geneid | 151195 |
---|---|
ensemblid | ENSG00000163249.13 |
hgncid | 26868 |
symbol | CCNYL1 |
name | cyclin Y like 1 |
refseq_nuc | NM_001330218.2 |
refseq_prot | NP_001317147.1 |
ensembl_nuc | ENST00000295414.8 |
ensembl_prot | ENSP00000295414.3 |
mane_status | MANE Select |
chr | chr2 |
start | 207711640 |
end | 207756174 |
strand | + |
ver | v1.2 |
region | chr2:207711640-207756174 |
region5000 | chr2:207706640-207761174 |
regionname0 | CCNYL1_chr2_207711640_207756174 |
regionname5000 | CCNYL1_chr2_207706640_207761174 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 359 | 352 | 88 | 64 | 146 | 14 | 38 | 105 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0002 | 0/0 | 359 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1080 | 345 | 85 | 63 | 146 | 14 | 35 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
c0002 | 0/0 | 1080 | 4 | 0 | 1 | 0 | 0 | 3 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
c0003 | 0/0 | 1080 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
c0004 | 0/0 | 1080 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
c0005 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2735 | 207 | 43 | 33 | 101 | 7 | 22 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0002 | 1/0 | 2734 | 109 | 17 | 26 | 45 | 6 | 14 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0003 | 0/0 | 2734 | 6 | 6 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0004 | 0/0 | 2735 | 5 | 0 | 3 | 1 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0005 | 0/0 | 2734 | 4 | 4 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0006 | 0/0 | 2735 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0007 | 0/0 | 2735 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0008 | 0/0 | 2735 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0009 | 0/0 | 2735 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0010 | 0/0 | 2735 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0011 | 0/0 | 2735 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0012 | 0/0 | 2735 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0013 | 0/0 | 2735 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0014 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0015 | 0/0 | 2734 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0016 | 0/0 | 2734 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0017 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0018 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0019 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0020 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0021 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
t0022 | 0/0 | 2735 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1080 | 345 | 85 | 63 | 146 | 14 | 35 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0002 | 0/0 | 1080 | 4 | 0 | 1 | 0 | 0 | 3 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0004 | 0/0 | 1080 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0005 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0002c0003 | 0/0 | 1080 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3814 | 200 | 42 | 32 | 99 | 7 | 19 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0002 | 1/0 | 3813 | 107 | 15 | 26 | 45 | 6 | 14 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0003 | 0/0 | 3813 | 6 | 6 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0004 | 0/0 | 3814 | 5 | 0 | 3 | 1 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0005 | 0/0 | 3813 | 4 | 4 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0006 | 0/0 | 3814 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0007 | 0/0 | 3814 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0008 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0009 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0010 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0011 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0012 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0013 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0014 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0015 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0016 | 0/0 | 3813 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0017 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0018 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0019 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0020 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0021 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0001t0022 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0002t0001 | 0/0 | 3814 | 4 | 0 | 1 | 0 | 0 | 3 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0004t0002 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0001c0005t0001 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
a0002c0003t0001 | 0/0 | 3814 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | copy fasta | chr2 | 207706640 | 207761174 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0010g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0013g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0015g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0016g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0017g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0018g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0019g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0020g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0021g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0001t0022g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0004t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0001c0005t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | GBR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00323 | hp1 | a0001 | c0001 | t0015 | g0121 | EUR | FIN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | FIN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00408 | hp2 | a0001 | c0001 | t0012 | g0175 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0222 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00741 | hp1 | a0001 | c0001 | t0016 | g0153 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0320 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0282 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0265 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01884 | hp2 | a0001 | c0001 | t0020 | g0174 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0149 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02074 | hp1 | a0002 | c0003 | t0001 | g0070 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0304 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | CDX | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0305 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02273 | hp1 | a0001 | c0001 | t0010 | g0221 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0142 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02630 | hp1 | a0001 | c0004 | t0002 | g0005 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02630 | hp2 | a0001 | c0001 | t0014 | g0019 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0204 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0327 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0328 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02886 | hp2 | a0001 | c0004 | t0002 | g0005 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02896 | hp1 | a0001 | c0001 | t0019 | g0303 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02970 | hp2 | a0001 | c0005 | t0001 | g0326 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0083 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0322 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0141 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0038 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03225 | hp2 | a0001 | c0001 | t0022 | g0004 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03486 | hp2 | a0001 | c0001 | t0017 | g0137 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | ESN | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0321 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG04115 | hp2 | a0001 | c0001 | t0013 | g0066 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | STU | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CHB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18984 | hp1 | a0002 | c0003 | t0001 | g0113 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19030 | hp1 | a0001 | c0001 | t0021 | g0128 | AFR | LWK | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | LWK | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | LWK | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | YRI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ASW | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ASW | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0247 | EUR | TSI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0314 | EUR | TSI | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0323 | SAS | GIH | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | CLM | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0039 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | USA | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | USA | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20300 | hp1 | a0001 | c0001 | t0018 | g0138 | AFR | USA | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | USA | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0264 | REF | REF | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0246 | REF | REF | CCNYL1_chr2_207706640_207761174 | CCNYL1 | chr2 | 207706640 | 207761174 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:207711991
|
T | G | 1 | a0002 | 2 | HG02074.hp1 NA18984.hp1 |
missense_variant | MODERATE | c.95T>G | p.Ile32Ser | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/10 | 352/3813 | 95/1080 | 32/359 | chr2 | 207711991 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:207712007
|
C | T | 1 | a0001c0002 | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
synonymous_variant | LOW | c.111C>T | p.Ser37Ser | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/10 | 368/3813 | 111/1080 | 37/359 | chr2 | 207712007 | ||
chr2:207742285
|
T | C | 1 | a0001c0005 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.582T>C | p.Phe194Phe | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/10 | 839/3813 | 582/1080 | 194/359 | chr2 | 207742285 | ||
chr2:207747073
|
T | C | 1 | a0001c0004 | 2 | HG02630.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.666T>C | p.Tyr222Tyr | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/10 | 923/3813 | 666/1080 | 222/359 | chr2 | 207747073 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:207753755
|
A | C | 1 | a0001c0001t0022 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 57 | chr2 | 207753755 | |||||
chr2:207753878
|
A | G | 1 | a0001c0001t0021 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*180A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 180 | chr2 | 207753878 | |||||
chr2:207753941
|
G | A | 1 | a0001c0001t0008 | 2 | HG02818.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*243G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 243 | chr2 | 207753941 | |||||
chr2:207754054
|
A | G | 1 | a0001c0001t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*356A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 356 | chr2 | 207754054 | |||||
chr2:207754112
|
C | G | 2 | a0001c0001t0007a0001c0001t0019 | 4 | HG02055.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 414 | chr2 | 207754112 | |||||
chr2:207754221
|
T | TA | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(11): Show | 227 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*524dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 525 | INFO_REALIGN_3_PRIME | chr2 | 207754221 | ||||
chr2:207754443
|
G | C | 1 | a0001c0001t0014 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 745 | chr2 | 207754443 | |||||
chr2:207754514
|
G | A | 1 | a0001c0001t0010 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*816G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 816 | chr2 | 207754514 | |||||
chr2:207754672
|
A | C | 1 | a0001c0001t0005 | 4 | HG02145.hp2 HG02280.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*974A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 974 | chr2 | 207754672 | |||||
chr2:207754916
|
G | A | 1 | a0001c0001t0004 | 5 | HG00738.hp1 HG01361.hp2 HG01981.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1218G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1218 | chr2 | 207754916 | |||||
chr2:207754988
|
G | A | 1 | a0001c0001t0015 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1290G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1290 | chr2 | 207754988 | |||||
chr2:207755056
|
C | G | 1 | a0001c0001t0013 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1358C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1358 | chr2 | 207755056 | |||||
chr2:207755350
|
A | G | 1 | a0001c0001t0018 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1652A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1652 | chr2 | 207755350 | |||||
chr2:207755358
|
C | T | 1 | a0001c0001t0006 | 3 | HG02976.hp1 HG03041.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1660C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 1660 | chr2 | 207755358 | |||||
chr2:207755854
|
C | G | 1 | a0001c0001t0012 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2156C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2156 | chr2 | 207755854 | |||||
chr2:207755892
|
A | C | 1 | a0001c0001t0017 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2194A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2194 | chr2 | 207755892 | |||||
chr2:207755923
|
A | G | 1 | a0001c0001t0011 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2225A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2225 | chr2 | 207755923 | |||||
chr2:207755932
|
A | G | 3 | a0001c0001t0003a0001c0001t0005a0001c0001t0019 | 11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2234A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2234 | chr2 | 207755932 | |||||
chr2:207756013
|
T | A | 1 | a0001c0001t0017 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2315T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2315 | chr2 | 207756013 | |||||
chr2:207756099
|
A | G | 1 | a0001c0001t0016 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2401A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2401 | chr2 | 207756099 | |||||
chr2:207756102
|
G | T | 1 | a0001c0001t0009 | 2 | HG02486.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2404G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 10/10 | 2404 | chr2 | 207756102 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:207712294
|
A | G | 1 | a0001c0001t0001g0330 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.220+178A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712294 | ||||||
