Item | Value |
---|---|
geneid | 4605 |
ensemblid | ENSG00000101057.16 |
hgncid | 7548 |
symbol | MYBL2 |
name | MYB proto-oncogene like 2 |
refseq_nuc | NM_002466.4 |
refseq_prot | NP_002457.1 |
ensembl_nuc | ENST00000217026.5 |
ensembl_prot | ENSP00000217026.4 |
mane_status | MANE Select |
chr | chr20 |
start | 43667114 |
end | 43716482 |
strand | + |
ver | v1.2 |
region | chr20:43667114-43716482 |
region5000 | chr20:43662114-43721482 |
regionname0 | MYBL2_chr20_43667114_43716482 |
regionname5000 | MYBL2_chr20_43662114_43721482 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 700 | 188 | 50 | 43 | 71 | 2 | 20 | 53 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0002 | 0/0 | 700 | 61 | 18 | 4 | 33 | 0 | 6 | 31 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0003 | 0/0 | 700 | 10 | 7 | 3 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0004 | 0/0 | 700 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0005 | 0/0 | 700 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0006 | 0/0 | 700 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0007 | 0/0 | 700 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0008 | 0/0 | 700 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0009 | 0/0 | 700 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0010 | 0/0 | 700 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2103 | 146 | 44 | 32 | 52 | 2 | 16 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0002 | 1/1 | 2103 | 38 | 4 | 11 | 17 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0003 | 0/0 | 2103 | 30 | 11 | 1 | 14 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0004 | 0/0 | 2103 | 25 | 2 | 2 | 19 | 0 | 2 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0005 | 0/0 | 2103 | 10 | 7 | 3 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0006 | 0/0 | 2103 | 6 | 5 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0007 | 0/0 | 2103 | 6 | 5 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0008 | 0/0 | 2103 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0009 | 0/0 | 2103 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0010 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0011 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0012 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0013 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0014 | 0/0 | 2103 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0015 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0016 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
c0017 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 566 | 258 | 70 | 50 | 108 | 2 | 26 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
t0002 | 0/0 | 566 | 9 | 8 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
t0003 | 0/0 | 564 | 6 | 5 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
t0004 | 0/0 | 566 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2103 | 146 | 44 | 32 | 52 | 2 | 16 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0002 | 1/1 | 2103 | 38 | 4 | 11 | 17 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0011 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0013 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0015 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0017 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0002c0003 | 0/0 | 2103 | 30 | 11 | 1 | 14 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0002c0004 | 0/0 | 2103 | 25 | 2 | 2 | 19 | 0 | 2 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0002c0007 | 0/0 | 2103 | 6 | 5 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0003c0005 | 0/0 | 2103 | 10 | 7 | 3 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0004c0006 | 0/0 | 2103 | 6 | 5 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0005c0008 | 0/0 | 2103 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0006c0009 | 0/0 | 2103 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0007c0016 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0008c0014 | 0/0 | 2103 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0009c0012 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0010c0010 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2668 | 143 | 41 | 32 | 52 | 2 | 16 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0001t0002 | 0/0 | 2668 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0001t0004 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0002t0001 | 1/1 | 2668 | 38 | 4 | 11 | 17 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0011t0001 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0013t0001 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0015t0001 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0001c0017t0002 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0002c0003t0001 | 0/0 | 2668 | 30 | 11 | 1 | 14 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0002c0004t0001 | 0/0 | 2668 | 25 | 2 | 2 | 19 | 0 | 2 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0002c0007t0001 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0002c0007t0003 | 0/0 | 2666 | 5 | 4 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0003c0005t0001 | 0/0 | 2668 | 10 | 7 | 3 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0004c0006t0002 | 0/0 | 2668 | 6 | 5 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0005c0008t0001 | 0/0 | 2668 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0006c0009t0001 | 0/0 | 2668 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0007c0016t0003 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0008c0014t0001 | 0/0 | 2668 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0009c0012t0001 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
a0010c0010t0001 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | copy fasta | chr20 | 43662114 | 43721482 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0011t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0013t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0015t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0001c0017t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0007t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0007t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0007t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0007t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0007t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0002c0007t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0003c0005t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0004c0006t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0004c0006t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0004c0006t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0004c0006t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0004c0006t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0005c0008t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0005c0008t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0005c0008t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0006c0009t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0006c0009t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0007c0016t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0008c0014t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0009c0012t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
a0010c0010t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | CHS | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG00741 | hp2 | a0003 | c0005 | t0001 | g0119 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01081 | hp1 | a0002 | c0004 | t0001 | g0163 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01081 | hp2 | a0002 | c0003 | t0001 | g0033 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01109 | hp2 | a0002 | c0004 | t0001 | g0084 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01167 | hp1 | a0003 | c0005 | t0001 | g0116 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01243 | hp1 | a0004 | c0006 | t0002 | g0101 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01243 | hp2 | a0008 | c0014 | t0001 | g0111 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01261 | hp2 | a0003 | c0005 | t0001 | g0121 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01361 | hp2 | a0002 | c0007 | t0003 | g0105 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01891 | hp2 | a0003 | c0005 | t0001 | g0260 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0263 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0262 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02055 | hp1 | a0004 | c0006 | t0002 | g0102 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02056 | hp1 | a0002 | c0004 | t0001 | g0075 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02083 | hp2 | a0002 | c0003 | t0001 | g0030 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | CDX | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0095 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02602 | hp2 | a0002 | c0004 | t0001 | g0011 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02615 | hp1 | a0002 | c0007 | t0003 | g0108 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02615 | hp2 | a0002 | c0004 | t0001 | g0010 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02622 | hp1 | a0001 | c0015 | t0001 | g0131 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02717 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02738 | hp2 | a0002 | c0004 | t0001 | g0012 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02818 | hp1 | a0003 | c0005 | t0001 | g0120 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02886 | hp1 | a0005 | c0008 | t0001 | g0115 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02886 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02895 | hp1 | a0003 | c0005 | t0001 | g0118 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02895 | hp2 | a0004 | c0006 | t0002 | g0103 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02896 | hp2 | a0004 | c0006 | t0002 | g0004 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02897 | hp1 | a0004 | c0006 | t0002 | g0004 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02897 | hp2 | a0002 | c0003 | t0001 | g0016 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02922 | hp1 | a0002 | c0007 | t0003 | g0107 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02922 | hp2 | a0004 | c0006 | t0002 | g0100 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02965 | hp2 | a0003 | c0005 | t0001 | g0122 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03041 | hp2 | a0002 | c0004 | t0001 | g0074 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0039 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03225 | hp1 | a0007 | c0016 | t0003 | g0254 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03453 | hp2 | a0005 | c0008 | t0001 | g0112 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03486 | hp1 | a0001 | c0017 | t0002 | g0123 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03491 | hp2 | a0002 | c0003 | t0001 | g0020 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03492 | hp2 | a0002 | c0003 | t0001 | g0021 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03540 | hp2 | a0002 | c0007 | t0003 | g0109 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03579 | hp2 | a0002 | c0003 | t0001 | g0036 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0237 | SAS | STU | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG04228 | hp1 | a0002 | c0003 | t0001 | g0037 | SAS | STU | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18612 | hp2 | a0001 | c0013 | t0001 | g0052 | EAS | CHB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18939 | hp2 | a0002 | c0004 | t0001 | g0086 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18946 | hp2 | a0002 | c0004 | t0001 | g0040 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18950 | hp1 | a0002 | c0004 | t0001 | g0077 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18952 | hp2 | a0002 | c0003 | t0001 | g0029 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18959 | hp1 | a0010 | c0010 | t0001 | g0053 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18963 | hp2 | a0002 | c0004 | t0001 | g0045 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18966 | hp1 | a0006 | c0009 | t0001 | g0172 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18966 | hp2 | a0002 | c0004 | t0001 | g0078 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0212 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18968 | hp1 | a0002 | c0004 | t0001 | g0079 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18971 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18972 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18975 | hp2 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18982 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18983 | hp2 | a0002 | c0004 | t0001 | g0096 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18984 | hp2 | a0002 | c0004 | t0001 | g0044 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18990 | hp1 | a0002 | c0004 | t0001 | g0041 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18992 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18993 | hp1 | a0002 | c0004 | t0001 | g0085 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18994 | hp2 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18995 | hp2 | a0002 | c0004 | t0001 | g0080 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19000 | hp2 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19003 | hp2 | a0006 | c0009 | t0001 | g0233 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19009 | hp2 | a0002 | c0004 | t0001 | g0047 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19011 | hp1 | a0002 | c0004 | t0001 | g0082 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19030 | hp2 | a0003 | c0005 | t0001 | g0261 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19043 | hp2 | a0002 | c0003 | t0001 | g0027 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19058 | hp1 | a0009 | c0012 | t0001 | g0245 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19058 | hp2 | a0002 | c0003 | t0001 | g0028 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19063 | hp2 | a0002 | c0003 | t0001 | g0032 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19068 | hp1 | a0001 | c0011 | t0001 | g0259 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19070 | hp1 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19077 | hp1 | a0002 | c0004 | t0001 | g0097 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19077 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19085 | hp2 | a0002 | c0004 | t0001 | g0083 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19089 | hp2 | a0002 | c0004 | t0001 | g0076 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19240 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA19240 | hp2 | a0002 | c0007 | t0003 | g0106 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ASW | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ASW | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0024 | SAS | GIH | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02109 | hp1 | a0003 | c0005 | t0001 | g0113 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02486 | hp1 | a0005 | c0008 | t0001 | g0114 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0034 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG06807 | hp1 | a0003 | c0005 | t0001 | g0117 | AFR | USA | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | USA | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA18955 | hp2 | a0002 | c0004 | t0001 | g0081 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | USA | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA20300 | hp2 | a0002 | c0007 | t0001 | g0110 | AFR | USA | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0058 | REF | REF | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0055 | REF | REF | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:43681809
|
G | A | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.140G>A | p.Arg47Lys | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/14 | 310/2668 | 140/2103 | 47/700 | chr20 | 43681809 | ||
chr20:43681838
|
C | A | 1 | a0010 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.169C>A | p.Leu57Met | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/14 | 339/2668 | 169/2103 | 57/700 | chr20 | 43681838 | ||
chr20:43692228
|
G | A | 1 | a0004 | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
missense_variant | MODERATE | c.572G>A | p.Ser191Asn | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/14 | 742/2668 | 572/2103 | 191/700 | chr20 | 43692228 | ||
chr20:43699914
|
C | T | 1 | a0008 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.821C>T | p.Pro274Leu | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/14 | 991/2668 | 821/2103 | 274/700 | chr20 | 43699914 | ||
chr20:43702560
|
A | G | 1 | a0005 | 3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1022A>G | p.Asn341Ser | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/14 | 1192/2668 | 1022/2103 | 341/700 | chr20 | 43702560 | ||
chr20:43702817
|
A | G | 4 | a0002a0003a0005others(1): Show | 75 | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(72): Show |
missense_variant | MODERATE | c.1279A>G | p.Ser427Gly | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/14 | 1449/2668 | 1279/2103 | 427/700 | chr20 | 43702817 | ||
chr20:43705358
|
C | T | 1 | a0009 | 1 | NA19058.hp1 | missense_variant&splice_region_variant | MODERATE | c.1505C>T | p.Ala502Val | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/14 | 1675/2668 | 1505/2103 | 502/700 | chr20 | 43705358 | ||
chr20:43713065
|
G | A | 2 | a0003a0008 | 11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
missense_variant | MODERATE | c.1783G>A | p.Val595Met | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/14 | 1953/2668 | 1783/2103 | 595/700 | chr20 | 43713065 | ||
chr20:43715137
|
A | G | 1 | a0006 | 2 | NA18966.hp1 NA19003.hp2 |
missense_variant | MODERATE | c.1828A>G | p.Thr610Ala | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/14 | 1998/2668 | 1828/2103 | 610/700 | chr20 | 43715137 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:43681786
|
C | T | 4 | a0001c0017a0002c0007a0004c0006others(1): Show | 14 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.117C>T | p.Asp39Asp | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/14 | 287/2668 | 117/2103 | 39/700 | chr20 | 43681786 | ||
chr20:43687052
|
C | T | 1 | a0001c0015 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.480C>T | p.Ile160Ile | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/14 | 650/2668 | 480/2103 | 160/700 | chr20 | 43687052 | ||
chr20:43692241
|
C | T | 1 | a0002c0004 | 25 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(22): Show |
synonymous_variant | LOW | c.585C>T | p.Asp195Asp | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/14 | 755/2668 | 585/2103 | 195/700 | chr20 | 43692241 | ||
chr20:43699999
|
T | C | 14 | a0001c0001a0001c0011a0001c0015others(11): Show | 234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
synonymous_variant | LOW | c.906T>C | p.Pro302Pro | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/14 | 1076/2668 | 906/2103 | 302/700 | chr20 | 43699999 | ||
chr20:43702756
|
G | A | 1 | a0001c0011 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.1218G>A | p.Pro406Pro | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/14 | 1388/2668 | 1218/2103 | 406/700 | chr20 | 43702756 | ||
chr20:43711565
|
C | T | 1 | a0001c0013 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.1683C>T | p.Asp561Asp | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/14 | 1853/2668 | 1683/2103 | 561/700 | chr20 | 43711565 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:43667258
|
A | G | 1 | a0001c0001t0004 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-26A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/14 | 26 | chr20 | 43667258 | |||||
chr20:43716105
|
G | A | 3 | a0001c0001t0002a0001c0017t0002a0004c0006t0002 | 9 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*18G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 14/14 | 18 | chr20 | 43716105 | |||||
chr20:43716215
|
ACT | A | 2 | a0002c0007t0003a0007c0016t0003 | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*132_*133delTC | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 14/14 | 132 | INFO_REALIGN_3_PRIME | chr20 | 43716215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:43667385
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.20+82C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667385 | ||||||
chr20:43667663
|
A | G | 4 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0262others(1): Show | 6 | HG01255.hp2 HG01496.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+360A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667663 | ||||||
chr20:43667788
|
G | T | 1 | a0003c0005t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.20+485G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667788 | ||||||
chr20:43667797
|
A | G | 1 | a0003c0005t0001g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.20+494A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667797 | ||||||
chr20:43667880
|
C | G | 1 | a0001c0011t0001g0259 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.20+577C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667880 | ||||||
chr20:43667902
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 167 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.20+599C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667902 | ||||||
chr20:43667911
|
T | C | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.20+608T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667911 | ||||||
chr20:43667924
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.20+621A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667924 | ||||||
chr20:43667933
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+630C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667933 | ||||||
chr20:43667952
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.20+649G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667952 | ||||||
chr20:43667998
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.20+695C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667998 | ||||||
chr20:43668004
|
A | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 147 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.20+701A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668004 | ||||||
chr20:43668042
|
C | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.20+739C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668042 | ||||||
chr20:43668075
|
T | G | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+772T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668075 | ||||||
chr20:43668096
|
T | A | 24 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(21): Show | 25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.20+793T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668096 | ||||||
chr20:43668194
|
C | CT | 15 | a0001c0001t0001g0087a0001c0002t0001g0088a0001c0002t0001g0089others(12): Show | 15 | HG01175.hp1 HG01192.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.20+915dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | |||||
chr20:43668194
|
CT | C | 14 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0048others(11): Show | 14 | HG02615.hp2 HG02717.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.20+915delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | |||||
chr20:43668194
|
CTT | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0227a0001c0001t0001g0228others(30): Show | 34 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.20+914_20+915delTT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | |||||
chr20:43668194
|
CTTT | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 138 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.20+913_20+915delTT others(1): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | |||||
chr20:43668194
|
CTTTT | C | 18 | a0001c0001t0001g0124a0003c0005t0001g0113a0003c0005t0001g0116others(15): Show | 19 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.20+912_20+915delTT others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | |||||
chr20:43668194
|
CTTTTTTT others(4): Show |
C | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.20+905_20+915delTT others(9): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | |||||
chr20:43668261
|
C | T | 24 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(21): Show | 25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.20+958C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668261 | ||||||
chr20:43668321
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.20+1018T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668321 | ||||||
chr20:43668324
|
C | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1021C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668324 | ||||||
chr20:43668340
|
T | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 160 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.20+1037T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668340 | ||||||
chr20:43668346
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 258 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(255): Show |
intron_variant | MODIFIER | c.20+1043A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668346 | ||||||
chr20:43668514
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1211C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668514 | ||||||
chr20:43668660
|
C | T | 1 | a0002c0003t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20+1357C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668660 | ||||||
chr20:43668664
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.20+1361C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668664 | ||||||
chr20:43668685
|
G | GT | 22 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0087others(19): Show | 24 | HG01255.hp2 HG01261.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.20+1402dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668685 | |||||
chr20:43668685
|
G | GTT | 23 | a0001c0001t0001g0043a0001c0002t0001g0263a0002c0003t0001g0002others(20): Show | 24 | HG01081.hp2 HG01934.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.20+1401_20+1402dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668685 | |||||
chr20:43668685
|
GT | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 142 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.20+1402delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668685 | |||||
chr20:43668726
|
A | C | 40 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0002g0049others(37): Show | 41 | HG01081.hp2 HG01361.hp2 HG02083.hp2 others(38): Show |
intron_variant | MODIFIER | c.20+1423A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668726 | ||||||
chr20:43668726
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0087 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.20+1423A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668726 | ||||||
chr20:43668771
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.20+1468C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668771 | ||||||
chr20:43668930
|
A | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1627A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668930 | ||||||
chr20:43669015
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1712C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669015 | ||||||
chr20:43669021
|
G | A | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1718G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669021 | ||||||
chr20:43669082
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0246 | 2 | HG03239.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.20+1779G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669082 | ||||||
chr20:43669138
|
G | A | 1 | a0004c0006t0002g0100 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.20+1835G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669138 | ||||||
chr20:43669202
|
A | G | 2 | a0001c0001t0001g0209a0009c0012t0001g0245 | 2 | NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.20+1899A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669202 | ||||||
chr20:43669347
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.20+2044G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669347 | ||||||
chr20:43669413
|
G | C | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0003c0005t0001g0261 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.20+2110G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669413 | ||||||
chr20:43669513
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.20+2210C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669513 | ||||||
chr20:43669806
|
A | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+2503A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669806 | ||||||
chr20:43669975
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | NA18967.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.20+2672G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669975 | ||||||
chr20:43669977
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0087 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.20+2674G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669977 | ||||||
chr20:43670023
|
T | G | 6 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0044others(3): Show | 6 | NA18946.hp2 NA18963.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+2720T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670023 | ||||||
chr20:43670109
|
T | TAAAC | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.20+2824_20+2827dup others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670109 | |||||
chr20:43670352
|
T | A | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+3049T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670352 | ||||||
chr20:43670469
|
A | C | 25 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(22): Show | 26 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.20+3166A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670469 | ||||||
chr20:43670639
|
A | G | 7 | a0003c0005t0001g0116a0003c0005t0001g0117a0003c0005t0001g0118others(4): Show | 7 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-3167A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670639 | ||||||
chr20:43670888
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.21-2918C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670888 | ||||||
chr20:43670953
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.21-2853A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670953 | ||||||
chr20:43670960
|
C | CT | 21 | a0001c0001t0002g0049a0001c0001t0002g0050a0002c0003t0001g0018others(18): Show | 21 | HG02083.hp2 HG02615.hp1 HG02723.hp2 others(18): Show |
intron_variant | MODIFIER | c.21-2838dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670960 | |||||
chr20:43670960
|
C | CTT | 9 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0032others(6): Show | 10 | HG01081.hp2 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-2839_21-2838dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670960 | |||||
chr20:43670960
|
CTTTTTTT others(8): Show |
C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 160 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.21-2837_21-2823del others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670960 | |||||
chr20:43670960
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0128 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.21-2837_21-2822del others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670960 | |||||
chr20:43670967
|
TTC | T | 8 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012others(5): Show | 9 | HG01243.hp1 HG02055.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-2837_21-2836del others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670967 | |||||
chr20:43670968
|
TC | T | 4 | a0002c0004t0001g0040a0002c0004t0001g0044a0002c0004t0001g0074others(1): Show | 4 | HG03041.hp2 NA18939.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-2837delC | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670968 | ||||||
chr20:43670969
|
C | T | 50 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0017t0002g0123others(47): Show | 51 | HG01081.hp2 HG01109.hp2 HG01361.hp2 others(48): Show |
intron_variant | MODIFIER | c.21-2837C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670969 | ||||||
chr20:43671093
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2713C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671093 | ||||||
chr20:43671188
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 161 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.21-2618G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671188 | ||||||
chr20:43671274
|
T | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 167 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.21-2532T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671274 | ||||||
chr20:43671451
|
C | T | 1 | a0002c0007t0003g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.21-2355C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671451 | ||||||
chr20:43671463
|
A | AT | 41 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0194others(38): Show | 41 | HG01167.hp2 HG01175.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.21-2319dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | |||||
chr20:43671463
|
A | ATT | 29 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0222others(26): Show | 29 | HG00741.hp2 HG01261.hp1 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.21-2320_21-2319dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | |||||
chr20:43671463
|
A | ATTT | 22 | a0001c0001t0001g0042a0002c0003t0001g0002a0002c0003t0001g0018others(19): Show | 23 | HG01081.hp2 HG01109.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.21-2321_21-2319dup others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | |||||
chr20:43671463
|
A | ATTTT | 8 | a0001c0001t0001g0043a0001c0001t0001g0087a0002c0003t0001g0017others(5): Show | 8 | HG01884.hp1 HG02083.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.21-2322_21-2319dup others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | |||||
chr20:43671463
|
A | ATTTTT | 6 | a0001c0001t0001g0051a0002c0003t0001g0013a0002c0003t0001g0014others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2323_21-2319dup others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | |||||
chr20:43671463
|
ATTTTTTT | A | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2325_21-2319del others(7): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | |||||
chr20:43671463
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0210 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.21-2331_21-2319del others(13): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | |||||
chr20:43671484
|
T | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2322T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671484 | ||||||
chr20:43671486
|
T | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2320T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671486 | ||||||
chr20:43671506
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.21-2300C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671506 | ||||||
chr20:43671622
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 213 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.21-2184A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671622 | ||||||
chr20:43671644
|
G | A | 1 | a0002c0004t0001g0075 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.21-2162G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671644 | ||||||
chr20:43671770
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | NA18941.hp2 NA18951.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-2036C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671770 | ||||||
chr20:43671841
|
T | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.21-1965T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671841 | ||||||
chr20:43671935
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.21-1871C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671935 | ||||||
chr20:43671947
|
C | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-1859C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671947 | ||||||
chr20:43671964
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.21-1842C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671964 | ||||||
chr20:43672085
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 167 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.21-1721T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672085 | ||||||
chr20:43672138
|
G | A | 1 | a0001c0013t0001g0052 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.21-1668G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672138 | ||||||
chr20:43672229
|
C | CTGTACAC others(40): Show |
163 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 169 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.21-1531_21-1530ins others(47): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43672229 | |||||
chr20:43672229
|
C | CTGTACTC others(40): Show |
1 | a0001c0001t0001g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.21-1572_21-1571ins others(47): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43672229 | |||||
chr20:43672427
|
CA | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 191 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.21-1365delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43672427 | |||||
chr20:43672454
|
A | G | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.21-1352A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672454 | ||||||
chr20:43672843
|
C | T | 1 | a0005c0008t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.21-963C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672843 | ||||||
chr20:43672855
|
T | G | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.21-951T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672855 | ||||||
chr20:43672897
|
C | T | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-909C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672897 | ||||||
chr20:43672900
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.21-906T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672900 | ||||||
chr20:43672915
|
C | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0242 | 3 | HG02055.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.21-891C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672915 | ||||||
chr20:43673246
|
C | CT | 20 | a0002c0004t0001g0041a0002c0004t0001g0044a0002c0004t0001g0045others(17): Show | 20 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(17): Show |
intron_variant | MODIFIER | c.21-544dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43673246 | |||||
chr20:43673246
|
CT | C | 45 | a0001c0001t0001g0062a0001c0001t0001g0187a0001c0001t0001g0188others(42): Show | 46 | HG00738.hp2 HG01081.hp2 HG01361.hp2 others(43): Show |
intron_variant | MODIFIER | c.21-544delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43673246 | |||||
chr20:43673246
|
CTT | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 158 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.21-545_21-544delTT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43673246 | |||||
chr20:43673511
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-295C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673511 | ||||||
chr20:43673561
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 119 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.21-245C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673561 | ||||||
chr20:43673679
|
A | C | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0003c0005t0001g0261 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.21-127A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673679 | ||||||
chr20:43673695
|
C | T | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.21-111C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673695 | ||||||
chr20:43673731
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.21-75C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673731 | ||||||
chr20:43673741
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | NA18967.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.21-65A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673741 | ||||||
chr20:43673742
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.21-64C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673742 | ||||||
chr20:43674018
|
G | T | 1 | a0003c0005t0001g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.114+119G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674018 | ||||||
chr20:43674101
|
