): Show | 138 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-181+3007C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940020 | ||||||
chr4:174940064
|
T | C | 69 | a0001c0001t0001g0121a0001c0001t0002g0001a0001c0001t0002g0007others(66): Show | 87 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-181+3051T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940064 | ||||||
chr4:174940337
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0177a0003c0003t0001g0171 | 3 | HG02027.hp2 HG02074.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-181+3324A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940337 | ||||||
chr4:174940362
|
G | A | 1 | a0002c0002t0001g0186 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-181+3349G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940362 | ||||||
chr4:174940514
|
G | GA | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+3507dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174940514 | |||||
chr4:174940531
|
A | C | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+3518A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940531 | ||||||
chr4:174940567
|
CT | C | 8 | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0006t0002g0032others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+3561delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174940567 | |||||
chr4:174940688
|
G | T | 1 | a0001c0001t0006g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+3675G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940688 | ||||||
chr4:174940753
|
T | A | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+3740T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940753 | ||||||
chr4:174940847
|
T | C | 1 | a0001c0009t0013g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-181+3834T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940847 | ||||||
chr4:174940898
|
C | T | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+3885C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940898 | ||||||
chr4:174940947
|
C | T | 1 | a0005c0007t0002g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-181+3934C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940947 | ||||||
chr4:174941000
|
A | G | 1 | a0004c0015t0002g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-181+3987A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941000 | ||||||
chr4:174941056
|
G | A | 3 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0016t0002g0037 | 3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-181+4043G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941056 | ||||||
chr4:174941126
|
A | G | 1 | a0002c0002t0004g0080 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-181+4113A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941126 | ||||||
chr4:174941252
|
T | C | 3 | a0002c0002t0004g0077a0002c0002t0004g0083a0002c0002t0004g0086 | 3 | HG01123.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-181+4239T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941252 | ||||||
chr4:174941349
|
G | C | 1 | a0004c0004t0002g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-181+4336G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941349 | ||||||
chr4:174941371
|
A | T | 41 | a0001c0001t0002g0035a0001c0001t0002g0193a0001c0001t0002g0232others(38): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-181+4358A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941371 | ||||||
chr4:174941763
|
T | C | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+4750T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941763 | ||||||
chr4:174941854
|
A | T | 2 | a0004c0015t0002g0229a0007c0012t0014g0031 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-181+4841A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941854 | ||||||
chr4:174941864
|
C | T | 2 | a0001c0008t0002g0097a0001c0008t0002g0098 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-181+4851C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941864 | ||||||
chr4:174942045
|
T | G | 1 | a0001c0001t0003g0041 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-181+5032T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942045 | ||||||
chr4:174942307
|
C | T | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+5294C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942307 | ||||||
chr4:174942425
|
C | T | 2 | a0005c0007t0002g0230a0005c0007t0002g0234 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-181+5412C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942425 | ||||||
chr4:174942426
|
G | A | 5 | a0001c0001t0001g0115a0002c0002t0003g0065a0002c0002t0003g0070others(2): Show | 5 | HG01074.hp1 HG01106.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-181+5413G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942426 | ||||||
chr4:174942470
|
G | C | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+5457G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942470 | ||||||
chr4:174942480
|
C | T | 1 | a0004c0004t0002g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-181+5467C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942480 | ||||||
chr4:174942488
|
ATCTGCCA others(5): Show |
A | 3 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0016t0002g0037 | 3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-181+5477_-181+548 others(16): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174942488 | |||||
chr4:174942562
|
T | TG | 8 | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0006t0002g0032others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+5551dupG | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174942562 | |||||
chr4:174942615
|
A | C | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-181+5602A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942615 | ||||||
chr4:174943046
|
A | G | 8 | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0006t0002g0032others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+6033A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943046 | ||||||
chr4:174943219
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-181+6206A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943219 | ||||||
chr4:174943259
|
A | T | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+6246A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943259 | ||||||
chr4:174943411
|
A | G | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+6398A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943411 | ||||||
chr4:174943482
|
G | A | 2 | a0004c0015t0002g0229a0007c0012t0014g0031 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-181+6469G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943482 | ||||||
chr4:174943526
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-181+6513G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943526 | ||||||
chr4:174943541
|
C | T | 1 | a0001c0001t0006g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+6528C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943541 | ||||||
chr4:174943590
|
G | A | 1 | a0002c0002t0012g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-181+6577G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943590 | ||||||
chr4:174943638
|
C | G | 2 | a0003c0003t0002g0263a0003c0003t0002g0265 | 2 | NA18981.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-181+6625C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943638 | ||||||
chr4:174943680
|
G | A | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+6667G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943680 | ||||||
chr4:174943701
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-181+6688C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943701 | ||||||
chr4:174943816
|
GA | G | 103 | a0001c0001t0001g0121a0001c0001t0002g0001a0001c0001t0002g0003others(100): Show | 128 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-181+6815delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174943816 | |||||
chr4:174943828
|
AG | A | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+6817delG | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174943828 | |||||
chr4:174943905
|
T | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0177a0003c0003t0001g0171 | 3 | HG02027.hp2 HG02074.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-181+6892T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943905 | ||||||
chr4:174944310
|
G | A | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+7297G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944310 | ||||||
chr4:174944391
|
C | G | 41 | a0001c0001t0002g0035a0001c0001t0002g0193a0001c0001t0002g0232others(38): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-181+7378C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944391 | ||||||
chr4:174944442
|
A | T | 262 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(259): Show | 301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-181+7429A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944442 | ||||||
chr4:174944477
|
A | G | 1 | a0001c0016t0002g0037 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-181+7464A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944477 | ||||||
chr4:174944540
|
T | C | 1 | a0001c0006t0002g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-181+7527T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944540 | ||||||
chr4:174944557
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-181+7544T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944557 | ||||||
chr4:174944600
|
G | T | 1 | a0002c0002t0001g0101 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-181+7587G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944600 | ||||||
chr4:174944612
|
T | C | 262 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(259): Show | 301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-181+7599T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944612 | ||||||
chr4:174944638
|
G | C | 1 | a0001c0001t0006g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+7625G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944638 | ||||||
chr4:174944968
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-181+7955C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944968 | ||||||
chr4:174944975
|
G | T | 41 | a0001c0001t0002g0035a0001c0001t0002g0193a0001c0001t0002g0232others(38): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-181+7962G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944975 | ||||||