chr2:207712407
|
A | G | 1 | a0001c0001t0002g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220+291A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712407 | ||||||
chr2:207712440
|
G | A | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220+324G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712440 | ||||||
chr2:207712670
|
A | G | 3 | a0001c0001t0008g0327a0001c0001t0008g0328a0001c0005t0001g0326 | 3 | HG02818.hp2 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.220+554A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712670 | ||||||
chr2:207712834
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.220+718C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712834 | ||||||
chr2:207712859
|
A | G | 1 | a0001c0001t0001g0324 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.220+743A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712859 | ||||||
chr2:207712889
|
C | T | 2 | a0001c0001t0008g0327a0001c0001t0008g0328 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.220+773C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712889 | ||||||
chr2:207712932
|
C | T | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+816C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207712932 | ||||||
chr2:207713114
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+998G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713114 | ||||||
chr2:207713172
|
G | A | 1 | a0001c0004t0002g0005 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.220+1056G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713172 | ||||||
chr2:207713306
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.220+1190G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713306 | ||||||
chr2:207713310
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.220+1194T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713310 | ||||||
chr2:207713687
|
A | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.220+1571A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713687 | ||||||
chr2:207713745
|
C | A | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220+1629C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713745 | ||||||
chr2:207713765
|
T | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+1649T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713765 | ||||||
chr2:207713787
|
A | T | 1 | a0001c0001t0001g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.220+1671A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713787 | ||||||
chr2:207713803
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.220+1687T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713803 | ||||||
chr2:207713811
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.220+1695T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713811 | ||||||
chr2:207713996
|
A | G | 1 | a0001c0001t0002g0318 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.220+1880A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207713996 | ||||||
chr2:207713996
|
ATACTTTC others(3): Show |
A | 1 | a0001c0001t0002g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220+1884_220+1893d others(12): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207713996 | |||||
chr2:207714058
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+1942G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207714058 | ||||||
chr2:207714312
|
C | CT | 14 | a0001c0001t0001g0117a0001c0001t0001g0306a0001c0001t0001g0307others(11): Show | 15 | HG00438.hp2 HG01891.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.220+2222dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | |||||
chr2:207714312
|
CT | C | 53 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0025others(50): Show | 54 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.220+2222delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | |||||
chr2:207714312
|
CTT | C | 16 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0114others(13): Show | 16 | HG00323.hp1 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+2221_220+2222d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | |||||
chr2:207714312
|
CTTT | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(73): Show | 84 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.220+2220_220+2222d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | |||||
chr2:207714312
|
CTTTT | C | 18 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(15): Show | 18 | HG01069.hp1 HG02015.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.220+2219_220+2222d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | |||||
chr2:207714312
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0027 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.220+2212_220+2222d others(13): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714312 | |||||
chr2:207714442
|
G | A | 1 | a0001c0001t0021g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220+2326G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207714442 | ||||||
chr2:207714632
|
A | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0009g0038others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+2516A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207714632 | ||||||
chr2:207714667
|
G | GATGATGA others(3): Show |
1 | a0001c0001t0020g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220+2553_220+2562d others(12): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207714667 | |||||
chr2:207714836
|
G | A | 1 | a0001c0001t0012g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.220+2720G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207714836 | ||||||
chr2:207715028
|
G | T | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220+2912G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715028 | ||||||
chr2:207715045
|
G | A | 1 | a0001c0001t0020g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220+2929G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715045 | ||||||
chr2:207715096
|
C | T | 10 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(7): Show | 11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+2980C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715096 | ||||||
chr2:207715097
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | NA19064.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.220+2981G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715097 | ||||||
chr2:207715268
|
AAAAC | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 201 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.220+3168_220+3171d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715268 | |||||
chr2:207715339
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220+3223C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715339 | ||||||
chr2:207715379
|
C | CT | 108 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(105): Show | 112 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.220+3285dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | |||||
chr2:207715379
|
C | CTT | 101 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0045others(98): Show | 111 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.220+3284_220+3285d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | |||||
chr2:207715379
|
C | CTTT | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(87): Show | 98 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.220+3283_220+3285d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | |||||
chr2:207715379
|
C | CTTTT | 10 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 10 | HG00597.hp2 HG02027.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+3282_220+3285d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | |||||
chr2:207715379
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.220+3274_220+3285d others(14): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715379 | |||||
chr2:207715436
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.220+3320A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715436 | ||||||
chr2:207715473
|
G | A | 3 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252 | 3 | NA18944.hp2 NA19005.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.220+3357G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715473 | ||||||
chr2:207715511
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+3395T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715511 | ||||||
chr2:207715624
|
G | T | 6 | a0001c0001t0002g0169a0001c0001t0002g0291a0001c0001t0002g0292others(3): Show | 6 | HG02015.hp1 HG03831.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+3508G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715624 | ||||||
chr2:207715676
|
G | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+3560G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715676 | ||||||
chr2:207715679
|
C | CT | 10 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(7): Show | 11 | HG01192.hp2 HG01261.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+3577dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715679 | |||||
chr2:207715679
|
CT | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 110 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.220+3577delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207715679 | |||||
chr2:207715696
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG00544.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.220+3580G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715696 | ||||||
chr2:207715745
|
C | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(95): Show | 101 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.220+3629C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715745 | ||||||
chr2:207715843
|
A | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0101others(1): Show | 4 | HG02735.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+3727A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207715843 | ||||||
chr2:207716106
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.220+3990A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716106 | ||||||
chr2:207716312
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.220+4196C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716312 | ||||||
chr2:207716339
|
C | CT | 9 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0096others(6): Show | 9 | HG00438.hp1 HG02486.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+4239dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207716339 | |||||
chr2:207716339
|
CT | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 106 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.220+4239delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207716339 | |||||
chr2:207716459
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.220+4343A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716459 | ||||||
chr2:207716574
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.220+4458C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716574 | ||||||
chr2:207716584
|
G | A | 1 | a0001c0001t0002g0010 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.220+4468G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716584 | ||||||
chr2:207716656
|
T | C | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.220+4540T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716656 | ||||||
chr2:207716662
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.220+4546A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716662 | ||||||
chr2:207716715
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(91): Show | 102 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.220+4599C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716715 | ||||||
chr2:207716739
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.220+4623G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716739 | ||||||
chr2:207716848
|
G | A | 1 | a0001c0004t0002g0005 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.220+4732G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716848 | ||||||
chr2:207716881
|
G | C | 1 | a0001c0001t0020g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220+4765G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716881 | ||||||
chr2:207716912
|
A | G | 6 | a0001c0001t0002g0119a0001c0001t0002g0139a0001c0001t0002g0140others(3): Show | 6 | HG01243.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+4796A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716912 | ||||||
chr2:207716926
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.220+4810G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207716926 | ||||||
chr2:207717108
|
C | CA | 32 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0053others(29): Show | 33 | HG00438.hp1 HG00597.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.220+5011dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207717108 | |||||
chr2:207717254
|
T | C | 3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0149 | 3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.220+5138T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717254 | ||||||
chr2:207717428
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 110 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.220+5312G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717428 | ||||||
chr2:207717435
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.220+5319G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717435 | ||||||
chr2:207717492
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 110 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.220+5376G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717492 | ||||||
chr2:207717625
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.220+5509G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717625 | ||||||
chr2:207717773
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG01169.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.220+5657G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717773 | ||||||
chr2:207717799
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.220+5683A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717799 | ||||||
chr2:207717906
|
C | CT | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.220+5805dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207717906 | |||||
chr2:207717943
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG00741.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+5827C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717943 | ||||||
chr2:207717946
|
C | T | 2 | a0001c0001t0002g0287a0001c0001t0002g0288 | 2 | NA18957.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.220+5830C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207717946 | ||||||
chr2:207718007
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.220+5891C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718007 | ||||||
