geneid | 1390 |
---|---|
ensemblid | ENSG00000095794.21 |
hgncid | 2352 |
symbol | CREM |
name | cAMP responsive element modulator |
refseq_nuc | NM_183011.2 |
refseq_prot | NP_898829.1 |
ensembl_nuc | ENST00000685392.1 |
ensembl_prot | ENSP00000509489.1 |
mane_status | MANE Select |
chr | chr10 |
start | 35126846 |
end | 35212953 |
strand | + |
ver | v1.2 |
region | chr10:35126846-35212953 |
region5000 | chr10:35121846-35217953 |
regionname0 | CREM_chr10_35126846_35212953 |
regionname5000 | CREM_chr10_35121846_35217953 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 299 | 292 | 79 | 54 | 102 | 14 | 41 | 78 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0002 | 0/0 | 299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0003 | 0/0 | 299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 900 | 277 | 69 | 49 | 102 | 14 | 41 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
c0002 | 0/0 | 900 | 12 | 9 | 3 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
c0003 | 0/0 | 900 | 2 | 1 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
c0004 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
c0005 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
c0006 | 0/0 | 900 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1958 | 154 | 53 | 23 | 48 | 8 | 21 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0002 | 0/0 | 1957 | 74 | 7 | 15 | 40 | 5 | 7 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0003 | 0/0 | 1958 | 32 | 2 | 9 | 8 | 1 | 12 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0004 | 0/0 | 1959 | 11 | 9 | 2 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0005 | 0/0 | 1958 | 4 | 4 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0006 | 0/0 | 1958 | 3 | 0 | 2 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0007 | 0/0 | 1957 | 2 | 2 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0008 | 0/0 | 1958 | 2 | 0 | 0 | 0 | 0 | 2 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0009 | 0/0 | 1958 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0010 | 0/1 | 1958 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0011 | 0/0 | 1958 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0012 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0013 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0014 | 0/0 | 1958 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0015 | 0/0 | 1958 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0016 | 0/0 | 1957 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0017 | 0/0 | 1958 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0018 | 0/0 | 1958 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0019 | 0/0 | 1958 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
t0020 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 900 | 277 | 69 | 49 | 102 | 14 | 41 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0002 | 0/0 | 900 | 12 | 9 | 3 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0003 | 0/0 | 900 | 2 | 1 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0004 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0002c0005 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0003c0006 | 0/0 | 900 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2857 | 153 | 52 | 23 | 48 | 8 | 21 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0002 | 0/0 | 2856 | 72 | 6 | 14 | 40 | 5 | 7 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0003 | 0/0 | 2857 | 31 | 2 | 9 | 8 | 1 | 11 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0005 | 0/0 | 2857 | 4 | 4 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0006 | 0/0 | 2857 | 3 | 0 | 2 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0007 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0008 | 0/0 | 2857 | 2 | 0 | 0 | 0 | 0 | 2 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0009 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0010 | 0/1 | 2857 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0011 | 0/0 | 2857 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0012 | 0/0 | 2857 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0014 | 0/0 | 2857 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0015 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0016 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0017 | 0/0 | 2857 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0018 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0001t0019 | 0/0 | 2857 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0002t0004 | 0/0 | 2858 | 11 | 9 | 2 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0002t0020 | 0/0 | 2857 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0003t0002 | 0/0 | 2856 | 2 | 1 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0001c0004t0013 | 0/0 | 2857 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0002c0005t0001 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
a0003c0006t0003 | 0/0 | 2857 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | copy fasta | chr10 | 35121846 | 35217953 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0010g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0012g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0014g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0016g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0017g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0018g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0001t0019g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0002t0020g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0003t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0001c0004t0013g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0002c0005t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
a0003c0006t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | FIN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | FIN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00735 | hp1 | a0001 | c0001 | t0012 | g0275 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0112 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01071 | hp1 | a0001 | c0002 | t0020 | g0291 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01099 | hp2 | a0001 | c0003 | t0002 | g0041 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01109 | hp1 | a0001 | c0002 | t0004 | g0116 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0141 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0103 | EUR | IBS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0023 | EUR | IBS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | IBS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01891 | hp1 | a0001 | c0001 | t0015 | g0263 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0140 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0111 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02572 | hp2 | a0001 | c0002 | t0004 | g0290 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02615 | hp2 | a0001 | c0002 | t0004 | g0117 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02647 | hp1 | a0001 | c0002 | t0004 | g0114 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02723 | hp1 | a0001 | c0002 | t0004 | g0118 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0113 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02965 | hp1 | a0001 | c0002 | t0004 | g0115 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03486 | hp1 | a0001 | c0001 | t0018 | g0288 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03579 | hp2 | a0001 | c0003 | t0002 | g0042 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03834 | hp2 | a0001 | c0001 | t0008 | g0248 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG04115 | hp2 | a0003 | c0006 | t0003 | g0031 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG04204 | hp2 | a0001 | c0001 | t0008 | g0246 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18941 | hp2 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18960 | hp1 | a0001 | c0001 | t0014 | g0200 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18960 | hp2 | a0001 | c0001 | t0019 | g0169 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18974 | hp1 | a0001 | c0001 | t0017 | g0136 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19043 | hp1 | a0002 | c0005 | t0001 | g0162 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19063 | hp2 | a0001 | c0001 | t0016 | g0203 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19089 | hp1 | a0001 | c0001 | t0011 | g0217 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0035 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ASW | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ASW | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0037 | EUR | TSI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | GIH | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | GIH | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01123 | hp1 | a0001 | c0004 | t0013 | g0272 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG02559 | hp2 | a0001 | c0001 | t0009 | g0289 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG03471 | hp2 | a0001 | c0002 | t0004 | g0109 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | USA | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | USA | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | USA | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0010 | g0245 | REF | REF | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0163 | REF | REF | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:35148447
|
G | C | 1 | a0002 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.124G>C | p.Val42Leu | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/8 | 526/2857 | 124/900 | 42/299 | chr10 | 35148447 | ||
chr10:35179265
|
C | A | 1 | a0003 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.398C>A | p.Thr133Lys | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/8 | 800/2857 | 398/900 | 133/299 | chr10 | 35179265 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:35148446
|
T | C | 1 | a0001c0004 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.123T>C | p.His41His | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/8 | 525/2857 | 123/900 | 41/299 | chr10 | 35148446 | ||
chr10:35179179
|
G | A | 1 | a0001c0002 | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
synonymous_variant | LOW | c.312G>A | p.Lys104Lys | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/8 | 714/2857 | 312/900 | 104/299 | chr10 | 35179179 | ||
chr10:35207028
|
A | G | 1 | a0001c0003 | 2 | HG01099.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.732A>G | p.Arg244Arg | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/8 | 1134/2857 | 732/900 | 244/299 | chr10 | 35207028 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:35126855
|
T | C | 1 | a0001c0001t0009 | 1 | HG02559.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-393T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | chr10 | 35126855 | ||||||
chr10:35126892
|
C | T | 1 | a0001c0001t0008 | 2 | HG03834.hp2 HG04204.hp2 |
5_prime_UTR_variant | MODIFIER | c.-356C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | 10944 | chr10 | 35126892 | |||||
chr10:35126922
|
G | T | 2 | a0001c0002t0004a0001c0002t0020 | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-326G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | 10914 | chr10 | 35126922 | |||||
chr10:35126939
|
C | T | 2 | a0001c0002t0004a0001c0002t0020 | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-309C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | chr10 | 35126939 | ||||||
chr10:35127047
|
G | A | 1 | a0001c0001t0005 | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-201G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | 10789 | chr10 | 35127047 | |||||
chr10:35127114
|
C | G | 1 | a0001c0001t0019 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-134C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | 10722 | chr10 | 35127114 | |||||
chr10:35137827
|
A | G | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(6): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-9A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/8 | chr10 | 35137827 | ||||||
chr10:35211582
|
G | A | 1 | a0001c0001t0010 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 184 | chr10 | 35211582 | |||||
chr10:35211766
|
C | A | 1 | a0001c0001t0011 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*368C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 368 | chr10 | 35211766 | |||||
chr10:35211846
|
T | C | 1 | a0001c0001t0012 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*448T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 448 | chr10 | 35211846 | |||||
chr10:35212007
|
G | A | 1 | a0001c0001t0006 | 3 | HG01261.hp1 HG01928.hp2 NA18941.hp2 |
3_prime_UTR_variant | MODIFIER | c.*609G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 609 | chr10 | 35212007 | |||||
chr10:35212054
|
C | T | 1 | a0001c0001t0017 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 656 | chr10 | 35212054 | |||||
chr10:35212068
|
C | A | 1 | a0001c0001t0007 | 2 | HG02280.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*670C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 670 | chr10 | 35212068 | |||||
chr10:35212193
|
T | A | 1 | a0001c0001t0018 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*795T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 795 | chr10 | 35212193 | |||||
chr10:35212303
|
T | TA | 1 | a0001c0002t0004 | 11 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*916dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 917 | INFO_REALIGN_3_PRIME | chr10 | 35212303 | ||||
chr10:35212303
|
TA | T | 4 | a0001c0001t0002a0001c0001t0007a0001c0001t0016others(1): Show | 77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*916delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 916 | INFO_REALIGN_3_PRIME | chr10 | 35212303 | ||||
chr10:35212394
|
G | A | 1 | a0001c0004t0013 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 996 | chr10 | 35212394 | |||||
chr10:35212510
|
A | G | 5 | a0001c0001t0002a0001c0001t0007a0001c0001t0016others(2): Show | 88 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1112A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 1112 | chr10 | 35212510 | |||||
chr10:35212727
|
G | A | 1 | a0001c0001t0014 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 1329 | chr10 | 35212727 | |||||
chr10:35212734
|
G | A | 1 | a0001c0001t0015 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1336G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 1336 | chr10 | 35212734 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:35127505
|
C | T | 2 | a0001c0002t0004g0290a0001c0002t0020g0291 | 2 | HG01071.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-55+312C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127505 | ||||||
chr10:35127527
|
A | G | 2 | a0001c0001t0009g0289a0001c0001t0018g0288 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-55+334A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127527 | ||||||
chr10:35127585
|
G | C | 117 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(114): Show | 117 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-55+392G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127585 | ||||||
chr10:35127641
|
G | A | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-55+448G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127641 | ||||||
chr10:35127744
|
G | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG00544.hp2 NA18965.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-55+551G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127744 | ||||||
chr10:35127854
|
C | CT | 115 | a0001c0001t0002g0040a0001c0001t0002g0043a0001c0001t0002g0044others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-55+672dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35127854 | |||||
chr10:35127857
|
T | TG | 3 | a0001c0002t0004g0035a0001c0002t0004g0290a0001c0002t0020g0291 | 3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-55+664_-55+665ins others(1): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127857 | ||||||
chr10:35128098
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-55+905A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128098 | ||||||
chr10:35128253
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-55+1060A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128253 | ||||||
chr10:35128274
|
C | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-55+1081C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128274 | ||||||
chr10:35128526
|
C | CT | 24 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0271others(21): Show | 24 | HG00735.hp1 HG00738.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-55+1350dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35128526 | |||||
chr10:35128526
|
CT | C | 101 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0036others(98): Show | 101 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-55+1350delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35128526 | |||||
chr10:35128545
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-55+1352A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128545 | ||||||
chr10:35128559
|
T | G | 1 | a0001c0001t0002g0040 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-55+1366T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128559 | ||||||
chr10:35128650
|
T | A | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-55+1457T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128650 | ||||||
chr10:35128794
|
G | A | 7 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 8 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-55+1601G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128794 | ||||||
chr10:35128854
|
G | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-55+1661G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128854 | ||||||
chr10:35128938
|
C | T | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-55+1745C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128938 | ||||||
chr10:35129024
|
A | G | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-55+1831A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129024 | ||||||
chr10:35129589
|
T | G | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-55+2396T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129589 | ||||||
chr10:35129598
|
G | A | 117 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(114): Show | 117 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-55+2405G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129598 | ||||||
chr10:35129641
|
G | A | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-55+2448G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129641 | ||||||
chr10:35129688
|
G | C | 141 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.-55+2495G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129688 | ||||||
chr10:35129776
|
C | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-55+2583C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129776 | ||||||
chr10:35129796
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-55+2603G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129796 | ||||||
chr10:35130052
|
C | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-55+2859C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130052 | ||||||
chr10:35130071
|
C | T | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-55+2878C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130071 | ||||||
chr10:35130112
|
C | G | 2 | a0001c0001t0002g0104a0001c0001t0002g0108 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-55+2919C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130112 | ||||||
chr10:35130190
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-55+2997C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130190 | ||||||
chr10:35130196
|
C | CA | 14 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(11): Show | 14 | HG00741.hp1 HG01358.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-55+3026dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35130196 | |||||
chr10:35130196
|
CA | C | 89 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(86): Show | 89 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-55+3026delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35130196 | |||||
chr10:35130219
|
AT | A | 10 | a0001c0001t0003g0034a0001c0001t0007g0038a0001c0002t0004g0109others(7): Show | 10 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-55+3034delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35130219 | |||||
chr10:35130220
|
T | A | 14 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG00438.hp1 HG00438.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-55+3027T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130220 | ||||||
chr10:35130265
|
A | G | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-55+3072A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130265 | ||||||
chr10:35130464
|
A | C | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-55+3271A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130464 | ||||||
chr10:35130720
|
A | G | 1 | a0001c0001t0003g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-55+3527A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130720 | ||||||
chr10:35130722
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-55+3529A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130722 | ||||||
chr10:35130781
|
T | C | 1 | a0001c0004t0013g0272 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-55+3588T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130781 | ||||||
chr10:35131081
|
G | A | 3 | a0001c0002t0004g0035a0001c0002t0004g0290a0001c0002t0020g0291 | 3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-55+3888G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131081 | ||||||
chr10:35131392
|
A | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-55+4199A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131392 | ||||||
chr10:35131631
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-55+4438A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131631 | ||||||
chr10:35131693
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-55+4500T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131693 | ||||||
chr10:35131924
|
G | A | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-55+4731G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131924 | ||||||
chr10:35131981
|
C | G | 1 | a0001c0001t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-55+4788C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131981 | ||||||
chr10:35132057
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-55+4864T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132057 | ||||||
chr10:35132076
|
G | C | 113 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0154others(110): Show | 113 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-55+4883G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132076 | ||||||
chr10:35132081
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-55+4888A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132081 | ||||||
chr10:35132156
|
G | A | 1 | a0001c0001t0006g0132 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-55+4963G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132156 | ||||||
chr10:35132201
|
CA | C | 7 | a0001c0001t0001g0250a0001c0001t0002g0282a0001c0001t0002g0283others(4): Show | 7 | HG01169.hp2 HG01192.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-55+5024delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35132201 | |||||
chr10:35132214
|
A | G | 3 | a0001c0002t0004g0109a0001c0002t0004g0116a0001c0002t0004g0118 | 3 | HG01109.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-55+5021A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132214 | ||||||
chr10:35132215
|
AAAG | A | 61 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0043others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-55+5025_-55+5027d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35132215 | |||||
chr10:35132216
|
AAG | A | 6 | a0001c0001t0002g0040a0001c0001t0002g0046a0001c0001t0002g0047others(3): Show | 6 | HG02486.hp1 HG03225.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.-55+5025_-55+5026d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35132216 | |||||
chr10:35132217
|
AG | A | 3 | a0001c0001t0003g0029a0001c0001t0003g0030a0003c0006t0003g0031 | 3 | HG03669.hp2 HG04115.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-55+5025delG | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132217 | ||||||
chr10:35132218
|
G | A | 29 | a0001c0001t0002g0045a0001c0001t0003g0004a0001c0001t0003g0005others(26): Show | 29 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.-55+5025G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132218 | ||||||
chr10:35132254
|
G | C | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-55+5061G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132254 | ||||||
chr10:35132476
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-55+5283G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132476 | ||||||
chr10:35132707
|
T | C | 2 | a0001c0003t0002g0041a0001c0003t0002g0042 | 2 | HG01099.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-54-5075T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132707 | ||||||
chr10:35132804
|
C | G | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-54-4978C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132804 | ||||||
chr10:35132907
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-54-4875T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132907 | ||||||
chr10:35133011
|
C | G | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-54-4771C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133011 | ||||||
chr10:35133175
|
G | A | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-54-4607G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133175 | ||||||
chr10:35133188
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-54-4594G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133188 | ||||||
chr10:35133263
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-54-4519G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133263 | ||||||
chr10:35133308
|
A | AT | 9 | a0001c0001t0001g0152a0001c0001t0001g0155a0001c0001t0001g0244others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-54-4457dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35133308 | |||||
chr10:35133308
|
AT | A | 19 | a0001c0001t0001g0121a0001c0001t0001g0156a0001c0001t0001g0157others(16): Show | 19 | HG01071.hp1 HG01109.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-54-4457delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35133308 | |||||
chr10:35133308
|
ATT | A | 99 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(96): Show | 99 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-54-4458_-54-4457d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35133308 | |||||
chr10:35133414
|
T | A | 1 | a0001c0001t0002g0050 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-54-4368T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133414 | ||||||
chr10:35133499