G | C | 24 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(21): Show | 25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.114+202G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674101 | ||||||
chr20:43674103
|
G | A | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0003c0005t0001g0261 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.114+204G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674103 | ||||||
chr20:43674127
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0185 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.114+228C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674127 | ||||||
chr20:43674224
|
T | TC | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0128others(38): Show | 43 | HG00280.hp1 HG00544.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.114+331dupC | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674224 | |||||
chr20:43674224
|
T | TCC | 41 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0127others(38): Show | 42 | HG00642.hp1 HG00642.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.114+330_114+331dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674224 | |||||
chr20:43674224
|
T | TCCC | 14 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(11): Show | 14 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+329_114+331dup others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674224 | |||||
chr20:43674230
|
CA | C | 7 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0118others(4): Show | 7 | HG00741.hp2 HG01167.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+332delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674230 | ||||||
chr20:43674231
|
A | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.114+332A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674231 | ||||||
chr20:43674234
|
C | CCCCT | 13 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+335_114+336ins others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674234 | ||||||
chr20:43674234
|
C | CCCT | 27 | a0001c0001t0001g0001a0001c0001t0001g0104a0001c0001t0001g0124others(24): Show | 29 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.114+335_114+336ins others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674234 | ||||||
chr20:43674234
|
C | CCT | 4 | a0001c0001t0001g0234a0004c0006t0002g0004a0004c0006t0002g0100others(1): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+335_114+336ins others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674234 | ||||||
chr20:43674234
|
C | CT | 25 | a0001c0001t0001g0051a0001c0001t0001g0087a0001c0002t0001g0003others(22): Show | 28 | HG00544.hp2 HG01255.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.114+354dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674234 | |||||
chr20:43674235
|
T | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0148a0001c0001t0001g0149others(9): Show | 13 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+336T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674235 | ||||||
chr20:43674370
|
G | A | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+471G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674370 | ||||||
chr20:43674391
|
AT | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 170 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.114+507delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674391 | |||||
chr20:43674417
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.114+518C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674417 | ||||||
chr20:43674467
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0210 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.114+568A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674467 | ||||||
chr20:43674559
|
T | C | 1 | a0002c0003t0001g0035 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.114+660T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674559 | ||||||
chr20:43674569
|
A | G | 1 | a0003c0005t0001g0121 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.114+670A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674569 | ||||||
chr20:43674616
|
G | A | 24 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(21): Show | 25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.114+717G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674616 | ||||||
chr20:43674663
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.114+764G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674663 | ||||||
chr20:43674675
|
T | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG02258.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.114+776T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674675 | ||||||
chr20:43674685
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.114+786C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674685 | ||||||
chr20:43674907
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | NA18967.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.114+1008T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674907 | ||||||
chr20:43674924
|
T | G | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.114+1025T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674924 | ||||||
chr20:43674988
|
T | A | 19 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(16): Show | 19 | HG00738.hp2 HG00741.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.114+1089T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674988 | ||||||
chr20:43675138
|
C | A | 1 | a0005c0008t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.114+1239C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675138 | ||||||
chr20:43675316
|
T | C | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+1417T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675316 | ||||||
chr20:43675322
|
C | CT | 5 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012others(2): Show | 5 | HG02602.hp2 HG02615.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1436dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675322 | |||||
chr20:43675322
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.114+1423C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675322 | ||||||
chr20:43675323
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.114+1424T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675323 | ||||||
chr20:43675336
|
G | T | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+1437G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675336 | ||||||
chr20:43675338
|
G | A | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+1439G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675338 | ||||||
chr20:43675340
|
T | C | 1 | a0001c0002t0001g0263 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.114+1441T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675340 | ||||||
chr20:43675761
|
T | TTG | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 150 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.114+1886_114+1887d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | |||||
chr20:43675761
|
T | TTGTG | 31 | a0001c0001t0001g0007a0001c0001t0001g0151a0001c0001t0001g0188others(28): Show | 33 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.114+1884_114+1887d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | |||||
chr20:43675761
|
T | TTGTGTG | 12 | a0001c0001t0001g0187a0001c0017t0002g0123a0002c0003t0001g0013others(9): Show | 12 | HG01361.hp2 HG02258.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114+1882_114+1887d others(8): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | |||||
chr20:43675761
|
T | TTGTGTGT others(1): Show |
3 | a0002c0007t0003g0107a0003c0005t0001g0122a0007c0016t0003g0254 | 3 | HG02922.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.114+1880_114+1887d others(10): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | |||||
chr20:43675761
|
T | TTGTGTGT others(3): Show |
9 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(6): Show | 9 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+1878_114+1887d others(12): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | |||||
chr20:43675894
|
G | A | 1 | a0001c0002t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.114+1995G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675894 | ||||||
chr20:43675911
|
G | GTT | 15 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(12): Show | 16 | HG00741.hp2 HG01167.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.114+2024_114+2025d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675911 | |||||
chr20:43675911
|
G | GTTT | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 146 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.114+2023_114+2025d others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675911 | |||||
chr20:43675935
|
C | T | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.114+2036C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675935 | ||||||
chr20:43675952
|
T | C | 1 | a0003c0005t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.114+2053T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675952 | ||||||
chr20:43676047
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114+2148G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676047 | ||||||
chr20:43676104
|
C | T | 1 | a0002c0003t0001g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114+2205C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676104 | ||||||
chr20:43676351
|
A | G | 1 | a0002c0004t0001g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.114+2452A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676351 | ||||||
chr20:43676601
|
T | C | 1 | a0002c0007t0003g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114+2702T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676601 | ||||||
chr20:43676613
|
C | T | 7 | a0002c0003t0001g0002a0002c0003t0001g0027a0002c0003t0001g0033others(4): Show | 8 | HG01081.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2714C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676613 | ||||||
chr20:43676616
|
T | A | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0003c0005t0001g0261 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.114+2717T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676616 | ||||||
chr20:43676874
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0210 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.114+2975T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676874 | ||||||
chr20:43676878
|
G | GT | 7 | a0001c0001t0001g0001a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 9 | HG00673.hp2 HG01255.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.114+2990dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43676878 | |||||
chr20:43676878
|
GT | G | 9 | a0001c0001t0002g0049a0001c0001t0002g0050a0003c0005t0001g0261others(6): Show | 10 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+2990delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43676878 | |||||
chr20:43677039
|
T | C | 21 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0044others(18): Show | 21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.114+3140T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677039 | ||||||
chr20:43677274
|
G | C | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.114+3375G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677274 | ||||||
chr20:43677289
|
G | C | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.114+3390G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677289 | ||||||
chr20:43677416
|
A | G | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+3517A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677416 | ||||||
chr20:43677427
|
G | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0258 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.114+3528G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677427 | ||||||
chr20:43677449
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.114+3550A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677449 | ||||||
chr20:43677547
|
A | G | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0003c0005t0001g0261 | 3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.114+3648A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677547 | ||||||
chr20:43677579
|
C | T | 1 | a0002c0007t0003g0105 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.114+3680C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677579 | ||||||
chr20:43677615
|
C | T | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+3716C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677615 | ||||||
chr20:43677620
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 166 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.114+3721A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677620 | ||||||
chr20:43677652
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.114+3753T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677652 | ||||||
chr20:43677667
|
A | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 166 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.114+3768A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677667 | ||||||
chr20:43677669
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.114+3770T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677669 | ||||||
chr20:43677769
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.114+3870C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677769 | ||||||
chr20:43677839
|
A | C | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.114+3940A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677839 | ||||||
chr20:43677896
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-3888G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677896 | ||||||
chr20:43678067
|