chr4:174945193
|
C | A | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+8180C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945193 | ||||||
chr4:174945301
|
AG | A | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+8291delG | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174945301 | |||||
chr4:174945396
|
C | A | 1 | a0001c0001t0002g0003 | 4 | HG02258.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+8383C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945396 | ||||||
chr4:174945407
|
T | G | 2 | a0001c0001t0005g0278a0001c0001t0005g0279 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-181+8394T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945407 | ||||||
chr4:174945652
|
C | T | 1 | a0001c0001t0006g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+8639C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945652 | ||||||
chr4:174945669
|
A | G | 1 | a0001c0001t0002g0233 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-181+8656A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945669 | ||||||
chr4:174945709
|
G | A | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+8696G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945709 | ||||||
chr4:174945759
|
C | T | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+8746C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945759 | ||||||
chr4:174945781
|
T | C | 1 | a0003c0003t0001g0187 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-181+8768T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945781 | ||||||
chr4:174945941
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0123 | 2 | HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-181+8928T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945941 | ||||||
chr4:174946105
|
G | T | 1 | a0001c0001t0001g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-181+9092G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946105 | ||||||
chr4:174946119
|
A | G | 1 | a0001c0001t0003g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-181+9106A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946119 | ||||||
chr4:174946291
|
C | T | 171 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(168): Show | 188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-181+9278C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946291 | ||||||
chr4:174946461
|
C | T | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+9448C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946461 | ||||||
chr4:174946587
|
G | A | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+9574G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946587 | ||||||
chr4:174946638
|
A | G | 2 | a0001c0001t0003g0043a0001c0001t0003g0046 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-181+9625A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946638 | ||||||
chr4:174946708
|
T | A | 1 | a0001c0001t0006g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+9695T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946708 | ||||||
chr4:174946880
|
T | C | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+9867T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946880 | ||||||
chr4:174947020
|
C | T | 4 | a0001c0008t0002g0097a0001c0008t0002g0098a0004c0015t0002g0229others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+10007C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947020 | ||||||
chr4:174947043
|
A | G | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+10030A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947043 | ||||||
chr4:174947073
|
A | G | 41 | a0001c0001t0002g0035a0001c0001t0002g0193a0001c0001t0002g0232others(38): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-181+10060A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947073 | ||||||
chr4:174947132
|
C | G | 1 | a0002c0002t0001g0206 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-181+10119C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947132 | ||||||
chr4:174947143
|
T | A | 1 | a0004c0004t0002g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-181+10130T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947143 | ||||||
chr4:174947158
|
G | A | 3 | a0001c0001t0003g0009a0001c0001t0003g0047a0001c0001t0003g0048 | 4 | HG00738.hp1 HG01257.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+10145G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947158 | ||||||
chr4:174947285
|
T | G | 1 | a0001c0001t0003g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-181+10272T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947285 | ||||||
chr4:174947289
|
A | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(123): Show | 138 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-181+10276A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947289 | ||||||
chr4:174947337
|
T | G | 1 | a0002c0002t0002g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-181+10324T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947337 | ||||||
chr4:174947555
|
G | C | 1 | a0001c0001t0004g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-181+10542G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947555 | ||||||
chr4:174947606
|
G | A | 69 | a0001c0001t0001g0121a0001c0001t0002g0001a0001c0001t0002g0007others(66): Show | 87 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-181+10593G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947606 | ||||||
chr4:174947884
|
A | C | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+10871A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947884 | ||||||
chr4:174947983
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-181+10970T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947983 | ||||||
chr4:174947995
|
T | G | 185 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(182): Show | 206 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.-181+10982T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947995 | ||||||
chr4:174948293
|
T | G | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-181+11280T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948293 | ||||||
chr4:174948472
|
G | T | 3 | a0002c0002t0004g0077a0002c0002t0004g0083a0002c0002t0004g0086 | 3 | HG01123.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-181+11459G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948472 | ||||||
chr4:174948877
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-181+11864G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948877 | ||||||
chr4:174948894
|
A | G | 1 | a0001c0001t0007g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-181+11881A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948894 | ||||||
chr4:174948906
|
G | T | 1 | a0003c0003t0002g0257 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-181+11893G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948906 | ||||||
chr4:174949122
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-181+12109C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949122 | ||||||
chr4:174949171
|
C | G | 42 | a0001c0001t0002g0035a0001c0001t0002g0193a0001c0001t0002g0232others(39): Show | 47 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-181+12158C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949171 | ||||||
chr4:174949279
|
G | A | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+12266G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949279 | ||||||
chr4:174949294
|
C | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(90): Show | 103 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-181+12281C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949294 | ||||||
chr4:174949299
|
A | G | 143 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(140): Show | 159 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.-181+12286A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949299 | ||||||
chr4:174949525
|
G | A | 36 | a0001c0001t0002g0035a0001c0001t0002g0193a0001c0001t0003g0005others(33): Show | 40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-181+12512G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949525 | ||||||
chr4:174949589
|
G | A | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+12576G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949589 | ||||||
chr4:174949593
|
A | G | 41 | a0001c0001t0001g0102a0001c0001t0001g0149a0001c0001t0001g0156others(38): Show | 43 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-181+12580A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949593 | ||||||
chr4:174949610
|
T | C | 178 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(175): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.-181+12597T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949610 | ||||||
chr4:174949666
|
C | T | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+12653C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949666 | ||||||
chr4:174949693
|
T | C | 107 | a0001c0001t0001g0121a0001c0001t0001g0134a0001c0001t0001g0217others(104): Show | 130 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-181+12680T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949693 | ||||||
chr4:174949711
|
C | T | 1 | a0004c0004t0002g0273 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-181+12698C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949711 | ||||||
chr4:174949763
|
T | C | 152 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(149): Show | 171 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-181+12750T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949763 | ||||||
chr4:174949771
|
C | T | 134 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(131): Show | 149 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.-181+12758C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949771 | ||||||
chr4:174949793
|
C | A | 144 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(141): Show | 160 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.-181+12780C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949793 | ||||||
chr4:174949827
|
C | A | 1 | a0001c0001t0001g0172 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-181+12814C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949827 | ||||||
chr4:174949853
|
T | C | 8 | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0006t0002g0032others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+12840T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949853 | ||||||