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-54-4283A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133499 | ||||||
chr10:35133571
|
T | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-54-4211T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133571 | ||||||
chr10:35133578
|
C | T | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-54-4204C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133578 | ||||||
chr10:35133591
|
G | A | 69 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-54-4191G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133591 | ||||||
chr10:35133614
|
T | A | 1 | a0001c0001t0003g0034 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-54-4168T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133614 | ||||||
chr10:35133784
|
G | T | 3 | a0001c0001t0006g0132a0001c0001t0006g0140a0001c0001t0006g0141 | 3 | HG01261.hp1 HG01928.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.-54-3998G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133784 | ||||||
chr10:35133812
|
C | T | 69 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-54-3970C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133812 | ||||||
chr10:35133939
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-54-3843G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133939 | ||||||
chr10:35134029
|
T | G | 109 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(106): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-54-3753T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134029 | ||||||
chr10:35134048
|
G | GT | 3 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0009g0289 | 3 | HG02280.hp1 HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-54-3728dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35134048 | |||||
chr10:35134055
|
G | GT | 37 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0243others(34): Show | 37 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-54-3712dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35134055 | |||||
chr10:35134055
|
G | T | 9 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0091others(6): Show | 9 | HG00423.hp2 HG01261.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54-3727G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134055 | ||||||
chr10:35134455
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-54-3327G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134455 | ||||||
chr10:35134546
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-54-3236A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134546 | ||||||
chr10:35134591
|
G | A | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54-3191G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134591 | ||||||
chr10:35134632
|
T | C | 22 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(19): Show | 22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-54-3150T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134632 | ||||||
chr10:35134641
|
A | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-54-3141A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134641 | ||||||
chr10:35134726
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-54-3056T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134726 | ||||||
chr10:35134931
|
A | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-54-2851A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134931 | ||||||
chr10:35134968
|
G | A | 1 | a0001c0002t0004g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-54-2814G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134968 | ||||||
chr10:35135016
|
C | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54-2766C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135016 | ||||||
chr10:35135033
|
G | A | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54-2749G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135033 | ||||||
chr10:35135119
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-54-2663G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135119 | ||||||
chr10:35135210
|
A | G | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-54-2572A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135210 | ||||||
chr10:35135245
|
A | C | 1 | a0001c0003t0002g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-54-2537A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135245 | ||||||
chr10:35135522
|
G | A | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-54-2260G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135522 | ||||||
chr10:35135721
|
GA | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-54-2039delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135721 | |||||
chr10:35135721
|
GAA | G | 22 | a0001c0001t0001g0121a0001c0001t0001g0138a0001c0001t0001g0143others(19): Show | 22 | HG00544.hp2 HG00621.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-54-2040_-54-2039d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135721 | |||||
chr10:35135737
|
AAAAAAAG others(2): Show |
A | 6 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(3): Show | 6 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54-2043_-54-2035d others(11): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135737 | |||||
chr10:35135738
|
AAAAAAGA others(1): Show |
A | 25 | a0001c0001t0002g0087a0001c0001t0003g0004a0001c0001t0003g0005others(22): Show | 25 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.-54-2042_-54-2035d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135738 | |||||
chr10:35135739
|
AAAAAGAG | A | 70 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(67): Show | 70 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-54-2041_-54-2035d others(9): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135739 | |||||
chr10:35135830
|
G | T | 1 | a0001c0001t0001g0235 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-54-1952G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135830 | ||||||
chr10:35135872
|
G | GTA | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(4): Show | 7 | HG02080.hp2 NA18612.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54-1909_-54-1908d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135872 | |||||
chr10:35135885
|
G | C | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-54-1897G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135885 | ||||||
chr10:35136208
|
C | CAAAAT | 110 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(107): Show | 110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-54-1573_-54-1572i others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35136208 | |||||
chr10:35136362
|
G | A | 4 | a0001c0001t0002g0043a0001c0001t0002g0051a0001c0001t0002g0052others(1): Show | 4 | NA18612.hp2 NA18953.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54-1420G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136362 | ||||||
chr10:35136426
|
C | T | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-54-1356C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136426 | ||||||
chr10:35136443
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-54-1339G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136443 | ||||||
chr10:35136484
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-54-1298T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136484 | ||||||
chr10:35136490
|
T | G | 1 | a0001c0001t0002g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-54-1292T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136490 | ||||||
chr10:35136585
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-54-1197T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136585 | ||||||
chr10:35136618
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-54-1164A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136618 | ||||||
chr10:35136622
|
C | T | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-54-1160C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136622 | ||||||
chr10:35136790
|
GT | G | 116 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(113): Show | 117 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-54-972delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35136790 | |||||
chr10:35136790
|
GTT | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54-973_-54-972del others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35136790 | |||||
chr10:35136790
|
GTTT | G | 11 | a0001c0001t0001g0236a0001c0002t0004g0035a0001c0002t0004g0109others(8): Show | 11 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-54-974_-54-972del others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35136790 | |||||
chr10:35136810
|
T | G | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54-972T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136810 | ||||||
chr10:35136890
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-54-892G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136890 | ||||||
chr10:35136891
|
G | T | 1 | a0001c0001t0002g0054 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-54-891G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136891 | ||||||
chr10:35136914
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-54-868G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136914 | ||||||
chr10:35137004
|
A | G | 2 | a0001c0002t0004g0290a0001c0002t0020g0291 | 2 | HG01071.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-54-778A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137004 | ||||||
chr10:35137030
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-54-752T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137030 | ||||||
chr10:35137040
|
C | G | 1 | a0001c0002t0004g0109 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-54-742C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137040 | ||||||
chr10:35137083
|
G | A | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-699G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137083 | ||||||
chr10:35137161
|
T | A | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-621T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137161 | ||||||
chr10:35137197
|
TAAAG | T | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54-583_-54-580del others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35137197 | |||||
chr10:35137282
|
T | C | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-54-500T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137282 | ||||||
chr10:35137308
|
A | G | 1 | a0002c0005t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-54-474A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137308 | ||||||
chr10:35137396
|
G | A | 122 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-54-386G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137396 | ||||||
chr10:35137686
|
T | C | 73 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-54-96T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137686 | ||||||
chr10:35137907
|
T | G | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+28T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35137907 | ||||||
chr10:35138326
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.44+447C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138326 | ||||||
chr10:35138467
|
G | A | 122 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+588G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138467 | ||||||
chr10:35138526
|
A | AT | 28 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0001g0223others(25): Show | 28 | HG00423.hp1 HG00738.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.44+666dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35138526 | |||||
chr10:35138682
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.44+803C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138682 | ||||||
chr10:35138697
|
T | A | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.44+818T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138697 | ||||||
chr10:35138733
|
T | A | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | HG02258.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.44+854T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138733 | ||||||
chr10:35138745
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0226a0001c0001t0001g0236 | 3 | HG00438.hp2 NA18974.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.44+866C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138745 | ||||||
chr10:35138746
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.44+867G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138746 | ||||||
chr10:35138786
|
G | T | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.44+907G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138786 | ||||||
chr10:35138872
|
T | C | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.44+993T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138872 | ||||||
chr10:35138876
|
A | G | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.44+997A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138876 | ||||||
chr10:35139122
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0244 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.44+1243T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139122 | ||||||
chr10:35139127
|
A | AT | 18 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(15): Show | 18 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.44+1262dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35139127 | |||||
chr10:35139127
|
AT | A | 108 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(105): Show | 108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.44+1262delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35139127 | |||||
chr10:35139135
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.44+1256T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139135 | ||||||
chr10:35139152
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.44+1273G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139152 | ||||||
chr10:35139272
|
G | A | 122 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+1393G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139272 | ||||||
chr10:35139304
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.44+1425G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139304 | ||||||
chr10:35139309
|
G | A | 1 | a0001c0001t0007g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.44+1430G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139309 | ||||||
chr10:35139327
|
C | G | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.44+1448C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139327 | ||||||
chr10:35139336
|
C | T | 110 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(107): Show | 110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.44+1457C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139336 | ||||||
chr10:35139368
|
C | G | 1 | a0001c0003t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.44+1489C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139368 | ||||||
chr10:35139666
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.44+1787G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139666 | ||||||
chr10:35139812
|
C | G | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.44+1933C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139812 | ||||||
chr10:35140072
|
A | G | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+2193A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140072 | ||||||
chr10:35140182
|
G | A | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+2303G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140182 | ||||||
chr10:35140198
|
C | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.44+2319C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140198 | ||||||
chr10:35140220
|
T | C | 1 | a0001c0001t0019g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.44+2341T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140220 | ||||||
chr10:35140528
|
G | C | 1 | a0001c0003t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.44+2649G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140528 | ||||||
chr10:35140577
|
A | G | 1 | a0001c0001t0009g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.44+2698A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140577 | ||||||
chr10:35140897
|
C | T | 122 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+3018C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140897 | ||||||
chr10:35141187
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.44+3308T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141187 | ||||||
chr10:35141227
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.44+3348T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141227 | ||||||
chr10:35141357
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.44+3478A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141357 | ||||||
chr10:35141519
|
C | T | 1 | a0001c0001t0007g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.44+3640C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141519 | ||||||
chr10:35141571
|
T | C | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+3692T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141571 | ||||||
chr10:35141634
|
G | A | 1 | a0001c0001t0003g0029 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.44+3755G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141634 | ||||||
chr10:35141636
|
T | C | 1 | a0001c0001t0003g0029 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.44+3757T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141636 | ||||||
chr10:35141934
|
ATGT | A | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+4059_44+4061del others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35141934 | |||||
chr10:35141982
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.44+4103A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141982 | ||||||
chr10:35142171
|
G | A | 1 | a0001c0004t0013g0272 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.44+4292G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142171 | ||||||
chr10:35142508
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.44+4629C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142508 | ||||||
chr10:35142708
|
T | C | 141 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.44+4829T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142708 | ||||||
chr10:35142756
|
T | C | 122 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+4877T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142756 | ||||||
chr10:35142782
|
T | C | 1 | a0001c0001t0002g0049 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.44+4903T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142782 | ||||||
chr10:35142887
|
C | T | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+5008C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142887 | ||||||
chr10:35142970
|
A | G | 1 | a0001c0001t0008g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.44+5091A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142970 | ||||||
chr10:35143035
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.44+5156A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143035 | ||||||
chr10:35143189
|
T | TTTA | 3 | a0001c0001t0001g0122a0001c0001t0001g0216a0001c0001t0011g0217 | 3 | NA18944.hp2 NA18975.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.45-5178_45-5176dup others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35143189 | |||||
chr10:35143422
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.45-4946G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143422 | ||||||
chr10:35143477
|
T | C | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.45-4891T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143477 | ||||||
chr10:35143484
|
A | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.45-4884A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143484 | ||||||
chr10:35143488
|
G | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45-4880G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143488 | ||||||
chr10:35143636
|
T | C | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-4732T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143636 | ||||||
chr10:35143793
|
G | T | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-4575G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143793 | ||||||
chr10:35143817
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45-4551C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143817 | ||||||
chr10:35143835
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.45-4533G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143835 | ||||||
chr10:35143836
|
T | G | 1 | a0001c0001t0001g0121 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.45-4532T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143836 | ||||||
chr10:35143837
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.45-4531G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143837 | ||||||
chr10:35143914
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45-4454T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143914 | ||||||
chr10:35143933
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.45-4435A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143933 | ||||||
chr10:35144090
|
T | A | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.45-4278T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144090 | ||||||
chr10:35144149
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45-4219C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144149 | ||||||
chr10:35144209
|
G | A | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.45-4159G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144209 | ||||||
chr10:35144271
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45-4097G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144271 | ||||||
chr10:35144551
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.45-3817A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144551 | ||||||
chr10:35144566
|
C | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 5 | HG00438.hp2 NA18972.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-3802C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144566 | ||||||
chr10:35144738
|
C | CT | 106 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0043others(103): Show | 106 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.45-3617dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35144738 | |||||
chr10:35144800
|
G | C | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.45-3568G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144800 | ||||||
chr10:35144818
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.45-3550G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144818 | ||||||
chr10:35145018
|
G | A | 1 | a0001c0002t0004g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45-3350G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145018 | ||||||
chr10:35145066
|
C | T | 69 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.45-3302C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145066 | ||||||
chr10:35145144
|
G | GAGCA | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-3221_45-3218dup others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145144 | |||||
chr10:35145160
|
C | CA | 18 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0130others(15): Show | 18 | HG01071.hp1 HG01175.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-3188dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | |||||
chr10:35145160
|
C | CAA | 66 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.45-3189_45-3188dup others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | |||||
chr10:35145160
|
C | CAAA | 13 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(10): Show | 13 | HG00733.hp2 HG01258.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.45-3190_45-3188dup others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | |||||
chr10:35145160
|
CA | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0230a0001c0001t0002g0282others(5): Show | 8 | HG01099.hp1 HG01192.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.45-3188delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | |||||
chr10:35145160
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0212 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.45-3197_45-3188del others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | |||||
chr10:35145168
|
A | AAG | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.45-3199_45-3198ins others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145168 | |||||
chr10:35145407
|
T | C | 1 | a0001c0003t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.45-2961T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145407 | ||||||
chr10:35145445
|
T | C | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-2923T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145445 | ||||||
chr10:35145513
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.45-2855C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145513 | ||||||
chr10:35145605
|
A | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0276others(1): Show | 4 | HG01123.hp1 HG02622.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-2763A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145605 | ||||||
chr10:35145609
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45-2759C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145609 | ||||||
chr10:35145676
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.45-2692G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145676 | ||||||
chr10:35145680
|
A | G | 141 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.45-2688A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145680 | ||||||
chr10:35145692
|
C | T | 2 | a0001c0003t0002g0041a0001c0003t0002g0042 | 2 | HG01099.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.45-2676C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145692 | ||||||
chr10:35145776
|
C | CA | 207 | a0001c0001t0001g0003a0001c0001t0001g0119a0001c0001t0001g0120others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.45-2569dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145776 | |||||
chr10:35145776
|
C | CAA | 28 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0145others(25): Show | 29 | HG00323.hp2 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.45-2570_45-2569dup others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145776 | |||||
chr10:35145776
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.45-2579_45-2569del others(11): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145776 | |||||
chr10:35145876
|
G | A | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.45-2492G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145876 | ||||||
chr10:35146009
|
A | G | 30 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(27): Show | 30 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.45-2359A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146009 | ||||||
chr10:35146080
|
T | C | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45-2288T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146080 | ||||||
chr10:35146158
|