chr2:207718008
|
G | A | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220+5892G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718008 | ||||||
chr2:207718017
|
G | A | 1 | a0001c0004t0002g0005 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.220+5901G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718017 | ||||||
chr2:207718088
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.220+5972T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718088 | ||||||
chr2:207718127
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(4): Show | 10 | HG02145.hp1 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+6011A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718127 | ||||||
chr2:207718161
|
C | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0126a0001c0001t0002g0148others(3): Show | 7 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+6045C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718161 | ||||||
chr2:207718200
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.220+6084G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718200 | ||||||
chr2:207718251
|
A | G | 2 | a0001c0001t0002g0119a0001c0001t0002g0329 | 2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.220+6135A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718251 | ||||||
chr2:207718323
|
A | G | 1 | a0001c0004t0002g0005 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.220+6207A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718323 | ||||||
chr2:207718349
|
A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.220+6233A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718349 | ||||||
chr2:207718356
|
A | G | 3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0149 | 3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.220+6240A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718356 | ||||||
chr2:207718429
|
G | C | 6 | a0001c0001t0002g0010a0001c0001t0002g0126a0001c0001t0002g0148others(3): Show | 7 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+6313G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718429 | ||||||
chr2:207718468
|
A | G | 2 | a0001c0001t0002g0125a0001c0001t0002g0290 | 2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.221-6332A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718468 | ||||||
chr2:207718503
|
C | CA | 6 | a0001c0001t0001g0117a0001c0001t0001g0248a0001c0001t0002g0289others(3): Show | 6 | HG01981.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-6284dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207718503 | |||||
chr2:207718704
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0248 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.221-6096G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718704 | ||||||
chr2:207718805
|
A | G | 1 | a0001c0001t0002g0286 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.221-5995A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718805 | ||||||
chr2:207718831
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.221-5969A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718831 | ||||||
chr2:207718906
|
A | G | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.221-5894A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207718906 | ||||||
chr2:207718975
|
T | TA | 9 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 9 | HG00733.hp2 HG00741.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-5811dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207718975 | |||||
chr2:207718975
|
TA | T | 8 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 8 | HG02015.hp2 HG02486.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-5811delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207718975 | |||||
chr2:207719028
|
G | T | 3 | a0001c0001t0008g0327a0001c0001t0008g0328a0001c0005t0001g0326 | 3 | HG02818.hp2 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.221-5772G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719028 | ||||||
chr2:207719049
|
CAAG | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG00438.hp1 NA18957.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-5750_221-5748d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719049 | ||||||
chr2:207719302
|
C | CT | 275 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.221-5482dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207719302 | |||||
chr2:207719302
|
C | CTT | 13 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(10): Show | 17 | HG01123.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.221-5483_221-5482d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207719302 | |||||
chr2:207719592
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.221-5208C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719592 | ||||||
chr2:207719597
|
G | A | 1 | a0001c0001t0002g0291 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.221-5203G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719597 | ||||||
chr2:207719749
|
G | T | 1 | a0001c0001t0002g0285 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.221-5051G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719749 | ||||||
chr2:207719775
|
C | T | 2 | a0001c0001t0002g0118a0001c0001t0002g0247 | 2 | HG03453.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.221-5025C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207719775 | ||||||
chr2:207720102
|
C | T | 4 | a0001c0001t0002g0144a0001c0001t0002g0284a0001c0001t0002g0295others(1): Show | 4 | NA18939.hp1 NA18970.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-4698C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720102 | ||||||
chr2:207720107
|
C | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 111 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.221-4693C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720107 | ||||||
chr2:207720129
|
A | G | 1 | a0001c0001t0001g0009 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.221-4671A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720129 | ||||||
chr2:207720171
|
G | C | 8 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0199others(5): Show | 8 | HG00438.hp2 HG00621.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-4629G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720171 | ||||||
chr2:207720187
|
C | CA | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 204 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.221-4591dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207720187 | |||||
chr2:207720187
|
C | CAA | 43 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0040others(40): Show | 43 | HG00438.hp1 HG00544.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.221-4592_221-4591d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207720187 | |||||
chr2:207720211
|
G | C | 2 | a0001c0001t0002g0014a0001c0001t0002g0155 | 3 | HG00735.hp1 HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.221-4589G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720211 | ||||||
chr2:207720288
|
T | A | 3 | a0001c0001t0005g0018a0001c0001t0005g0298a0001c0001t0005g0304 | 4 | HG02145.hp2 HG02280.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-4512T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720288 | ||||||
chr2:207720298
|
C | G | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.221-4502C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720298 | ||||||
chr2:207720393
|
C | CT | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0088others(5): Show | 8 | HG00597.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-4392dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207720393 | |||||
chr2:207720408
|
T | C | 1 | a0001c0001t0002g0253 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.221-4392T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720408 | ||||||
chr2:207720417
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.221-4383T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720417 | ||||||
chr2:207720558
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0235 | 2 | NA18944.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.221-4242G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720558 | ||||||
chr2:207720841
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.221-3959C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720841 | ||||||
chr2:207720892
|
C | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-3908C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720892 | ||||||
chr2:207720901
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.221-3899G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720901 | ||||||
chr2:207720961
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0009g0038others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-3839G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720961 | ||||||
chr2:207720978
|
G | GT | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 111 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.221-3822_221-3821i others(3): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720978 | ||||||
chr2:207720997
|
T | G | 1 | a0001c0001t0002g0156 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.221-3803T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207720997 | ||||||
chr2:207721184
|
A | C | 1 | a0001c0001t0001g0033 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.221-3616A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721184 | ||||||
chr2:207721365
|
C | T | 1 | a0001c0001t0020g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.221-3435C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721365 | ||||||
chr2:207721734
|
G | GT | 10 | a0001c0001t0001g0185a0001c0001t0001g0194a0001c0001t0001g0197others(7): Show | 10 | HG01261.hp2 HG01515.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-3052dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207721734 | |||||
chr2:207721734
|
GT | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(104): Show | 116 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.221-3052delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207721734 | |||||
chr2:207721737
|
T | G | 1 | a0001c0001t0002g0157 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.221-3063T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721737 | ||||||
chr2:207721911
|
T | C | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-2889T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721911 | ||||||
chr2:207721912
|
T | C | 3 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0313 | 3 | NA18966.hp1 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.221-2888T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721912 | ||||||
chr2:207721916
|
T | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0190others(2): Show | 5 | HG00544.hp1 NA18942.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-2884T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721916 | ||||||
chr2:207721930
|
C | G | 1 | a0001c0001t0001g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.221-2870C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207721930 | ||||||
chr2:207722073
|
A | AT | 97 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(94): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.221-2710dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207722073 | |||||
chr2:207722073
|
A | ATT | 9 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0184others(6): Show | 9 | HG00544.hp1 HG01255.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-2711_221-2710d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207722073 | |||||
chr2:207722073
|
AT | A | 9 | a0001c0001t0001g0049a0001c0001t0001g0093a0001c0001t0001g0097others(6): Show | 9 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-2710delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207722073 | |||||
chr2:207722179
|
T | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-2621T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722179 | ||||||
chr2:207722198
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.221-2602G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722198 | ||||||
chr2:207722203
|
G | T | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.221-2597G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722203 | ||||||
chr2:207722221
|
C | T | 1 | a0001c0001t0017g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.221-2579C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722221 | ||||||
chr2:207722229
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.221-2571C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722229 | ||||||
chr2:207722402
|
A | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-2398A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722402 | ||||||
chr2:207722457
|
C | T | 2 | a0001c0001t0020g0174a0001c0001t0021g0128 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.221-2343C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722457 | ||||||
chr2:207722581
|
T | G | 1 | a0001c0001t0021g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.221-2219T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722581 | ||||||
chr2:207722848
|
A | T | 1 | a0001c0004t0002g0005 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.221-1952A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722848 | ||||||
chr2:207722955
|
C | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-1845C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207722955 | ||||||
chr2:207722961
|
G | GA | 6 | a0001c0001t0001g0097a0001c0001t0001g0170a0001c0001t0001g0239others(3): Show | 6 | HG02818.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-1826dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207722961 | |||||
chr2:207723251
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0233 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.221-1549A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723251 | ||||||
chr2:207723330
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-1470C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723330 | ||||||
chr2:207723364
|
C | G | 1 | a0001c0001t0002g0261 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.221-1436C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723364 | ||||||
chr2:207723492
|
A | G | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-1308A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723492 | ||||||
chr2:207723695
|
G | A | 1 | a0001c0005t0001g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.221-1105G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723695 | ||||||
chr2:207723829
|
C | T | 1 | a0001c0001t0021g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.221-971C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723829 | ||||||
chr2:207723874
|
C | CA | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(106): Show | 117 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.221-905dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207723874 | |||||
