geneid | 9541 |
---|---|
ensemblid | ENSG00000138433.16 |
hgncid | 24217 |
symbol | CIR1 |
name | corepressor interacting with RBPJ, CIR1 |
refseq_nuc | NM_004882.4 |
refseq_prot | NP_004873.3 |
ensembl_nuc | ENST00000342016.8 |
ensembl_prot | ENSP00000339723.3 |
mane_status | MANE Select |
chr | chr2 |
start | 174348022 |
end | 174395712 |
strand | - |
ver | v1.2 |
region | chr2:174348022-174395712 |
region5000 | chr2:174343022-174400712 |
regionname0 | CIR1_chr2_174348022_174395712 |
regionname5000 | CIR1_chr2_174343022_174400712 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 450 | 325 | 70 | 62 | 131 | 14 | 46 | 103 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0002 | 0/0 | 450 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0003 | 0/0 | 450 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0004 | 0/0 | 450 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0005 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0006 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0007 | 0/0 | 450 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1353 | 325 | 70 | 62 | 131 | 14 | 46 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
c0002 | 0/0 | 1353 | 16 | 15 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
c0003 | 0/0 | 1353 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
c0004 | 0/0 | 1353 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
c0005 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
c0006 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
c0007 | 0/0 | 1353 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 566 | 180 | 17 | 42 | 82 | 12 | 27 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
t0002 | 1/1 | 566 | 133 | 51 | 15 | 48 | 2 | 15 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
t0003 | 0/0 | 566 | 17 | 15 | 1 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
t0004 | 0/0 | 566 | 7 | 0 | 6 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
t0005 | 0/0 | 566 | 5 | 5 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
t0006 | 0/0 | 566 | 2 | 0 | 0 | 0 | 0 | 2 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
t0007 | 0/0 | 566 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
t0008 | 0/0 | 566 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
t0009 | 0/0 | 566 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1353 | 325 | 70 | 62 | 131 | 14 | 46 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0002c0002 | 0/0 | 1353 | 16 | 15 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0003c0004 | 0/0 | 1353 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0004c0003 | 0/0 | 1353 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0005c0005 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0006c0006 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0007c0007 | 0/0 | 1353 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1918 | 174 | 15 | 41 | 79 | 12 | 27 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0001c0001t0002 | 1/1 | 1918 | 132 | 50 | 15 | 48 | 2 | 15 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0001c0001t0003 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0001c0001t0004 | 0/0 | 1918 | 7 | 0 | 6 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0001c0001t0005 | 0/0 | 1918 | 5 | 5 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0001c0001t0006 | 0/0 | 1918 | 2 | 0 | 0 | 0 | 0 | 2 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0001c0001t0007 | 0/0 | 1918 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0001c0001t0008 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0001c0001t0009 | 0/0 | 1918 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0002c0002t0003 | 0/0 | 1918 | 16 | 15 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0003c0004t0001 | 0/0 | 1918 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0004c0003t0001 | 0/0 | 1918 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0005c0005t0002 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0006c0006t0001 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
a0007c0007t0001 | 0/0 | 1918 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | copy fasta | chr2 | 174343022 | 174400712 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0001c0001t0009g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0002c0002t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0003c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0003c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0004c0003t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0005c0005t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0006c0006t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
a0007c0007t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00408 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00735 | hp1 | a0002 | c0002 | t0003 | g0010 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0213 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01952 | hp1 | a0007 | c0007 | t0001 | g0122 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0317 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02630 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02647 | hp1 | a0002 | c0002 | t0003 | g0037 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02698 | hp2 | a0001 | c0001 | t0009 | g0291 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02735 | hp2 | a0001 | c0001 | t0006 | g0229 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0231 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02809 | hp1 | a0002 | c0002 | t0003 | g0054 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02886 | hp1 | a0002 | c0002 | t0003 | g0056 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02896 | hp2 | a0002 | c0002 | t0003 | g0237 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02922 | hp2 | a0002 | c0002 | t0003 | g0052 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02965 | hp1 | a0002 | c0002 | t0003 | g0316 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02976 | hp2 | a0002 | c0002 | t0003 | g0055 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03209 | hp1 | a0004 | c0003 | t0001 | g0011 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03225 | hp2 | a0002 | c0002 | t0003 | g0050 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0096 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03540 | hp2 | a0004 | c0003 | t0001 | g0011 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0026 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18522 | hp1 | a0005 | c0005 | t0002 | g0209 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18906 | hp1 | a0002 | c0002 | t0003 | g0238 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18948 | hp1 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19004 | hp1 | a0006 | c0006 | t0001 | g0311 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19030 | hp1 | a0002 | c0002 | t0003 | g0059 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19056 | hp1 | a0003 | c0004 | t0001 | g0299 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19057 | hp2 | a0001 | c0001 | t0007 | g0147 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19058 | hp2 | a0003 | c0004 | t0001 | g0301 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA20129 | hp2 | a0002 | c0002 | t0003 | g0082 | AFR | ASW | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | GIH | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | GIH | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | USA | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
NA21309 | hp2 | a0002 | c0002 | t0003 | g0010 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0243 | REF | REF | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0175 | REF | REF | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:174348679
|
G | A | 1 | a0006 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.1171C>T | p.Arg391Trp | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 1261/1918 | 1171/1353 | 391/450 | chr2 | 174348679 | ||
chr2:174348917
|
G | C | 1 | a0002 | 16 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(13): Show |
missense_variant | MODERATE | c.933C>G | p.Asp311Glu | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 1023/1918 | 933/1353 | 311/450 | chr2 | 174348917 | ||
chr2:174349123
|
T | C | 1 | a0004 | 2 | HG03209.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.727A>G | p.Lys243Glu | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 817/1918 | 727/1353 | 243/450 | chr2 | 174349123 | ||
chr2:174349141
|
T | C | 1 | a0003 | 2 | NA19056.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.709A>G | p.Lys237Glu | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 799/1918 | 709/1353 | 237/450 | chr2 | 174349141 | ||
chr2:174378931
|
T | C | 1 | a0007 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.476A>G | p.Asp159Gly | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/10 | 566/1918 | 476/1353 | 159/450 | chr2 | 174378931 | ||
chr2:174378941
|
C | T | 1 | a0005 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.466G>A | p.Val156Ile | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/10 | 556/1918 | 466/1353 | 156/450 | chr2 | 174378941 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:174348127
|
T | C | 1 | a0001c0001t0006 | 2 | HG02735.hp2 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*370A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 370 | chr2 | 174348127 | |||||
chr2:174348135
|
A | T | 2 | a0001c0001t0003a0002c0002t0003 | 17 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*362T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 362 | chr2 | 174348135 | |||||
chr2:174348244
|
A | C | 1 | a0001c0001t0005 | 5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*253T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 253 | chr2 | 174348244 | |||||
chr2:174348313
|
T | C | 9 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(6): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*184A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 184 | chr2 | 174348313 | |||||
chr2:174348471
|
T | C | 1 | a0001c0001t0007 | 2 | NA18948.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*26A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 26 | chr2 | 174348471 | |||||
chr2:174348475
|
G | A | 1 | a0001c0001t0009 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 22 | chr2 | 174348475 | |||||
chr2:174395627
|
G | T | 1 | a0001c0001t0004 | 7 | HG00733.hp2 HG01261.hp1 HG01361.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-5C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/10 | 5 | chr2 | 174395627 | |||||
chr2:174395646
|
C | T | 1 | a0001c0001t0008 | 1 | HG00408.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/10 | 24 | chr2 | 174395646 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:174349275
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.678-103A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349275 | ||||||
chr2:174349538
|
T | A | 196 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(193): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.678-366A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349538 | ||||||
chr2:174349564
|
T | TA | 7 | a0001c0001t0002g0178a0001c0001t0002g0198a0001c0001t0002g0222others(4): Show | 7 | HG00673.hp2 HG02027.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.678-393dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349564 | ||||||
chr2:174349564
|
TA | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0165a0001c0001t0001g0217others(62): Show | 73 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.678-393delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349564 | ||||||
chr2:174349564
|
TAA | T | 172 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(169): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.678-394_678-393del others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349564 | ||||||
chr2:174349741
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.678-569A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349741 | ||||||
chr2:174349859
|
A | G | 5 | a0001c0001t0005g0049a0001c0001t0005g0096a0001c0001t0005g0111others(2): Show | 5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-687T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349859 | ||||||
chr2:174350050
|
T | G | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.677+610A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174350050 | ||||||
chr2:174350168
|
ACT | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(95): Show | 106 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.677+490_677+491del others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174350168 | ||||||
chr2:174350202
|
A | G | 10 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0035others(7): Show | 12 | HG00408.hp1 HG00642.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.677+458T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174350202 | ||||||
chr2:174350559
|
G | A | 29 | a0001c0001t0001g0217a0001c0001t0002g0001a0001c0001t0002g0038others(26): Show | 33 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.677+101C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174350559 | ||||||
chr2:174351006
|
C | G | 1 | a0001c0001t0002g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.592-261G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351006 | ||||||
chr2:174351058
|
T | A | 198 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(195): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.592-313A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351058 | ||||||
chr2:174351098
|
A | T | 1 | a0001c0001t0002g0188 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.592-353T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351098 | ||||||
chr2:174351272
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.591+347T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351272 | ||||||
chr2:174351303
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.591+316T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351303 | ||||||
chr2:174351463
|
T | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0210a0001c0001t0001g0211others(10): Show | 14 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.591+156A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351463 | ||||||
chr2:174351498
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591+121A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351498 | ||||||
chr2:174351801
|
G | A | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-76C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174351801 | ||||||
chr2:174351886
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.485-161T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174351886 | ||||||
chr2:174352205
|
T | TCA | 63 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(60): Show | 76 | HG00558.hp2 HG00673.hp2 HG01884.hp1 others(73): Show |
intron_variant | MODIFIER | c.485-482_485-481dup others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352205 | ||||||
chr2:174352205
|
TCA | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-482_485-481del others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352205 | ||||||