C | T | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-2210C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146158 | ||||||
chr10:35146190
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0247 | 2 | HG01109.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.45-2178G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146190 | ||||||
chr10:35146304
|
GGTTT | G | 7 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 8 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-2058_45-2055del others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35146304 | |||||
chr10:35146313
|
G | A | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-2055G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146313 | ||||||
chr10:35146348
|
G | A | 1 | a0001c0001t0002g0087 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.45-2020G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146348 | ||||||
chr10:35146387
|
T | C | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-1981T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146387 | ||||||
chr10:35146544
|
C | T | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.45-1824C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146544 | ||||||
chr10:35146690
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45-1678C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146690 | ||||||
chr10:35146780
|
T | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG00621.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.45-1588T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146780 | ||||||
chr10:35146948
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.45-1420T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146948 | ||||||
chr10:35146999
|
A | T | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-1369A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146999 | ||||||
chr10:35147041
|
G | GT | 76 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0131others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.45-1300dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35147041 | |||||
chr10:35147041
|
G | GTT | 17 | a0001c0001t0001g0151a0001c0001t0001g0160a0001c0001t0001g0168others(14): Show | 17 | HG00280.hp1 HG00621.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.45-1301_45-1300dup others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35147041 | |||||
chr10:35147041
|
GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0002g0084a0001c0001t0003g0012a0001c0001t0003g0017 | 3 | HG00639.hp1 HG06807.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.45-1309_45-1300del others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35147041 | |||||
chr10:35147041
|
GTTTTTTT others(4): Show |
G | 101 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(98): Show | 101 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.45-1310_45-1300del others(11): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35147041 | |||||
chr10:35147055
|
T | G | 9 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(6): Show | 10 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-1313T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147055 | ||||||
chr10:35147067
|
T | C | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-1301T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147067 | ||||||
chr10:35147146
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.45-1222G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147146 | ||||||
chr10:35147152
|
G | T | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.45-1216G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147152 | ||||||
chr10:35147210
|
C | T | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.45-1158C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147210 | ||||||
chr10:35147211
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.45-1157G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147211 | ||||||
chr10:35147215
|
G | A | 1 | a0001c0003t0002g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.45-1153G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147215 | ||||||
chr10:35147275
|
G | A | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-1093G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147275 | ||||||
chr10:35147348
|
C | T | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.45-1020C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147348 | ||||||
chr10:35147931
|
G | A | 1 | a0001c0001t0003g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.45-437G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147931 | ||||||
chr10:35147942
|
A | G | 1 | a0001c0002t0004g0290 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.45-426A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147942 | ||||||
chr10:35147946
|
T | G | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-422T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147946 | ||||||
chr10:35147981
|
G | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0122others(60): Show | 64 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.45-387G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147981 | ||||||
chr10:35148061
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.45-307A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35148061 | ||||||
chr10:35148165
|
A | G | 5 | a0001c0001t0002g0048a0001c0001t0002g0081a0001c0001t0002g0082others(2): Show | 5 | HG02040.hp1 HG02135.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-203A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35148165 | ||||||
chr10:35148295
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.45-73G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35148295 | ||||||
chr10:35148311
|
A | AT | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.45-54dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35148311 | |||||
chr10:35148592
|
C | G | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+101C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148592 | ||||||
chr10:35148644
|
G | GTAAT | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+156_168+159dup others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35148644 | |||||
chr10:35148689
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.168+198C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148689 | ||||||
chr10:35148929
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.168+438C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148929 | ||||||
chr10:35148964
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.168+473T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148964 | ||||||
chr10:35148974
|
A | G | 11 | a0001c0001t0001g0137a0001c0001t0001g0145a0001c0001t0001g0170others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+483A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148974 | ||||||
chr10:35149018
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+527T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149018 | ||||||
chr10:35149031
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.168+540T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149031 | ||||||
chr10:35149409
|
T | C | 109 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(106): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.168+918T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149409 | ||||||
chr10:35149486
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+995T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149486 | ||||||
chr10:35149582
|
G | A | 1 | a0001c0001t0019g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.168+1091G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149582 | ||||||
chr10:35149888
|
AAACACAC others(10): Show |
A | 2 | a0001c0001t0002g0040a0001c0001t0002g0093 | 2 | NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.168+1399_168+1415d others(19): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149888 | |||||
chr10:35149889
|
A | AAC | 16 | a0001c0001t0001g0186a0001c0001t0001g0196a0001c0001t0001g0239others(13): Show | 16 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.168+1447_168+1448d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACAC | 16 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0205others(13): Show | 16 | HG00544.hp2 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+1445_168+1448d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACAC | 21 | a0001c0001t0001g0149a0001c0001t0001g0160a0001c0001t0001g0168others(18): Show | 21 | HG00741.hp2 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.168+1443_168+1448d others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACACA others(1): Show |
15 | a0001c0001t0001g0144a0001c0001t0001g0154a0001c0001t0001g0191others(12): Show | 15 | HG00558.hp1 HG01109.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+1441_168+1448d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACACA others(3): Show |
16 | a0001c0001t0001g0126a0001c0001t0001g0138a0001c0001t0001g0139others(13): Show | 16 | HG00099.hp2 HG01261.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.168+1439_168+1448d others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACACA others(5): Show |
29 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0123others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.168+1437_168+1448d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACACA others(7): Show |
16 | a0001c0001t0001g0124a0001c0001t0001g0135a0001c0001t0001g0152others(13): Show | 16 | HG00438.hp1 HG02135.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+1435_168+1448d others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACACA others(9): Show |
14 | a0001c0001t0001g0003a0001c0001t0001g0119a0001c0001t0001g0137others(11): Show | 15 | HG00438.hp2 HG00621.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+1433_168+1448d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACACA others(11): Show |
7 | a0001c0001t0001g0143a0001c0001t0001g0182a0001c0001t0001g0195others(4): Show | 7 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+1431_168+1448d others(20): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACACA others(13): Show |
5 | a0001c0001t0001g0134a0001c0001t0001g0153a0001c0001t0001g0181others(2): Show | 5 | HG00099.hp1 HG00738.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+1429_168+1448d others(22): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACACA others(15): Show |
1 | a0001c0001t0001g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.168+1427_168+1448d others(24): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | AACACACA others(17): Show |
2 | a0001c0001t0001g0180a0001c0001t0001g0206 | 2 | HG03453.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.168+1425_168+1448d others(26): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0011g0217 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.168+1398_168+1399i others(15): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149889 | ||||||
chr10:35149889
|
AAC | A | 12 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+1447_168+1448d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
AACAC | A | 11 | a0001c0001t0001g0151a0001c0001t0001g0177a0001c0001t0001g0255others(8): Show | 11 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+1445_168+1448d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
AACACAC | A | 7 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0002t0004g0111others(4): Show | 7 | HG00738.hp2 HG01071.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+1443_168+1448d others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.168+1439_168+1448d others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
AACACACA others(5): Show |
A | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG02015.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.168+1437_168+1448d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
AACACACA others(7): Show |
A | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+1435_168+1448d others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
AACACACA others(9): Show |
A | 31 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0047others(28): Show | 31 | HG00323.hp1 HG00544.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.168+1433_168+1448d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149889
|
AACACACA others(11): Show |
A | 35 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0045others(32): Show | 35 | HG00280.hp2 HG00423.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.168+1431_168+1448d others(20): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | |||||
chr10:35149924
|
ACACACAC others(8): Show |
A | 1 | a0001c0001t0002g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.168+1435_168+1449d others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149924 | |||||
chr10:35149938
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.168+1448_168+1449i others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149938 | |||||
chr10:35149938
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0156 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.168+1448_168+1449i others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149938 | |||||
chr10:35149938
|
A | ACACACAC others(3): Show |
3 | a0001c0001t0001g0121a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | NA19057.hp1 NA19076.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.168+1448_168+1449i others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149938 | |||||
chr10:35149938
|
A | ACACC | 2 | a0001c0001t0001g0185a0001c0001t0005g0001 | 3 | HG00558.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.168+1448_168+1449i others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149938 | |||||
chr10:35149939
|
C | CACACACA others(8): Show |
1 | a0001c0001t0001g0187 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.168+1448_168+1449i others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149939 | ||||||
chr10:35149939
|
C | CACACACA others(10): Show |
1 | a0001c0001t0001g0214 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.168+1448_168+1449i others(19): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149939 | ||||||
chr10:35150224
|
T | G | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+1733T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150224 | ||||||
chr10:35150232
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.168+1741T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150232 | ||||||
chr10:35150261
|
T | C | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.168+1770T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150261 | ||||||
chr10:35150333
|
A | G | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+1842A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150333 | ||||||
chr10:35150696
|
C | CTGT | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+2206_168+2208d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35150696 | |||||
chr10:35150828
|
AAAAGTGT others(58): Show |
A | 141 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.168+2403_168+2467d others(67): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35150828 | |||||
chr10:35150953
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.168+2462G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150953 | ||||||
chr10:35151072
|
A | G | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+2581A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151072 | ||||||
chr10:35151100
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.168+2609C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151100 | ||||||
chr10:35151194
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.168+2703A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151194 | ||||||
chr10:35151213
|
G | A | 141 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.168+2722G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151213 | ||||||
chr10:35151257
|
A | G | 1 | a0002c0005t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.168+2766A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151257 | ||||||
chr10:35151285
|
T | C | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.168+2794T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151285 | ||||||
chr10:35151365
|
G | A | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+2874G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151365 | ||||||
chr10:35151399
|
A | G | 110 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(107): Show | 110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.168+2908A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151399 | ||||||
chr10:35151404
|
A | G | 122 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.168+2913A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151404 | ||||||
chr10:35151444
|
C | G | 9 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+2953C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151444 | ||||||
chr10:35151501
|
G | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+3010G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151501 | ||||||
chr10:35151509
|
G | A | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+3018G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151509 | ||||||
chr10:35151530
|
C | A | 9 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+3039C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151530 | ||||||
chr10:35151532
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+3041C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151532 | ||||||
chr10:35151653
|
T | C | 122 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.168+3162T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151653 | ||||||
chr10:35151758
|
C | A | 1 | a0001c0001t0002g0054 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.168+3267C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151758 | ||||||
chr10:35151808
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.168+3317A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151808 | ||||||
chr10:35151941
|
A | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0276others(1): Show | 4 | HG01123.hp1 HG02622.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+3450A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151941 | ||||||
chr10:35152072
|
T | A | 1 | a0001c0001t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.168+3581T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152072 | ||||||
chr10:35152113
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+3622G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152113 | ||||||
chr10:35152241
|
A | G | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+3750A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152241 | ||||||
chr10:35152284
|
T | G | 1 | a0001c0004t0013g0272 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.168+3793T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152284 | ||||||
chr10:35152297
|
A | C | 1 | a0001c0001t0001g0261 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.168+3806A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152297 | ||||||
chr10:35152314
|
A | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+3823A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152314 | ||||||
chr10:35152540
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.168+4049C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152540 | ||||||
chr10:35152584
|
C | T | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+4093C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152584 | ||||||
chr10:35152671
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+4180G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152671 | ||||||
chr10:35152783
|
GTACAA | G | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+4298_168+4302d others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35152783 | |||||
chr10:35152825
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01261.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.168+4334C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152825 | ||||||
chr10:35153067
|
TAAA | T | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+4580_168+4582d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35153067 | |||||
chr10:35153089
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+4598A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153089 | ||||||
chr10:35153153
|
TGGATTGC others(9): Show |
T | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.168+4666_168+4681d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35153153 | |||||
chr10:35153535
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0016g0203 | 2 | NA18947.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.168+5044G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153535 | ||||||
chr10:35153681
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+5190C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153681 | ||||||
chr10:35153891
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.168+5400A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153891 | ||||||
chr10:35153920
|
G | T | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+5429G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153920 | ||||||
chr10:35154112
|
G | A | 8 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+5621G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154112 | ||||||
chr10:35154292
|
A | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+5801A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154292 | ||||||
chr10:35154389
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+5898C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154389 | ||||||
chr10:35154403
|
G | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+5912G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154403 | ||||||
chr10:35154422
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168+5931T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154422 | ||||||
chr10:35154543
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.168+6052A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154543 | ||||||
chr10:35154715
|
A | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+6224A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154715 | ||||||
chr10:35154985
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0210a0001c0001t0001g0229 | 3 | HG02145.hp1 HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.168+6494C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154985 | ||||||
chr10:35155054
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.168+6563T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155054 | ||||||
chr10:35155055
|
G | A | 1 | a0001c0004t0013g0272 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.168+6564G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155055 | ||||||
chr10:35155214
|
G | A | 1 | a0001c0001t0007g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+6723G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155214 | ||||||
chr10:35155529
|
CA | C | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+7046delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35155529 | |||||
chr10:35155630
|
TC | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(4): Show | 7 | HG01071.hp1 HG01123.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+7140delC | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155630 | ||||||
chr10:35155631
|
C | T | 26 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(23): Show | 26 | HG00621.hp1 HG00738.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.168+7140C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155631 | ||||||
chr10:35155631
|
CT | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.168+7151delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35155631 | |||||
chr10:35155632
|
T | A | 1 | a0001c0001t0003g0008 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.168+7141T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155632 | ||||||
chr10:35155733
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0271a0001c0001t0017g0136 | 3 | HG00438.hp1 HG02080.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.168+7242A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155733 | ||||||
chr10:35155859
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.168+7368G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155859 | ||||||
chr10:35155945
|
CT | C | 103 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(100): Show | 103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.168+7466delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35155945 | |||||
chr10:35155963
|
A | G | 110 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(107): Show | 110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.168+7472A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155963 | ||||||
chr10:35156253
|
C | CT | 106 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0002g0036others(103): Show | 106 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.168+7773dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35156253 | |||||
chr10:35156291
|
C | G | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+7800C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156291 | ||||||
chr10:35156467
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0228 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.168+7976C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156467 | ||||||
chr10:35156660
|
A | T | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+8169A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156660 | ||||||
chr10:35156665
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.168+8174A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156665 | ||||||
chr10:35156727
|
G | C | 3 | a0001c0002t0004g0035a0001c0002t0004g0290a0001c0002t0020g0291 | 3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168+8236G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156727 | ||||||
chr10:35156924
|
A | G | 33 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(30): Show | 33 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.168+8433A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156924 | ||||||
chr10:35156958
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.168+8467T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156958 | ||||||
chr10:35157276
|
C | CAACT | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+8789_168+8792d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157276 | |||||
chr10:35157447
|
C | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0247 | 2 | HG01109.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.168+8956C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157447 | ||||||
chr10:35157635
|
C | CA | 12 | a0001c0001t0001g0131a0001c0001t0001g0231a0001c0001t0001g0260others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+9165dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157635 | |||||
chr10:35157635
|
CA | C | 111 | a0001c0001t0001g0202a0001c0001t0001g0250a0001c0001t0002g0036others(108): Show | 111 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.168+9165delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157635 | |||||