TGCAAGAT others(26): Show |
T | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.115-3713_115-3681d others(35): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678067 | |||||
chr20:43678092
|
C | T | 1 | a0003c0005t0001g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.115-3692C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678092 | ||||||
chr20:43678173
|
C | T | 1 | a0002c0007t0003g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.115-3611C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678173 | ||||||
chr20:43678212
|
T | C | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-3572T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678212 | ||||||
chr20:43678275
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.115-3509C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678275 | ||||||
chr20:43678303
|
AAAAT | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0166a0001c0001t0001g0187others(45): Show | 50 | HG00738.hp2 HG00741.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.115-3473_115-3470d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678303 | |||||
chr20:43678311
|
T | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 119 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.115-3473T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678311 | ||||||
chr20:43678311
|
TAAAG | T | 11 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(8): Show | 11 | HG01884.hp1 HG02602.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-3453_115-3450d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678311 | |||||
chr20:43678319
|
GAAAGAAA others(10): Show |
G | 2 | a0001c0001t0001g0148a0001c0001t0001g0208 | 2 | HG01071.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.115-3461_115-3445d others(19): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678319 | |||||
chr20:43678323
|
GAAAGAAA others(6): Show |
G | 7 | a0001c0001t0001g0138a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 7 | HG00642.hp1 HG00642.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-3457_115-3445d others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678323 | |||||
chr20:43678327
|
GAAAGAAA others(2): Show |
G | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 115 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.115-3453_115-3445d others(11): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678327 | |||||
chr20:43678327
|
GAAAGAAA others(3): Show |
G | 2 | a0001c0001t0001g0164a0001c0001t0001g0232 | 2 | HG01346.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.115-3453_115-3444d others(12): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678327 | |||||
chr20:43678331
|
GAAAAA | G | 32 | a0001c0001t0001g0007a0001c0001t0001g0147a0001c0001t0001g0166others(29): Show | 33 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.115-3442_115-3438d others(7): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678331 | |||||
chr20:43678332
|
A | AAAG | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-3450_115-3449i others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678332 | |||||
chr20:43678349
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.115-3435A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678349 | ||||||
chr20:43678452
|
A | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 166 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.115-3332A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678452 | ||||||
chr20:43678466
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115-3318C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678466 | ||||||
chr20:43678505
|
A | G | 1 | a0003c0005t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.115-3279A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678505 | ||||||
chr20:43678791
|
A | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-2993A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678791 | ||||||
chr20:43678835
|
C | A | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115-2949C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678835 | ||||||
chr20:43678857
|
C | CA | 5 | a0001c0001t0001g0221a0004c0006t0002g0004a0004c0006t0002g0100others(2): Show | 6 | HG01243.hp1 HG01255.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-2910dupA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678857 | |||||
chr20:43678871
|
AAAAG | A | 37 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0002g0049others(34): Show | 38 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(35): Show |
intron_variant | MODIFIER | c.115-2909_115-2906d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678871 | |||||
chr20:43678873
|
AAG | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0151a0001c0001t0001g0161others(3): Show | 6 | HG01081.hp1 HG01167.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-2909_115-2908d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678873 | |||||
chr20:43678874
|
AG | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 129 | HG00280.hp1 HG00544.hp1 HG00673.hp1 others(126): Show |
intron_variant | MODIFIER | c.115-2909delG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678874 | ||||||
chr20:43678875
|
G | A | 29 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0140others(26): Show | 30 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.115-2909G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678875 | ||||||
chr20:43678883
|
CAT | C | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-2897_115-2896d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678883 | |||||
chr20:43678929
|
G | A | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-2855G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678929 | ||||||
chr20:43678951
|
A | C | 10 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0017t0002g0123others(7): Show | 10 | HG01361.hp2 HG02615.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-2833A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678951 | ||||||
chr20:43679000
|
T | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG00673.hp1 HG01109.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-2784T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679000 | ||||||
chr20:43679072
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.115-2712A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679072 | ||||||
chr20:43679194
|
T | C | 7 | a0003c0005t0001g0116a0003c0005t0001g0117a0003c0005t0001g0118others(4): Show | 7 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-2590T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679194 | ||||||
chr20:43679195
|
A | T | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.115-2589A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679195 | ||||||
chr20:43679268
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0197 | 2 | NA18959.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.115-2516C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679268 | ||||||
chr20:43679325
|
G | A | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-2459G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679325 | ||||||
chr20:43679473
|
GA | G | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.115-2308delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43679473 | |||||
chr20:43679517
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.115-2267C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679517 | ||||||
chr20:43679535
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.115-2249G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679535 | ||||||
chr20:43679577
|
T | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 213 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.115-2207T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679577 | ||||||
chr20:43679707
|
C | G | 1 | a0002c0003t0001g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.115-2077C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679707 | ||||||
chr20:43679727
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0168 | 2 | HG01109.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.115-2057T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679727 | ||||||
chr20:43679851
|
CGG | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 211 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.115-1930_115-1929d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43679851 | |||||
chr20:43679853
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.115-1931G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679853 | ||||||
chr20:43679912
|
CA | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 158 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.115-1859delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43679912 | |||||
chr20:43679928
|
A | T | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115-1856A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679928 | ||||||
chr20:43680024
|
TTTTA | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.115-1748_115-1745d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43680024 | |||||
chr20:43680075
|
T | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 213 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.115-1709T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680075 | ||||||
chr20:43680089
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.115-1695G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680089 | ||||||
chr20:43680176
|
G | A | 6 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(3): Show | 7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-1608G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680176 | ||||||
chr20:43680182
|
C | G | 3 | a0005c0008t0001g0112a0005c0008t0001g0114a0005c0008t0001g0115 | 3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.115-1602C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680182 | ||||||
chr20:43680308
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.115-1476A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680308 | ||||||
chr20:43680373
|
A | G | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.115-1411A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680373 | ||||||
chr20:43680514
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.115-1270T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680514 | ||||||
chr20:43680644
|
A | G | 1 | a0009c0012t0001g0245 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.115-1140A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680644 | ||||||
chr20:43680739
|
C | T | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115-1045C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680739 | ||||||
chr20:43680740
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.115-1044A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680740 | ||||||
chr20:43680906
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-878C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680906 | ||||||
chr20:43680945
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 158 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.115-839C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680945 | ||||||
chr20:43680981
|
A | G | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-803A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680981 | ||||||
chr20:43681168
|
T | C | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-616T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681168 | ||||||
chr20:43681276
|
C | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.115-508C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681276 | ||||||
chr20:43681292
|
C | G | 1 | a0004c0006t0002g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.115-492C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681292 | ||||||
chr20:43681359
|
C | G | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-425C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681359 | ||||||
chr20:43681374
|
A | G | 24 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(21): Show | 25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.115-410A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681374 | ||||||
chr20:43681378
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.115-406A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681378 | ||||||
chr20:43681608
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.115-176G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681608 | ||||||
chr20:43681657
|
T | C | 21 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0044others(18): Show | 21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.115-127T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681657 | ||||||
chr20:43681869
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.186+14T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43681869 | ||||||
chr20:43681886
|
G | A | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.186+31G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43681886 | ||||||
chr20:43682036
|
G | T | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.186+181G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682036 | ||||||
chr20:43682171
|
A | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 158 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.186+316A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682171 | ||||||
chr20:43682244
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0167a0001c0001t0001g0200others(1): Show | 4 | HG00280.hp2 HG01175.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+389G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682244 | ||||||
chr20:43682249
|
C | CACATTCG others(298): Show |