chr4:174949950
|
C | A | 2 | a0001c0008t0002g0097a0001c0008t0002g0098 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-181+12937C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949950 | ||||||
chr4:174950298
|
A | G | 141 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(138): Show | 157 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-181+13285A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950298 | ||||||
chr4:174950411
|
A | G | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-181+13398A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950411 | ||||||
chr4:174950473
|
G | A | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+13460G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950473 | ||||||
chr4:174950843
|
G | A | 4 | a0001c0001t0002g0136a0001c0006t0002g0032a0001c0006t0002g0033others(1): Show | 4 | HG02886.hp2 HG03225.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+13830G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950843 | ||||||
chr4:174950926
|
A | G | 145 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(142): Show | 160 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-181+13913A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950926 | ||||||
chr4:174950980
|
G | C | 143 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(140): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.-181+13967G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950980 | ||||||
chr4:174951052
|
A | C | 147 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(144): Show | 162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-181+14039A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951052 | ||||||
chr4:174951119
|
T | G | 1 | a0001c0001t0003g0041 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-181+14106T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951119 | ||||||
chr4:174951202
|
C | A | 129 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(126): Show | 157 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.-181+14189C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951202 | ||||||
chr4:174951341
|
G | A | 147 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(144): Show | 162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-181+14328G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951341 | ||||||
chr4:174951411
|
C | T | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+14398C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951411 | ||||||
chr4:174951438
|
G | T | 1 | a0001c0001t0004g0078 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-181+14425G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951438 | ||||||
chr4:174951489
|
A | G | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+14476A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951489 | ||||||
chr4:174951541
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0255others(1): Show | 4 | HG01496.hp2 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+14528A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951541 | ||||||
chr4:174951715
|
A | G | 136 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(133): Show | 165 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.-181+14702A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951715 | ||||||
chr4:174951749
|
A | G | 82 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(79): Show | 99 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-181+14736A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951749 | ||||||
chr4:174951858
|
C | T | 1 | a0007c0012t0014g0031 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-181+14845C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951858 | ||||||
chr4:174951899
|
T | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+14886T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951899 | ||||||
chr4:174951953
|
C | A | 1 | a0001c0009t0013g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-181+14940C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951953 | ||||||
chr4:174951977
|
T | C | 1 | a0001c0001t0005g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-181+14964T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951977 | ||||||
chr4:174951996
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+14983C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951996 | ||||||
chr4:174952146
|
G | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+15133G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952146 | ||||||
chr4:174952350
|
C | CCA | 21 | a0001c0001t0001g0126a0001c0001t0001g0144a0001c0001t0001g0217others(18): Show | 26 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.-181+15367_-181+15 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | |||||
chr4:174952350
|
C | CCACA | 14 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0244others(11): Show | 16 | HG01109.hp2 HG01496.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-181+15365_-181+15 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | |||||
chr4:174952350
|
CCA | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0106others(74): Show | 96 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-181+15367_-181+15 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | |||||
chr4:174952350
|
CCACA | C | 9 | a0001c0001t0002g0136a0001c0001t0006g0073a0001c0001t0008g0099others(6): Show | 9 | HG01891.hp1 HG02622.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.-181+15365_-181+15 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | |||||
chr4:174952350
|
CCACACA | C | 13 | a0001c0001t0001g0142a0001c0001t0002g0233a0001c0001t0002g0277others(10): Show | 14 | HG00408.hp2 HG00642.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-181+15363_-181+15 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | |||||
chr4:174952444
|
G | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+15431G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952444 | ||||||
chr4:174952713
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+15700C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952713 | ||||||
chr4:174952739
|
AG | A | 122 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(119): Show | 149 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-181+15727delG | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952739 | ||||||
chr4:174952786
|
T | C | 2 | a0002c0002t0001g0174a0002c0002t0001g0183 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-181+15773T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952786 | ||||||
chr4:174952846
|
A | T | 122 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(119): Show | 149 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-181+15833A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952846 | ||||||
chr4:174952861
|
C | T | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+15848C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952861 | ||||||
chr4:174952992
|
A | G | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+15979A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952992 | ||||||
chr4:174953012
|
C | T | 1 | a0002c0002t0004g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-181+15999C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953012 | ||||||
chr4:174953142
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16129C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953142 | ||||||
chr4:174953172
|
G | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16159G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953172 | ||||||
chr4:174953214
|
A | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16201A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953214 | ||||||
chr4:174953216
|
G | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16203G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953216 | ||||||
chr4:174953229
|
T | G | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16216T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953229 | ||||||
chr4:174953255
|
T | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16242T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953255 | ||||||
chr4:174953280
|
T | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16267T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953280 | ||||||
chr4:174953333
|
A | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16320A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953333 | ||||||
chr4:174953368
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-181+16355A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953368 | ||||||
chr4:174953426
|
G | T | 1 | a0001c0001t0003g0064 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-181+16413G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953426 | ||||||
chr4:174953574
|
T | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16561T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953574 | ||||||
chr4:174953722
|
T | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16709T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953722 | ||||||
chr4:174953775
|
A | G | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16762A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953775 | ||||||
chr4:174953845
|
G | A | 3 | a0001c0001t0002g0136a0001c0006t0002g0032a0001c0006t0002g0033 | 3 | HG03225.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-181+16832G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953845 | ||||||
chr4:174953913
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16900C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953913 | ||||||
chr4:174953991
|
T | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16978T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953991 | ||||||
chr4:174953999
|
G | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16986G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953999 | ||||||
chr4:174954079
|
T | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17066T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954079 | ||||||
chr4:174954093
|
C | T | 3 | a0001c0001t0002g0136a0001c0006t0002g0032a0001c0006t0002g0033 | 3 | HG03225.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-181+17080C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954093 | ||||||
chr4:174954207
|
A | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17194A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954207 | ||||||
chr4:174954239
|
A | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17226A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954239 | ||||||
chr4:174954248
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17235C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954248 | ||||||
chr4:174954252
|
G | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17239G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954252 | ||||||
chr4:174954335
|
C | T | 1 | a0001c0001t0005g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-181+17322C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954335 | ||||||
chr4:174954453
|
T | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17440T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954453 | ||||||
chr4:174954474
|
G | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17461G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954474 | ||||||
chr4:174954477
|
T | C | 124 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(121): Show | 152 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-181+17464T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954477 | ||||||
chr4:174954496
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0232a0001c0001t0006g0082 | 6 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-181+17483C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954496 | ||||||
chr4:174954566
|
A | G | 1 | a0003c0003t0002g0167 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-181+17553A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954566 | ||||||
chr4:174954604
|
C | T | 1 | a0001c0009t0011g0095 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-181+17591C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954604 | ||||||
chr4:174954635
|
T | C | 6 | a0001c0001t0001g0149a0001c0001t0001g0172a0001c0001t0001g0188others(3): Show | 6 | HG01255.hp1 HG02523.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-181+17622T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954635 | ||||||
chr4:174954737
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-181+17724G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954737 | ||||||
chr4:174954863
|
A | G | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17850A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954863 | ||||||
chr4:174954911
|
C | G | 1 | a0003c0003t0001g0192 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-181+17898C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954911 | ||||||
chr4:174955002
|
A | C | 134 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(131): Show | 163 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.-181+17989A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955002 | ||||||
chr4:174955083
|
AT | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18078delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174955083 | |||||
chr4:174955172
|
T | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18159T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955172 | ||||||
chr4:174955173
|
G | A | 1 | a0004c0004t0002g0242 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-181+18160G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955173 | ||||||
chr4:174955198
|
G | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18185G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955198 | ||||||
chr4:174955205
|
A | G | 2 | a0001c0001t0001g0108a0003c0003t0001g0222 | 2 | HG01975.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-181+18192A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955205 | ||||||
chr4:174955222
|
G | A | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+18209G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955222 | ||||||
chr4:174955322
|
T | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18309T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955322 | ||||||
chr4:174955443
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-181+18430G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955443 | ||||||
chr4:174955516
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18503C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955516 | ||||||
chr4:174955661
|
C | CTTATT | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18651_-181+18 others(11): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174955661 | |||||
chr4:174955727
|
G | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18714G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955727 | ||||||
chr4:174955901
|
C | T | 83 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(80): Show | 100 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-181+18888C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955901 | ||||||
chr4:174956025
|
T | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+19012T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956025 | ||||||
chr4:174956044
|
A | G | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+19031A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956044 | ||||||
chr4:174956150
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-181+19137C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956150 | ||||||
chr4:174956209
|
G | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-19137G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956209 | ||||||
chr4:174956227
|
A | C | 3 | a0002c0002t0004g0077a0002c0002t0004g0083a0002c0002t0004g0086 | 3 | HG01123.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-180-19119A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956227 | ||||||
chr4:174956327
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-180-19019G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956327 | ||||||
chr4:174956406
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-18940C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956406 | ||||||
chr4:174956420
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-18926C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956420 | ||||||
chr4:174956440
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-18906C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956440 | ||||||
chr4:174956445
|
C | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0255 | 3 | HG01496.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-180-18901C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956445 | ||||||
chr4:174956448
|
T | G | 1 | a0001c0001t0002g0270 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-180-18898T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956448 | ||||||
chr4:174956475
|
G | GGT | 3 | a0003c0003t0001g0170a0003c0003t0002g0265a0004c0004t0002g0034 | 3 | HG02572.hp1 NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-180-18854_-180-18 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174956475 | |||||
chr4:174956508
|
T | G | 123 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(120): Show | 151 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-180-18838T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956508 | ||||||
chr4:174956510
|
G | T | 123 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(120): Show | 151 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-180-18836G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956510 | ||||||
chr4:174956513
|
A | T | 123 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(120): Show | 151 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-180-18833A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956513 | ||||||
chr4:174956522
|
GA | G | 124 | a0001c0001t0001g0102a0001c0001t0001g0124a0001c0001t0001g0133others(121): Show | 152 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-180-18816delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174956522 | |||||
chr4:174956551
|
A | G | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-18795A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956551 | ||||||
chr4:174956654
|
A | G | 1 | a0001c0016t0002g0037 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-180-18692A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956654 | ||||||
chr4:174956742
|
C | A | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-18604C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956742 | ||||||
chr4:174956766
|
A | G | 3 | a0001c0001t0002g0136a0001c0006t0002g0032a0001c0006t0002g0033 | 3 | HG03225.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-180-18580A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956766 | ||||||
chr4:174956887
|
A | G | 78 | a0001c0001t0001g0102a0001c0001t0001g0149a0001c0001t0001g0156others(75): Show | 92 | HG00544.hp1 HG00642.hp2 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.-180-18459A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956887 | ||||||
chr4:174956905
|
A | C | 2 | a0001c0001t0008g0099a0001c0001t0008g0100 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-180-18441A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956905 | ||||||
chr4:174957013
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-180-18333A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957013 | ||||||
chr4:174957413
|
C | T | 3 | a0001c0001t0008g0099a0001c0001t0008g0100a0004c0004t0002g0228 | 3 | HG03130.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-180-17933C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957413 | ||||||
chr4:174957414
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-17932C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957414 | ||||||
chr4:174957542
|
A | T | 1 | a0001c0001t0001g0112 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-180-17804A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957542 | ||||||
chr4:174957577
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-180-17769C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957577 | ||||||
chr4:174957767
|
T | C | 124 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(121): Show | 152 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-180-17579T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957767 | ||||||
chr4:174957771
|
T | C | 1 | a0001c0001t0005g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-180-17575T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957771 | ||||||
chr4:174958018
|