chr2:207723874
|
C | CAA | 8 | a0001c0001t0001g0067a0001c0001t0001g0088a0001c0001t0001g0096others(5): Show | 8 | HG00438.hp1 HG00597.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-906_221-905dup others(2): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 207723874 | |||||
chr2:207723978
|
T | G | 1 | a0001c0001t0009g0038 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.221-822T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207723978 | ||||||
chr2:207724273
|
C | A | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.221-527C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724273 | ||||||
chr2:207724379
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.221-421A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724379 | ||||||
chr2:207724469
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.221-331T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724469 | ||||||
chr2:207724496
|
A | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | NA19005.hp1 NA19068.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.221-304A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724496 | ||||||
chr2:207724611
|
G | A | 1 | a0001c0001t0013g0066 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.221-189G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724611 | ||||||
chr2:207724679
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.221-121A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724679 | ||||||
chr2:207724778
|
T | C | 10 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(7): Show | 11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-22T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 1/9 | chr2 | 207724778 | ||||||
chr2:207724926
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0194 | 2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.295+52A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207724926 | ||||||
chr2:207725126
|
A | AT | 126 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0088others(123): Show | 138 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.295+269dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 207725126 | |||||
chr2:207725126
|
A | ATT | 101 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.295+268_295+269dup others(2): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 207725126 | |||||
chr2:207725183
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.295+309A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725183 | ||||||
chr2:207725228
|
G | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.295+354G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725228 | ||||||
chr2:207725232
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.295+358T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725232 | ||||||
chr2:207725269
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0022g0004 | 3 | HG03225.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.295+395G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725269 | ||||||
chr2:207725600
|
A | G | 1 | a0001c0001t0019g0303 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.295+726A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725600 | ||||||
chr2:207725737
|
A | G | 10 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(7): Show | 11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+863A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725737 | ||||||
chr2:207725815
|
A | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.295+941A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725815 | ||||||
chr2:207725825
|
T | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.295+951T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725825 | ||||||
chr2:207725960
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.296-882A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207725960 | ||||||
chr2:207726144
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.296-698G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726144 | ||||||
chr2:207726203
|
C | A | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-639C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726203 | ||||||
chr2:207726358
|
C | G | 2 | a0001c0001t0007g0142a0001c0001t0007g0149 | 2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.296-484C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726358 | ||||||
chr2:207726365
|
A | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0232 | 2 | NA18988.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.296-477A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726365 | ||||||
chr2:207726537
|
C | A | 1 | a0001c0001t0001g0009 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.296-305C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726537 | ||||||
chr2:207726554
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.296-288T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726554 | ||||||
chr2:207726726
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.296-116T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726726 | ||||||
chr2:207726799
|
G | A | 7 | a0001c0001t0001g0131a0001c0001t0001g0183a0001c0001t0001g0203others(4): Show | 7 | HG01070.hp2 HG01081.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-43G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 2/9 | chr2 | 207726799 | ||||||
chr2:207726978
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(97): Show | 108 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.330+102A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207726978 | ||||||
chr2:207727042
|
G | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.330+166G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727042 | ||||||
chr2:207727063
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.330+187A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727063 | ||||||
chr2:207727322
|
A | T | 1 | a0001c0001t0001g0051 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.330+446A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727322 | ||||||
chr2:207727365
|
C | T | 1 | a0001c0001t0002g0279 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.330+489C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727365 | ||||||
chr2:207727388
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.330+512G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727388 | ||||||
chr2:207727439
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.330+563C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727439 | ||||||
chr2:207727465
|
C | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG00741.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+589C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727465 | ||||||
chr2:207727533
|
T | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.330+657T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727533 | ||||||
chr2:207727558
|
A | G | 1 | a0001c0001t0002g0247 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.330+682A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727558 | ||||||
chr2:207727706
|
TC | T | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+832delC | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207727706 | |||||
chr2:207727880
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.330+1004A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207727880 | ||||||
chr2:207727952
|
TTCTC | T | 3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0149 | 3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.330+1086_330+1089d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207727952 | |||||
chr2:207727964
|
CT | C | 16 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0036others(13): Show | 16 | HG01070.hp1 HG01169.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.330+1104delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207727964 | |||||
chr2:207728049
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.330+1173T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728049 | ||||||
chr2:207728183
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.330+1307C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728183 | ||||||
chr2:207728206
|
T | C | 1 | a0001c0001t0001g0011 | 2 | HG02074.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.330+1330T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728206 | ||||||
chr2:207728261
|
CT | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(88): Show | 99 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.330+1400delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207728261 | |||||
chr2:207728273
|
T | C | 2 | a0001c0001t0002g0119a0001c0001t0002g0329 | 2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.330+1397T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728273 | ||||||
chr2:207728276
|
T | A | 1 | a0001c0001t0002g0015 | 2 | HG00099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.330+1400T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728276 | ||||||
chr2:207728277
|
C | A | 1 | a0001c0001t0002g0015 | 2 | HG00099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.330+1401C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728277 | ||||||
chr2:207728278
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.330+1402T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728278 | ||||||
chr2:207728428
|
A | G | 3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0149 | 3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.330+1552A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728428 | ||||||
chr2:207728676
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.330+1800A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728676 | ||||||
chr2:207728765
|
G | A | 1 | a0001c0001t0015g0121 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.330+1889G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728765 | ||||||
chr2:207728808
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.330+1932T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728808 | ||||||
chr2:207728849
|
T | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.330+1973T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728849 | ||||||
chr2:207728852
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.330+1976A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728852 | ||||||
chr2:207728858
|
G | A | 3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0149 | 3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.330+1982G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728858 | ||||||
chr2:207728877
|
A | G | 1 | a0001c0001t0005g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.330+2001A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207728877 | ||||||
chr2:207729044
|
G | A | 1 | a0001c0001t0010g0221 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.330+2168G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729044 | ||||||
chr2:207729052
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.330+2176G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729052 | ||||||
chr2:207729142
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.330+2266C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729142 | ||||||
chr2:207729186
|
T | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0009g0038others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+2310T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729186 | ||||||
chr2:207729201
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.330+2325T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729201 | ||||||
chr2:207729247
|
TCCGCCCC others(17): Show |
T | 4 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0091others(1): Show | 5 | HG01891.hp2 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+2374_330+2397d others(26): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729247 | |||||
chr2:207729247
|
TCCGCCCC others(18): Show |
T | 2 | a0001c0001t0001g0003a0001c0001t0001g0056 | 4 | HG03139.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+2374_330+2398d others(27): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729247 | |||||
chr2:207729248
|
CCGCCCCC others(16): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.330+2374_330+2396d others(25): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729248 | |||||
chr2:207729250
|
G | C | 1 | a0001c0001t0001g0048 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.330+2374G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729250 | ||||||
chr2:207729250
|
G | GC | 97 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0025others(94): Show | 101 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.330+2383dupC | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729250 | |||||
chr2:207729251
|
CCCCCCCC others(13): Show |
C | 3 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0061 | 4 | NA18945.hp2 NA18974.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+2384_330+2403d others(22): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729251 | |||||
chr2:207729252
|
C | A | 6 | a0001c0001t0001g0296a0001c0001t0002g0169a0001c0001t0002g0269others(3): Show | 6 | HG02015.hp1 HG02132.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+2376C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729252 | ||||||
chr2:207729252
|
CCCCCCCC others(12): Show |
C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0081 | 3 | HG03540.hp1 NA19010.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.330+2384_330+2402d others(21): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729252 | |||||
chr2:207729252
|
CCCCCCCC others(21): Show |
C | 3 | a0001c0001t0001g0232a0001c0001t0002g0279a0001c0001t0002g0285 | 3 | NA18961.hp1 NA19074.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.330+2386_330+2413d others(30): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729252 | |||||
chr2:207729253
|
CCCCCCCG others(11): Show |
C | 1 | a0001c0001t0009g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.330+2384_330+2401d others(20): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729253 | |||||
chr2:207729253
|
CCCCCCCG others(20): Show |
C | 1 | a0001c0001t0001g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.330+2384_330+2410d others(29): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729253 | |||||
chr2:207729254
|
CCCCCCGC others(10): Show |
C | 2 | a0001c0001t0001g0065a0001c0001t0009g0038 | 2 | HG03139.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.330+2384_330+2400d others(19): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729254 | |||||
chr2:207729255
|
CCCCCGCC others(4): Show |
C | 14 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0045others(11): Show | 15 | HG00673.hp1 HG01169.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.330+2384_330+2394d others(13): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729255 | |||||