chr2:174352228
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.485-503A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352228 | ||||||
chr2:174352447
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.485-722T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352447 | ||||||
chr2:174352470
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.485-745A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352470 | ||||||
chr2:174352508
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(195): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.485-783T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352508 | ||||||
chr2:174352559
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.485-834T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352559 | ||||||
chr2:174352616
|
G | T | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-891C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352616 | ||||||
chr2:174352617
|
C | G | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-892G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352617 | ||||||
chr2:174352944
|
C | A | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-1219G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352944 | ||||||
chr2:174352963
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-1238G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352963 | ||||||
chr2:174353113
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.485-1388G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353113 | ||||||
chr2:174353114
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0163 | 2 | HG01257.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.485-1389C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353114 | ||||||
chr2:174353188
|
G | T | 1 | a0004c0003t0001g0011 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.485-1463C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353188 | ||||||
chr2:174353225
|
C | A | 1 | a0001c0001t0002g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.485-1500G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353225 | ||||||
chr2:174353312
|
T | C | 1 | a0002c0002t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.485-1587A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353312 | ||||||
chr2:174353429
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.485-1704G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353429 | ||||||
chr2:174353470
|
T | G | 1 | a0001c0001t0001g0281 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.485-1745A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353470 | ||||||
chr2:174353555
|
C | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0136 | 3 | HG03704.hp2 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.485-1830G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353555 | ||||||
chr2:174353603
|
G | T | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-1878C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353603 | ||||||
chr2:174353605
|
T | C | 14 | a0001c0001t0002g0043a0001c0001t0002g0102a0001c0001t0002g0103others(11): Show | 14 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-1880A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353605 | ||||||
chr2:174353640
|
G | A | 3 | a0002c0002t0003g0017a0002c0002t0003g0237a0002c0002t0003g0238 | 4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-1915C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353640 | ||||||
chr2:174353640
|
G | C | 14 | a0001c0001t0002g0043a0001c0001t0002g0102a0001c0001t0002g0103others(11): Show | 14 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-1915C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353640 | ||||||
chr2:174353706
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.485-1981A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353706 | ||||||
chr2:174353745
|
C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-2020G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353745 | ||||||
chr2:174353932
|
C | G | 3 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062 | 3 | HG02615.hp2 HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.485-2207G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353932 | ||||||
chr2:174353979
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.485-2254G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353979 | ||||||
chr2:174354205
|
T | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-2480A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354205 | ||||||
chr2:174354266
|
C | T | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-2541G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354266 | ||||||
chr2:174354310
|
A | C | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-2585T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354310 | ||||||
chr2:174354382
|
TA | T | 3 | a0001c0001t0002g0095a0001c0001t0002g0100a0001c0001t0002g0101 | 3 | HG02559.hp2 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.485-2658delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354382 | ||||||
chr2:174354413
|
A | AT | 13 | a0002c0002t0003g0010a0002c0002t0003g0017a0002c0002t0003g0037others(10): Show | 15 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.485-2689dupA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354413 | ||||||
chr2:174354414
|
TATAA | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0257a0002c0002t0003g0050 | 3 | HG01123.hp1 HG03225.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.485-2693_485-2690d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354414 | ||||||
chr2:174354431
|
G | A | 198 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(195): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.485-2706C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354431 | ||||||
chr2:174354435
|
TATATA | T | 7 | a0001c0001t0002g0079a0001c0001t0002g0102a0001c0001t0002g0103others(4): Show | 7 | HG01074.hp2 HG02717.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-2715_485-2711d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354435 | ||||||
chr2:174354441
|
ATATAT | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.485-2721_485-2717d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354441 | ||||||
chr2:174354442
|
TATATTAT others(3): Show |
T | 1 | a0001c0001t0001g0145 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.485-2727_485-2718d others(12): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354442 | ||||||
chr2:174354446
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.485-2721A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354446 | ||||||
chr2:174354447
|
T | A | 13 | a0001c0001t0002g0039a0001c0001t0003g0206a0002c0002t0003g0010others(10): Show | 15 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.485-2722A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354447 | ||||||
chr2:174354447
|
TATATA | T | 7 | a0001c0001t0002g0043a0001c0001t0002g0112a0001c0001t0002g0207others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.485-2727_485-2723d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354447 | ||||||
chr2:174354454
|
TATA | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0127a0001c0001t0002g0174others(5): Show | 10 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.485-2732_485-2730d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354454 | ||||||
chr2:174354491
|
TATAAATT others(14): Show |
T | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0020others(81): Show | 88 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.485-2787_485-2767d others(23): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354491 | ||||||
chr2:174354495
|
A | AATTATAT others(42): Show |
1 | a0001c0001t0001g0217 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.485-2819_485-2771d others(51): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354495 | ||||||
chr2:174354495
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.485-2770T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354495 | ||||||
chr2:174354505
|
TATATATC | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0019others(93): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.485-2787_485-2781d others(9): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354505 | ||||||
chr2:174354517
|
A | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-2792T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354517 | ||||||
chr2:174354538
|
A | AATATATA others(30): Show |
34 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0016others(31): Show | 39 | HG00558.hp2 HG00673.hp2 HG02027.hp1 others(36): Show |
intron_variant | MODIFIER | c.485-2850_485-2814d others(39): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354538 | ||||||
chr2:174354538
|
A | AATATATA others(27): Show |
1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-2814_485-2813i others(36): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354538 | ||||||
chr2:174354541
|
ATATAT | A | 10 | a0001c0001t0003g0206a0002c0002t0003g0010a0002c0002t0003g0037others(7): Show | 11 | HG00735.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.485-2821_485-2817d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354541 | ||||||
chr2:174354561
|
TTTATATA others(40): Show |
T | 179 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(176): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.485-2883_485-2837d others(49): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354561 | ||||||
chr2:174354562
|
T | TTATATAT others(56): Show |
1 | a0001c0001t0002g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485-2838_485-2837i others(65): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354562 | ||||||
chr2:174354562
|
T | TTATATAT others(58): Show |
2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-2838_485-2837i others(67): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354562 | ||||||
chr2:174354562
|
T | TTATATAT others(28): Show |
6 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0244others(3): Show | 6 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.485-2872_485-2838d others(37): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354562 | ||||||
chr2:174354575
|
T | G | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-2850A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354575 | ||||||
chr2:174354575
|
T | TATATATA others(30): Show |
4 | a0001c0001t0002g0007a0001c0001t0002g0032a0001c0001t0002g0183others(1): Show | 5 | NA18942.hp2 NA18954.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-2851_485-2850i others(39): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354575 | ||||||
chr2:174354575
|
T | TATATATA others(88): Show |
1 | a0001c0001t0002g0030 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.485-2851_485-2850i others(97): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354575 | ||||||
chr2:174354575
|
T | TATATATT others(28): Show |
2 | a0001c0001t0002g0248a0001c0001t0002g0249 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.485-2851_485-2850i others(37): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354575 | ||||||
chr2:174354578
|
ATAT | A | 5 | a0001c0001t0005g0049a0001c0001t0005g0096a0001c0001t0005g0111others(2): Show | 5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-2856_485-2854d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354578 | ||||||
chr2:174354583
|
A | ATATATCA others(26): Show |
2 | a0001c0001t0002g0039a0001c0001t0002g0113 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.485-2859_485-2858i others(35): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354583 | ||||||
chr2:174354583
|
ATATATAT others(28): Show |
A | 3 | a0002c0002t0003g0017a0002c0002t0003g0237a0002c0002t0003g0238 | 4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-2893_485-2859d others(37): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354583 | ||||||
chr2:174354591
|
C | A | 5 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0003g0206others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-2866G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354591 | ||||||
chr2:174354615
|
A | ATTTTATA others(24): Show |
8 | a0002c0002t0003g0010a0002c0002t0003g0037a0002c0002t0003g0050others(5): Show | 9 | HG00735.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.485-2921_485-2891d others(33): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354615 | ||||||
chr2:174354626
|
T | A | 3 | a0002c0002t0003g0017a0002c0002t0003g0237a0002c0002t0003g0238 | 4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-2901A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354626 | ||||||
chr2:174354626
|
T | C | 3 | a0001c0001t0002g0038a0001c0001t0002g0101a0001c0001t0002g0104 | 3 | HG02055.hp2 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.485-2901A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354626 | ||||||
chr2:174354689
|
T | A | 1 | a0001c0001t0002g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.485-2964A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354689 | ||||||
chr2:174354764
|
A | G | 3 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099 | 3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.485-3039T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354764 | ||||||
chr2:174354768
|
A | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0061 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.485-3043T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354768 | ||||||
chr2:174354769
|
TA | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0116a0001c0001t0001g0141others(2): Show | 5 | HG00438.hp1 HG02738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-3045delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354769 | ||||||
chr2:174354770
|
A | T | 57 | a0001c0001t0001g0217a0001c0001t0002g0001a0001c0001t0002g0008others(54): Show | 64 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.485-3045T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354770 | ||||||
chr2:174354770
|
AT | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(172): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.485-3046delA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354770 | ||||||
chr2:174354771
|
T | TA | 5 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0176others(2): Show | 5 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-3047_485-3046i others(3): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354771 | ||||||
chr2:174354772
|
T | A | 15 | a0001c0001t0001g0132a0001c0001t0002g0003a0001c0001t0002g0006others(12): Show | 20 | HG00673.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-3047A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354772 | ||||||
chr2:174354773
|
T | A | 4 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0302others(1): Show | 4 | HG01099.hp2 HG01169.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-3048A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354773 | ||||||
chr2:174354847
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.485-3122G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354847 | ||||||
chr2:174354882
|
G | A | 1 | a0001c0001t0005g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.485-3157C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354882 | ||||||