A | T | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-17328A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958018 | ||||||
chr4:174958064
|
A | T | 1 | a0001c0001t0007g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-180-17282A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958064 | ||||||
chr4:174958120
|
G | A | 2 | a0002c0002t0001g0101a0002c0002t0001g0189 | 2 | NA18970.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-180-17226G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958120 | ||||||
chr4:174958135
|
T | G | 2 | a0001c0008t0002g0097a0001c0008t0002g0098 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-180-17211T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958135 | ||||||
chr4:174958184
|
C | T | 2 | a0001c0001t0003g0069a0001c0001t0003g0071 | 2 | HG02738.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-180-17162C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958184 | ||||||
chr4:174958243
|
G | A | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-17103G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958243 | ||||||
chr4:174958245
|
G | GA | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-17101_-180-17 others(7): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958245 | ||||||
chr4:174958356
|
A | G | 132 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(129): Show | 161 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-180-16990A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958356 | ||||||
chr4:174958472
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16874C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958472 | ||||||
chr4:174958527
|
C | T | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16819C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958527 | ||||||
chr4:174958608
|
C | T | 1 | a0001c0001t0004g0092 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-180-16738C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958608 | ||||||
chr4:174958643
|
A | C | 1 | a0007c0012t0014g0031 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-180-16703A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958643 | ||||||
chr4:174958726
|
CTTTT | C | 15 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0122others(12): Show | 17 | HG00323.hp1 HG00323.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.-180-16616_-180-16 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174958726 | |||||
chr4:174958727
|
T | C | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16619T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958727 | ||||||
chr4:174958750
|
A | G | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16596A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958750 | ||||||
chr4:174958791
|
T | A | 1 | a0001c0001t0006g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-180-16555T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958791 | ||||||
chr4:174958859
|
A | C | 1 | a0001c0006t0002g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-180-16487A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958859 | ||||||
chr4:174958983
|
A | ATTG | 125 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16361_-180-16 others(9): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174958983 | |||||
chr4:174959044
|
A | T | 1 | a0001c0001t0002g0284 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-180-16302A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959044 | ||||||
chr4:174959205
|
T | A | 7 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(4): Show | 8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-16141T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959205 | ||||||
chr4:174959317
|
C | A | 1 | a0001c0001t0001g0139 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-180-16029C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959317 | ||||||
chr4:174959317
|
C | T | 3 | a0001c0001t0004g0011a0004c0004t0004g0074a0004c0004t0006g0050 | 4 | HG03098.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-16029C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959317 | ||||||
chr4:174959340
|
T | C | 7 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(4): Show | 8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-16006T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959340 | ||||||
chr4:174959417
|
A | G | 9 | a0001c0001t0002g0270a0004c0004t0002g0025a0004c0004t0002g0178others(6): Show | 10 | HG00741.hp1 HG01433.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-180-15929A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959417 | ||||||
chr4:174959457
|
C | CTG | 53 | a0001c0001t0001g0110a0001c0001t0001g0133a0001c0001t0001g0149others(50): Show | 67 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-180-15863_-180-15 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959457 | |||||
chr4:174959457
|
C | CTGTG | 30 | a0001c0001t0001g0102a0001c0001t0001g0140a0001c0001t0001g0156others(27): Show | 33 | HG01069.hp1 HG01070.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-180-15865_-180-15 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959457 | |||||
chr4:174959457
|
CTG | C | 15 | a0001c0001t0002g0136a0001c0001t0002g0252a0001c0001t0002g0258others(12): Show | 16 | HG00639.hp1 HG01109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.-180-15863_-180-15 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959457 | |||||
chr4:174959457
|
CTGTG | C | 4 | a0001c0016t0002g0037a0002c0002t0004g0002a0003c0003t0002g0119others(1): Show | 8 | HG02135.hp1 HG02818.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.-180-15865_-180-15 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959457 | |||||
chr4:174959477
|
GTGTGTGT others(1): Show |
G | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-15853_-180-15 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959477 | |||||
chr4:174959485
|
T | G | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-15861T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959485 | ||||||
chr4:174959503
|
C | G | 1 | a0001c0008t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-180-15843C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959503 | ||||||
chr4:174959504
|
T | C | 1 | a0001c0016t0002g0037 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-180-15842T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959504 | ||||||
chr4:174959604
|
A | G | 7 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(4): Show | 8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-15742A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959604 | ||||||
chr4:174959915
|
G | T | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-15431G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959915 | ||||||
chr4:174959954
|
G | A | 20 | a0001c0001t0002g0270a0001c0001t0004g0011a0004c0004t0001g0184others(17): Show | 24 | HG00741.hp1 HG01109.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-180-15392G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959954 | ||||||
chr4:174960025
|
G | A | 1 | a0001c0001t0007g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-180-15321G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960025 | ||||||
chr4:174960154
|
T | C | 7 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(4): Show | 8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-15192T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960154 | ||||||
chr4:174960191
|
G | C | 1 | a0001c0001t0002g0247 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-180-15155G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960191 | ||||||
chr4:174960193
|
G | T | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-15153G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960193 | ||||||
chr4:174960477
|
A | G | 2 | a0001c0016t0002g0037a0004c0004t0002g0034 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-180-14869A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960477 | ||||||
chr4:174960580
|
T | C | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-14766T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960580 | ||||||
chr4:174960685
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-180-14661T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960685 | ||||||
chr4:174960789
|
T | C | 7 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(4): Show | 8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-14557T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960789 | ||||||
chr4:174960934
|
T | C | 2 | a0004c0004t0009g0240a0004c0004t0009g0241 | 2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-180-14412T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960934 | ||||||
chr4:174960990
|
C | T | 130 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(127): Show | 159 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.-180-14356C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960990 | ||||||
chr4:174961040
|
A | G | 1 | a0001c0016t0002g0037 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-180-14306A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961040 | ||||||
chr4:174961226
|
A | G | 14 | a0001c0001t0005g0278a0001c0001t0005g0279a0001c0009t0011g0095others(11): Show | 18 | HG00544.hp1 HG01123.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-180-14120A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961226 | ||||||
chr4:174961319
|
T | C | 3 | a0005c0005t0002g0022a0005c0005t0002g0231a0005c0005t0002g0235 | 4 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-14027T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961319 | ||||||
chr4:174961728
|
G | A | 131 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(128): Show | 160 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.-180-13618G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961728 | ||||||
chr4:174961794
|
A | G | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-13552A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961794 | ||||||
chr4:174961938
|
T | C | 14 | a0001c0001t0005g0278a0001c0001t0005g0279a0001c0009t0011g0095others(11): Show | 18 | HG00544.hp1 HG01123.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-180-13408T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961938 | ||||||
chr4:174962034
|
G | A | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-13312G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962034 | ||||||