chr10:35157635
|
CAA | C | 6 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 6 | HG00639.hp1 HG01071.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+9164_168+9165d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157635 | |||||
chr10:35157800
|
A | G | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG02015.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.168+9309A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157800 | ||||||
chr10:35157822
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.168+9331G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157822 | ||||||
chr10:35157875
|
A | AT | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+9385dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157875 | |||||
chr10:35157910
|
C | A | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+9419C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157910 | ||||||
chr10:35157917
|
T | C | 1 | a0001c0001t0003g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.168+9426T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157917 | ||||||
chr10:35157937
|
A | G | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+9446A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157937 | ||||||
chr10:35157950
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.168+9459G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157950 | ||||||
chr10:35158347
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.168+9856C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158347 | ||||||
chr10:35158615
|
G | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01261.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.168+10124G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158615 | ||||||
chr10:35158794
|
T | C | 32 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(29): Show | 32 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.168+10303T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158794 | ||||||
chr10:35158798
|
GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0002g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168+10318_168+1034 others(28): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35158798 | |||||
chr10:35158799
|
T | TG | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+10308_168+1030 others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158799 | ||||||
chr10:35158800
|
T | G | 2 | a0001c0001t0009g0289a0001c0001t0018g0288 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.168+10309T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158800 | ||||||
chr10:35158805
|
TTTTGTTG others(5): Show |
T | 24 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.168+10321_168+1033 others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35158805 | |||||
chr10:35158806
|
TTTGTTGT others(4): Show |
T | 36 | a0001c0001t0002g0036a0001c0001t0002g0044a0001c0001t0002g0045others(33): Show | 36 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.168+10318_168+1032 others(15): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35158806 | |||||
chr10:35158807
|
T | G | 13 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(10): Show | 13 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+10316T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158807 | ||||||
chr10:35158807
|
TTGTTGTT others(3): Show |
T | 23 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0043others(20): Show | 23 | HG00280.hp2 HG00544.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.168+10318_168+1032 others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35158807 | |||||
chr10:35158808
|
TGTTGTTT others(6): Show |
T | 20 | a0001c0001t0002g0077a0001c0001t0003g0004a0001c0001t0003g0005others(17): Show | 20 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.168+10318_168+1033 others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158808 | ||||||
chr10:35158809
|
G | T | 35 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(32): Show | 35 | HG00621.hp1 HG00738.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.168+10318G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158809 | ||||||
chr10:35158812
|
G | T | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+10321G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158812 | ||||||
chr10:35158817
|
G | T | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+10326G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158817 | ||||||
chr10:35158818
|
T | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+10327T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158818 | ||||||
chr10:35158821
|
G | T | 103 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(100): Show | 103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.168+10330G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158821 | ||||||
chr10:35158942
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+10451G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158942 | ||||||
chr10:35159121
|
G | A | 3 | a0001c0002t0004g0035a0001c0002t0004g0290a0001c0002t0020g0291 | 3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168+10630G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159121 | ||||||
chr10:35159260
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.168+10769C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159260 | ||||||
chr10:35159262
|
C | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+10771C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159262 | ||||||
chr10:35159440
|
C | T | 1 | a0001c0001t0009g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168+10949C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159440 | ||||||
chr10:35159476
|
G | A | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+10985G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159476 | ||||||
chr10:35159527
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.168+11036C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159527 | ||||||
chr10:35159792
|
G | A | 69 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.168+11301G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159792 | ||||||
chr10:35159907
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.168+11416C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159907 | ||||||
chr10:35159910
|
G | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+11419G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159910 | ||||||
chr10:35159979
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.168+11488T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159979 | ||||||
chr10:35160261
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.168+11770C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160261 | ||||||
chr10:35160281
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.168+11790G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160281 | ||||||
chr10:35160300
|
A | G | 109 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(106): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.168+11809A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160300 | ||||||
chr10:35160349
|
C | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0220 | 2 | NA18954.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.168+11858C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160349 | ||||||
chr10:35160350
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.168+11859G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160350 | ||||||
chr10:35160387
|
A | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+11896A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160387 | ||||||
chr10:35160409
|
C | CT | 40 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(37): Show | 40 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.168+11927dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35160409 | |||||
chr10:35160433
|
C | G | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.168+11942C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160433 | ||||||
chr10:35160511
|
G | C | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+12020G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160511 | ||||||
chr10:35160660
|
C | T | 1 | a0001c0003t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.168+12169C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160660 | ||||||
chr10:35160694
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.168+12203A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160694 | ||||||
chr10:35160695
|
TAAC | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+12206_168+1220 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35160695 | |||||
chr10:35160752
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+12261A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160752 | ||||||
chr10:35160899
|
TCATATCC others(5): Show |
T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+12412_168+1242 others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35160899 | |||||
chr10:35160985
|
C | T | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.168+12494C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160985 | ||||||
chr10:35160989
|
G | A | 7 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 8 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+12498G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160989 | ||||||
chr10:35161187
|
T | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+12696T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161187 | ||||||
chr10:35161205
|
C | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+12714C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161205 | ||||||
chr10:35161206
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.168+12715G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161206 | ||||||
chr10:35161211
|
A | G | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+12720A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161211 | ||||||
chr10:35161218
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+12727C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161218 | ||||||
chr10:35161219
|
C | T | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+12728C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161219 | ||||||
chr10:35161222
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+12731C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161222 | ||||||
chr10:35161244
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+12753C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161244 | ||||||
chr10:35161262
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0219 | 2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.168+12771G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161262 | ||||||
chr10:35161350
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.168+12859G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161350 | ||||||
chr10:35161368
|
G | A | 1 | a0001c0001t0016g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.168+12877G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161368 | ||||||
chr10:35161398
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+12907G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161398 | ||||||
chr10:35161495
|
A | T | 1 | a0001c0002t0004g0116 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.168+13004A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161495 | ||||||
chr10:35161663
|
CA | C | 121 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.168+13183delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35161663 | |||||
chr10:35161679
|
G | A | 121 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.168+13188G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161679 | ||||||
chr10:35161680
|
A | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+13189A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161680 | ||||||
chr10:35161827
|
G | C | 3 | a0001c0002t0004g0035a0001c0002t0004g0290a0001c0002t0020g0291 | 3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168+13336G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161827 | ||||||
chr10:35161929
|
A | G | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+13438A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161929 | ||||||
chr10:35161937
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+13446G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161937 | ||||||
chr10:35161940
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+13449A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161940 | ||||||
chr10:35162012
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+13521C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162012 | ||||||
chr10:35162024
|
C | T | 1 | a0001c0001t0003g0023 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.168+13533C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162024 | ||||||
chr10:35162208
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.168+13717A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162208 | ||||||
chr10:35162378
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+13887A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162378 | ||||||
chr10:35162405
|
T | C | 1 | a0001c0001t0007g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+13914T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162405 | ||||||
chr10:35162415
|
A | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0143a0001c0001t0001g0151others(7): Show | 11 | HG00741.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+13924A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162415 | ||||||
chr10:35162424
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.168+13933T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162424 | ||||||
chr10:35162670
|
G | A | 9 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+14179G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162670 | ||||||
chr10:35162673
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+14182G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162673 | ||||||
chr10:35162728
|
G | C | 1 | a0001c0001t0001g0197 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.168+14237G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162728 | ||||||
chr10:35162770
|
C | T | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+14279C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162770 | ||||||
chr10:35162865
|
T | A | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+14374T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162865 | ||||||
chr10:35162896
|
A | C | 1 | a0001c0001t0001g0201 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.168+14405A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162896 | ||||||
chr10:35163018
|
C | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+14527C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163018 | ||||||
chr10:35163045
|
C | CA | 71 | a0001c0001t0001g0142a0001c0001t0002g0036a0001c0001t0002g0037others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+14565dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35163045 | |||||
chr10:35163159
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+14668G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163159 | ||||||
chr10:35163177
|
T | G | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.168+14686T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163177 | ||||||
chr10:35163213
|
G | A | 109 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(106): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.168+14722G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163213 | ||||||
chr10:35163261
|
G | C | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+14770G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163261 | ||||||
chr10:35163333
|
CTT | C | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+14845_168+1484 others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35163333 | |||||
chr10:35163396
|
A | T | 1 | a0001c0001t0002g0087 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.168+14905A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163396 | ||||||
chr10:35163420
|
A | G | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+14929A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163420 | ||||||
chr10:35163428
|
A | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+14937A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163428 | ||||||
chr10:35163435
|
A | G | 1 | a0001c0001t0002g0047 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.168+14944A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163435 | ||||||
chr10:35163441
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.168+14950T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163441 | ||||||
chr10:35163449
|
C | T | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+14958C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163449 | ||||||
chr10:35163450
|
G | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG00544.hp2 NA18965.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.168+14959G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163450 | ||||||
chr10:35163478
|
GTTCGAGA others(5): Show |
G | 1 | a0001c0001t0002g0106 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.168+14988_168+1499 others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163478 | ||||||
chr10:35163482
|
G | C | 5 | a0001c0002t0004g0111a0001c0002t0004g0112a0001c0002t0004g0113others(2): Show | 5 | HG00738.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+14991G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163482 | ||||||
chr10:35163558
|
G | A | 6 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG03098.hp2 HG03579.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+15067G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163558 | ||||||
chr10:35163580
|
A | G | 121 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.168+15089A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163580 | ||||||
chr10:35163752
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.169-15137C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163752 | ||||||
chr10:35163917
|
G | A | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-14972G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163917 | ||||||
chr10:35163974
|
C | CA | 9 | a0001c0001t0001g0145a0001c0001t0001g0215a0001c0001t0001g0231others(6): Show | 10 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-14902dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35163974 | |||||
chr10:35164053
|
AAGT | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0170a0001c0001t0001g0212 | 3 | HG01258.hp1 HG02273.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.169-14832_169-1483 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35164053 | |||||
chr10:35164282
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.169-14607G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164282 | ||||||
chr10:35164473
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-14416G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164473 | ||||||
chr10:35164526
|
T | C | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-14363T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164526 | ||||||
chr10:35164577
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.169-14312A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164577 | ||||||
chr10:35164614
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-14275C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164614 | ||||||
chr10:35164773
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.169-14116G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164773 | ||||||
chr10:35165056
|
C | CAA | 9 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(6): Show | 9 | HG01884.hp2 HG02559.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-13812_169-1381 others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | |||||
chr10:35165056
|
C | CAAA | 7 | a0001c0001t0002g0057a0001c0001t0002g0061a0001c0001t0002g0073others(4): Show | 7 | HG01516.hp2 HG01975.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-13813_169-1381 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | |||||
chr10:35165056
|
C | CAAAA | 64 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.169-13814_169-1381 others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | |||||
chr10:35165056
|
C | CAAAAA | 6 | a0001c0001t0002g0055a0001c0001t0002g0074a0001c0001t0002g0078others(3): Show | 6 | HG00544.hp1 HG01069.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-13815_169-1381 others(9): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | |||||
chr10:35165056
|
C | CAAAAAAA | 21 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0008others(18): Show | 21 | HG00639.hp1 HG00735.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.169-13817_169-1381 others(11): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | |||||
chr10:35165056
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0016others(4): Show | 7 | HG00741.hp2 NA18959.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-13818_169-1381 others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | |||||
chr10:35165056
|
CAA | C | 8 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0113others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-13812_169-1381 others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | |||||
chr10:35165057
|
A | C | 1 | a0001c0002t0004g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.169-13832A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165057 | ||||||
chr10:35165058
|
A | T | 1 | a0001c0002t0004g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.169-13831A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165058 | ||||||
chr10:35165066
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.169-13823A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165066 | ||||||
chr10:35165069
|
A | T | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.169-13820A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165069 | ||||||
chr10:35165070
|
A | AT | 7 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0198others(4): Show | 7 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-13819_169-1381 others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165070 | ||||||
chr10:35165070
|
A | T | 7 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0149others(4): Show | 7 | HG00735.hp1 HG02015.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-13819A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165070 | ||||||
chr10:35165074
|
A | AT | 10 | a0001c0001t0001g0121a0001c0001t0001g0139a0001c0001t0001g0151others(7): Show | 10 | HG01261.hp2 HG02572.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-13815_169-1381 others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165074 | ||||||
chr10:35165074
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.169-13815A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165074 | ||||||
chr10:35165074
|
A | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.169-13815A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165074 | ||||||
chr10:35165078
|
A | AAAG | 10 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0264others(7): Show | 10 | HG00621.hp1 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-13811_169-1381 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165078 | ||||||
chr10:35165079
|
G | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0191 | 2 | HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.169-13810G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165079 | ||||||
chr10:35165178
|
T | C | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-13711T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165178 | ||||||
chr10:35165271
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-13618A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165271 | ||||||
chr10:35165369
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.169-13520C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165369 | ||||||
chr10:35165422
|
A | C | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-13467A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165422 | ||||||
chr10:35165477
|
A | C | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-13412A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165477 | ||||||
chr10:35165590
|
A | T | 3 | a0001c0002t0004g0109a0001c0002t0004g0116a0001c0002t0004g0118 | 3 | HG01109.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169-13299A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165590 | ||||||
chr10:35165712
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02258.hp1 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-13177T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165712 | ||||||
chr10:35166048
|
C | T | 121 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.169-12841C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166048 | ||||||
chr10:35166050
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.169-12839A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166050 | ||||||
chr10:35166166
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.169-12723C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166166 | ||||||
chr10:35166266
|
C | CA | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-12615dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35166266 | |||||
chr10:35166359
|
C | T | 6 | a0001c0001t0001g0198a0001c0001t0002g0282a0001c0001t0002g0283others(3): Show | 6 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-12530C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166359 | ||||||
chr10:35166378
|
T | C | 1 | a0001c0003t0002g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.169-12511T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166378 | ||||||
chr10:35166408
|
A | G | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-12481A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166408 | ||||||
chr10:35166564
|
C | CA | 14 | a0001c0001t0001g0154a0001c0001t0001g0269a0001c0001t0002g0061others(11): Show | 14 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-12310dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35166564 | |||||
chr10:35166564
|
C | CAA | 74 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(71): Show | 74 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.169-12311_169-1231 others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35166564 | |||||
chr10:35166564
|
C | CAAA | 30 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(27): Show | 30 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.169-12312_169-1231 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35166564 | |||||
chr10:35166600
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-12289G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166600 | ||||||
chr10:35166701
|
C | T | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-12188C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166701 | ||||||
chr10:35166831
|
A | G | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.169-12058A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166831 | ||||||