chr2:174354928
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.485-3203G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354928 | ||||||
chr2:174355073
|
C | A | 1 | a0001c0001t0001g0012 | 2 | NA19005.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.485-3348G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355073 | ||||||
chr2:174355218
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0003g0206 | 2 | HG01928.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.485-3493C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355218 | ||||||
chr2:174355228
|
T | C | 15 | a0001c0001t0002g0018a0002c0002t0003g0010a0002c0002t0003g0017others(12): Show | 18 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.485-3503A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355228 | ||||||
chr2:174355247
|
C | A | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-3522G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355247 | ||||||
chr2:174355361
|
T | A | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-3636A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355361 | ||||||
chr2:174355425
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.485-3700T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355425 | ||||||
chr2:174355563
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.485-3838A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355563 | ||||||
chr2:174355688
|
G | A | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-3963C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355688 | ||||||
chr2:174355792
|
T | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-4067A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355792 | ||||||
chr2:174355853
|
T | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-4128A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355853 | ||||||
chr2:174355866
|
G | C | 2 | a0001c0001t0001g0308a0001c0001t0001g0315 | 2 | NA18956.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.485-4141C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355866 | ||||||
chr2:174355877
|
A | G | 5 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0072others(2): Show | 5 | HG00609.hp2 HG02083.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-4152T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355877 | ||||||
chr2:174355915
|
ACTTGTGT others(26): Show |
A | 1 | a0001c0001t0001g0125 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.485-4223_485-4191d others(35): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355915 | ||||||
chr2:174355956
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.485-4231G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355956 | ||||||
chr2:174356008
|
G | A | 4 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(1): Show | 4 | HG02015.hp1 HG02040.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-4283C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356008 | ||||||
chr2:174356076
|
A | G | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-4351T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356076 | ||||||
chr2:174356185
|
G | T | 1 | a0001c0001t0002g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485-4460C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356185 | ||||||
chr2:174356191
|
C | T | 1 | a0001c0001t0005g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.485-4466G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356191 | ||||||
chr2:174356215
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0074 | 2 | HG00438.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.485-4490G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356215 | ||||||
chr2:174356503
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.485-4778C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356503 | ||||||
chr2:174356522
|
A | AGGAAGGA others(6): Show |
1 | a0001c0001t0001g0309 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.485-4798_485-4797i others(15): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356522 | ||||||
chr2:174356522
|
A | AGGAAGGA others(10): Show |
1 | a0001c0001t0001g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.485-4798_485-4797i others(19): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356522 | ||||||
chr2:174356526
|
A | AG | 4 | a0001c0001t0001g0076a0001c0001t0001g0117a0001c0001t0001g0128others(1): Show | 4 | HG02165.hp1 HG03017.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-4802dupC | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | ||||||
chr2:174356526
|
A | AGGAAG | 78 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(75): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.485-4802_485-4801i others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | ||||||
chr2:174356526
|
A | AGGAAGGA others(2): Show |
10 | a0001c0001t0001g0064a0001c0001t0001g0071a0001c0001t0001g0078others(7): Show | 10 | HG00408.hp2 HG00597.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.485-4802_485-4801i others(11): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | ||||||
chr2:174356526
|
A | AGGAAGGA others(6): Show |
60 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(57): Show | 66 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.485-4802_485-4801i others(15): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | ||||||
chr2:174356526
|
A | AGGAAGGA others(10): Show |
21 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0115others(18): Show | 23 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.485-4802_485-4801i others(19): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | ||||||
chr2:174356526
|
A | AGGAAGGA others(14): Show |
2 | a0001c0001t0001g0132a0001c0001t0001g0137 | 2 | HG00280.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.485-4802_485-4801i others(23): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | ||||||
chr2:174356526
|
A | AGGAAGGA others(22): Show |
1 | a0001c0001t0001g0133 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.485-4802_485-4801i others(31): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | ||||||
chr2:174356526
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0309 | 2 | HG00609.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.485-4801T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | ||||||
chr2:174356531
|
A | AAAGGAAG others(17): Show |
1 | a0001c0001t0002g0041 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.485-4807_485-4806i others(26): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356531 | ||||||
chr2:174356531
|
A | AAAGGAAG others(29): Show |
2 | a0001c0001t0002g0040a0001c0001t0002g0099 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.485-4807_485-4806i others(38): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356531 | ||||||
chr2:174356531
|
A | AAAGGAAG others(17): Show |
1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-4807_485-4806i others(26): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356531 | ||||||
chr2:174356531
|
A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(176): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.485-4806T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356531 | ||||||
chr2:174356533
|
A | AGGAAGGA others(13): Show |
14 | a0002c0002t0003g0010a0002c0002t0003g0017a0002c0002t0003g0037others(11): Show | 16 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-4809_485-4808i others(22): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356533 | ||||||
chr2:174356601
|
GGGAA | G | 3 | a0002c0002t0003g0017a0002c0002t0003g0237a0002c0002t0003g0238 | 4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-4880_485-4877d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356601 | ||||||
chr2:174356603
|
G | GAGGA | 178 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(175): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.485-4879_485-4878i others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356603 | ||||||
chr2:174356605
|
A | G | 305 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(302): Show | 333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.485-4880T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356605 | ||||||
chr2:174356620
|
AGAAGGG | A | 3 | a0001c0001t0002g0216a0001c0001t0002g0218a0001c0001t0002g0220 | 3 | HG00639.hp2 HG01109.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.485-4901_485-4896d others(8): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356620 | ||||||
chr2:174356675
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.485-4950G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356675 | ||||||
chr2:174356677
|
C | G | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-4952G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356677 | ||||||
chr2:174356680
|
A | C | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-4955T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356680 | ||||||
chr2:174356808
|
G | A | 1 | a0001c0001t0002g0008 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.485-5083C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356808 | ||||||
chr2:174356831
|
T | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG00639.hp1 HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.485-5106A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356831 | ||||||
chr2:174356926
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.485-5201A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356926 | ||||||
chr2:174356981
|
C | G | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099others(15): Show | 20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-5256G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356981 | ||||||
chr2:174357106
|
T | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-5381A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357106 | ||||||
chr2:174357288
|
T | G | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-5563A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357288 | ||||||
chr2:174357322
|
T | A | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-5597A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357322 | ||||||
chr2:174357348
|
A | G | 14 | a0001c0001t0002g0043a0001c0001t0002g0102a0001c0001t0002g0103others(11): Show | 14 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-5623T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357348 | ||||||
chr2:174357486
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.485-5761A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357486 | ||||||
chr2:174357513
|
T | C | 3 | a0001c0001t0001g0287a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | NA18947.hp1 NA18968.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.485-5788A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357513 | ||||||
chr2:174357558
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0039a0001c0001t0002g0045others(2): Show | 6 | HG01891.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-5833G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357558 | ||||||
chr2:174357690
|
T | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(195): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.485-5965A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357690 | ||||||
chr2:174357820
|
A | G | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099others(15): Show | 20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-6095T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357820 | ||||||
chr2:174357873
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.485-6148A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357873 | ||||||
chr2:174357974
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.485-6249A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357974 | ||||||
chr2:174358383
|
C | T | 2 | a0001c0001t0002g0241a0001c0001t0002g0244 | 2 | HG00735.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.485-6658G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358383 | ||||||
chr2:174358399
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-6674G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358399 | ||||||
chr2:174358401
|
G | C | 1 | a0001c0001t0002g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.485-6676C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358401 | ||||||
chr2:174358524
|
C | T | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099others(15): Show | 20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-6799G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358524 | ||||||
chr2:174358568
|
T | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-6843A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358568 | ||||||
chr2:174358675
|
G | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0298 | 2 | NA18956.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.485-6950C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358675 | ||||||
chr2:174358869
|
C | T | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0176others(1): Show | 4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-7144G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358869 | ||||||
chr2:174358917
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.485-7192C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358917 | ||||||
chr2:174358927
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.485-7202C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358927 | ||||||
chr2:174358963
|
G | A | 14 | a0002c0002t0003g0010a0002c0002t0003g0017a0002c0002t0003g0037others(11): Show | 16 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-7238C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358963 | ||||||
chr2:174358963
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.485-7238C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358963 | ||||||
chr2:174358973
|
C | T | 8 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0244others(5): Show | 8 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.485-7248G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358973 | ||||||
chr2:174359030
|
A | T | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0176others(1): Show | 4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-7305T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359030 | ||||||
chr2:174359111
|
T | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-7386A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359111 | ||||||
chr2:174359130
|
T | TAAG | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099others(15): Show | 20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-7408_485-7406d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359130 | ||||||
chr2:174359207
|
T | A | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-7482A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359207 | ||||||
chr2:174359278
|
T | A | 1 | a0001c0001t0002g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.485-7553A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359278 | ||||||
chr2:174359334
|
TA | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(200): Show | 218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.485-7610delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359334 | ||||||