chr4:174962187
|
C | G | 2 | a0001c0008t0002g0097a0001c0008t0002g0098 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-180-13159C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962187 | ||||||
chr4:174962249
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0127others(5): Show | 10 | HG01255.hp2 HG01346.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-180-13097T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962249 | ||||||
chr4:174962264
|
T | C | 2 | a0001c0001t0002g0246a0001c0001t0002g0256 | 2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-180-13082T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962264 | ||||||
chr4:174962293
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-180-13053T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962293 | ||||||
chr4:174962318
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-180-13028T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962318 | ||||||
chr4:174962319
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-180-13027G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962319 | ||||||
chr4:174962380
|
G | C | 5 | a0001c0001t0002g0003a0001c0001t0002g0232a0001c0001t0006g0082others(2): Show | 8 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-180-12966G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962380 | ||||||
chr4:174962396
|
C | T | 2 | a0001c0006t0002g0032a0001c0006t0002g0033 | 2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-180-12950C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962396 | ||||||
chr4:174962441
|
A | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0255 | 3 | HG01496.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-180-12905A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962441 | ||||||
chr4:174962444
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0255others(1): Show | 4 | HG01496.hp2 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-12902A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962444 | ||||||
chr4:174962482
|
A | T | 1 | a0002c0002t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-180-12864A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962482 | ||||||
chr4:174962506
|
C | T | 2 | a0001c0001t0001g0211a0004c0004t0002g0027 | 3 | HG01109.hp1 NA18906.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-180-12840C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962506 | ||||||
chr4:174962511
|
C | CA | 22 | a0001c0001t0001g0194a0001c0001t0002g0244a0001c0001t0002g0277others(19): Show | 22 | HG01070.hp2 HG01928.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-180-12818dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174962511 | |||||
chr4:174962511
|
CA | C | 7 | a0001c0001t0001g0148a0001c0001t0002g0003a0001c0001t0002g0232others(4): Show | 10 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-180-12818delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174962511 | |||||
chr4:174962540
|
T | G | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-12806T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962540 | ||||||
chr4:174962784
|
GA | G | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-12553delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174962784 | |||||
chr4:174962994
|
A | G | 137 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(134): Show | 165 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.-180-12352A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962994 | ||||||
chr4:174963097
|
A | T | 1 | a0002c0002t0001g0114 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-180-12249A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963097 | ||||||
chr4:174963661
|
C | T | 2 | a0001c0001t0006g0073a0007c0012t0014g0031 | 2 | HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-180-11685C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963661 | ||||||
chr4:174963667
|
G | A | 112 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(109): Show | 135 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.-180-11679G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963667 | ||||||
chr4:174963690
|
AT | A | 112 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(109): Show | 135 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.-180-11648delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174963690 | |||||
chr4:174963841
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-180-11505C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963841 | ||||||
chr4:174963882
|
G | C | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-11464G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963882 | ||||||
chr4:174963891
|
G | A | 19 | a0001c0001t0002g0270a0004c0004t0001g0184a0004c0004t0002g0025others(16): Show | 22 | HG00741.hp1 HG01109.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-180-11455G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963891 | ||||||
chr4:174963905
|
G | A | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-11441G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963905 | ||||||
chr4:174963922
|
A | G | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-11424A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963922 | ||||||
chr4:174963951
|
G | A | 1 | a0007c0012t0014g0031 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-180-11395G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963951 | ||||||
chr4:174964087
|
A | C | 1 | a0001c0009t0013g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-180-11259A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964087 | ||||||
chr4:174964238
|
T | A | 1 | a0001c0009t0013g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-180-11108T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964238 | ||||||
chr4:174964289
|
A | T | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-11057A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964289 | ||||||
chr4:174964319
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-180-11027A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964319 | ||||||
chr4:174964426
|
C | T | 6 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-10920C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964426 | ||||||
chr4:174964508
|
A | G | 2 | a0002c0002t0001g0203a0002c0002t0001g0206 | 2 | NA19062.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-180-10838A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964508 | ||||||
chr4:174964548
|
A | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0201a0001c0001t0015g0153 | 3 | HG00558.hp2 HG00673.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-180-10798A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964548 | ||||||
chr4:174964882
|
GTGTT | G | 4 | a0001c0001t0001g0212a0001c0001t0002g0003a0001c0008t0002g0097others(1): Show | 7 | HG01891.hp1 HG02132.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-10461_-180-10 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174964882 | |||||
chr4:174964899
|
T | C | 1 | a0001c0016t0002g0037 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-180-10447T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964899 | ||||||
chr4:174964912
|
T | A | 1 | a0001c0009t0013g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-180-10434T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964912 | ||||||
chr4:174964926
|
C | T | 1 | a0002c0002t0001g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-180-10420C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964926 | ||||||
chr4:174965167
|
G | T | 1 | a0001c0001t0003g0010 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-180-10179G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965167 | ||||||
chr4:174965244
|
A | AAG | 120 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0127others(117): Show | 143 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-180-10092_-180-10 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965244 | |||||
chr4:174965412
|
A | T | 1 | a0002c0002t0003g0072 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-180-9934A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965412 | ||||||
chr4:174965446
|
A | C | 106 | a0001c0001t0001g0006a0001c0001t0001g0142a0001c0001t0001g0143others(103): Show | 127 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-180-9900A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965446 | ||||||
chr4:174965454
|
T | C | 1 | a0002c0002t0001g0168 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-180-9892T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965454 | ||||||
chr4:174965457
|
G | C | 1 | a0001c0001t0006g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-180-9889G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965457 | ||||||
chr4:174965484
|
C | CATCT | 89 | a0001c0001t0001g0015a0001c0001t0001g0129a0001c0001t0001g0143others(86): Show | 101 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.-180-9826_-180-982 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | |||||
chr4:174965484
|
C | CATCTATC others(1): Show |
45 | a0001c0001t0001g0122a0001c0001t0001g0134a0001c0001t0001g0138others(42): Show | 52 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-180-9830_-180-982 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | |||||
chr4:174965484
|
C | CATCTATC others(5): Show |
2 | a0001c0001t0003g0059a0006c0010t0003g0058 | 2 | HG01981.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-180-9834_-180-982 others(16): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | |||||
chr4:174965484
|
CATCT | C | 12 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0137others(9): Show | 15 | HG00609.hp2 HG01074.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-180-9826_-180-982 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | |||||
chr4:174965484
|
CATCTATC others(1): Show |
C | 4 | a0001c0001t0002g0264a0001c0001t0003g0045a0001c0001t0006g0073others(1): Show | 4 | HG00642.hp2 HG00741.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-9830_-180-982 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | |||||
chr4:174965508
|
T | TATCTATC others(8): Show |
1 | a0001c0001t0002g0233 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-180-9830_-180-981 others(19): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965508 | |||||
chr4:174965537
|
T | C | 1 | a0001c0001t0003g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-180-9809T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965537 | ||||||