chr10:35166863
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-12026C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166863 | ||||||
chr10:35167001
|
C | T | 2 | a0001c0001t0003g0110a0001c0001t0009g0289 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.169-11888C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167001 | ||||||
chr10:35167150
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0014g0200 | 2 | NA18960.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.169-11739A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167150 | ||||||
chr10:35167230
|
C | T | 6 | a0001c0001t0001g0137a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG00438.hp2 NA18972.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-11659C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167230 | ||||||
chr10:35167287
|
G | A | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-11602G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167287 | ||||||
chr10:35167306
|
A | G | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-11583A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167306 | ||||||
chr10:35167314
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.169-11575C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167314 | ||||||
chr10:35167367
|
C | T | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-11522C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167367 | ||||||
chr10:35167461
|
G | T | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-11428G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167461 | ||||||
chr10:35167476
|
C | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.169-11413C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167476 | ||||||
chr10:35167785
|
A | T | 1 | a0001c0002t0004g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.169-11104A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167785 | ||||||
chr10:35167890
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-10999A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167890 | ||||||
chr10:35167980
|
A | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-10909A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167980 | ||||||
chr10:35167983
|
CT | C | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169-10899delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35167983 | |||||
chr10:35168158
|
C | T | 2 | a0001c0001t0003g0014a0001c0001t0003g0033 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.169-10731C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168158 | ||||||
chr10:35168247
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.169-10642C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168247 | ||||||
chr10:35168269
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.169-10620C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168269 | ||||||
chr10:35168286
|
G | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-10603G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168286 | ||||||
chr10:35168335
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.169-10554T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168335 | ||||||
chr10:35168385
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.169-10504T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168385 | ||||||
chr10:35168528
|
T | C | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-10361T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168528 | ||||||
chr10:35168545
|
G | C | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-10344G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168545 | ||||||
chr10:35168591
|
T | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.169-10298T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168591 | ||||||
chr10:35168677
|
C | G | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.169-10212C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168677 | ||||||
chr10:35168754
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-10135C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168754 | ||||||
chr10:35168850
|
A | G | 1 | a0001c0001t0002g0047 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.169-10039A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168850 | ||||||
chr10:35168971
|
A | C | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-9918A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168971 | ||||||
chr10:35169114
|
G | GT | 5 | a0001c0001t0001g0157a0001c0001t0002g0078a0001c0001t0002g0085others(2): Show | 5 | HG01169.hp1 HG01993.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-9769dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35169114 | |||||
chr10:35169232
|
A | G | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.169-9657A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169232 | ||||||
chr10:35169263
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0197 | 2 | HG02015.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.169-9626T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169263 | ||||||
chr10:35169332
|
T | A | 1 | a0001c0001t0001g0241 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.169-9557T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169332 | ||||||
chr10:35169376
|
C | T | 1 | a0001c0002t0004g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.169-9513C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169376 | ||||||
chr10:35169390
|
C | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-9499C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169390 | ||||||
chr10:35169597
|
G | C | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-9292G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169597 | ||||||
chr10:35169845
|
G | A | 43 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(40): Show | 43 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.169-9044G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169845 | ||||||
chr10:35169852
|
A | T | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-9037A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169852 | ||||||
chr10:35169893
|
G | T | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-8996G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169893 | ||||||
chr10:35169965
|
C | CT | 85 | a0001c0001t0001g0149a0001c0001t0001g0260a0001c0001t0001g0261others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.169-8909dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35169965 | |||||
chr10:35169965
|
C | CTT | 10 | a0001c0001t0001g0259a0001c0001t0003g0005a0001c0001t0003g0024others(7): Show | 10 | HG02145.hp2 HG03491.hp1 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-8910_169-8909d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35169965 | |||||
chr10:35169965
|
C | CTTT | 22 | a0001c0001t0001g0194a0001c0001t0003g0004a0001c0001t0003g0006others(19): Show | 22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.169-8911_169-8909d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35169965 | |||||
chr10:35169994
|
G | A | 2 | a0001c0001t0003g0030a0003c0006t0003g0031 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.169-8895G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169994 | ||||||
chr10:35170014
|
G | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-8875G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170014 | ||||||
chr10:35170064
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-8825G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170064 | ||||||
chr10:35170111
|
C | T | 1 | a0002c0005t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169-8778C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170111 | ||||||
chr10:35170189
|
T | G | 1 | a0001c0001t0007g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-8700T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170189 | ||||||
chr10:35170201
|
G | A | 9 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(6): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-8688G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170201 | ||||||
chr10:35170209
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.169-8680C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170209 | ||||||
chr10:35170335
|
C | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-8554C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170335 | ||||||
chr10:35170359
|
C | A | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-8530C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170359 | ||||||
chr10:35170524
|
T | C | 1 | a0001c0001t0003g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.169-8365T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170524 | ||||||
chr10:35170569
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.169-8320A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170569 | ||||||
chr10:35170747
|
T | A | 3 | a0001c0002t0004g0109a0001c0002t0004g0116a0001c0002t0004g0118 | 3 | HG01109.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169-8142T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170747 | ||||||
chr10:35170768
|
G | C | 22 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(19): Show | 22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.169-8121G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170768 | ||||||
chr10:35171048
|
G | A | 141 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.169-7841G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171048 | ||||||
chr10:35171147
|
A | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-7742A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171147 | ||||||
chr10:35171161
|
C | CT | 55 | a0001c0001t0001g0133a0001c0001t0001g0146a0001c0001t0001g0147others(52): Show | 56 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.169-7703dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | |||||
chr10:35171161
|
C | CTT | 35 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0149others(32): Show | 35 | HG00438.hp1 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.169-7704_169-7703d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | |||||
chr10:35171161
|
C | CTTT | 61 | a0001c0001t0002g0037a0001c0001t0002g0043a0001c0001t0002g0044others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.169-7705_169-7703d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | |||||
chr10:35171161
|
C | CTTTT | 12 | a0001c0001t0002g0036a0001c0001t0002g0040a0001c0001t0002g0047others(9): Show | 12 | HG00733.hp2 HG01168.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-7706_169-7703d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | |||||
chr10:35171161
|
CT | C | 10 | a0001c0001t0001g0142a0001c0001t0001g0255a0001c0001t0001g0256others(7): Show | 10 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-7703delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | |||||
chr10:35171161
|
CTT | C | 7 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(4): Show | 7 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-7704_169-7703d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | |||||
chr10:35171161
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0167others(1): Show | 5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-7713_169-7703d others(13): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | |||||
chr10:35171295
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.169-7594A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171295 | ||||||
chr10:35171296
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.169-7593T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171296 | ||||||
chr10:35171299
|
G | T | 69 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.169-7590G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171299 | ||||||
chr10:35171309
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.169-7580T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171309 | ||||||
chr10:35171392
|
G | C | 2 | a0001c0002t0004g0290a0001c0002t0020g0291 | 2 | HG01071.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.169-7497G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171392 | ||||||
chr10:35171419
|
G | C | 1 | a0001c0001t0002g0047 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.169-7470G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171419 | ||||||
chr10:35171424
|
G | A | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.169-7465G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171424 | ||||||
chr10:35171491
|
T | C | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.169-7398T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171491 | ||||||
chr10:35171578
|
A | G | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG00639.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.169-7311A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171578 | ||||||
chr10:35171849
|
A | G | 1 | a0001c0001t0007g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.169-7040A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171849 | ||||||
chr10:35171850
|
T | G | 1 | a0001c0001t0001g0197 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.169-7039T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171850 | ||||||
chr10:35172011
|
T | C | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-6878T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172011 | ||||||
chr10:35172046
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.169-6843G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172046 | ||||||
chr10:35172082
|
G | A | 1 | a0001c0001t0009g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169-6807G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172082 | ||||||
chr10:35172110
|
T | C | 126 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(123): Show | 126 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.169-6779T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172110 | ||||||
chr10:35172129
|
CTTTGTTT others(3): Show |
C | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.169-6751_169-6742d others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35172129 | |||||
chr10:35172203
|
C | G | 1 | a0001c0001t0001g0201 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.169-6686C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172203 | ||||||
chr10:35172332
|
A | G | 10 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0008others(7): Show | 10 | HG01123.hp2 HG01981.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-6557A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172332 | ||||||
chr10:35172385
|
G | A | 7 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0198others(4): Show | 7 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-6504G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172385 | ||||||
chr10:35172414
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.169-6475C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172414 | ||||||
chr10:35172419
|
A | G | 2 | a0001c0001t0003g0030a0003c0006t0003g0031 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.169-6470A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172419 | ||||||
chr10:35172470
|
CAG | C | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169-6418_169-6417d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172470 | ||||||
chr10:35172572
|
GT | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(279): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.169-6304delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35172572 | |||||
chr10:35172574
|
T | A | 1 | a0001c0001t0002g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.169-6315T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172574 | ||||||
chr10:35172690
|
T | A | 2 | a0001c0001t0008g0246a0001c0001t0008g0248 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.169-6199T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172690 | ||||||
chr10:35172709
|
A | AC | 82 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.169-6173dupC | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35172709 | |||||
chr10:35172820
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-6069C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172820 | ||||||
chr10:35172875
|
A | T | 1 | a0001c0001t0001g0237 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.169-6014A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172875 | ||||||
chr10:35173022
|
G | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.169-5867G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173022 | ||||||
chr10:35173030
|
T | G | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-5859T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173030 | ||||||
chr10:35173351
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.169-5538A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173351 | ||||||
chr10:35173432
|
A | G | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169-5457A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173432 | ||||||
chr10:35173474
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-5415G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173474 | ||||||
chr10:35173711
|
A | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-5178A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173711 | ||||||
chr10:35173983
|
C | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-4906C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173983 | ||||||
chr10:35174134
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.169-4755A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174134 | ||||||
chr10:35174243
|
G | C | 1 | a0001c0002t0004g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.169-4646G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174243 | ||||||
chr10:35174798
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-4091G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174798 | ||||||
chr10:35174821
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-4068C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174821 | ||||||
chr10:35174880
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.169-4009G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174880 | ||||||
chr10:35175031
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.169-3858G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175031 | ||||||
chr10:35175173
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.169-3716T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175173 | ||||||
chr10:35175240
|
G | A | 129 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(126): Show | 129 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.169-3649G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175240 | ||||||
chr10:35175244
|
G | A | 131 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(128): Show | 131 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.169-3645G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175244 | ||||||
chr10:35175260
|
A | AC | 39 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(36): Show | 39 | HG00621.hp1 HG00738.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.169-3629_169-3628i others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175260 | ||||||
chr10:35175261
|
T | A | 39 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(36): Show | 39 | HG00621.hp1 HG00738.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.169-3628T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175261 | ||||||
chr10:35175262
|
G | T | 39 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(36): Show | 39 | HG00621.hp1 HG00738.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.169-3627G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175262 | ||||||
chr10:35175274
|
G | A | 1 | a0001c0001t0009g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169-3615G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175274 | ||||||
chr10:35175307
|
G | A | 7 | a0001c0001t0002g0054a0001c0001t0002g0056a0001c0001t0002g0058others(4): Show | 7 | HG01258.hp2 HG01358.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-3582G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175307 | ||||||
chr10:35175445
|
C | CA | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-3434dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35175445 | |||||
chr10:35175503
|
G | T | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-3386G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175503 | ||||||
chr10:35175547
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0018g0288 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.169-3342G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175547 | ||||||
chr10:35175610
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.169-3279C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175610 | ||||||
chr10:35175744
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-3145G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175744 | ||||||
chr10:35175850
|
C | T | 73 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.169-3039C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175850 | ||||||
chr10:35175905
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.169-2984T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175905 | ||||||
chr10:35176060
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.169-2829C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176060 | ||||||
chr10:35176173
|
G | A | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169-2716G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176173 | ||||||
chr10:35176243
|
C | T | 8 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-2646C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176243 | ||||||
chr10:35176251
|
G | A | 5 | a0001c0001t0002g0043a0001c0001t0002g0051a0001c0001t0002g0052others(2): Show | 5 | HG02129.hp1 NA18612.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-2638G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176251 | ||||||
chr10:35176262
|
T | A | 109 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(106): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.169-2627T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176262 | ||||||
chr10:35176351
|
G | C | 102 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(99): Show | 102 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.169-2538G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176351 | ||||||
chr10:35176409
|
CT | C | 11 | a0001c0001t0001g0129a0001c0001t0001g0165a0001c0001t0001g0201others(8): Show | 11 | HG00558.hp1 HG01884.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-2464delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35176409 | |||||
chr10:35176424
|
T | G | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-2465T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176424 | ||||||
chr10:35176469
|
A | G | 109 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(106): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.169-2420A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176469 | ||||||
chr10:35176508
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169-2381C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176508 | ||||||
chr10:35176533
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.169-2356G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176533 | ||||||
chr10:35176535
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.169-2354G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176535 | ||||||
chr10:35176630
|
T | A | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-2259T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176630 | ||||||
chr10:35176671
|
A | C | 2 | a0001c0001t0002g0057a0001c0001t0002g0072 | 2 | NA18946.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.169-2218A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176671 | ||||||
chr10:35176688
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-2201C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176688 | ||||||
chr10:35176818
|
G | A | 109 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(106): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.169-2071G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176818 | ||||||
chr10:35176848
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.169-2041C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176848 | ||||||
chr10:35176952
|
T | C | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1937T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176952 | ||||||
chr10:35177077
|
CA | C | 59 | a0001c0001t0001g0148a0001c0001t0001g0180a0001c0001t0001g0182others(56): Show | 59 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.169-1801delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35177077 | |||||
chr10:35177132
|
T | C | 1 | a0001c0001t0007g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.169-1757T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177132 | ||||||
chr10:35177222
|
A | G | 1 | a0001c0001t0001g0285 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.169-1667A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177222 | ||||||
chr10:35177257
|
T | G | 121 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.169-1632T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177257 | ||||||
chr10:35177259
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.169-1630C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177259 | ||||||
chr10:35177305
|
T | C | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-1584T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177305 | ||||||
chr10:35177451
|
A | G | 33 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(30): Show | 33 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.169-1438A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177451 | ||||||
chr10:35177554
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.169-1335C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177554 | ||||||
chr10:35177568
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.169-1321G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177568 | ||||||
chr10:35177843
|
G | T | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.169-1046G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177843 | ||||||
chr10:35177999
|
G | A | 4 | a0001c0001t0001g0259a0001c0001t0001g0262a0001c0001t0001g0264others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-890G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177999 | ||||||
chr10:35178139
|
T | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.169-750T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35178139 | ||||||
chr10:35178434
|
T | C | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0276 | 3 | HG02622.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.169-455T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35178434 | ||||||
chr10:35178743
|
C | T | 125 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(122): Show | 125 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.169-146C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35178743 | ||||||
chr10:35179342
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.409+66A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35179342 | ||||||