chr2:174359334
|
TAA | T | 11 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(8): Show | 11 | HG00323.hp2 HG00597.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.485-7611_485-7610d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359334 | ||||||
chr2:174359334
|
TAAA | T | 16 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099others(13): Show | 18 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.485-7612_485-7610d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359334 | ||||||
chr2:174359351
|
A | G | 1 | a0001c0001t0002g0243 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.485-7626T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359351 | ||||||
chr2:174359491
|
T | C | 4 | a0001c0001t0001g0263a0001c0001t0001g0267a0001c0001t0001g0269others(1): Show | 4 | HG01256.hp1 HG01981.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-7766A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359491 | ||||||
chr2:174359535
|
G | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0298 | 2 | NA18956.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.485-7810C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359535 | ||||||
chr2:174359536
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.485-7811G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359536 | ||||||
chr2:174359593
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0003g0206 | 2 | HG03195.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.485-7868G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359593 | ||||||
chr2:174359595
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.485-7870G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359595 | ||||||
chr2:174359670
|
G | A | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099others(15): Show | 20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-7945C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359670 | ||||||
chr2:174359844
|
A | T | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8119T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359844 | ||||||
chr2:174359845
|
T | C | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8120A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359845 | ||||||
chr2:174359863
|
T | A | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8138A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359863 | ||||||
chr2:174359864
|
G | T | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8139C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359864 | ||||||
chr2:174359871
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.485-8146A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359871 | ||||||
chr2:174359970
|
A | G | 1 | a0001c0001t0002g0061 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.485-8245T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359970 | ||||||
chr2:174360021
|
G | A | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0176others(1): Show | 4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-8296C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360021 | ||||||
chr2:174360140
|
C | A | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8415G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360140 | ||||||
chr2:174360183
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.485-8458T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360183 | ||||||
chr2:174360201
|
A | G | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-8476T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360201 | ||||||
chr2:174360219
|
A | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0129 | 3 | NA18977.hp2 NA18986.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.485-8494T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360219 | ||||||
chr2:174360245
|
TTTA | T | 15 | a0001c0001t0003g0206a0002c0002t0003g0010a0002c0002t0003g0017others(12): Show | 17 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.485-8523_485-8521d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360245 | ||||||
chr2:174360290
|
C | T | 6 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0244others(3): Show | 6 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.485-8565G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360290 | ||||||
chr2:174360326
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0112 | 2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.485-8601A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360326 | ||||||
chr2:174360479
|
G | T | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8754C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360479 | ||||||
chr2:174360753
|
T | A | 1 | a0001c0001t0002g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-9028A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360753 | ||||||
chr2:174360898
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(195): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.485-9173T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360898 | ||||||
chr2:174360986
|
G | T | 14 | a0002c0002t0003g0010a0002c0002t0003g0017a0002c0002t0003g0037others(11): Show | 16 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-9261C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360986 | ||||||
chr2:174361071
|
AATCAACT others(3): Show |
A | 8 | a0001c0001t0002g0008a0001c0001t0002g0039a0001c0001t0002g0045others(5): Show | 9 | HG01891.hp2 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.485-9356_485-9347d others(12): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361071 | ||||||
chr2:174361380
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-9655C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361380 | ||||||
chr2:174361522
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0003g0206 | 3 | HG02965.hp2 HG03139.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.485-9797C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361522 | ||||||
chr2:174361561
|
G | A | 5 | a0001c0001t0005g0049a0001c0001t0005g0096a0001c0001t0005g0111others(2): Show | 5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-9836C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361561 | ||||||
chr2:174361647
|
C | A | 1 | a0001c0001t0001g0290 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.485-9922G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361647 | ||||||
chr2:174361914
|
T | G | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-10189A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361914 | ||||||
chr2:174362086
|
C | A | 1 | a0001c0001t0001g0132 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.485-10361G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362086 | ||||||
chr2:174362090
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.485-10365C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362090 | ||||||
chr2:174362107
|
G | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-10382C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362107 | ||||||
chr2:174362108
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0145a0001c0001t0001g0159 | 3 | HG00280.hp1 HG01981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.485-10383C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362108 | ||||||
chr2:174362155
|
A | C | 6 | a0001c0001t0003g0206a0002c0002t0003g0017a0002c0002t0003g0237others(3): Show | 7 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-10430T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362155 | ||||||
chr2:174362366
|
A | ATAACT | 90 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(87): Show | 95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.485-10642_485-1064 others(9): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362366 | ||||||
chr2:174362556
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.485-10831C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362556 | ||||||
chr2:174362652
|
A | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0071 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.485-10927T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362652 | ||||||
chr2:174362685
|
TCA | T | 43 | a0001c0001t0001g0042a0001c0001t0001g0066a0001c0001t0001g0070others(40): Show | 43 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.485-10962_485-1096 others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362685 | ||||||
chr2:174362685
|
TCAA | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(131): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.485-10963_485-1096 others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362685 | ||||||
chr2:174362686
|
C | CA | 68 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(65): Show | 82 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.485-10962dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362686 | ||||||
chr2:174362686
|
C | CAA | 24 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0058others(21): Show | 25 | HG00673.hp2 HG01891.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.485-10963_485-1096 others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362686 | ||||||
chr2:174362718
|
TTACATTT others(1): Show |
T | 178 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(175): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.485-11001_485-1099 others(12): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362718 | ||||||
chr2:174362773
|
G | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 105 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.485-11048C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362773 | ||||||
chr2:174363029
|
G | A | 9 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099others(6): Show | 10 | HG02258.hp2 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.485-11304C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363029 | ||||||
chr2:174363086
|
A | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.485-11361T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363086 | ||||||
chr2:174363089
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.485-11364A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363089 | ||||||
chr2:174363205
|
C | G | 11 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0009others(8): Show | 16 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-11480G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363205 | ||||||
chr2:174363334
|
T | C | 22 | a0001c0001t0001g0217a0001c0001t0002g0001a0001c0001t0002g0182others(19): Show | 26 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.485-11609A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363334 | ||||||
chr2:174363501
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.485-11776G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363501 | ||||||
chr2:174363752
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.485-12027G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363752 | ||||||
chr2:174363773
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0192 | 3 | HG02965.hp2 HG03139.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.485-12048C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363773 | ||||||
chr2:174363809
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.485-12084T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363809 | ||||||
chr2:174363811
|
G | T | 6 | a0001c0001t0003g0206a0002c0002t0003g0017a0002c0002t0003g0237others(3): Show | 7 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-12086C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363811 | ||||||
chr2:174363882
|
G | A | 1 | a0005c0005t0002g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.485-12157C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363882 | ||||||
chr2:174363915
|
C | T | 1 | a0001c0001t0008g0022 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.485-12190G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363915 | ||||||
chr2:174363925
|
C | A | 14 | a0001c0001t0002g0043a0001c0001t0002g0102a0001c0001t0002g0103others(11): Show | 14 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-12200G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363925 | ||||||
chr2:174363941
|
A | G | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.485-12216T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363941 | ||||||
chr2:174364180
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.485-12455A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364180 | ||||||
chr2:174364201
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.485-12476C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364201 | ||||||
chr2:174364269
|
T | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-12544A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364269 | ||||||
chr2:174364360
|
G | A | 5 | a0002c0002t0003g0017a0002c0002t0003g0237a0002c0002t0003g0238others(2): Show | 6 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-12635C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364360 | ||||||
chr2:174364480
|
T | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-12755A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364480 | ||||||
chr2:174364656
|
C | T | 1 | a0001c0001t0008g0022 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.485-12931G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364656 | ||||||
chr2:174364876
|
T | C | 58 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(55): Show | 70 | HG00558.hp2 HG00673.hp2 HG01884.hp1 others(67): Show |
intron_variant | MODIFIER | c.485-13151A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364876 | ||||||
chr2:174364883
|
TTC | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0039a0001c0001t0002g0045others(2): Show | 6 | HG01891.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-13160_485-1315 others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364883 | ||||||
chr2:174364904
|
C | T | 310 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(307): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.485-13179G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364904 | ||||||
chr2:174364925
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.485-13200A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364925 | ||||||
chr2:174364934
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.485-13209C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364934 | ||||||
chr2:174364990
|
T | C | 21 | a0001c0001t0002g0005a0001c0001t0002g0173a0001c0001t0002g0177others(18): Show | 23 | HG00558.hp2 HG00673.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.485-13265A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364990 | ||||||
chr2:174365046
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.485-13321G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365046 | ||||||
chr2:174365289
|
C | T | 5 | a0001c0001t0005g0049a0001c0001t0005g0096a0001c0001t0005g0111others(2): Show | 5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-13564G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365289 | ||||||
chr2:174365705
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.484+13218C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365705 | ||||||