chr2:207729255
|
CCCCCGCC others(9): Show |
C | 2 | a0001c0001t0001g0109a0002c0003t0001g0070 | 2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.330+2384_330+2399d others(18): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729255 | |||||
chr2:207729256
|
CCCCGCCC others(3): Show |
C | 9 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0067others(6): Show | 9 | HG02129.hp2 HG02647.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+2384_330+2393d others(12): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729256 | |||||
chr2:207729256
|
CCCCGCCC others(8): Show |
C | 5 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0060others(2): Show | 5 | HG00544.hp2 NA18983.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+2384_330+2398d others(17): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729256 | |||||
chr2:207729256
|
CCCCGCCC others(17): Show |
C | 3 | a0001c0001t0001g0052a0001c0001t0001g0082a0001c0001t0001g0104 | 3 | HG01346.hp2 HG02145.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.330+2384_330+2407d others(26): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729256 | |||||
chr2:207729257
|
CCCGCCCC others(7): Show |
C | 6 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0034others(3): Show | 6 | HG00408.hp1 HG00597.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+2384_330+2397d others(16): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729257 | |||||
chr2:207729257
|
CCCGCCCC others(16): Show |
C | 1 | a0001c0001t0001g0062 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.330+2384_330+2406d others(25): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729257 | |||||
chr2:207729258
|
CCGCCCCC others(6): Show |
C | 10 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0037others(7): Show | 12 | HG01069.hp1 HG02071.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.330+2384_330+2396d others(15): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729258 | |||||
chr2:207729259
|
CGCCCCCA others(5): Show |
C | 13 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0036others(10): Show | 13 | HG01256.hp2 HG02818.hp1 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.330+2384_330+2395d others(14): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729259 | ||||||
chr2:207729260
|
G | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0043a0001c0001t0001g0069others(4): Show | 7 | HG02896.hp1 HG03041.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+2384G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729260 | ||||||
chr2:207729265
|
C | G | 1 | a0001c0004t0002g0005 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.330+2389C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729265 | ||||||
chr2:207729265
|
CACCCCA | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0093 | 3 | NA18956.hp1 NA18956.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.330+2390_330+2395d others(8): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729265 | ||||||
chr2:207729266
|
A | C | 8 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0096others(5): Show | 9 | HG00438.hp1 HG02630.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+2390A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729266 | ||||||
chr2:207729271
|
A | AC | 61 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0024others(58): Show | 62 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.330+2403dupC | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729271 | |||||
chr2:207729271
|
A | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0027others(37): Show | 42 | HG00438.hp1 HG00673.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.330+2395A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729271 | ||||||
chr2:207729279
|
C | A | 2 | a0001c0001t0003g0299a0001c0001t0005g0018 | 3 | HG03516.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.330+2403C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729279 | ||||||
chr2:207729280
|
A | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(100): Show | 112 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.330+2404A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729280 | ||||||
chr2:207729285
|
C | G | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+2409C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729285 | ||||||
chr2:207729288
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0102 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.330+2412G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729288 | ||||||
chr2:207729288
|
G | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0101 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.330+2412G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729288 | ||||||
chr2:207729384
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 111 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.330+2508A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729384 | ||||||
chr2:207729386
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.330+2510G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729386 | ||||||
chr2:207729395
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0009g0038others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+2519G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729395 | ||||||
chr2:207729550
|
C | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0248 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.330+2674C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729550 | ||||||
chr2:207729550
|
C | G | 2 | a0001c0001t0008g0327a0001c0001t0008g0328 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.330+2674C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729550 | ||||||
chr2:207729671
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0233 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.330+2795C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729671 | ||||||
chr2:207729744
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | NA19064.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.330+2868C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729744 | ||||||
chr2:207729804
|
C | G | 10 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(7): Show | 11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.330+2928C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729804 | ||||||
chr2:207729814
|
C | A | 1 | a0001c0001t0003g0302 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.330+2938C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729814 | ||||||
chr2:207729882
|
AT | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(97): Show | 108 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.330+3019delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207729882 | |||||
chr2:207729916
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.330+3040G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729916 | ||||||
chr2:207729965
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(97): Show | 108 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.330+3089A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207729965 | ||||||
chr2:207730079
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.330+3203G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730079 | ||||||
chr2:207730215
|
C | A | 1 | a0001c0001t0001g0011 | 2 | HG02074.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.330+3339C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730215 | ||||||
chr2:207730266
|
G | A | 330 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(327): Show | 353 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.330+3390G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730266 | ||||||
chr2:207730268
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.330+3392C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730268 | ||||||
chr2:207730448
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.331-3499T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730448 | ||||||
chr2:207730480
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.331-3467G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730480 | ||||||
chr2:207730493
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.331-3454C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730493 | ||||||
chr2:207730587
|
G | A | 1 | a0001c0004t0002g0005 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.331-3360G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730587 | ||||||
chr2:207730733
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.331-3214G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730733 | ||||||
chr2:207730806
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.331-3141A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730806 | ||||||
chr2:207730807
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.331-3140C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730807 | ||||||
chr2:207730906
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.331-3041A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730906 | ||||||
chr2:207730928
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.331-3019C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730928 | ||||||
chr2:207730955
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0056others(1): Show | 6 | HG02976.hp2 HG03139.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-2992A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207730955 | ||||||
chr2:207731083
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331-2864A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731083 | ||||||
chr2:207731243
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.331-2704C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731243 | ||||||
chr2:207731290
|
A | AGGTACTT others(7): Show |
1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.331-2656_331-2643d others(16): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731290 | |||||
chr2:207731455
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.331-2492C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731455 | ||||||
chr2:207731458
|
A | G | 1 | a0001c0001t0002g0143 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.331-2489A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731458 | ||||||
chr2:207731718
|
T | C | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.331-2229T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731718 | ||||||
chr2:207731721
|
T | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.331-2226T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731721 | ||||||
chr2:207731806
|
CT | C | 205 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(202): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.331-2120delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731806 | |||||
chr2:207731806
|
CTT | C | 7 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0076others(4): Show | 7 | HG01169.hp2 HG01496.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-2121_331-2120d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731806 | |||||
chr2:207731806
|
CTTT | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 97 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.331-2122_331-2120d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731806 | |||||
chr2:207731806
|
CTTTT | C | 10 | a0001c0001t0001g0037a0001c0001t0001g0075a0001c0001t0001g0089others(7): Show | 10 | HG01256.hp2 HG02083.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.331-2123_331-2120d others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207731806 | |||||
chr2:207731840
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.331-2107C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731840 | ||||||
chr2:207731873
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-2074A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731873 | ||||||
chr2:207731917
|
C | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0241 | 2 | HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.331-2030C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731917 | ||||||
chr2:207731926
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.331-2021C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731926 | ||||||
chr2:207731966
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0076 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.331-1981C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207731966 | ||||||
chr2:207732010
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.331-1937A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732010 | ||||||
chr2:207732100
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG01884.hp1 HG01891.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.331-1847G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732100 | ||||||
chr2:207732123
|
T | C | 1 | a0001c0004t0002g0005 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.331-1824T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732123 | ||||||
chr2:207732263
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(94): Show | 105 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.331-1684G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732263 | ||||||
chr2:207732417
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.331-1530G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732417 | ||||||
chr2:207732422
|
T | G | 1 | a0001c0001t0001g0059 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.331-1525T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732422 | ||||||
chr2:207732444
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-1503G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732444 | ||||||
chr2:207732594
|
G | GT | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(101): Show | 112 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.331-1343dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207732594 | |||||
chr2:207732636
|
T | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.331-1311T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732636 | ||||||
chr2:207732693
|
CCTT | C | 10 | a0001c0001t0002g0124a0001c0001t0002g0127a0001c0001t0002g0152others(7): Show | 10 | HG01099.hp2 HG01168.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.331-1250_331-1248d others(5): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207732693 | |||||
chr2:207732830
|
A | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-1117A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732830 | ||||||
chr2:207732861
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.331-1086T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732861 | ||||||
chr2:207732880
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-1067T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732880 | ||||||
chr2:207732894
|