chr10:35180112
|
A | T | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.409+836A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180112 | ||||||
chr10:35180157
|
G | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | NA18984.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.409+881G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180157 | ||||||
chr10:35180250
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.409+974G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180250 | ||||||
chr10:35180734
|
G | A | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.409+1458G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180734 | ||||||
chr10:35180769
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0177 | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+1493G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180769 | ||||||
chr10:35180845
|
G | A | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+1569G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180845 | ||||||
chr10:35181047
|
T | G | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.409+1771T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181047 | ||||||
chr10:35181214
|
C | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.409+1938C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181214 | ||||||
chr10:35181215
|
A | C | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.409+1939A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181215 | ||||||
chr10:35181221
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.409+1945C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181221 | ||||||
chr10:35181373
|
A | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0033 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.409+2097A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181373 | ||||||
chr10:35181518
|
G | T | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.409+2242G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181518 | ||||||
chr10:35181525
|
G | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02258.hp1 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+2249G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181525 | ||||||
chr10:35181656
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.409+2380T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181656 | ||||||
chr10:35181830
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.409+2554A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181830 | ||||||
chr10:35181913
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.409+2637A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181913 | ||||||
chr10:35181997
|
A | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.409+2721A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181997 | ||||||
chr10:35182023
|
C | T | 3 | a0001c0002t0004g0109a0001c0002t0004g0116a0001c0002t0004g0118 | 3 | HG01109.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.409+2747C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182023 | ||||||
chr10:35182154
|
A | G | 1 | a0001c0001t0009g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.409+2878A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182154 | ||||||
chr10:35182175
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.409+2899G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182175 | ||||||
chr10:35182355
|
A | G | 1 | a0001c0003t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.409+3079A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182355 | ||||||
chr10:35182369
|
C | T | 5 | a0001c0002t0004g0111a0001c0002t0004g0112a0001c0002t0004g0113others(2): Show | 5 | HG00738.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.409+3093C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182369 | ||||||
chr10:35182382
|
A | AT | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.409+3114dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35182382 | |||||
chr10:35182443
|
C | T | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+3167C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182443 | ||||||
chr10:35182482
|
T | G | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0265 | 3 | HG00621.hp1 HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.409+3206T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182482 | ||||||
chr10:35182668
|
GACTT | G | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.409+3396_409+3399d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35182668 | |||||
chr10:35182672
|
T | G | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.409+3396T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182672 | ||||||
chr10:35182793
|
A | G | 8 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.409+3517A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182793 | ||||||
chr10:35182813
|
A | G | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.409+3537A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182813 | ||||||
chr10:35182945
|
G | A | 141 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(138): Show | 141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.409+3669G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182945 | ||||||
chr10:35183222
|
T | C | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.409+3946T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183222 | ||||||
chr10:35183271
|
A | G | 122 | a0001c0001t0001g0147a0001c0001t0002g0036a0001c0001t0002g0037others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.409+3995A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183271 | ||||||
chr10:35183504
|
T | C | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.409+4228T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183504 | ||||||
chr10:35183546
|
A | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.409+4270A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183546 | ||||||
chr10:35183627
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.409+4351C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183627 | ||||||
chr10:35183813
|
G | A | 1 | a0001c0001t0002g0087 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.410-4387G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183813 | ||||||
chr10:35183817
|
G | A | 1 | a0001c0002t0004g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.410-4383G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183817 | ||||||
chr10:35183827
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.410-4373C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183827 | ||||||
chr10:35183891
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.410-4309A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183891 | ||||||
chr10:35183905
|
T | C | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-4295T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183905 | ||||||
chr10:35184107
|
G | A | 121 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.410-4093G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184107 | ||||||
chr10:35184116
|
C | T | 2 | a0001c0001t0005g0001a0001c0001t0005g0128 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.410-4084C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184116 | ||||||
chr10:35184128
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.410-4072T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184128 | ||||||
chr10:35184185
|
C | A | 4 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-4015C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184185 | ||||||
chr10:35184557
|
G | A | 22 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(19): Show | 22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.410-3643G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184557 | ||||||
chr10:35184624
|
T | C | 3 | a0001c0002t0004g0035a0001c0002t0004g0290a0001c0002t0020g0291 | 3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.410-3576T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184624 | ||||||
chr10:35184707
|
G | T | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.410-3493G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184707 | ||||||
chr10:35184786
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.410-3414C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184786 | ||||||
chr10:35184797
|
AAAAG | A | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.410-3397_410-3394d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35184797 | |||||
chr10:35184814
|
G | A | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.410-3386G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184814 | ||||||
chr10:35184880
|
A | G | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.410-3320A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184880 | ||||||
chr10:35184950
|
T | G | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.410-3250T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184950 | ||||||
chr10:35184985
|
A | G | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.410-3215A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184985 | ||||||
chr10:35184999
|
T | G | 109 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(106): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.410-3201T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184999 | ||||||
chr10:35185033
|
C | CCATT | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(145): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.410-3137_410-3134d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185033 | |||||
chr10:35185033
|
C | CCATTCAT others(1): Show |
12 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0151others(9): Show | 12 | HG00423.hp1 HG00621.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.410-3141_410-3134d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185033 | |||||
chr10:35185033
|
CCATT | C | 3 | a0001c0001t0003g0009a0001c0001t0003g0110a0001c0001t0018g0288 | 3 | HG01081.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.410-3137_410-3134d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185033 | |||||
chr10:35185033
|
CCATTCAT others(1): Show |
C | 103 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(100): Show | 103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.410-3141_410-3134d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185033 | |||||
chr10:35185067
|
T | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.410-3133T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185067 | ||||||
chr10:35185085
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.410-3115T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185085 | ||||||
chr10:35185101
|
T | C | 9 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-3099T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185101 | ||||||
chr10:35185106
|
CT | C | 115 | a0001c0001t0001g0184a0001c0001t0001g0287a0001c0001t0002g0036others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.410-3078delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185106 | |||||
chr10:35185189
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.410-3011G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185189 | ||||||
chr10:35185205
|
C | T | 1 | a0001c0001t0014g0200 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.410-2995C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185205 | ||||||
chr10:35185292
|
C | T | 5 | a0001c0001t0001g0149a0001c0001t0001g0208a0001c0001t0003g0030others(2): Show | 5 | HG03669.hp2 HG04115.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.410-2908C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185292 | ||||||
chr10:35185350
|
A | C | 121 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.410-2850A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185350 | ||||||
chr10:35185462
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.410-2738C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185462 | ||||||
chr10:35185493
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.410-2707A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185493 | ||||||
chr10:35185628
|
A | G | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.410-2572A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185628 | ||||||
chr10:35185631
|
A | G | 1 | a0001c0001t0003g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.410-2569A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185631 | ||||||
chr10:35185708
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.410-2492A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185708 | ||||||
chr10:35185771
|
T | C | 121 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.410-2429T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185771 | ||||||
chr10:35185835
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.410-2365C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185835 | ||||||
chr10:35185889
|
T | C | 1 | a0002c0005t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.410-2311T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185889 | ||||||
chr10:35185978
|
C | T | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.410-2222C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185978 | ||||||
chr10:35186111
|
C | A | 1 | a0001c0001t0001g0239 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.410-2089C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186111 | ||||||
chr10:35186112
|
T | C | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.410-2088T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186112 | ||||||
chr10:35186190
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.410-2010T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186190 | ||||||
chr10:35186222
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.410-1978G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186222 | ||||||
chr10:35186234
|
T | C | 1 | a0001c0003t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.410-1966T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186234 | ||||||
chr10:35186380
|
T | G | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1820T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186380 | ||||||
chr10:35186382
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1818A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186382 | ||||||
chr10:35186383
|
G | C | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1817G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186383 | ||||||
chr10:35186387
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1813T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186387 | ||||||
chr10:35186390
|
A | C | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1810A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186390 | ||||||
chr10:35186393
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1807G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186393 | ||||||
chr10:35186394
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1806A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186394 | ||||||
chr10:35186395
|
A | T | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1805A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186395 | ||||||
chr10:35186650
|
A | G | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.410-1550A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186650 | ||||||
chr10:35186656
|
C | T | 1 | a0001c0003t0002g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.410-1544C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186656 | ||||||
chr10:35186671
|
A | G | 63 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0122others(60): Show | 64 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.410-1529A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186671 | ||||||
chr10:35186707
|
A | T | 1 | a0001c0001t0002g0091 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.410-1493A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186707 | ||||||
chr10:35186713
|
CAT | C | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-1481_410-1480d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186713 | |||||
chr10:35186723
|
T | TATATATA others(46): Show |
1 | a0001c0001t0001g0222 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.410-1475_410-1423d others(55): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186723 | |||||
chr10:35186828
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0244 | 3 | HG03195.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.410-1372A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186828 | ||||||
chr10:35186843
|
T | C | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.410-1357T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186843 | ||||||
chr10:35186845
|
C | G | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.410-1355C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186845 | ||||||
chr10:35186846
|
G | C | 121 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.410-1354G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186846 | ||||||
chr10:35186902
|
TATA | T | 104 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.410-1292_410-1290d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186902 | |||||
chr10:35186909
|
A | G | 27 | a0001c0001t0002g0044a0001c0001t0002g0048a0001c0001t0002g0050others(24): Show | 27 | HG00544.hp1 HG02015.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.410-1291A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186909 | ||||||
chr10:35186947
|
T | TTA | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.410-1244_410-1243d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186947 | |||||
chr10:35186981
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-1219G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186981 | ||||||
chr10:35186984
|
ATATATAT others(51): Show |
A | 1 | a0001c0001t0001g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.410-1208_410-1151d others(60): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186984 | |||||
chr10:35186999
|
T | C | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.410-1201T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186999 | ||||||
chr10:35186999
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.410-1188_410-1177d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186999 | |||||
chr10:35187001
|
TATATA | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0244 | 3 | HG03195.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.410-1188_410-1184d others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187001 | |||||
chr10:35187004
|
A | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-1196A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187004 | ||||||
chr10:35187005
|
T | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-1195T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187005 | ||||||
chr10:35187006
|
A | G | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.410-1194A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187006 | ||||||
chr10:35187006
|
A | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-1194A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187006 | ||||||
chr10:35187029
|
C | T | 88 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(85): Show | 88 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.410-1171C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187029 | ||||||
chr10:35187049
|
T | A | 1 | a0001c0001t0002g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.410-1151T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187049 | ||||||
chr10:35187060
|
T | TA | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.410-1139dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187060 | |||||
chr10:35187075
|
AAT | A | 9 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(6): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-1117_410-1116d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187075 | |||||
chr10:35187077
|
TATATATA others(7): Show |
T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.410-1115_410-1102d others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187077 | |||||
chr10:35187082
|
ATAATATA others(4): Show |
A | 22 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0007others(19): Show | 22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.410-1117_410-1107d others(13): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187082 | ||||||
chr10:35187084
|
A | C | 1 | a0001c0001t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.410-1116A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187084 | ||||||
chr10:35187092
|
A | ATAATT | 73 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.410-1106_410-1105i others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187092 | |||||
chr10:35187099
|
TGA | T | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.410-1100_410-1099d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187099 | ||||||
chr10:35187100
|
G | A | 32 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(29): Show | 32 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.410-1100G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187100 | ||||||
chr10:35187100
|
G | T | 73 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.410-1100G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187100 | ||||||
chr10:35187101
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.410-1099A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187101 | ||||||
chr10:35187108
|
T | A | 1 | a0001c0001t0009g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.410-1092T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187108 | ||||||
chr10:35187119
|
T | C | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.410-1081T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187119 | ||||||
chr10:35187122
|
A | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.410-1078A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187122 | ||||||
chr10:35187130
|
T | A | 6 | a0001c0001t0001g0142a0001c0002t0004g0111a0001c0002t0004g0112others(3): Show | 6 | HG00738.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.410-1070T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187130 | ||||||
chr10:35187130
|
TAATATAT others(18): Show |
T | 1 | a0001c0001t0002g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1068_410-1044d others(27): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187130 | |||||
chr10:35187131
|
A | T | 108 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(105): Show | 108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.410-1069A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187131 | ||||||
chr10:35187131
|
AAT | A | 4 | a0001c0002t0004g0035a0001c0002t0004g0115a0001c0002t0004g0290others(1): Show | 4 | HG01071.hp1 HG02572.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-1064_410-1063d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187131 | |||||
chr10:35187136
|
AT | A | 8 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-1062delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187136 | |||||
chr10:35187142
|
A | G | 72 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.410-1058A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187142 | ||||||
chr10:35187147
|
A | T | 9 | a0001c0001t0001g0176a0001c0002t0004g0109a0001c0002t0004g0111others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-1053A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187147 | ||||||
chr10:35187148
|
TATATATA others(39): Show |
T | 1 | a0001c0001t0001g0149 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.410-1028_410-983de others(47): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187148 | |||||
chr10:35187152
|
TATAATAT others(49): Show |
T | 72 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.410-1047_410-992de others(57): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187152 | ||||||
chr10:35187155
|
A | T | 60 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(57): Show | 60 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.410-1045A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187155 | ||||||
chr10:35187156
|
A | T | 8 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-1044A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187156 | ||||||
chr10:35187162
|
A | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.410-1038A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187162 | ||||||
chr10:35187163
|
T | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.410-1037T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187163 | ||||||
chr10:35187163
|
TTATATAT others(9): Show |
T | 35 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(32): Show | 35 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.410-1030_410-1015d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187163 | |||||
chr10:35187165
|
AT | A | 8 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-1034delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187165 | ||||||
chr10:35187170
|
T | A | 1 | a0001c0001t0002g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1030T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187170 | ||||||
chr10:35187171
|
T | A | 1 | a0001c0001t0002g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1029T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187171 | ||||||
chr10:35187172
|
A | T | 1 | a0001c0001t0002g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1028A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187172 | ||||||
chr10:35187176
|
T | TATAATAT others(8): Show |
1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.410-1024_410-1023i others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187176 | ||||||
chr10:35187176
|
T | TATTTATA others(26): Show |
8 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-1024_410-1023i others(35): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187176 | ||||||
chr10:35187177
|
T | A | 1 | a0001c0001t0002g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1023T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187177 | ||||||
chr10:35187179
|
A | ATATATTT others(32): Show |
1 | a0001c0002t0004g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.410-1016_410-1015i others(41): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187179 | |||||
chr10:35187179
|
A | ATATATTT others(32): Show |
3 | a0001c0002t0004g0115a0001c0002t0004g0290a0001c0002t0020g0291 | 3 | HG01071.hp1 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.410-1016_410-1015i others(41): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187179 | |||||
chr10:35187179
|
A | T | 9 | a0001c0001t0003g0110a0001c0002t0004g0109a0001c0002t0004g0111others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-1021A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187179 | ||||||
chr10:35187185
|
A | T | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 9 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.410-1015A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187185 | ||||||
chr10:35187186
|
A | T | 1 | a0001c0001t0002g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1014A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187186 | ||||||