chr4:174965665
|
C | T | 1 | a0001c0001t0005g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-180-9681C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965665 | ||||||
chr4:174965686
|
A | T | 2 | a0001c0001t0002g0233a0004c0004t0002g0228 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-180-9660A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965686 | ||||||
chr4:174965701
|
C | T | 3 | a0001c0006t0002g0032a0001c0006t0002g0033a0007c0012t0014g0031 | 3 | HG03225.hp2 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-180-9645C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965701 | ||||||
chr4:174965759
|
T | C | 131 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(128): Show | 157 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.-180-9587T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965759 | ||||||
chr4:174966064
|
C | A | 4 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0255others(1): Show | 4 | HG01496.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-9282C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966064 | ||||||
chr4:174966096
|
G | A | 1 | a0002c0002t0002g0266 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-180-9250G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966096 | ||||||
chr4:174966107
|
A | G | 2 | a0001c0009t0011g0095a0001c0009t0013g0039 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-9239A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966107 | ||||||
chr4:174966311
|
G | C | 143 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(140): Show | 172 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-180-9035G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966311 | ||||||
chr4:174966312
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-180-9034C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966312 | ||||||
chr4:174966313
|
A | T | 2 | a0001c0009t0011g0095a0001c0009t0013g0039 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-9033A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966313 | ||||||
chr4:174966328
|
T | C | 5 | a0001c0001t0002g0024a0001c0001t0002g0116a0001c0001t0002g0154others(2): Show | 6 | HG02040.hp2 NA18949.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-9018T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966328 | ||||||
chr4:174966329
|
T | C | 1 | a0008c0014t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-9017T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966329 | ||||||
chr4:174966332
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-180-9014A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966332 | ||||||
chr4:174966493
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-180-8853G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966493 | ||||||
chr4:174966519
|
C | T | 2 | a0001c0001t0003g0043a0001c0001t0003g0046 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-180-8827C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966519 | ||||||
chr4:174966598
|
A | T | 2 | a0001c0009t0011g0095a0001c0009t0013g0039 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-8748A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966598 | ||||||
chr4:174966708
|
G | A | 84 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(81): Show | 102 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-180-8638G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966708 | ||||||
chr4:174966747
|
T | G | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-8599T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966747 | ||||||
chr4:174966788
|
C | T | 2 | a0001c0008t0002g0097a0001c0008t0002g0098 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-180-8558C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966788 | ||||||
chr4:174966872
|
A | G | 2 | a0001c0001t0002g0233a0001c0016t0002g0037 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-180-8474A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966872 | ||||||
chr4:174966995
|
C | T | 2 | a0001c0009t0011g0095a0001c0009t0013g0039 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-8351C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966995 | ||||||
chr4:174967046
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-180-8300G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967046 | ||||||
chr4:174967321
|
TTTATTA | T | 52 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(49): Show | 67 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-180-8015_-180-801 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174967321 | |||||
chr4:174967355
|
T | C | 52 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(49): Show | 67 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-180-7991T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967355 | ||||||
chr4:174967523
|
TA | T | 52 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(49): Show | 67 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-180-7822delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967523 | ||||||
chr4:174967576
|
T | G | 8 | a0001c0006t0002g0032a0001c0006t0002g0033a0005c0005t0002g0022others(5): Show | 9 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-180-7770T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967576 | ||||||
chr4:174967590
|
G | A | 1 | a0004c0015t0002g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-180-7756G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967590 | ||||||
chr4:174967591
|
G | GA | 3 | a0001c0001t0001g0134a0001c0001t0003g0069a0001c0001t0003g0071 | 3 | HG02738.hp1 HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-180-7752dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174967591 | |||||
chr4:174967829
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-180-7517T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967829 | ||||||
chr4:174968123
|
C | T | 1 | a0001c0001t0006g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-180-7223C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968123 | ||||||
chr4:174968154
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-180-7192T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968154 | ||||||
chr4:174968646
|
C | A | 25 | a0002c0002t0002g0029a0002c0002t0002g0030a0004c0004t0001g0184others(22): Show | 28 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-180-6700C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968646 | ||||||
chr4:174968771
|
C | A | 1 | a0001c0001t0003g0052 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-180-6575C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968771 | ||||||
chr4:174968771
|
C | CA | 4 | a0001c0001t0001g0134a0001c0001t0001g0161a0001c0001t0003g0047others(1): Show | 4 | HG00323.hp1 HG01099.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-6575_-180-657 others(5): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968771 | ||||||
chr4:174968771
|
C | CCA | 22 | a0001c0001t0001g0162a0001c0001t0001g0204a0001c0001t0002g0193others(19): Show | 23 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-180-6540_-180-653 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | |||||
chr4:174968771
|
C | CCACA | 3 | a0001c0001t0001g0124a0001c0001t0003g0010a0001c0001t0003g0068 | 4 | HG01884.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-6542_-180-653 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | |||||
chr4:174968771
|
CCA | C | 8 | a0001c0001t0001g0176a0001c0001t0001g0225a0001c0001t0002g0252others(5): Show | 8 | HG00438.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-6540_-180-653 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | |||||
chr4:174968771
|
CCACA | C | 7 | a0001c0001t0001g0138a0001c0001t0002g0232a0001c0001t0002g0270others(4): Show | 7 | HG01243.hp1 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-180-6542_-180-653 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | |||||
chr4:174968771
|
CCACACA | C | 4 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(1): Show | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-180-6544_-180-653 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | |||||
chr4:174968771
|
CCACACAC others(1): Show |
C | 7 | a0001c0001t0002g0003a0001c0006t0002g0032a0001c0006t0002g0033others(4): Show | 10 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-180-6546_-180-653 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | |||||
chr4:174968771
|
CCACACAC others(3): Show |
C | 12 | a0001c0001t0001g0188a0001c0001t0002g0036a0001c0001t0002g0038others(9): Show | 12 | HG01255.hp1 HG01496.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-180-6548_-180-653 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | |||||
chr4:174968771
|
CCACACAC others(5): Show |
C | 121 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(118): Show | 146 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-180-6550_-180-653 others(16): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | |||||
chr4:174968773
|
A | C | 1 | a0001c0001t0001g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-180-6573A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968773 | ||||||
chr4:174968824
|
A | G | 44 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(41): Show | 51 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-180-6522A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968824 | ||||||
chr4:174968976
|
G | A | 141 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(138): Show | 170 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.-180-6370G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968976 | ||||||
chr4:174969008
|
A | AAAAG | 90 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(87): Show | 109 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-180-6332_-180-632 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174969008 | |||||
chr4:174969367
|
T | C | 2 | a0001c0006t0002g0032a0001c0006t0002g0033 | 2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-180-5979T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969367 | ||||||
chr4:174969601
|
A | G | 18 | a0002c0002t0001g0113a0002c0002t0001g0173a0002c0002t0001g0191others(15): Show | 22 | HG00544.hp1 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-180-5745A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969601 | ||||||
chr4:174969679
|