3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.186+408_186+409ins others(305): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43682249 | |||||
chr20:43682263
|
T | TA | 8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(5): Show | 8 | HG01884.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+409dupA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43682263 | |||||
chr20:43682430
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.187-364C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682430 | ||||||
chr20:43682448
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.187-346T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682448 | ||||||
chr20:43682479
|
T | C | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-315T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682479 | ||||||
chr20:43682511
|
G | A | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.187-283G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682511 | ||||||
chr20:43682582
|
A | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.187-212A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682582 | ||||||
chr20:43682947
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.279+61C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43682947 | ||||||
chr20:43683215
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.279+329T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683215 | ||||||
chr20:43683383
|
C | G | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+497C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683383 | ||||||
chr20:43683389
|
G | T | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+503G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683389 | ||||||
chr20:43683479
|
C | A | 5 | a0001c0001t0001g0140a0001c0001t0001g0171a0001c0001t0001g0182others(2): Show | 5 | HG02735.hp1 NA18965.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+593C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683479 | ||||||
chr20:43683549
|
G | GC | 13 | a0001c0001t0001g0104a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.279+664dupC | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683549 | |||||
chr20:43683550
|
C | CCT | 5 | a0003c0005t0001g0116a0003c0005t0001g0117a0003c0005t0001g0118others(2): Show | 5 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+664_279+665ins others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683550 | ||||||
chr20:43683550
|
CA | C | 5 | a0001c0001t0001g0125a0001c0001t0001g0226a0005c0008t0001g0112others(2): Show | 5 | HG02486.hp1 HG02886.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+665delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683550 | ||||||
chr20:43683551
|
A | AT | 6 | a0001c0002t0001g0071a0001c0002t0001g0099a0002c0004t0001g0047others(3): Show | 6 | HG00544.hp2 HG02056.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+685dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | |||||
chr20:43683551
|
A | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 140 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.279+665A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683551 | ||||||
chr20:43683551
|
A | T | 19 | a0001c0001t0001g0104a0001c0001t0001g0144a0001c0001t0001g0145others(16): Show | 19 | HG00741.hp2 HG01167.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.279+665A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683551 | ||||||
chr20:43683551
|
AT | A | 9 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(6): Show | 9 | HG01884.hp1 HG02630.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.279+685delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | |||||
chr20:43683551
|
ATT | A | 26 | a0001c0001t0002g0049a0002c0003t0001g0002a0002c0003t0001g0014others(23): Show | 27 | HG01081.hp2 HG01361.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.279+684_279+685del others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | |||||
chr20:43683551
|
ATTT | A | 5 | a0002c0007t0001g0110a0002c0007t0003g0106a0002c0007t0003g0107others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+683_279+685del others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | |||||
chr20:43683551
|
ATTTT | A | 6 | a0001c0017t0002g0123a0004c0006t0002g0004a0004c0006t0002g0100others(3): Show | 7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+682_279+685del others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | |||||
chr20:43683552
|
T | C | 5 | a0001c0001t0001g0125a0001c0001t0001g0226a0005c0008t0001g0112others(2): Show | 5 | HG02486.hp1 HG02886.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+666T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683552 | ||||||
chr20:43683607
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(1): Show | 4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+721G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683607 | ||||||
chr20:43683614
|
C | T | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+728C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683614 | ||||||
chr20:43683646
|
C | T | 3 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0093 | 3 | HG01099.hp2 HG01175.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.279+760C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683646 | ||||||
chr20:43683657
|
G | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 147 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.279+771G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683657 | ||||||
chr20:43683664
|
G | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.279+778G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683664 | ||||||
chr20:43683720
|
A | AT | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+841dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683720 | |||||
chr20:43683782
|
C | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(5): Show | 8 | HG01884.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+896C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683782 | ||||||
chr20:43683843
|
C | T | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.279+957C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683843 | ||||||
chr20:43683979
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.279+1093G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683979 | ||||||
chr20:43684013
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.279+1127C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684013 | ||||||
chr20:43684038
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.279+1152C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684038 | ||||||
chr20:43684052
|
T | C | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+1166T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684052 | ||||||
chr20:43684208
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 163 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.279+1322T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684208 | ||||||
chr20:43684226
|
C | CT | 36 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(33): Show | 37 | HG01081.hp2 HG01884.hp1 HG02083.hp2 others(34): Show |
intron_variant | MODIFIER | c.279+1353dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684226 | |||||
chr20:43684276
|
C | T | 1 | a0003c0005t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.279+1390C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684276 | ||||||
chr20:43684294
|
A | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1408A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684294 | ||||||
chr20:43684423
|
G | A | 3 | a0002c0003t0001g0027a0002c0003t0001g0033a0002c0003t0001g0035 | 3 | HG01081.hp2 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.279+1537G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684423 | ||||||
chr20:43684449
|
C | G | 2 | a0001c0001t0001g0209a0009c0012t0001g0245 | 2 | NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.279+1563C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684449 | ||||||
chr20:43684515
|
G | A | 21 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0044others(18): Show | 21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+1629G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684515 | ||||||
chr20:43684530
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.279+1644C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684530 | ||||||
chr20:43684534
|
C | CT | 42 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(39): Show | 44 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.279+1665dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684534 | |||||
chr20:43684534
|
C | CTT | 8 | a0001c0017t0002g0123a0002c0003t0001g0025a0002c0007t0001g0110others(5): Show | 8 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+1664_279+1665d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684534 | |||||
chr20:43684615
|
A | G | 21 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0044others(18): Show | 21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+1729A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684615 | ||||||
chr20:43684707
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG02083.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.279+1821G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684707 | ||||||
chr20:43684752
|
G | C | 21 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0044others(18): Show | 21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+1866G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684752 | ||||||
chr20:43684770
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.279+1884G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684770 | ||||||
chr20:43684774
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.279+1888T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684774 | ||||||
chr20:43684787
|
C | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0072others(1): Show | 4 | HG00544.hp2 HG02027.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+1901C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684787 | ||||||
chr20:43684801
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.279+1915T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684801 | ||||||
chr20:43684838
|
TA | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 211 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.279+1965delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684838 | |||||
chr20:43684850
|
A | C | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+1964A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684850 | ||||||
chr20:43684854
|
CAAAAG | C | 46 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(43): Show | 47 | HG01081.hp2 HG01109.hp2 HG02056.hp1 others(44): Show |
intron_variant | MODIFIER | c.279+1973_279+1977d others(7): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684854 | |||||
chr20:43684912
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.280-1940T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684912 | ||||||
chr20:43684980
|
C | T | 21 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0044others(18): Show | 21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.280-1872C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684980 | ||||||
chr20:43685059
|
A | G | 3 | a0002c0003t0001g0002a0002c0003t0001g0034a0002c0003t0001g0036 | 4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-1793A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685059 | ||||||
chr20:43685108
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 150 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.280-1744T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685108 | ||||||
chr20:43685147
|
CA | C | 7 | a0001c0001t0001g0216a0001c0017t0002g0123a0004c0006t0002g0004others(4): Show | 8 | HG01074.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.280-1689delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43685147 | |||||
chr20:43685147
|
CAA | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.280-1690_280-1689d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43685147 | |||||
chr20:43685214
|
C | G | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.280-1638C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685214 | ||||||
chr20:43685427
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.280-1425T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685427 | ||||||
chr20:43685456
|
C | T | 3 | a0005c0008t0001g0112a0005c0008t0001g0114a0005c0008t0001g0115 | 3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.280-1396C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685456 | ||||||
chr20:43685697
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.280-1155G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685697 | ||||||
chr20:43685710
|
G | A | 2 | a0001c0001t0001g0209a0009c0012t0001g0245 | 2 | NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.280-1142G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685710 | ||||||
chr20:43685916
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.280-936A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685916 | ||||||
chr20:43686069
|
A | T | 2 | a0001c0001t0001g0209a0009c0012t0001g0245 | 2 | NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.280-783A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686069 | ||||||
chr20:43686263
|
T | C | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-589T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686263 | ||||||
chr20:43686273
|
G | A | 1 | a0001c0002t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.280-579G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686273 | ||||||