A | G | 3 | a0001c0001t0008g0327a0001c0001t0008g0328a0001c0005t0001g0326 | 3 | HG02818.hp2 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.331-1053A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207732894 | ||||||
chr2:207733083
|
G | GT | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.331-858dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 207733083 | |||||
chr2:207733172
|
G | A | 1 | a0001c0001t0017g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.331-775G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733172 | ||||||
chr2:207733266
|
C | G | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-681C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733266 | ||||||
chr2:207733275
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.331-672T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733275 | ||||||
chr2:207733282
|
A | C | 1 | a0001c0001t0021g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.331-665A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733282 | ||||||
chr2:207733523
|
G | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.331-424G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733523 | ||||||
chr2:207733536
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG00741.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-411A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733536 | ||||||
chr2:207733640
|
A | G | 1 | a0001c0004t0002g0005 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.331-307A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733640 | ||||||
chr2:207733854
|
T | A | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.331-93T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 3/9 | chr2 | 207733854 | ||||||
chr2:207734118
|
G | C | 2 | a0001c0001t0002g0119a0001c0001t0002g0329 | 2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.431+71G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734118 | ||||||
chr2:207734393
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.431+346T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734393 | ||||||
chr2:207734412
|
G | C | 1 | a0001c0001t0021g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.431+365G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734412 | ||||||
chr2:207734579
|
CCAA | C | 100 | a0001c0001t0001g0257a0001c0001t0001g0266a0001c0001t0001g0271others(97): Show | 110 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.431+541_431+543del others(3): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 207734579 | |||||
chr2:207734665
|
C | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.431+618C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734665 | ||||||
chr2:207734683
|
T | A | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.431+636T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734683 | ||||||
chr2:207734736
|
T | C | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.431+689T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207734736 | ||||||
chr2:207734772
|
C | CT | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 97 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.431+735dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 207734772 | |||||
chr2:207735274
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.431+1227T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735274 | ||||||
chr2:207735327
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.431+1280A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735327 | ||||||
chr2:207735370
|
A | T | 11 | a0001c0001t0002g0001a0001c0001t0002g0136a0001c0001t0002g0158others(8): Show | 15 | HG00621.hp1 HG02027.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.431+1323A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735370 | ||||||
chr2:207735399
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG00438.hp1 NA18957.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.431+1352C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735399 | ||||||
chr2:207735498
|
A | T | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.431+1451A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735498 | ||||||
chr2:207735499
|
T | A | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.431+1452T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735499 | ||||||
chr2:207735727
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(94): Show | 105 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.431+1680C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735727 | ||||||
chr2:207735731
|
G | A | 1 | a0001c0001t0018g0138 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.432-1680G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735731 | ||||||
chr2:207735803
|
G | A | 1 | a0001c0001t0021g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-1608G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735803 | ||||||
chr2:207735822
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.432-1589C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735822 | ||||||
chr2:207735874
|
C | A | 1 | a0001c0001t0001g0069 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.432-1537C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207735874 | ||||||
chr2:207736598
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.432-813T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736598 | ||||||
chr2:207736621
|
C | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0009g0038others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-790C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736621 | ||||||
chr2:207736728
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.432-683T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736728 | ||||||
chr2:207736852
|
A | T | 1 | a0001c0001t0001g0232 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.432-559A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736852 | ||||||
chr2:207736860
|
A | C | 1 | a0001c0001t0002g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.432-551A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207736860 | ||||||
chr2:207736918
|
G | GT | 16 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0069others(13): Show | 16 | HG01109.hp1 HG01361.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.432-478dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 207736918 | |||||
chr2:207737018
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.432-393C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737018 | ||||||
chr2:207737077
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.432-334G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737077 | ||||||
chr2:207737105
|
C | T | 3 | a0001c0001t0002g0325a0001c0001t0017g0137a0001c0001t0018g0138 | 3 | HG02615.hp2 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.432-306C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737105 | ||||||
chr2:207737116
|
C | T | 91 | a0001c0001t0001g0257a0001c0001t0001g0266a0001c0001t0001g0271others(88): Show | 101 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.432-295C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737116 | ||||||
chr2:207737127
|
G | A | 1 | a0001c0001t0020g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.432-284G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737127 | ||||||
chr2:207737313
|
G | A | 1 | a0001c0002t0001g0321 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.432-98G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737313 | ||||||
chr2:207737381
|
G | A | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-30G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737381 | ||||||
chr2:207737386
|
AAATAATT others(9): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.432-24_432-9delAAT others(13): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 4/9 | chr2 | 207737386 | ||||||
chr2:207737507
|
C | T | 1 | a0001c0001t0002g0268 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.467+61C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737507 | ||||||
chr2:207737599
|
G | T | 3 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0173 | 3 | HG02735.hp2 HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.467+153G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737599 | ||||||
chr2:207737690
|
A | AT | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(89): Show | 100 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.467+247dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207737690 | |||||
chr2:207737693
|
T | TA | 22 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0103others(19): Show | 24 | HG00597.hp2 HG01243.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.467+258dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207737693 | |||||
chr2:207737693
|
TA | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0208others(11): Show | 16 | HG00609.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.467+258delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207737693 | |||||
chr2:207737861
|
T | A | 1 | a0001c0001t0002g0325 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.467+415T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737861 | ||||||
chr2:207737865
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0248 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.467+419C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737865 | ||||||
chr2:207737901
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.467+455C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207737901 | ||||||
chr2:207738042
|
A | G | 2 | a0001c0001t0002g0277a0001c0001t0002g0312 | 2 | NA18978.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.467+596A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738042 | ||||||
chr2:207738182
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.467+736C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738182 | ||||||
chr2:207738231
|
G | GT | 106 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(103): Show | 109 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.467+793dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207738231 | |||||
chr2:207738231
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.467+785G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738231 | ||||||
chr2:207738346
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.467+900G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738346 | ||||||
chr2:207738449
|
G | A | 10 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(7): Show | 11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.467+1003G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738449 | ||||||
chr2:207738594
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.467+1148T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738594 | ||||||
chr2:207738714
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.467+1268C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207738714 | ||||||
chr2:207738718
|
CT | C | 329 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(326): Show | 352 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.467+1282delT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207738718 | |||||
chr2:207739225
|
T | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0009g0038others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.468-1430T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739225 | ||||||
chr2:207739273
|
C | T | 1 | a0001c0001t0002g0318 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.468-1382C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739273 | ||||||
chr2:207739538
|
C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 110 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.468-1117C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739538 | ||||||
chr2:207739653
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.468-1002C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739653 | ||||||
chr2:207739673
|
T | G | 1 | a0001c0001t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.468-982T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739673 | ||||||
chr2:207739872
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.468-783G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739872 | ||||||
chr2:207739939
|
T | G | 1 | a0001c0001t0018g0138 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.468-716T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739939 | ||||||
chr2:207739941
|
C | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.468-714C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739941 | ||||||
chr2:207739951
|
A | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.468-704A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207739951 | ||||||
chr2:207740075
|
C | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.468-580C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740075 | ||||||
chr2:207740084
|
G | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.468-571G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740084 | ||||||
chr2:207740173
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.468-482A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740173 | ||||||
chr2:207740202
|
A | T | 1 | a0001c0001t0012g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.468-453A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740202 | ||||||
chr2:207740470
|
G | A | 3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0149 | 3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.468-185G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | chr2 | 207740470 | ||||||
chr2:207740577
|
G | GC | 4 | a0001c0001t0002g0144a0001c0001t0002g0284a0001c0001t0002g0295others(1): Show | 4 | NA18939.hp1 NA18970.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.468-76dupC | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 207740577 | |||||
chr2:207740768
|
G | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.519+62G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207740768 | ||||||
chr2:207740840
|
T | C | 3 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252 | 3 | NA18944.hp2 NA19005.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.519+134T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207740840 | ||||||
chr2:207740870
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(94): Show | 105 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.519+164T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207740870 | ||||||
chr2:207741147
|
T | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(102): Show | 114 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.519+441T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741147 | ||||||
chr2:207741252
|
CA | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.519+558delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207741252 | |||||
chr2:207741259