chr10:35187190
|
TA | T | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.410-1009delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187190 | ||||||
chr10:35187193
|
T | A | 1 | a0001c0001t0001g0271 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.410-1007T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187193 | ||||||
chr10:35187197
|
A | G | 1 | a0001c0001t0002g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1003A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187197 | ||||||
chr10:35187209
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.410-991T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187209 | ||||||
chr10:35187210
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0016g0203 | 2 | NA18947.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.410-990T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187210 | ||||||
chr10:35187218
|
T | A | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.410-982T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187218 | ||||||
chr10:35187235
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.410-965T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187235 | ||||||
chr10:35187271
|
GT | G | 73 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.410-918delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187271 | |||||
chr10:35187273
|
T | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.410-927T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187273 | ||||||
chr10:35187385
|
G | A | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.410-815G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187385 | ||||||
chr10:35187395
|
G | A | 1 | a0001c0001t0009g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.410-805G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187395 | ||||||
chr10:35187506
|
T | C | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.410-694T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187506 | ||||||
chr10:35187540
|
G | T | 1 | a0001c0001t0002g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.410-660G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187540 | ||||||
chr10:35187822
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.410-378A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187822 | ||||||
chr10:35187925
|
T | G | 1 | a0001c0001t0001g0279 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.410-275T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187925 | ||||||
chr10:35187991
|
A | G | 2 | a0001c0001t0001g0277a0001c0001t0012g0275 | 2 | HG00735.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.410-209A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187991 | ||||||
chr10:35188004
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0122others(62): Show | 66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.410-196T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35188004 | ||||||
chr10:35188424
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.598+36A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188424 | ||||||
chr10:35188574
|
C | T | 30 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(27): Show | 30 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.598+186C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188574 | ||||||
chr10:35188642
|
G | A | 1 | a0001c0001t0009g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.598+254G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188642 | ||||||
chr10:35188659
|
A | AT | 14 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0249others(11): Show | 14 | HG00621.hp1 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.598+289dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35188659 | |||||
chr10:35188659
|
AT | A | 116 | a0001c0001t0001g0230a0001c0001t0001g0236a0001c0001t0001g0253others(113): Show | 116 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.598+289delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35188659 | |||||
chr10:35188672
|
T | G | 2 | a0001c0001t0001g0277a0001c0001t0012g0275 | 2 | HG00735.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.598+284T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188672 | ||||||
chr10:35188685
|
A | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0033 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.598+297A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188685 | ||||||
chr10:35188691
|
G | A | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.598+303G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188691 | ||||||
chr10:35188847
|
G | A | 9 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(6): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+459G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188847 | ||||||
chr10:35188937
|
G | A | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+549G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188937 | ||||||
chr10:35188974
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.598+586A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188974 | ||||||
chr10:35189132
|
T | G | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+744T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189132 | ||||||
chr10:35189177
|
G | GT | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.598+798dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35189177 | |||||
chr10:35189183
|
T | G | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+795T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189183 | ||||||
chr10:35189187
|
G | T | 114 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(111): Show | 114 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.598+799G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189187 | ||||||
chr10:35189195
|
G | GT | 9 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(6): Show | 9 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+814dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35189195 | |||||
chr10:35189199
|
T | G | 1 | a0001c0001t0002g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.598+811T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189199 | ||||||
chr10:35189333
|
C | T | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+945C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189333 | ||||||
chr10:35189463
|
A | G | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+1075A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189463 | ||||||
chr10:35189469
|
A | G | 1 | a0001c0002t0004g0118 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.598+1081A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189469 | ||||||
chr10:35189481
|
TTTGC | T | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+1101_598+1104d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35189481 | |||||
chr10:35189489
|
CTTGT | C | 74 | a0001c0001t0001g0213a0001c0001t0002g0036a0001c0001t0002g0037others(71): Show | 74 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.598+1116_598+1119d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35189489 | |||||
chr10:35189582
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.598+1194C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189582 | ||||||
chr10:35189601
|
C | T | 108 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(105): Show | 108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.598+1213C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189601 | ||||||
chr10:35189725
|
A | C | 1 | a0001c0001t0003g0034 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.598+1337A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189725 | ||||||
chr10:35189726
|
G | A | 1 | a0001c0001t0003g0034 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.598+1338G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189726 | ||||||
chr10:35189852
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.598+1464A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189852 | ||||||
chr10:35190044
|
C | G | 7 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0053others(4): Show | 7 | HG00280.hp2 HG01081.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+1656C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190044 | ||||||
chr10:35190184
|
C | T | 2 | a0001c0001t0003g0014a0001c0001t0003g0033 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.598+1796C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190184 | ||||||
chr10:35190336
|
G | T | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+1948G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190336 | ||||||
chr10:35190562
|
A | G | 1 | a0001c0003t0002g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.598+2174A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190562 | ||||||
chr10:35190576
|
G | T | 110 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(107): Show | 110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.598+2188G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190576 | ||||||
chr10:35190669
|
A | AT | 6 | a0001c0001t0001g0213a0001c0001t0002g0282a0001c0001t0002g0283others(3): Show | 6 | HG01192.hp1 HG02129.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+2291dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35190669 | |||||
chr10:35190780
|
G | C | 72 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.598+2392G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190780 | ||||||
chr10:35190915
|
G | A | 1 | a0001c0001t0002g0049 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.598+2527G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190915 | ||||||
chr10:35190958
|
A | G | 109 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(106): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.598+2570A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190958 | ||||||
chr10:35191086
|
T | TTTTATTT others(1): Show |
151 | a0001c0001t0001g0003a0001c0001t0001g0119a0001c0001t0001g0120others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.598+2713_598+2720d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | |||||
chr10:35191086
|
T | TTTTATTT others(5): Show |
18 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0176others(15): Show | 19 | HG00621.hp1 HG01071.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.598+2709_598+2720d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | |||||
chr10:35191086
|
T | TTTTATTT others(9): Show |
30 | a0001c0001t0001g0177a0001c0001t0003g0004a0001c0001t0003g0007others(27): Show | 30 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.598+2705_598+2720d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | |||||
chr10:35191086
|
T | TTTTATTT others(13): Show |
16 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0081others(13): Show | 16 | HG00733.hp2 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.598+2701_598+2720d others(22): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | |||||
chr10:35191086
|
T | TTTTATTT others(17): Show |
55 | a0001c0001t0002g0037a0001c0001t0002g0043a0001c0001t0002g0044others(52): Show | 55 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.598+2720_598+2721i others(26): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | |||||
chr10:35191086
|
T | TTTTATTT others(21): Show |
16 | a0001c0001t0002g0040a0001c0001t0002g0047a0001c0001t0002g0049others(13): Show | 16 | HG00423.hp2 HG02040.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.598+2720_598+2721i others(30): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | |||||
chr10:35191086
|
T | TTTTATTT others(25): Show |
1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+2720_598+2721i others(34): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | |||||
chr10:35191086
|
T | TTTTATTT others(25): Show |
1 | a0001c0001t0002g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.598+2720_598+2721i others(34): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | |||||
chr10:35191086
|
T | TTTTTTTT others(25): Show |
1 | a0001c0001t0007g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.598+2701_598+2702i others(34): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | |||||
chr10:35191147
|
C | A | 1 | a0001c0001t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.598+2759C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191147 | ||||||
chr10:35191150
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0220 | 2 | NA18954.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.598+2762G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191150 | ||||||
chr10:35191383
|
T | C | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+2995T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191383 | ||||||
chr10:35191444
|
T | A | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+3056T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191444 | ||||||
chr10:35191652
|
C | A | 1 | a0001c0003t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.598+3264C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191652 | ||||||
chr10:35191688
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.598+3300C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191688 | ||||||
chr10:35191694
|
T | G | 1 | a0001c0002t0004g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+3306T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191694 | ||||||
chr10:35191821
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.598+3433C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191821 | ||||||
chr10:35191822
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+3434G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191822 | ||||||
chr10:35191938
|
C | CCCACCTG others(3): Show |
120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.598+3551_598+3552i others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191938 | |||||
chr10:35192054
|
C | G | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+3666C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192054 | ||||||
chr10:35192238
|
G | C | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+3850G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192238 | ||||||
chr10:35192241
|
A | G | 72 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.598+3853A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192241 | ||||||
chr10:35192351
|
C | T | 1 | a0001c0001t0003g0017 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.598+3963C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192351 | ||||||
chr10:35192484
|
G | T | 1 | a0001c0001t0002g0048 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.598+4096G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192484 | ||||||
chr10:35192613
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.598+4225T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192613 | ||||||
chr10:35192791
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598+4403A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192791 | ||||||
chr10:35192811
|
C | T | 2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG01123.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.598+4423C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192811 | ||||||
chr10:35192844
|
T | A | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+4456T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192844 | ||||||
chr10:35193037
|
G | T | 121 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.598+4649G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193037 | ||||||
chr10:35193039
|
TC | T | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+4655delC | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35193039 | |||||
chr10:35193121
|
T | G | 1 | a0001c0001t0006g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.598+4733T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193121 | ||||||
chr10:35193264
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.598+4876G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193264 | ||||||
chr10:35193379
|
T | A | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.598+4991T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193379 | ||||||
chr10:35193382
|
T | C | 1 | a0001c0002t0004g0116 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.598+4994T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193382 | ||||||
chr10:35193498
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.598+5110C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193498 | ||||||
chr10:35193610
|
C | A | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+5222C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193610 | ||||||
chr10:35193624
|
T | TA | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+5238dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35193624 | |||||
chr10:35193634
|
G | T | 9 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(6): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+5246G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193634 | ||||||
chr10:35193636
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.598+5248C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193636 | ||||||
chr10:35193683
|
T | C | 72 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.598+5295T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193683 | ||||||
chr10:35193702
|
G | C | 1 | a0001c0001t0002g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.598+5314G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193702 | ||||||
chr10:35194001
|
G | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+5613G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194001 | ||||||
chr10:35194097
|
C | CA | 45 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(42): Show | 45 | HG00438.hp1 HG00558.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.598+5736dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAA | 8 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+5732_598+5736d others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(3): Show |
8 | a0001c0001t0002g0040a0001c0001t0002g0047a0001c0001t0002g0066others(5): Show | 8 | HG00423.hp2 HG01515.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+5727_598+5736d others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(4): Show |
17 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0049others(14): Show | 17 | HG00733.hp2 HG01081.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.598+5726_598+5736d others(13): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(5): Show |
32 | a0001c0001t0002g0045a0001c0001t0002g0048a0001c0001t0002g0050others(29): Show | 32 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.598+5725_598+5736d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(6): Show |
25 | a0001c0001t0002g0044a0001c0001t0002g0062a0001c0001t0002g0064others(22): Show | 25 | HG01074.hp1 HG01081.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.598+5724_598+5736d others(15): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0026others(1): Show | 4 | HG00639.hp1 HG03492.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+5723_598+5736d others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0002g0088a0001c0001t0003g0024a0001c0001t0003g0025 | 3 | HG03688.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.598+5722_598+5736d others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0005 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.598+5721_598+5736d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0002g0065 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.598+5720_598+5736d others(19): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0003g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.598+5719_598+5736d others(20): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0002g0053a0001c0001t0003g0032 | 2 | HG00280.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.598+5718_598+5736d others(21): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
C | CAAAAAAA others(13): Show |
1 | a0003c0006t0003g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.598+5717_598+5736d others(22): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194097
|
CA | C | 7 | a0001c0001t0001g0159a0001c0001t0001g0179a0001c0001t0001g0184others(4): Show | 7 | HG01167.hp2 HG01168.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+5736delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | |||||
chr10:35194322
|
TA | T | 120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.598+5942delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194322 | |||||
chr10:35194426
|
A | G | 1 | a0001c0002t0004g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+6038A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194426 | ||||||
chr10:35194450
|
A | G | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+6062A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194450 | ||||||
chr10:35194515
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+6127C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194515 | ||||||
chr10:35194611
|
T | G | 1 | a0001c0001t0001g0222 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.598+6223T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194611 | ||||||
chr10:35194741
|
GT | G | 16 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0177others(13): Show | 16 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.598+6367delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194741 | |||||
chr10:35194741
|
GTT | G | 107 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(104): Show | 107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.598+6366_598+6367d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194741 | |||||
chr10:35194841
|
A | G | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+6453A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194841 | ||||||
chr10:35194899
|
G | A | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+6511G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194899 | ||||||
chr10:35194901
|
C | CATT | 32 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(29): Show | 33 | HG00621.hp1 HG01168.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.598+6538_598+6540d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194901 | |||||
chr10:35194901
|
C | CATTATT | 4 | a0001c0001t0001g0178a0001c0001t0001g0206a0001c0001t0003g0026others(1): Show | 4 | HG03453.hp2 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+6535_598+6540d others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194901 | |||||
chr10:35194901
|
CATT | C | 92 | a0001c0001t0001g0259a0001c0001t0002g0036a0001c0001t0002g0037others(89): Show | 92 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.598+6538_598+6540d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194901 | |||||
chr10:35195053
|
T | C | 1 | a0001c0002t0004g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.598+6665T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195053 | ||||||
chr10:35195261
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.598+6873T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195261 | ||||||
chr10:35195292
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.598+6904G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195292 | ||||||
chr10:35195491
|
C | G | 4 | a0001c0001t0001g0259a0001c0001t0001g0262a0001c0001t0001g0264others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+7103C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195491 | ||||||
chr10:35195549
|
G | C | 1 | a0001c0001t0002g0097 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.598+7161G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195549 | ||||||
chr10:35195598
|
A | G | 1 | a0001c0001t0007g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.598+7210A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195598 | ||||||
chr10:35195622
|
G | C | 1 | a0001c0001t0011g0217 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.598+7234G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195622 | ||||||
chr10:35195801
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.598+7413G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195801 | ||||||
chr10:35196021
|
T | G | 127 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(124): Show | 127 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.598+7633T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196021 | ||||||
chr10:35196135
|
T | C | 1 | a0001c0001t0016g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.598+7747T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196135 | ||||||
chr10:35196469
|
A | C | 1 | a0001c0001t0002g0103 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.598+8081A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196469 | ||||||
chr10:35196585
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.598+8197A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196585 | ||||||
chr10:35196607
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.598+8219G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196607 | ||||||
chr10:35196710
|
C | T | 1 | a0001c0001t0002g0049 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.598+8322C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196710 | ||||||
chr10:35196736
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.598+8348A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196736 | ||||||
chr10:35196761
|
A | T | 123 | a0001c0001t0001g0262a0001c0001t0002g0036a0001c0001t0002g0037others(120): Show | 123 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.598+8373A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196761 | ||||||
chr10:35196808
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.598+8420G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196808 | ||||||
chr10:35196822
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.598+8434C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196822 | ||||||
chr10:35196865
|
C | CT | 18 | a0001c0001t0001g0123a0001c0001t0001g0156a0001c0001t0001g0177others(15): Show | 18 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.598+8499dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | |||||
chr10:35196865
|
C | CTT | 10 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(7): Show | 10 | HG00621.hp1 HG01884.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.598+8498_598+8499d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | |||||
chr10:35196865
|
C | CTTT | 12 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+8497_598+8499d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | |||||
chr10:35196865
|
C | CTTTTTT | 68 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0044others(65): Show | 68 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.598+8494_598+8499d others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | |||||
chr10:35196865
|
C | CTTTTTTT | 31 | a0001c0001t0001g0262a0001c0001t0002g0040a0001c0001t0002g0043others(28): Show | 31 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.598+8493_598+8499d others(9): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | |||||
chr10:35196895
|
G | A | 123 | a0001c0001t0001g0262a0001c0001t0002g0036a0001c0001t0002g0037others(120): Show | 123 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.598+8507G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196895 | ||||||