chr20:43686349
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.280-503C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686349 | ||||||
chr20:43686350
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.280-502G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686350 | ||||||
chr20:43686371
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 150 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.280-481C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686371 | ||||||
chr20:43686428
|
G | C | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-424G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686428 | ||||||
chr20:43686451
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 211 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.280-401G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686451 | ||||||
chr20:43686467
|
T | C | 8 | a0003c0005t0001g0116a0003c0005t0001g0117a0003c0005t0001g0118others(5): Show | 8 | HG00741.hp2 HG01167.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-385T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686467 | ||||||
chr20:43686636
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.280-216T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686636 | ||||||
chr20:43686640
|
T | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-212T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686640 | ||||||
chr20:43686652
|
G | A | 1 | a0001c0002t0001g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.280-200G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686652 | ||||||
chr20:43687254
|
C | T | 1 | a0002c0003t0001g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.500+182C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687254 | ||||||
chr20:43687319
|
C | T | 2 | a0002c0007t0003g0109a0003c0005t0001g0118 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.500+247C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687319 | ||||||
chr20:43687391
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.500+319T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687391 | ||||||
chr20:43687434
|
C | G | 1 | a0001c0002t0001g0069 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.500+362C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687434 | ||||||
chr20:43687460
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.500+388A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687460 | ||||||
chr20:43687770
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0127others(7): Show | 11 | HG00642.hp2 HG00741.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.500+698C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687770 | ||||||
chr20:43687942
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 175 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.500+870G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687942 | ||||||
chr20:43687998
|
C | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0227a0001c0001t0001g0228others(10): Show | 14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.500+926C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687998 | ||||||
chr20:43688010
|
C | CA | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 144 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.500+955dupA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43688010 | |||||
chr20:43688010
|
C | CAA | 8 | a0001c0001t0001g0140a0001c0001t0001g0198a0001c0001t0001g0206others(5): Show | 8 | HG02027.hp1 HG03225.hp2 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.500+954_500+955dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43688010 | |||||
chr20:43688047
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.500+975C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688047 | ||||||
chr20:43688196
|
T | G | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.500+1124T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688196 | ||||||
chr20:43688248
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.500+1176C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688248 | ||||||
chr20:43688263
|
G | A | 2 | a0001c0002t0001g0061a0001c0002t0001g0092 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.500+1191G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688263 | ||||||
chr20:43688450
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.500+1378C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688450 | ||||||
chr20:43688779
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.500+1707A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688779 | ||||||
chr20:43688800
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 235 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(232): Show |
intron_variant | MODIFIER | c.500+1728T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688800 | ||||||
chr20:43688812
|
C | T | 49 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(46): Show | 50 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.500+1740C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688812 | ||||||
chr20:43688851
|
A | C | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+1779A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688851 | ||||||
chr20:43689028
|
G | T | 1 | a0002c0004t0001g0075 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.500+1956G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689028 | ||||||
chr20:43689043
|
GGCCTCCC others(1786): Show |
G | 1 | a0001c0002t0001g0069 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.500+1979_501-1314d others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43689043 | |||||
chr20:43689118
|
C | T | 10 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.500+2046C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689118 | ||||||
chr20:43689176
|
C | G | 1 | a0002c0003t0001g0017 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.500+2104C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689176 | ||||||
chr20:43689892
|
G | C | 7 | a0003c0005t0001g0116a0003c0005t0001g0117a0003c0005t0001g0118others(4): Show | 7 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.501-2265G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689892 | ||||||
chr20:43689961
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.501-2196G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689961 | ||||||
chr20:43690164
|
C | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-1993C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690164 | ||||||
chr20:43690192
|
G | T | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.501-1965G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690192 | ||||||
chr20:43690192
|
GT | G | 58 | a0001c0001t0001g0140a0001c0017t0002g0123a0002c0003t0001g0002others(55): Show | 60 | HG00741.hp2 HG01081.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.501-1952delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43690192 | |||||
chr20:43690194
|
T | G | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-1963T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690194 | ||||||
chr20:43690202
|
T | G | 32 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0124others(29): Show | 35 | HG00544.hp2 HG01167.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.501-1955T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690202 | ||||||
chr20:43690293
|
C | T | 7 | a0001c0017t0002g0123a0002c0007t0001g0110a0002c0007t0003g0105others(4): Show | 7 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-1864C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690293 | ||||||
chr20:43690325
|
C | G | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.501-1832C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690325 | ||||||
chr20:43690362
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.501-1795C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690362 | ||||||
chr20:43690366
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.501-1791T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690366 | ||||||
chr20:43690735
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.501-1422A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690735 | ||||||
chr20:43690873
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.501-1284C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690873 | ||||||
chr20:43690876
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 235 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(232): Show |
intron_variant | MODIFIER | c.501-1281G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690876 | ||||||
chr20:43690984
|
C | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 235 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(232): Show |
intron_variant | MODIFIER | c.501-1173C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690984 | ||||||
chr20:43691229
|
T | C | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(1): Show | 4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-928T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691229 | ||||||
chr20:43691257
|
G | C | 3 | a0001c0002t0001g0003a0001c0002t0001g0067a0001c0002t0001g0069 | 4 | NA18941.hp1 NA18945.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-900G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691257 | ||||||
chr20:43691300
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.501-857A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691300 | ||||||
chr20:43691308
|
T | A | 29 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(26): Show | 31 | HG01081.hp2 HG01243.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.501-849T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691308 | ||||||
chr20:43691309
|
A | T | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.501-848A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691309 | ||||||
chr20:43691313
|
T | A | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-844T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691313 | ||||||
chr20:43691479
|
G | A | 3 | a0002c0004t0001g0010a0002c0004t0001g0011a0002c0004t0001g0012 | 3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.501-678G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691479 | ||||||
chr20:43691491
|
C | A | 11 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(8): Show | 11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.501-666C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691491 | ||||||
chr20:43691492
|
C | T | 11 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(8): Show | 11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.501-665C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691492 | ||||||
chr20:43691543
|
A | AT | 145 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 151 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.501-600dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43691543 | |||||
chr20:43691543
|
A | ATT | 9 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0168others(6): Show | 9 | HG01109.hp1 HG01952.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-601_501-600dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43691543 | |||||
chr20:43691566
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.501-591A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691566 | ||||||
chr20:43691603
|
C | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0253others(1): Show | 4 | HG01891.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-554C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691603 | ||||||
chr20:43691639
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.501-518A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691639 | ||||||
chr20:43691768
|
A | G | 1 | a0002c0003t0001g0030 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.501-389A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691768 | ||||||
chr20:43691785
|
C | T | 1 | a0010c0010t0001g0053 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.501-372C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691785 | ||||||
chr20:43691842
|
A | AT | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-300dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43691842 | |||||
chr20:43691970
|
T | C | 12 | a0001c0017t0002g0123a0002c0007t0001g0110a0002c0007t0003g0105others(9): Show | 13 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.501-187T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691970 | ||||||
chr20:43692582
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+263A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43692582 | ||||||
chr20:43692982
|
A | G | 1 | a0003c0005t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.663+663A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43692982 | ||||||
chr20:43693011
|
T | C | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.663+692T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43693011 | ||||||
chr20:43693188
|
C | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.663+869C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43693188 | ||||||
chr20:43693579
|
C | T | 1 | a0002c0004t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.663+1260C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43693579 | ||||||
chr20:43693948
|
T | TGAGGTGG others(19): Show |
1 | a0002c0004t0001g0086 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.663+1640_663+1665d others(28): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43693948 | |||||
chr20:43693991
|
T | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.663+1672T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43693991 | ||||||
chr20:43694071
|