A | G | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-5667A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969679 | ||||||
chr4:174969722
|
T | C | 55 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(52): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-180-5624T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969722 | ||||||
chr4:174969944
|
T | G | 1 | a0001c0001t0002g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-180-5402T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969944 | ||||||
chr4:174969954
|
A | C | 7 | a0001c0001t0002g0270a0001c0001t0002g0280a0001c0001t0002g0285others(4): Show | 7 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-180-5392A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969954 | ||||||
chr4:174970013
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-180-5333C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970013 | ||||||
chr4:174970021
|
C | G | 1 | a0002c0002t0001g0114 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-180-5325C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970021 | ||||||
chr4:174970145
|
G | T | 2 | a0001c0009t0011g0095a0001c0009t0013g0039 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-5201G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970145 | ||||||
chr4:174970162
|
A | G | 2 | a0002c0002t0002g0029a0002c0002t0002g0030 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-180-5184A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970162 | ||||||
chr4:174970192
|
G | C | 2 | a0001c0009t0011g0095a0001c0009t0013g0039 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-5154G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970192 | ||||||
chr4:174970197
|
AT | A | 25 | a0002c0002t0002g0029a0002c0002t0002g0030a0004c0004t0001g0184others(22): Show | 28 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-180-5147delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174970197 | |||||
chr4:174970253
|
T | C | 2 | a0004c0004t0002g0034a0004c0004t0002g0228 | 2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-180-5093T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970253 | ||||||
chr4:174970341
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0148 | 3 | NA18945.hp1 NA18947.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-180-5005G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970341 | ||||||
chr4:174970446
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-180-4900C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970446 | ||||||
chr4:174970563
|
C | T | 45 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(42): Show | 52 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-180-4783C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970563 | ||||||
chr4:174970794
|
C | T | 55 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(52): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-180-4552C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970794 | ||||||
chr4:174970897
|
T | C | 1 | a0001c0009t0013g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-180-4449T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970897 | ||||||
chr4:174970991
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0213 | 2 | HG03453.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-180-4355A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970991 | ||||||
chr4:174971263
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-180-4083G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971263 | ||||||
chr4:174971415
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-180-3931C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971415 | ||||||
chr4:174971425
|
TTTTG | T | 45 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(42): Show | 52 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-180-3917_-180-391 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174971425 | |||||
chr4:174971537
|
C | T | 25 | a0002c0002t0002g0029a0002c0002t0002g0030a0004c0004t0001g0184others(22): Show | 28 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-180-3809C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971537 | ||||||
chr4:174971581
|
G | T | 80 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(77): Show | 98 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-180-3765G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971581 | ||||||
chr4:174971738
|
T | G | 46 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(43): Show | 53 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-180-3608T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971738 | ||||||
chr4:174971800
|
T | A | 1 | a0001c0001t0002g0024 | 2 | HG02040.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-180-3546T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971800 | ||||||
chr4:174972014
|
G | A | 27 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(24): Show | 30 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.-180-3332G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972014 | ||||||
chr4:174972152
|
T | G | 1 | a0004c0004t0002g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-3194T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972152 | ||||||
chr4:174972212
|
G | C | 1 | a0001c0001t0002g0256 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-180-3134G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972212 | ||||||
chr4:174972340
|
C | A | 5 | a0005c0005t0002g0022a0005c0005t0002g0231a0005c0005t0002g0235others(2): Show | 6 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-180-3006C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972340 | ||||||
chr4:174972710
|
T | C | 1 | a0004c0004t0006g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-2636T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972710 | ||||||
chr4:174972830
|
C | A | 3 | a0001c0001t0002g0233a0001c0001t0006g0073a0001c0016t0002g0037 | 3 | HG02818.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-180-2516C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972830 | ||||||
chr4:174973015
|
C | T | 5 | a0005c0005t0002g0022a0005c0005t0002g0231a0005c0005t0002g0235others(2): Show | 6 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-180-2331C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973015 | ||||||
chr4:174973195
|
T | C | 2 | a0001c0006t0002g0032a0001c0006t0002g0033 | 2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-180-2151T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973195 | ||||||
chr4:174973229
|
C | A | 88 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(85): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-180-2117C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973229 | ||||||
chr4:174973237
|
G | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0201 | 2 | HG00558.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.-180-2109G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973237 | ||||||
chr4:174973247
|
C | G | 133 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(130): Show | 158 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.-180-2099C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973247 | ||||||
chr4:174973682
|
T | G | 5 | a0005c0005t0002g0022a0005c0005t0002g0231a0005c0005t0002g0235others(2): Show | 6 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-180-1664T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973682 | ||||||
chr4:174973776
|
C | G | 1 | a0001c0001t0002g0256 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-180-1570C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973776 | ||||||
chr4:174973835
|
C | T | 80 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(77): Show | 98 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-180-1511C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973835 | ||||||
chr4:174973903
|
C | T | 2 | a0001c0009t0011g0095a0001c0009t0013g0039 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-1443C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973903 | ||||||
chr4:174973921
|
G | C | 142 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(139): Show | 171 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-180-1425G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973921 | ||||||
chr4:174974156
|
A | G | 3 | a0001c0001t0002g0003a0001c0008t0002g0097a0001c0008t0002g0098 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-1190A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974156 | ||||||
chr4:174974251
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0127others(5): Show | 10 | HG00323.hp2 HG01255.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-180-1095A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974251 | ||||||
chr4:174974413
|
A | C | 5 | a0005c0005t0002g0022a0005c0005t0002g0231a0005c0005t0002g0235others(2): Show | 6 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-180-933A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974413 | ||||||
chr4:174974483
|
C | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0255others(1): Show | 4 | HG01496.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-863C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974483 | ||||||
chr4:174974484
|
C | T | 2 | a0005c0007t0002g0230a0005c0007t0002g0234 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-180-862C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974484 | ||||||
chr4:174974747
|
A | C | 55 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0157others(52): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-180-599A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974747 | ||||||
chr4:174974798
|
C | T | 3 | a0002c0002t0004g0077a0002c0002t0004g0083a0002c0002t0004g0086 | 3 | HG01123.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-180-548C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974798 | ||||||
chr4:174974832
|
T | C | 3 | a0001c0001t0002g0233a0001c0001t0006g0073a0001c0016t0002g0037 | 3 | HG02818.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-180-514T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974832 | ||||||
chr4:174975029
|
A | G | 1 | a0004c0004t0006g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-317A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174975029 | ||||||
chr4:174975106
|
C | T | 1 | a0003c0003t0002g0250 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-180-240C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174975106 |