chr2:174365712
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.484+13211G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365712 | ||||||
chr2:174365928
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.484+12995T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365928 | ||||||
chr2:174366092
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.484+12831A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366092 | ||||||
chr2:174366134
|
G | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.484+12789C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366134 | ||||||
chr2:174366552
|
C | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.484+12371G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366552 | ||||||
chr2:174366718
|
A | G | 1 | a0001c0001t0004g0023 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.484+12205T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366718 | ||||||
chr2:174366846
|
A | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(214): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.484+12077T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366846 | ||||||
chr2:174366869
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.484+12054G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366869 | ||||||
chr2:174366887
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(219): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.484+12036G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366887 | ||||||
chr2:174366934
|
C | T | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+11989G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366934 | ||||||
chr2:174366957
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.484+11966T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366957 | ||||||
chr2:174367011
|
C | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(219): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.484+11912G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367011 | ||||||
chr2:174367056
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.484+11867T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367056 | ||||||
chr2:174367228
|
A | C | 1 | a0001c0001t0001g0200 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.484+11695T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367228 | ||||||
chr2:174367260
|
G | A | 3 | a0002c0002t0003g0017a0002c0002t0003g0237a0002c0002t0003g0238 | 4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+11663C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367260 | ||||||
chr2:174367296
|
G | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.484+11627C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367296 | ||||||
chr2:174367302
|
G | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.484+11621C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367302 | ||||||
chr2:174367329
|
C | G | 1 | a0005c0005t0002g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.484+11594G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367329 | ||||||
chr2:174367355
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.484+11568C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367355 | ||||||
chr2:174367488
|
G | A | 90 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(87): Show | 95 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.484+11435C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367488 | ||||||
chr2:174367493
|
T | C | 1 | a0001c0001t0002g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.484+11430A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367493 | ||||||
chr2:174367495
|
G | A | 1 | a0001c0001t0007g0169 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.484+11428C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367495 | ||||||
chr2:174367715
|
C | T | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.484+11208G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367715 | ||||||
chr2:174367745
|
T | TA | 104 | a0001c0001t0001g0078a0001c0001t0001g0161a0001c0001t0001g0212others(101): Show | 121 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.484+11177dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367745 | ||||||
chr2:174367745
|
T | TAA | 13 | a0001c0001t0002g0018a0001c0001t0002g0039a0001c0001t0002g0051others(10): Show | 14 | HG01884.hp1 HG02080.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.484+11176_484+1117 others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367745 | ||||||
chr2:174367745
|
TA | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0120others(5): Show | 8 | HG00609.hp2 HG01069.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.484+11177delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367745 | ||||||
chr2:174367752
|
AAAAAAAA others(22): Show |
A | 2 | a0001c0001t0002g0043a0001c0001t0002g0112 | 2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.484+11142_484+1117 others(33): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367752 | ||||||
chr2:174367781
|
TA | T | 9 | a0001c0001t0001g0294a0001c0001t0002g0240a0001c0001t0002g0241others(6): Show | 9 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.484+11141delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367781 | ||||||
chr2:174367830
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.484+11093T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367830 | ||||||
chr2:174367843
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484+11080A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367843 | ||||||
chr2:174367884
|
G | A | 2 | a0001c0001t0002g0228a0001c0001t0002g0230 | 2 | HG00733.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.484+11039C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367884 | ||||||
chr2:174368043
|
A | G | 316 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(313): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.484+10880T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368043 | ||||||
chr2:174368132
|
T | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(175): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.484+10791A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368132 | ||||||
chr2:174368164
|
T | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(214): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.484+10759A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368164 | ||||||
chr2:174368235
|
TAATAG | T | 81 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(78): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.484+10683_484+1068 others(9): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368235 | ||||||
chr2:174368355
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.484+10568C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368355 | ||||||
chr2:174368545
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.484+10378C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368545 | ||||||
chr2:174368548
|
G | A | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.484+10375C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368548 | ||||||
chr2:174368971
|
C | A | 1 | a0001c0001t0002g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.484+9952G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368971 | ||||||
chr2:174369087
|
T | C | 1 | a0001c0001t0002g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.484+9836A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369087 | ||||||
chr2:174369107
|
T | C | 14 | a0001c0001t0002g0008a0001c0001t0002g0039a0001c0001t0002g0045others(11): Show | 16 | HG00735.hp1 HG01891.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.484+9816A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369107 | ||||||
chr2:174369132
|
T | C | 5 | a0002c0002t0003g0017a0002c0002t0003g0237a0002c0002t0003g0238others(2): Show | 6 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.484+9791A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369132 | ||||||
chr2:174369140
|
A | C | 311 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(308): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.484+9783T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369140 | ||||||
chr2:174369168
|
CTGGAGAA others(21): Show |
C | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+9727_484+9754d others(30): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369168 | ||||||
chr2:174369489
|
T | C | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099others(15): Show | 20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.484+9434A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369489 | ||||||
chr2:174369629
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.484+9294A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369629 | ||||||
chr2:174369762
|
C | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.484+9161G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369762 | ||||||
chr2:174369835
|
A | C | 1 | a0001c0001t0002g0176 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.484+9088T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369835 | ||||||
chr2:174369931
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.484+8992C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369931 | ||||||
chr2:174369942
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.484+8981G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369942 | ||||||
chr2:174370123
|
G | A | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+8800C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370123 | ||||||
chr2:174370164
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.484+8759C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370164 | ||||||
chr2:174370264
|
T | C | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.484+8659A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370264 | ||||||
chr2:174370284
|
G | C | 1 | a0002c0002t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.484+8639C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370284 | ||||||
chr2:174370467
|
A | G | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0176others(1): Show | 4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+8456T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370467 | ||||||
chr2:174370629
|
T | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(219): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.484+8294A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370629 | ||||||
chr2:174370632
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.484+8291C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370632 | ||||||
chr2:174370783
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.484+8140G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370783 | ||||||
chr2:174370789
|
T | C | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+8134A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370789 | ||||||
chr2:174370882
|
T | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(220): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.484+8041A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370882 | ||||||
chr2:174370910
|
C | CA | 226 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(223): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.484+8012dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370910 | ||||||
chr2:174370910
|
CA | C | 34 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0090others(31): Show | 35 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.484+8012delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370910 | ||||||
chr2:174370921
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.484+8002T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370921 | ||||||
chr2:174370944
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.484+7979G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370944 | ||||||
chr2:174370970
|
T | TCA | 3 | a0001c0001t0001g0014a0001c0001t0001g0129a0001c0001t0001g0134 | 4 | HG00558.hp1 NA18977.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+7951_484+7952d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370970 | ||||||
chr2:174370995
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.484+7928C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370995 | ||||||
chr2:174371012
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484+7911T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371012 | ||||||
chr2:174371139
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.484+7784C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371139 | ||||||
chr2:174371269
|
T | C | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+7654A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371269 | ||||||
chr2:174371288
|
G | A | 192 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.484+7635C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371288 | ||||||
chr2:174371288
|
G | T | 20 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0090others(17): Show | 20 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.484+7635C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371288 | ||||||
chr2:174371598
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.484+7325G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371598 | ||||||
chr2:174371599
|
C | G | 95 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 100 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.484+7324G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371599 | ||||||
chr2:174372329
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.484+6594T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174372329 | ||||||
chr2:174372635
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.484+6288A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174372635 | ||||||
chr2:174372773
|
G | C | 2 | a0001c0001t0002g0083a0001c0001t0002g0191 | 2 | NA18942.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.484+6150C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174372773 | ||||||
chr2:174373027
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0272 | 2 | HG01074.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.484+5896C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373027 | ||||||
chr2:174373066
|
A | C | 3 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099 | 3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.484+5857T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373066 | ||||||
chr2:174373236
|
C | T | 3 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099 | 3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.484+5687G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373236 | ||||||
chr2:174373276
|
A | G | 4 | a0001c0001t0002g0018a0001c0001t0002g0036a0001c0001t0002g0039others(1): Show | 5 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.484+5647T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373276 | ||||||
chr2:174373299
|
T | TA | 174 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(171): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.484+5623dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373299 | ||||||
chr2:174373448
|