chr10:35196930
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0167others(1): Show | 5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+8542C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196930 | ||||||
chr10:35196932
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.598+8544C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196932 | ||||||
chr10:35197218
|
A | G | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+8830A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197218 | ||||||
chr10:35197346
|
T | A | 5 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+8958T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197346 | ||||||
chr10:35197416
|
C | CTTTA | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0147others(27): Show | 32 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.598+9076_598+9079d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | |||||
chr10:35197416
|
CTTTA | C | 142 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0129others(139): Show | 142 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.598+9076_598+9079d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | |||||
chr10:35197416
|
CTTTATTT others(1): Show |
C | 10 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0276others(7): Show | 10 | HG01258.hp2 HG01261.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.598+9072_598+9079d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | |||||
chr10:35197416
|
CTTTATTT others(5): Show |
C | 9 | a0001c0001t0001g0124a0001c0001t0001g0206a0001c0001t0002g0089others(6): Show | 10 | HG00423.hp2 HG01175.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.598+9068_598+9079d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | |||||
chr10:35197416
|
CTTTATTT others(9): Show |
C | 4 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0209others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+9064_598+9079d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | |||||
chr10:35197416
|
CTTTATTT others(13): Show |
C | 1 | a0001c0001t0002g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+9060_598+9079d others(22): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | |||||
chr10:35197452
|
ATTTATTT others(9): Show |
A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.598+9065_598+9080d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197452 | ||||||
chr10:35197468
|
T | A | 3 | a0001c0001t0001g0255a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | HG01884.hp2 HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.598+9080T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197468 | ||||||
chr10:35197470
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.598+9082T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197470 | ||||||
chr10:35197492
|
G | A | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.598+9104G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197492 | ||||||
chr10:35197543
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.598+9155C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197543 | ||||||
chr10:35197549
|
T | C | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.598+9161T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197549 | ||||||
chr10:35197618
|
A | T | 5 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG00438.hp1 HG00738.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+9230A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197618 | ||||||
chr10:35197631
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.598+9243T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197631 | ||||||
chr10:35198102
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.599-8793C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198102 | ||||||
chr10:35198263
|
G | T | 1 | a0001c0003t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.599-8632G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198263 | ||||||
chr10:35198295
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599-8600C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198295 | ||||||
chr10:35198368
|
C | T | 14 | a0001c0001t0002g0040a0001c0001t0002g0043a0001c0001t0002g0047others(11): Show | 14 | HG02040.hp2 HG02129.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.599-8527C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198368 | ||||||
chr10:35198384
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.599-8511G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198384 | ||||||
chr10:35198676
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.599-8219G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198676 | ||||||
chr10:35198678
|
C | G | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-8217C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198678 | ||||||
chr10:35198795
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.599-8100T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198795 | ||||||
chr10:35198887
|
C | T | 1 | a0001c0001t0003g0010 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.599-8008C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198887 | ||||||
chr10:35199333
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.599-7562A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199333 | ||||||
chr10:35199334
|
T | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.599-7561T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199334 | ||||||
chr10:35199336
|
C | T | 120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.599-7559C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199336 | ||||||
chr10:35199341
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-7554C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199341 | ||||||
chr10:35199515
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.599-7380G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199515 | ||||||
chr10:35199551
|
C | T | 6 | a0001c0001t0003g0009a0001c0001t0003g0019a0001c0001t0003g0020others(3): Show | 6 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-7344C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199551 | ||||||
chr10:35199576
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-7319G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199576 | ||||||
chr10:35199664
|
A | T | 1 | a0001c0001t0002g0058 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.599-7231A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199664 | ||||||
chr10:35199864
|
ATTATT | A | 70 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(67): Show | 70 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.599-7027_599-7023d others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35199864 | |||||
chr10:35199887
|
C | CT | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.599-6989dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35199887 | |||||
chr10:35199887
|
C | CTT | 51 | a0001c0001t0001g0172a0001c0001t0001g0196a0001c0001t0001g0205others(48): Show | 51 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.599-6990_599-6989d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35199887 | |||||
chr10:35199887
|
C | CTTT | 66 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0043others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.599-6991_599-6989d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35199887 | |||||
chr10:35199973
|
T | C | 1 | a0001c0002t0004g0290 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.599-6922T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199973 | ||||||
chr10:35200326
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-6569G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200326 | ||||||
chr10:35200411
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-6484A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200411 | ||||||
chr10:35200431
|
G | T | 1 | a0002c0005t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.599-6464G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200431 | ||||||
chr10:35200485
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.599-6410T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200485 | ||||||
chr10:35200651
|
A | C | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-6244A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200651 | ||||||
chr10:35200714
|
C | G | 1 | a0001c0002t0004g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.599-6181C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200714 | ||||||
chr10:35200947
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0224 | 2 | NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.599-5948C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200947 | ||||||
chr10:35200996
|
G | GT | 30 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(27): Show | 30 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.599-5890dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35200996 | |||||
chr10:35201084
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-5811A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201084 | ||||||
chr10:35201136
|
T | C | 1 | a0001c0003t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.599-5759T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201136 | ||||||
chr10:35201243
|
G | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-5652G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201243 | ||||||
chr10:35201483
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.599-5412G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201483 | ||||||
chr10:35201597
|
G | A | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.599-5298G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201597 | ||||||
chr10:35201679
|
G | T | 1 | a0001c0001t0002g0054 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.599-5216G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201679 | ||||||
chr10:35201921
|
C | T | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-4974C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201921 | ||||||
chr10:35201954
|
C | T | 1 | a0001c0002t0004g0290 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.599-4941C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201954 | ||||||
chr10:35202144
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.599-4751C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202144 | ||||||
chr10:35202187
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.599-4708C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202187 | ||||||
chr10:35202566
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-4329A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202566 | ||||||
chr10:35202598
|
T | G | 1 | a0001c0002t0004g0113 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.599-4297T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202598 | ||||||
chr10:35202692
|
C | G | 11 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(8): Show | 11 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-4203C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202692 | ||||||
chr10:35202730
|
G | A | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.599-4165G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202730 | ||||||
chr10:35202794
|
A | T | 72 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.599-4101A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202794 | ||||||
chr10:35203096
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-3799T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203096 | ||||||
chr10:35203198
|
A | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-3697A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203198 | ||||||
chr10:35203363
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.599-3532C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203363 | ||||||
chr10:35203415
|
C | T | 1 | a0001c0001t0002g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.599-3480C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203415 | ||||||
chr10:35203672
|
G | A | 1 | a0001c0001t0009g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.599-3223G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203672 | ||||||
chr10:35203686
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-3209T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203686 | ||||||
chr10:35203904
|
A | G | 120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.599-2991A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203904 | ||||||
chr10:35203936
|
A | G | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.599-2959A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203936 | ||||||
chr10:35203963
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.599-2932G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203963 | ||||||
chr10:35204050
|
C | G | 72 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.599-2845C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204050 | ||||||
chr10:35204240
|
A | T | 1 | a0001c0001t0001g0172 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.599-2655A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204240 | ||||||
chr10:35204328
|
A | G | 120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.599-2567A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204328 | ||||||
chr10:35204487
|
CTACTCGG others(37): Show |
C | 1 | a0001c0001t0001g0185 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.599-2407_599-2364d others(46): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204487 | ||||||
chr10:35204492
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.599-2403C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204492 | ||||||
chr10:35204590
|
A | C | 120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.599-2305A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204590 | ||||||
chr10:35204596
|
C | CA | 7 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0158others(4): Show | 7 | HG02280.hp2 HG03942.hp2 NA19030.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-2278dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35204596 | |||||
chr10:35204596
|
CA | C | 42 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0204others(39): Show | 42 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.599-2278delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35204596 | |||||
chr10:35204596
|
CAA | C | 73 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(70): Show | 73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.599-2279_599-2278d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35204596 | |||||
chr10:35205204
|
A | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.599-1691A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205204 | ||||||
chr10:35205380
|
T | C | 2 | a0001c0001t0002g0099a0001c0001t0016g0203 | 2 | NA19005.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.599-1515T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205380 | ||||||
chr10:35205624
|
G | T | 1 | a0001c0003t0002g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.599-1271G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205624 | ||||||
chr10:35205680
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-1215C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205680 | ||||||
chr10:35205684
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.599-1211C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205684 | ||||||
chr10:35205710
|
A | G | 2 | a0001c0003t0002g0041a0001c0003t0002g0042 | 2 | HG01099.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.599-1185A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205710 | ||||||
chr10:35206031
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.599-864G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206031 | ||||||
chr10:35206079
|
T | C | 70 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(67): Show | 70 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.599-816T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206079 | ||||||
chr10:35206087
|
A | T | 1 | a0001c0001t0003g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-808A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206087 | ||||||
chr10:35206109
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.599-786G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206109 | ||||||
chr10:35206234
|
C | T | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(9): Show | 12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-661C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206234 | ||||||
chr10:35206260
|
AT | A | 68 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(65): Show | 68 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.599-634delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206260 | ||||||
chr10:35206261
|
T | A | 2 | a0001c0001t0002g0095a0001c0001t0002g0108 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.599-634T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206261 | ||||||
chr10:35206280
|
G | A | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.599-615G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206280 | ||||||
chr10:35206367
|
T | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-528T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206367 | ||||||
chr10:35206417
|
G | A | 5 | a0001c0002t0004g0111a0001c0002t0004g0112a0001c0002t0004g0113others(2): Show | 5 | HG00738.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-478G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206417 | ||||||
chr10:35206542
|
A | T | 1 | a0001c0001t0018g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-353A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206542 | ||||||
chr10:35206685
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.599-210G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206685 | ||||||
chr10:35206770
|
A | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0143a0001c0001t0001g0151others(7): Show | 11 | HG00741.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.599-125A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206770 | ||||||
chr10:35207167
|
C | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG00544.hp2 NA18965.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.755+116C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207167 | ||||||
chr10:35207197
|
C | G | 1 | a0001c0001t0002g0097 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.755+146C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207197 | ||||||
chr10:35207326
|
G | A | 72 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.755+275G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207326 | ||||||
chr10:35207343
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.755+292A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207343 | ||||||
chr10:35207381
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.755+330G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207381 | ||||||
chr10:35207425
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.755+374T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207425 | ||||||
chr10:35207458
|
C | T | 120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.755+407C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207458 | ||||||
chr10:35207461
|
TAAATAA | T | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.755+427_755+432del others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 35207461 | |||||
chr10:35207512
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.755+461C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207512 | ||||||
chr10:35207513
|
C | T | 29 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(26): Show | 29 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.755+462C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207513 | ||||||
chr10:35207540
|
T | C | 119 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(116): Show | 119 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.755+489T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207540 | ||||||
chr10:35207545
|
G | A | 11 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(8): Show | 11 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.755+494G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207545 | ||||||
chr10:35207546
|
C | A | 7 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0198others(4): Show | 7 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+495C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207546 | ||||||
chr10:35207551
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.755+500A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207551 | ||||||
chr10:35207564
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.755+513A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207564 | ||||||
chr10:35207594
|
C | T | 11 | a0001c0001t0001g0259a0001c0001t0001g0262a0001c0001t0001g0264others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.755+543C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207594 | ||||||
chr10:35207667
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.755+616G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207667 | ||||||
chr10:35207698
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0119others(146): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.755+647C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207698 | ||||||
chr10:35207699
|
G | A | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.755+648G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207699 | ||||||
chr10:35207729
|
G | A | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(2): Show | 5 | HG01884.hp2 HG02293.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+678G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207729 | ||||||
chr10:35207766
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.755+715C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207766 | ||||||
chr10:35207771
|
TA | T | 31 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.755+732delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 35207771 | |||||
chr10:35207797
|
A | T | 1 | a0001c0001t0003g0017 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.755+746A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207797 | ||||||
chr10:35207802
|
A | G | 121 | a0001c0001t0001g0206a0001c0001t0002g0036a0001c0001t0002g0037others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.755+751A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207802 | ||||||
chr10:35207835
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.755+784A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207835 | ||||||
chr10:35207927
|
A | G | 1 | a0001c0001t0003g0018 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.755+876A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207927 | ||||||
chr10:35207940
|
G | A | 120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.755+889G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207940 | ||||||
chr10:35207944
|
T | C | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG02015.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.755+893T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207944 | ||||||
chr10:35208018
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0122others(49): Show | 53 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.755+967G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208018 | ||||||
chr10:35208503
|
C | T | 9 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.755+1452C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208503 | ||||||
chr10:35208528
|
A | G | 9 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.755+1477A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208528 | ||||||
chr10:35208605
|
C | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0244 | 3 | HG03195.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.755+1554C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208605 | ||||||
chr10:35208606
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.755+1555G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208606 | ||||||
chr10:35208631
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.755+1580A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208631 | ||||||
chr10:35208808
|
C | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+1757C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208808 | ||||||
chr10:35209176
|
G | A | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.756-2078G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209176 | ||||||
chr10:35209221
|
T | C | 11 | a0001c0002t0004g0035a0001c0002t0004g0109a0001c0002t0004g0111others(8): Show | 11 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.756-2033T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209221 | ||||||
chr10:35209530
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0191 | 2 | HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.756-1724A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209530 | ||||||
chr10:35209609
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.756-1645C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209609 | ||||||
chr10:35209610
|
G | A | 120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.756-1644G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209610 | ||||||
chr10:35209860
|
T | A | 124 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(121): Show | 124 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.756-1394T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209860 | ||||||
chr10:35209919
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0242 | 3 | HG00741.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.756-1335A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209919 | ||||||
chr10:35209961
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.756-1293G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209961 | ||||||
chr10:35210065
|
T | TA | 16 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0126others(13): Show | 17 | HG01081.hp2 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.756-1173dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 35210065 | |||||
chr10:35210115
|
G | A | 120 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0040others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.756-1139G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210115 | ||||||
chr10:35210139
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.756-1115T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210139 | ||||||
chr10:35210223
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.756-1031A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210223 | ||||||
chr10:35210350
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.756-904G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210350 | ||||||
chr10:35210555
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.756-699A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210555 | ||||||
chr10:35211075
|
C | T | 8 | a0001c0002t0004g0109a0001c0002t0004g0111a0001c0002t0004g0112others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.756-179C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35211075 |