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.519+553A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741259 | ||||||
chr2:207741264
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.519+558A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741264 | ||||||
chr2:207741271
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(4): Show | 10 | HG02145.hp1 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+565A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741271 | ||||||
chr2:207741359
|
A | G | 99 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(96): Show | 102 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.519+653A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741359 | ||||||
chr2:207741444
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.519+738A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741444 | ||||||
chr2:207741651
|
C | T | 6 | a0001c0001t0001g0257a0001c0001t0001g0266a0001c0001t0001g0271others(3): Show | 6 | NA18954.hp2 NA18962.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-572C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741651 | ||||||
chr2:207741710
|
T | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.520-513T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741710 | ||||||
chr2:207741833
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.520-390A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741833 | ||||||
chr2:207741843
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0206a0001c0001t0001g0241 | 3 | HG01109.hp1 HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.520-380C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741843 | ||||||
chr2:207741845
|
CA | C | 14 | a0001c0001t0001g0274a0001c0001t0001g0330a0001c0001t0002g0140others(11): Show | 15 | HG01168.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-362delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207741845 | |||||
chr2:207741873
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.520-350G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741873 | ||||||
chr2:207741890
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.520-333C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741890 | ||||||
chr2:207741927
|
G | A | 1 | a0001c0001t0020g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520-296G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | chr2 | 207741927 | ||||||
chr2:207742151
|
C | CA | 6 | a0001c0001t0002g0119a0001c0001t0002g0139a0001c0001t0002g0140others(3): Show | 6 | HG01243.hp1 HG02015.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-55dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207742151 | |||||
chr2:207742151
|
CA | C | 6 | a0001c0001t0001g0063a0001c0001t0001g0081a0001c0001t0001g0274others(3): Show | 6 | HG03486.hp2 HG03942.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-55delA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207742151 | |||||
chr2:207742151
|
CAA | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(95): Show | 106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.520-56_520-55delAA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 207742151 | |||||
chr2:207742421
|
A | G | 1 | a0001c0001t0002g0283 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.639+79A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742421 | ||||||
chr2:207742480
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.639+138C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742480 | ||||||
chr2:207742552
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.639+210A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742552 | ||||||
chr2:207742712
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.639+370G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742712 | ||||||
chr2:207742752
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.639+410C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207742752 | ||||||
chr2:207743123
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.639+781G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743123 | ||||||
chr2:207743141
|
T | C | 2 | a0001c0001t0002g0279a0001c0001t0002g0285 | 2 | NA18961.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.639+799T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743141 | ||||||
chr2:207743538
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.639+1196G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743538 | ||||||
chr2:207743576
|
C | T | 2 | a0001c0001t0017g0137a0001c0001t0018g0138 | 2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.639+1234C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743576 | ||||||
chr2:207743720
|
G | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0248 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.639+1378G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743720 | ||||||
chr2:207743763
|
C | T | 1 | a0001c0001t0002g0294 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.639+1421C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743763 | ||||||
chr2:207743769
|
A | T | 1 | a0001c0001t0020g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.639+1427A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743769 | ||||||
chr2:207743806
|
T | TTTTTTG | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(95): Show | 106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.639+1487_639+1492d others(8): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207743806 | |||||
chr2:207743806
|
T | TTTTTTGT others(5): Show |
1 | a0001c0001t0001g0031 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.639+1481_639+1492d others(14): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207743806 | |||||
chr2:207743806
|
TTTTTTGT others(5): Show |
T | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.639+1481_639+1492d others(14): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207743806 | |||||
chr2:207743812
|
G | T | 1 | a0001c0001t0002g0285 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.639+1470G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743812 | ||||||
chr2:207743912
|
C | G | 3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0149 | 3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.639+1570C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743912 | ||||||
chr2:207743915
|
G | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0009g0038others(5): Show | 8 | HG01069.hp1 HG02486.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.639+1573G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207743915 | ||||||
chr2:207744053
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0245 | 2 | NA18970.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.639+1711A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744053 | ||||||
chr2:207744065
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.639+1723A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744065 | ||||||
chr2:207744080
|
G | A | 1 | a0001c0001t0009g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.639+1738G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744080 | ||||||
chr2:207744092
|
T | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(46): Show | 53 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.639+1750T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744092 | ||||||
chr2:207744095
|
C | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(110): Show | 123 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.639+1753C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744095 | ||||||
chr2:207744117
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.639+1775G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744117 | ||||||
chr2:207744218
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.639+1876C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744218 | ||||||
chr2:207744228
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.639+1886T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744228 | ||||||
chr2:207744228
|
T | TTG | 10 | a0001c0001t0001g0063a0001c0001t0001g0131a0001c0001t0001g0183others(7): Show | 10 | HG01070.hp2 HG01081.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.639+1906_639+1907d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744228 | |||||
chr2:207744228
|
T | TTGTGTG | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0115others(4): Show | 7 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.639+1902_639+1907d others(8): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744228 | |||||
chr2:207744228
|
T | TTGTGTGT others(1): Show |
90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(87): Show | 98 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.639+1900_639+1907d others(10): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744228 | |||||
chr2:207744228
|
T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0013g0066 | 3 | HG00408.hp1 HG04115.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.639+1898_639+1907d others(12): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744228 | |||||
chr2:207744295
|
G | C | 1 | a0001c0005t0001g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.639+1953G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744295 | ||||||
chr2:207744326
|
G | A | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.639+1984G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744326 | ||||||
chr2:207744401
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.639+2059A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744401 | ||||||
chr2:207744530
|
A | AT | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(105): Show | 117 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.639+2206dupT | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207744530 | |||||
chr2:207744600
|
C | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(103): Show | 109 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.639+2258C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744600 | ||||||
chr2:207744612
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 106 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.639+2270C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744612 | ||||||
chr2:207744940
|
A | G | 6 | a0001c0001t0001g0257a0001c0001t0001g0266a0001c0001t0001g0271others(3): Show | 6 | NA18954.hp2 NA18962.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.640-2107A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207744940 | ||||||
chr2:207745072
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0108 | 2 | NA18973.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.640-1975C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745072 | ||||||
chr2:207745265
|
G | A | 1 | a0001c0001t0021g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640-1782G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745265 | ||||||
chr2:207745331
|
G | C | 4 | a0001c0001t0002g0119a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG01243.hp1 HG02895.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-1716G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745331 | ||||||
chr2:207745408
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.640-1639C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745408 | ||||||
chr2:207745475
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.640-1572G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745475 | ||||||
chr2:207745810
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-1237G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207745810 | ||||||
chr2:207746077
|
A | G | 102 | a0001c0001t0001g0257a0001c0001t0001g0264a0001c0001t0001g0266others(99): Show | 112 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.640-970A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746077 | ||||||
chr2:207746128
|
C | T | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.640-919C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746128 | ||||||
chr2:207746216
|
T | C | 1 | a0001c0001t0010g0221 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.640-831T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746216 | ||||||
chr2:207746278
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.640-769A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746278 | ||||||
chr2:207746294
|
C | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.640-753C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746294 | ||||||
chr2:207746361
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.640-686G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746361 | ||||||
chr2:207746553
|
G | A | 95 | a0001c0001t0001g0257a0001c0001t0001g0264a0001c0001t0001g0266others(92): Show | 105 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.640-494G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746553 | ||||||
chr2:207746584
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.640-463T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746584 | ||||||
chr2:207746663
|
T | C | 108 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0185others(105): Show | 118 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.640-384T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746663 | ||||||
chr2:207746717
|
C | T | 3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0149 | 3 | HG02055.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.640-330C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746717 | ||||||
chr2:207746899
|
C | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG01169.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.640-148C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746899 | ||||||
chr2:207746962
|
T | C | 1 | a0001c0001t0001g0009 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.640-85T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746962 | ||||||
chr2:207746971
|
G | A | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-76G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | chr2 | 207746971 | ||||||
chr2:207746975
|
C | CA | 17 | a0001c0001t0001g0021a0001c0001t0001g0130a0001c0001t0001g0232others(14): Show | 18 | HG00738.hp1 HG00738.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.640-57dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 207746975 | |||||
chr2:207747307
|
A | G | 1 | a0001c0001t0012g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.806+94A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747307 | ||||||
chr2:207747358
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0248 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.806+145A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747358 | ||||||
chr2:207747501
|
TTACAAG | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.806+291_806+296del others(6): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 207747501 | |||||
chr2:207747506
|
A | G | 1 | a0001c0001t0007g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.806+293A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747506 | ||||||