C | A | 14 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0090others(11): Show | 14 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.484+5475G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373448 | ||||||
chr2:174373689
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.484+5234A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373689 | ||||||
chr2:174373764
|
TA | T | 15 | a0001c0001t0001g0125a0001c0001t0001g0134a0001c0001t0001g0137others(12): Show | 15 | HG00280.hp1 HG00558.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.484+5158delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373764 | ||||||
chr2:174373828
|
C | CTG | 18 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0090others(15): Show | 18 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.484+5093_484+5094d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373828 | ||||||
chr2:174373828
|
C | CTGTG | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0099others(15): Show | 20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.484+5091_484+5094d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373828 | ||||||
chr2:174373828
|
CT | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(171): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.484+5094delA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373828 | ||||||
chr2:174373856
|
T | TTTC | 311 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(308): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.484+5064_484+5066d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373856 | ||||||
chr2:174374019
|
G | C | 1 | a0001c0001t0001g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.484+4904C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374019 | ||||||
chr2:174374111
|
A | G | 1 | a0001c0001t0002g0083 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.484+4812T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374111 | ||||||
chr2:174374196
|
T | C | 14 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0090others(11): Show | 14 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.484+4727A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374196 | ||||||
chr2:174374346
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.484+4577G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374346 | ||||||
chr2:174374347
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.484+4576C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374347 | ||||||
chr2:174374354
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(76): Show | 84 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.484+4569A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374354 | ||||||
chr2:174374457
|
A | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(171): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.484+4466T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374457 | ||||||
chr2:174374534
|
CA | C | 8 | a0002c0002t0003g0010a0002c0002t0003g0037a0002c0002t0003g0050others(5): Show | 9 | HG00735.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.484+4388delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374534 | ||||||
chr2:174374597
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.484+4326G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374597 | ||||||
chr2:174374730
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.484+4193A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374730 | ||||||
chr2:174374790
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.484+4133T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374790 | ||||||
chr2:174375080
|
A | G | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0176others(1): Show | 4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+3843T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375080 | ||||||
chr2:174375189
|
A | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(171): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.484+3734T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375189 | ||||||
chr2:174375225
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0039a0001c0001t0002g0113 | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+3698C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375225 | ||||||
chr2:174375279
|
A | G | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.484+3644T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375279 | ||||||
chr2:174375425
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484+3498A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375425 | ||||||
chr2:174375564
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(170): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.484+3359G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375564 | ||||||
chr2:174375761
|
T | C | 75 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(72): Show | 77 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.484+3162A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375761 | ||||||
chr2:174375890
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.484+3033C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375890 | ||||||
chr2:174376133
|
T | C | 1 | a0001c0001t0002g0008 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.484+2790A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376133 | ||||||
chr2:174376319
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.484+2604T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376319 | ||||||
chr2:174376655
|
A | G | 317 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(314): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.484+2268T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376655 | ||||||
chr2:174376706
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.484+2217C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376706 | ||||||
chr2:174376729
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.484+2194G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376729 | ||||||
chr2:174376730
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0210a0001c0001t0001g0211others(13): Show | 17 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.484+2193C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376730 | ||||||
chr2:174376737
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0009g0291 | 2 | HG02698.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.484+2186C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376737 | ||||||
chr2:174376754
|
T | C | 127 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(124): Show | 133 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.484+2169A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376754 | ||||||
chr2:174376801
|
GA | G | 76 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.484+2121delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376801 | ||||||
chr2:174376802
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.484+2121T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376802 | ||||||
chr2:174376803
|
A | G | 40 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063others(37): Show | 41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.484+2120T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376803 | ||||||
chr2:174376804
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0149 | 2 | HG02015.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.484+2119T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376804 | ||||||
chr2:174376838
|
G | A | 14 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0090others(11): Show | 14 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.484+2085C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376838 | ||||||
chr2:174376960
|
C | G | 1 | a0002c0002t0003g0316 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.484+1963G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376960 | ||||||
chr2:174377353
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.484+1570C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377353 | ||||||
chr2:174377376
|
G | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0280others(6): Show | 11 | HG00673.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.484+1547C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377376 | ||||||
chr2:174377407
|
G | T | 2 | a0001c0001t0002g0191a0001c0001t0003g0206 | 2 | NA18942.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.484+1516C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377407 | ||||||
chr2:174377426
|
T | C | 5 | a0001c0001t0002g0041a0001c0001t0002g0207a0001c0001t0002g0239others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.484+1497A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377426 | ||||||
chr2:174377476
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.484+1447T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377476 | ||||||
chr2:174377539
|
A | G | 1 | a0001c0001t0002g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.484+1384T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377539 | ||||||
chr2:174377717
|
C | T | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0135others(2): Show | 5 | HG00738.hp2 HG01496.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.484+1206G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377717 | ||||||
chr2:174377753
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.484+1170T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377753 | ||||||
chr2:174377761
|
G | C | 2 | a0001c0001t0002g0127a0001c0001t0002g0201 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.484+1162C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377761 | ||||||
chr2:174377781
|
C | T | 1 | a0001c0001t0002g0018 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.484+1142G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377781 | ||||||
chr2:174377824
|
C | CA | 76 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(73): Show | 84 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.484+1098dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | ||||||
chr2:174377824
|
C | CAA | 17 | a0001c0001t0001g0131a0001c0001t0001g0163a0001c0001t0001g0200others(14): Show | 17 | HG01106.hp2 HG01109.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.484+1097_484+1098d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | ||||||
chr2:174377824
|
C | CAAA | 13 | a0001c0001t0001g0012a0001c0001t0001g0097a0001c0001t0001g0114others(10): Show | 16 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.484+1096_484+1098d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | ||||||
chr2:174377824
|
C | CAAAA | 67 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0020others(64): Show | 71 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.484+1095_484+1098d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | ||||||
chr2:174377824
|
C | CAAAAA | 43 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.484+1094_484+1098d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | ||||||
chr2:174377875
|
C | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.484+1048G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377875 | ||||||
chr2:174377913
|
G | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(48): Show | 56 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.484+1010C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377913 | ||||||
chr2:174378113
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.484+810A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378113 | ||||||
chr2:174378320
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.484+603C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378320 | ||||||
chr2:174378496
|
G | C | 16 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(13): Show | 16 | HG00140.hp1 HG00280.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.484+427C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378496 | ||||||
chr2:174378523
|
TTTG | T | 107 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(104): Show | 114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.484+397_484+399del others(3): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378523 | ||||||
chr2:174378577
|
C | A | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.484+346G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378577 | ||||||
chr2:174378692
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0002g0043others(1): Show | 7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+231C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378692 | ||||||
chr2:174378693
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.484+230C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378693 | ||||||
chr2:174378697
|
T | G | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.484+226A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378697 | ||||||
chr2:174378773
|
T | C | 66 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063others(63): Show | 70 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.484+150A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378773 | ||||||
chr2:174378796
|
T | G | 1 | a0002c0002t0003g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.484+127A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378796 | ||||||
chr2:174379321
|
C | T | 1 | a0004c0003t0001g0011 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.367-281G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379321 | ||||||
chr2:174379394
|
C | T | 1 | a0002c0002t0003g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.367-354G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379394 | ||||||
chr2:174379473
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.367-433A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379473 | ||||||
chr2:174379479
|
C | A | 1 | a0002c0002t0003g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.367-439G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379479 | ||||||
chr2:174379716
|
C | CT | 35 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063others(32): Show | 36 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.366+485dupA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379716 | ||||||
chr2:174379716
|
C | CTT | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG01517.hp2 HG02572.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+484_366+485dup others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379716 | ||||||
chr2:174379716
|
CT | C | 140 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(137): Show | 153 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.366+485delA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379716 | ||||||
chr2:174379716
|
CTTTT | C | 14 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.366+482_366+485del others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379716 | ||||||
chr2:174379739
|
T | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.366+463A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379739 | ||||||
chr2:174379754
|
C | T | 47 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063others(44): Show | 50 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.366+448G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379754 | ||||||
chr2:174379809
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.366+393G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379809 | ||||||
chr2:174379869
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.366+333C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379869 | ||||||
chr2:174380028
|
T | C | 304 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(301): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.366+174A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174380028 | ||||||
chr2:174380344
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.318-94T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 5/9 | chr2 | 174380344 | ||||||
chr2:174380443
|
T | C | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.318-193A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 5/9 | chr2 | 174380443 | ||||||
chr2:174380514
|
A | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(35): Show | 42 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.317+137T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 5/9 | chr2 | 174380514 | ||||||
chr2:174380899
|
TATC | T | 107 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(104): Show | 114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.242-88_242-86delGA others(1): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174380899 | ||||||
chr2:174380980
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.242-166A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174380980 | ||||||
chr2:174380986
|
G | A | 1 | a0001c0001t0002g0016 | 2 | NA18983.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.242-172C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174380986 | ||||||
chr2:174381016
|
T | C | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.242-202A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381016 | ||||||
chr2:174381045
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.242-231A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381045 | ||||||
chr2:174381101
|
A | G | 1 | a0002c0002t0003g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.242-287T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381101 | ||||||
chr2:174381102
|
A | G | 1 | a0002c0002t0003g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.242-288T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381102 | ||||||
chr2:174381330
|
G | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(229): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.241+374C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381330 | ||||||
chr2:174382195
|
T | A | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(114): Show | 124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.168-418A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382195 | ||||||
chr2:174382325
|
G | C | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.168-548C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382325 | ||||||
chr2:174382362
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.168-585C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382362 | ||||||
chr2:174382393
|
C | T | 1 | a0001c0001t0002g0222 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.168-616G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382393 | ||||||
chr2:174382510
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.168-733C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382510 | ||||||
chr2:174382567
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0002g0043others(1): Show | 7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-790T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382567 | ||||||
chr2:174382587
|
C | T | 3 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0201 | 3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168-810G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382587 | ||||||
chr2:174382650
|
T | C | 312 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(309): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.168-873A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382650 | ||||||
chr2:174382794
|
G | C | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.168-1017C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382794 | ||||||
chr2:174382972
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(106): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.168-1195A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382972 | ||||||
chr2:174383038
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.168-1261T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383038 | ||||||
chr2:174383312
|
T | G | 1 | a0001c0001t0002g0083 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.168-1535A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383312 | ||||||
chr2:174383366
|
TAAAAA | T | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 127 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.168-1594_168-1590d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383366 | ||||||
chr2:174383548
|
C | T | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.168-1771G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383548 | ||||||
chr2:174383632
|
A | G | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 127 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.168-1855T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383632 | ||||||
chr2:174383668
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.168-1891G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383668 | ||||||
chr2:174383677
|
A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(176): Show | 191 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.168-1900T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383677 | ||||||
chr2:174383701
|
T | C | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.168-1924A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383701 | ||||||
chr2:174383711
|
C | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG01934.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.168-1934G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383711 | ||||||
chr2:174383719
|
C | CA | 17 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(14): Show | 17 | HG00140.hp1 HG00280.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-1943dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383719 | ||||||
chr2:174383719
|
CA | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(151): Show | 166 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.168-1943delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383719 | ||||||
chr2:174383719
|
CAA | C | 11 | a0001c0001t0001g0242a0001c0001t0002g0240a0001c0001t0002g0241others(8): Show | 11 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.168-1944_168-1943d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383719 | ||||||
chr2:174383835
|
GGCTA | G | 2 | a0001c0001t0002g0015a0001c0001t0002g0174 | 3 | HG02055.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168-2062_168-2059d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383835 | ||||||
chr2:174383849
|
C | CA | 62 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(59): Show | 68 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.168-2073dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383849 | ||||||
chr2:174383849
|
C | CAA | 11 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(8): Show | 11 | HG01109.hp1 HG01192.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.168-2074_168-2073d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383849 | ||||||
chr2:174383849
|
CAAAAA | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0203a0001c0001t0002g0204others(1): Show | 6 | HG01891.hp1 HG02257.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-2077_168-2073d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383849 | ||||||
chr2:174383849
|
CAAAAAA | C | 109 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.168-2078_168-2073d others(8): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383849 | ||||||
chr2:174383894
|
T | G | 2 | a0001c0001t0003g0206a0002c0002t0003g0037 | 2 | HG02647.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.168-2117A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383894 | ||||||
chr2:174384067
|
A | G | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.168-2290T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384067 | ||||||
chr2:174384162
|
G | A | 4 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(1): Show | 4 | HG02015.hp1 HG02040.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-2385C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384162 | ||||||
chr2:174384482
|
C | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0103 | 2 | HG03942.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.168-2705G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384482 | ||||||
chr2:174384542
|
A | C | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.168-2765T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384542 | ||||||
chr2:174384607
|
T | A | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.168-2830A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384607 | ||||||
chr2:174384715
|
C | T | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.168-2938G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384715 | ||||||
chr2:174384741
|
T | A | 135 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063others(132): Show | 150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.167+2944A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384741 | ||||||
chr2:174384952
|
G | A | 4 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225others(1): Show | 4 | HG00642.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+2733C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384952 | ||||||
chr2:174385215
|
C | CA | 8 | a0001c0001t0001g0110a0001c0001t0001g0200a0001c0001t0001g0275others(5): Show | 8 | HG01106.hp2 HG02080.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+2469dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385215 | ||||||
chr2:174385215
|
CA | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.167+2469delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385215 | ||||||
chr2:174385225
|
A | C | 1 | a0001c0001t0002g0003 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.167+2460T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385225 | ||||||
chr2:174385233
|
A | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(151): Show | 165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.167+2452T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385233 | ||||||
chr2:174385437
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(174): Show | 189 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.167+2248G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385437 | ||||||
chr2:174385502
|
G | T | 1 | a0001c0001t0002g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.167+2183C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385502 | ||||||
chr2:174385561
|
T | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(174): Show | 189 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.167+2124A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385561 | ||||||
chr2:174385672
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.167+2013C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385672 | ||||||
chr2:174385722
|
A | T | 2 | a0001c0001t0001g0121a0007c0007t0001g0122 | 2 | HG01952.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.167+1963T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385722 | ||||||
chr2:174385743
|
T | C | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.167+1942A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385743 | ||||||
chr2:174385753
|
A | G | 2 | a0001c0001t0001g0121a0007c0007t0001g0122 | 2 | HG01952.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.167+1932T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385753 | ||||||
chr2:174385810
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0002g0249 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.167+1875A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385810 | ||||||
chr2:174385833
|
C | A | 1 | a0001c0001t0001g0276 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.167+1852G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385833 | ||||||
chr2:174385958
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.167+1727A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385958 | ||||||
chr2:174385973
|
G | C | 1 | a0001c0001t0002g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.167+1712C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385973 | ||||||
chr2:174386011
|
A | T | 1 | a0001c0001t0002g0030 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.167+1674T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386011 | ||||||
chr2:174386147
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.167+1538C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386147 | ||||||
chr2:174386212
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(33): Show | 40 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.167+1473C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386212 | ||||||
chr2:174386254
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.167+1431A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386254 | ||||||
chr2:174386257
|
G | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(175): Show | 190 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.167+1428C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386257 | ||||||
chr2:174386293
|
T | C | 5 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(2): Show | 6 | HG02109.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.167+1392A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386293 | ||||||
chr2:174386328
|
T | G | 1 | a0001c0001t0001g0308 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.167+1357A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386328 | ||||||
chr2:174386418
|
G | A | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.167+1267C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386418 | ||||||
chr2:174386474
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.167+1211C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386474 | ||||||
chr2:174386586
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.167+1099C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386586 | ||||||
chr2:174386707
|
A | C | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.167+978T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386707 | ||||||
chr2:174386892
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.167+793A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386892 | ||||||
chr2:174387099
|
G | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(175): Show | 190 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.167+586C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387099 | ||||||
chr2:174387114
|
T | C | 1 | a0001c0001t0001g0309 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.167+571A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387114 | ||||||
chr2:174387310
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.167+375G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387310 | ||||||