chr2:207747602
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.806+389G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747602 | ||||||
chr2:207747801
|
G | T | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+588G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747801 | ||||||
chr2:207747811
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.806+598G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747811 | ||||||
chr2:207747907
|
T | TTTCA | 5 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0005g0018others(2): Show | 6 | HG02145.hp2 HG02280.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+717_806+720dup others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 207747907 | |||||
chr2:207747981
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.806+768A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207747981 | ||||||
chr2:207748076
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.806+863T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748076 | ||||||
chr2:207748211
|
C | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.806+998C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748211 | ||||||
chr2:207748243
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.806+1030C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748243 | ||||||
chr2:207748289
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0290 | 2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.806+1076C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748289 | ||||||
chr2:207748290
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG00741.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+1077G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748290 | ||||||
chr2:207748379
|
G | A | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+1166G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748379 | ||||||
chr2:207748455
|
T | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.806+1242T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748455 | ||||||
chr2:207748466
|
G | A | 1 | a0001c0001t0021g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.806+1253G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748466 | ||||||
chr2:207748512
|
T | G | 1 | a0001c0001t0003g0299 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.806+1299T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748512 | ||||||
chr2:207748603
|
T | A | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.806+1390T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748603 | ||||||
chr2:207748770
|
C | A | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.806+1557C>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748770 | ||||||
chr2:207748783
|
T | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.806+1570T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748783 | ||||||
chr2:207748794
|
T | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.806+1581T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748794 | ||||||
chr2:207748799
|
C | G | 1 | a0001c0001t0008g0327 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.806+1586C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748799 | ||||||
chr2:207748905
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0009g0038others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+1692G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748905 | ||||||
chr2:207748926
|
A | G | 1 | a0001c0001t0002g0016 | 2 | NA19007.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.806+1713A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748926 | ||||||
chr2:207748926
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.806+1713A>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748926 | ||||||
chr2:207748983
|
A | G | 1 | a0001c0001t0020g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.806+1770A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207748983 | ||||||
chr2:207749022
|
C | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 89 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.806+1809C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749022 | ||||||
chr2:207749030
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.806+1817C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749030 | ||||||
chr2:207749345
|
G | A | 1 | a0001c0001t0018g0138 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.807-1612G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749345 | ||||||
chr2:207749447
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.807-1510C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749447 | ||||||
chr2:207749502
|
A | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.807-1455A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749502 | ||||||
chr2:207749529
|
C | G | 1 | a0001c0001t0002g0260 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.807-1428C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749529 | ||||||
chr2:207749547
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.807-1410T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749547 | ||||||
chr2:207749572
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.807-1385T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749572 | ||||||
chr2:207749842
|
G | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0009g0038others(5): Show | 8 | HG01069.hp1 HG02486.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.807-1115G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749842 | ||||||
chr2:207749891
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(93): Show | 99 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.807-1066T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749891 | ||||||
chr2:207749954
|
A | C | 1 | a0001c0001t0002g0260 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.807-1003A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207749954 | ||||||
chr2:207750075
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.807-882T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750075 | ||||||
chr2:207750079
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.807-878A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750079 | ||||||
chr2:207750101
|
G | A | 3 | a0001c0002t0001g0320a0001c0002t0001g0322a0001c0002t0001g0323 | 3 | HG01069.hp1 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.807-856G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750101 | ||||||
chr2:207750267
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.807-690G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750267 | ||||||
chr2:207750354
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.807-603C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750354 | ||||||
chr2:207750656
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0190others(2): Show | 5 | HG00544.hp1 NA18942.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.807-301G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750656 | ||||||
chr2:207750661
|
G | T | 1 | a0001c0001t0021g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.807-296G>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750661 | ||||||
chr2:207750800
|
T | G | 4 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp1 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.807-157T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750800 | ||||||
chr2:207750813
|
C | T | 1 | a0001c0001t0002g0279 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.807-144C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 8/9 | chr2 | 207750813 | ||||||
chr2:207751138
|
T | G | 1 | a0001c0001t0002g0316 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.969+19T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751138 | ||||||
chr2:207751322
|
A | C | 105 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0185others(102): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.969+203A>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751322 | ||||||
chr2:207751573
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.969+454G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751573 | ||||||
chr2:207751580
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.969+461C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751580 | ||||||
chr2:207751581
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 101 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.969+462G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751581 | ||||||
chr2:207751593
|
G | A | 1 | a0001c0001t0014g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.969+474G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751593 | ||||||
chr2:207751621
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+502G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751621 | ||||||
chr2:207751637
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.969+518C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751637 | ||||||
chr2:207751704
|
A | G | 1 | a0001c0001t0018g0138 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.969+585A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751704 | ||||||
chr2:207751809
|
G | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(211): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.969+690G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751809 | ||||||
chr2:207751841
|
C | T | 4 | a0001c0001t0002g0144a0001c0001t0002g0284a0001c0001t0002g0295others(1): Show | 4 | NA18939.hp1 NA18970.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+722C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751841 | ||||||
chr2:207751854
|
CAAAA | C | 27 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0135others(24): Show | 29 | HG00597.hp1 HG00609.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.969+749_969+752del others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207751854 | |||||
chr2:207751945
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.969+826G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751945 | ||||||
chr2:207751967
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.969+848G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751967 | ||||||
chr2:207751976
|
A | G | 1 | a0001c0001t0020g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.969+857A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751976 | ||||||
chr2:207751995
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0319 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.969+876G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207751995 | ||||||
chr2:207752082
|
A | G | 10 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(7): Show | 11 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.969+963A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752082 | ||||||
chr2:207752121
|
A | ATT | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.969+1002_969+1003i others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752121 | ||||||
chr2:207752224
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.969+1105G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752224 | ||||||
chr2:207752351
|
T | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.969+1232T>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752351 | ||||||
chr2:207752392
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.970-1196A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752392 | ||||||
chr2:207752437
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.970-1151G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752437 | ||||||
chr2:207752442
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.970-1146G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752442 | ||||||
chr2:207752534
|
C | CA | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(94): Show | 106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.970-1041dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207752534 | |||||
chr2:207752534
|
C | CAA | 6 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 6 | HG02074.hp1 HG03831.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.970-1042_970-1041d others(4): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207752534 | |||||
chr2:207752548
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.970-1040T>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752548 | ||||||
chr2:207752758
|
G | C | 74 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(71): Show | 76 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.970-830G>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752758 | ||||||
chr2:207752803
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.970-785G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752803 | ||||||
chr2:207752811
|
CG | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.970-774delG | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207752811 | |||||
chr2:207752812
|
G | A | 18 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0187others(15): Show | 18 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.970-776G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752812 | ||||||
chr2:207752914
|
C | CTGT | 99 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0185others(96): Show | 109 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.970-673_970-671dup others(3): Show |
CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207752914 | |||||
chr2:207752974
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.970-614G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752974 | ||||||
chr2:207752981
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(98): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.970-607A>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207752981 | ||||||
chr2:207753027
|
C | CA | 6 | a0001c0001t0006g0044a0001c0001t0020g0174a0001c0002t0001g0320others(3): Show | 6 | HG01069.hp1 HG01884.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.970-549dupA | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 207753027 | |||||
chr2:207753076
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.970-512C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753076 | ||||||
chr2:207753245
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.970-343C>T | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753245 | ||||||
chr2:207753468
|
T | C | 1 | a0001c0001t0002g0273 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.970-120T>C | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753468 | ||||||
chr2:207753501
|
C | G | 1 | a0001c0001t0001g0239 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.970-87C>G | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753501 | ||||||
chr2:207753537
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.970-51G>A | CCNYL1 | ENSG00000163249.13 | transcript | ENST00000295414.8 | protein_coding | 9/9 | chr2 | 207753537 |