chr2:174387320
|
A | T | 5 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0234others(2): Show | 5 | HG00673.hp2 NA18945.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.167+365T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387320 | ||||||
chr2:174387522
|
T | C | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.167+163A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387522 | ||||||
chr2:174387803
|
A | G | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.73-24T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174387803 | ||||||
chr2:174387944
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.73-165C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174387944 | ||||||
chr2:174388157
|
C | T | 1 | a0002c0002t0003g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-378G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388157 | ||||||
chr2:174388263
|
A | C | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.73-484T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388263 | ||||||
chr2:174388322
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.73-543G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388322 | ||||||
chr2:174388525
|
G | T | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.73-746C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388525 | ||||||
chr2:174388544
|
T | A | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.73-765A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388544 | ||||||
chr2:174388700
|
C | A | 4 | a0001c0001t0002g0228a0001c0001t0002g0230a0001c0001t0006g0229others(1): Show | 4 | HG00733.hp1 HG00741.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-921G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388700 | ||||||
chr2:174388703
|
G | A | 2 | a0001c0001t0001g0310a0006c0006t0001g0311 | 2 | NA19004.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.73-924C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388703 | ||||||
chr2:174388766
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.73-987G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388766 | ||||||
chr2:174388790
|
C | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0002g0043others(1): Show | 7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-1011G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388790 | ||||||
chr2:174388829
|
G | A | 2 | a0001c0001t0002g0312a0001c0001t0002g0313 | 2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.73-1050C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388829 | ||||||
chr2:174388849
|
T | C | 5 | a0001c0001t0002g0006a0001c0001t0002g0171a0001c0001t0002g0203others(2): Show | 7 | HG01891.hp1 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1070A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388849 | ||||||
chr2:174388998
|
A | G | 1 | a0001c0001t0002g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.73-1219T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388998 | ||||||
chr2:174389096
|
A | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(225): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.73-1317T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389096 | ||||||
chr2:174389137
|
G | A | 5 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(2): Show | 6 | HG02109.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-1358C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389137 | ||||||
chr2:174389255
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-1476T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389255 | ||||||
chr2:174389299
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(227): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.73-1520A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389299 | ||||||
chr2:174389354
|
G | C | 1 | a0001c0001t0007g0169 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.73-1575C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389354 | ||||||
chr2:174389473
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(32): Show | 39 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.73-1694A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389473 | ||||||
chr2:174389556
|
G | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(229): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.73-1777C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389556 | ||||||
chr2:174389645
|
C | T | 3 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062 | 3 | HG02615.hp2 HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.73-1866G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389645 | ||||||
chr2:174389690
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73-1911C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389690 | ||||||
chr2:174389700
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.73-1921G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389700 | ||||||
chr2:174389714
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0314 | 3 | NA18954.hp1 NA18991.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.73-1935C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389714 | ||||||
chr2:174389783
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(32): Show | 39 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.73-2004A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389783 | ||||||
chr2:174389792
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.73-2013C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389792 | ||||||
chr2:174389844
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.73-2065C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389844 | ||||||
chr2:174389867
|
T | G | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 127 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.73-2088A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389867 | ||||||
chr2:174390031
|
T | C | 64 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063others(61): Show | 68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.73-2252A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390031 | ||||||
chr2:174390087
|
C | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(229): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.73-2308G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390087 | ||||||
chr2:174390145
|
T | C | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.73-2366A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390145 | ||||||
chr2:174390225
|
G | A | 1 | a0001c0001t0003g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.73-2446C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390225 | ||||||
chr2:174390239
|
A | G | 13 | a0001c0001t0002g0009a0001c0001t0002g0051a0001c0001t0002g0053others(10): Show | 15 | HG00735.hp1 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.73-2460T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390239 | ||||||
chr2:174390290
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.73-2511C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390290 | ||||||
chr2:174390358
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.73-2579C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390358 | ||||||
chr2:174390470
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.73-2691T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390470 | ||||||
chr2:174390690
|
G | GT | 72 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063others(69): Show | 76 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.73-2912dupA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390690 | ||||||
chr2:174390731
|
G | A | 6 | a0001c0001t0002g0036a0001c0001t0002g0104a0001c0001t0002g0113others(3): Show | 6 | HG02257.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-2952C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390731 | ||||||
chr2:174390756
|
G | A | 1 | a0001c0001t0008g0022 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.73-2977C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390756 | ||||||
chr2:174390959
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.73-3180T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390959 | ||||||
chr2:174391040
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.73-3261T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391040 | ||||||
chr2:174391213
|
T | C | 25 | a0001c0001t0001g0019a0001c0001t0001g0254a0001c0001t0001g0255others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.73-3434A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391213 | ||||||
chr2:174391255
|
G | A | 25 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(22): Show | 29 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.73-3476C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391255 | ||||||
chr2:174391734
|
A | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02080.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.72+3817T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391734 | ||||||
chr2:174391791
|
G | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.72+3760C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391791 | ||||||
chr2:174391882
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0002g0043others(1): Show | 7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+3669A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391882 | ||||||
chr2:174391944
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.72+3607G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391944 | ||||||
chr2:174392059
|
G | A | 5 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0234others(2): Show | 5 | HG00673.hp2 NA18945.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+3492C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392059 | ||||||
chr2:174392142
|
C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02738.hp1 NA18945.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+3409G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392142 | ||||||
chr2:174392401
|
T | C | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG03704.hp2 HG03834.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+3150A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392401 | ||||||
chr2:174392563
|
G | C | 3 | a0002c0002t0003g0017a0002c0002t0003g0237a0002c0002t0003g0238 | 4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+2988C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392563 | ||||||
chr2:174392611
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.72+2940C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392611 | ||||||
chr2:174392791
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.72+2760A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392791 | ||||||
chr2:174392915
|
G | A | 4 | a0001c0001t0002g0036a0001c0001t0005g0111a0001c0001t0005g0278others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+2636C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392915 | ||||||
chr2:174392948
|
G | T | 1 | a0001c0001t0002g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.72+2603C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392948 | ||||||
chr2:174393206
|
G | C | 10 | a0001c0001t0001g0242a0001c0001t0002g0240a0001c0001t0002g0241others(7): Show | 10 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+2345C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393206 | ||||||
chr2:174393212
|
T | G | 5 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(2): Show | 6 | HG02109.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+2339A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393212 | ||||||
chr2:174393405
|
C | A | 3 | a0001c0001t0005g0111a0001c0001t0005g0278a0001c0001t0005g0279 | 3 | HG02896.hp1 HG02897.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.72+2146G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393405 | ||||||
chr2:174393534
|
TG | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0002g0043others(1): Show | 7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+2016delC | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393534 | ||||||
chr2:174393556
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.72+1995A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393556 | ||||||
chr2:174393691
|
A | T | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.72+1860T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393691 | ||||||
chr2:174394166
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0039 | 3 | HG02965.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.72+1385T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394166 | ||||||
chr2:174394198
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.72+1353A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394198 | ||||||
chr2:174394337
|
A | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(106): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.72+1214T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394337 | ||||||
chr2:174394375
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.72+1176T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394375 | ||||||
chr2:174394479
|
C | A | 1 | a0001c0001t0008g0022 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.72+1072G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394479 | ||||||
chr2:174394688
|
G | C | 25 | a0001c0001t0001g0019a0001c0001t0001g0254a0001c0001t0001g0255others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.72+863C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394688 | ||||||
chr2:174394696
|
G | A | 2 | a0001c0001t0005g0278a0001c0001t0005g0279 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.72+855C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394696 | ||||||
chr2:174394995
|
C | T | 1 | a0002c0002t0003g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.72+556G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394995 | ||||||
chr2:174395074
|
A | G | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.72+477T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395074 | ||||||
chr2:174395163
|
A | C | 1 | a0001c0001t0002g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+388T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395163 | ||||||
chr2:174395282
|
T | C | 39 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0035others(36): Show | 41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.72+269A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395282 | ||||||
chr2:174395311
|
T | C | 2 | a0002c0002t0003g0316a0002c0002t0003g0317 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.72+240A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395311 | ||||||
chr2:174395380
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.72+171G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395380 | ||||||
chr2:174395486
|
C | A | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.72+65G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395486 | ||||||
chr2:174395496
|
C | T | 6 | a0001c0001t0002g0007a0001c0001t0002g0030a0001c0001t0002g0031others(3): Show | 7 | NA18954.hp2 NA18963.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+55G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395496 |