G | T | 6 | a0002c0007t0001g0110a0002c0007t0003g0105a0002c0007t0003g0106others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.663+1752G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694071 | ||||||
chr20:43694115
|
G | A | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663+1796G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694115 | ||||||
chr20:43694245
|
T | G | 1 | a0002c0003t0001g0212 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.663+1926T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694245 | ||||||
chr20:43694294
|
T | G | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663+1975T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694294 | ||||||
chr20:43694325
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.663+2006C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694325 | ||||||
chr20:43694343
|
A | G | 3 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0093 | 3 | HG01099.hp2 HG01175.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.663+2024A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694343 | ||||||
chr20:43694373
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.663+2054T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694373 | ||||||
chr20:43694394
|
A | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+2075A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694394 | ||||||
chr20:43694396
|
T | TTA | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+2077_663+2078i others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694396 | ||||||
chr20:43694414
|
C | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+2095C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694414 | ||||||
chr20:43694530
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.663+2211G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694530 | ||||||
chr20:43694699
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.663+2380G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694699 | ||||||
chr20:43694843
|
C | T | 1 | a0002c0004t0001g0044 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.663+2524C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694843 | ||||||
chr20:43695037
|
A | AT | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.663+2733dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43695037 | |||||
chr20:43695095
|
G | A | 1 | a0004c0006t0002g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.663+2776G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695095 | ||||||
chr20:43695190
|
C | T | 1 | a0002c0004t0001g0075 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.663+2871C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695190 | ||||||
chr20:43695191
|
G | A | 24 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(21): Show | 25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.663+2872G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695191 | ||||||
chr20:43695240
|
C | T | 16 | a0001c0017t0002g0123a0002c0003t0001g0013a0002c0003t0001g0014others(13): Show | 17 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.663+2921C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695240 | ||||||
chr20:43695382
|
T | C | 1 | a0002c0004t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.663+3063T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695382 | ||||||
chr20:43695427
|
A | G | 3 | a0002c0003t0001g0002a0002c0003t0001g0034a0002c0003t0001g0036 | 4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+3108A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695427 | ||||||
chr20:43695466
|
T | C | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(1): Show | 4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+3147T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695466 | ||||||
chr20:43695550
|
G | A | 1 | a0002c0003t0001g0030 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.663+3231G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695550 | ||||||
chr20:43695578
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.663+3259A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695578 | ||||||
chr20:43695594
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.663+3275G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695594 | ||||||
chr20:43695617
|
C | G | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663+3298C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695617 | ||||||
chr20:43695686
|
CA | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+3381delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43695686 | |||||
chr20:43695695
|
A | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 147 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.663+3376A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695695 | ||||||
chr20:43695752
|
A | AG | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 148 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.663+3435dupG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43695752 | |||||
chr20:43695767
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.663+3448G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695767 | ||||||
chr20:43695902
|
C | G | 1 | a0002c0004t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.663+3583C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695902 | ||||||
chr20:43695950
|
G | A | 1 | a0001c0002t0001g0057 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.663+3631G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695950 | ||||||
chr20:43695977
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.663+3658T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695977 | ||||||
chr20:43696095
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.664-3662G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696095 | ||||||
chr20:43696107
|
A | T | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664-3650A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696107 | ||||||
chr20:43696243
|
CT | C | 11 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(8): Show | 11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.664-3500delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43696243 | |||||
chr20:43696263
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.664-3494G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696263 | ||||||
chr20:43696484
|
A | G | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664-3273A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696484 | ||||||
chr20:43696486
|
A | ACTGGGAT others(1001): Show |
4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.664-2994_664-2993i others(1010): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43696486 | |||||
chr20:43696486
|
A | ACTGGGAT others(497): Show |
40 | a0002c0003t0001g0002a0002c0003t0001g0018a0002c0003t0001g0019others(37): Show | 41 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(38): Show |
intron_variant | MODIFIER | c.664-2907_664-2906i others(506): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43696486 | |||||
chr20:43696486
|
A | ACTGGGAT others(498): Show |
141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 146 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.664-3017_664-3016i others(507): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43696486 | |||||
chr20:43696764
|
G | C | 16 | a0001c0017t0002g0123a0002c0003t0001g0013a0002c0003t0001g0014others(13): Show | 17 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.664-2993G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696764 | ||||||
chr20:43696851
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.664-2906T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696851 | ||||||
chr20:43696972
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.664-2785G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696972 | ||||||
chr20:43697021
|
G | A | 5 | a0002c0004t0001g0011a0002c0004t0001g0012a0005c0008t0001g0112others(2): Show | 5 | HG02486.hp1 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-2736G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697021 | ||||||
chr20:43697180
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.664-2577G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697180 | ||||||
chr20:43697424
|
A | G | 11 | a0003c0005t0001g0113a0003c0005t0001g0116a0003c0005t0001g0117others(8): Show | 11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.664-2333A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697424 | ||||||
chr20:43697593
|
A | T | 1 | a0003c0005t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.664-2164A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697593 | ||||||
chr20:43697661
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.664-2096T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697661 | ||||||
chr20:43697784
|
G | A | 1 | a0002c0004t0001g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.664-1973G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697784 | ||||||
chr20:43697875
|
A | G | 4 | a0002c0007t0001g0110a0002c0007t0003g0107a0002c0007t0003g0108others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-1882A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697875 | ||||||
chr20:43697891
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.664-1866G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697891 | ||||||
chr20:43697900
|
G | A | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.664-1857G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697900 | ||||||
chr20:43697914
|
C | CA | 31 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0213others(28): Show | 32 | HG01081.hp2 HG01175.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.664-1825dupA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43697914 | |||||
chr20:43697914
|
C | CAA | 11 | a0001c0017t0002g0123a0002c0007t0001g0110a0002c0007t0003g0105others(8): Show | 12 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.664-1826_664-1825d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43697914 | |||||
chr20:43697937
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.664-1820G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697937 | ||||||
chr20:43698061
|
CT | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 136 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.664-1677delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698061 | |||||
chr20:43698061
|
CTT | C | 20 | a0002c0003t0001g0017a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 20 | HG02083.hp2 HG02486.hp1 HG02886.hp1 others(17): Show |
intron_variant | MODIFIER | c.664-1678_664-1677d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698061 | |||||
chr20:43698080
|
T | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 215 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.664-1677T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698080 | ||||||
chr20:43698080
|
T | TG | 7 | a0001c0001t0001g0241a0002c0007t0001g0110a0002c0007t0003g0105others(4): Show | 7 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-1677_664-1676i others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698080 | ||||||
chr20:43698080
|
T | TTG | 4 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0102others(1): Show | 5 | HG02055.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-1677_664-1676i others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698080 | ||||||
chr20:43698240
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 148 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.664-1517A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698240 | ||||||
chr20:43698258
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-1499C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698258 | ||||||
chr20:43698347
|
G | A | 1 | a0002c0004t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.664-1410G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698347 | ||||||
chr20:43698349
|
A | G | 1 | a0002c0004t0001g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.664-1408A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698349 | ||||||
chr20:43698351
|
A | ATTTTTTT others(6): Show |
1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.664-1374_664-1362d others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
A | ATTTTTTT others(13): Show |
2 | a0001c0002t0001g0061a0001c0002t0001g0065 | 2 | HG03516.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.664-1381_664-1362d others(22): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTT | A | 5 | a0001c0002t0001g0054a0001c0002t0001g0057a0001c0002t0001g0059others(2): Show | 5 | HG01099.hp2 HG02257.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-1365_664-1362d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTTTTT others(3): Show |
A | 8 | a0001c0002t0001g0009a0001c0002t0001g0067a0001c0002t0001g0069others(5): Show | 9 | HG01934.hp2 HG01952.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.664-1371_664-1362d others(12): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTTTTT others(4): Show |
A | 5 | a0001c0002t0001g0008a0001c0002t0001g0070a0001c0002t0001g0071others(2): Show | 6 | HG00544.hp2 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-1372_664-1362d others(13): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0002t0001g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.664-1374_664-1362d others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTTTTT others(8): Show |
A | 12 | a0001c0001t0001g0042a0002c0003t0001g0013a0002c0003t0001g0014others(9): Show | 12 | HG01361.hp2 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.664-1376_664-1362d others(17): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTTTTT others(9): Show |
A | 20 | a0001c0001t0001g0051a0001c0001t0001g0087a0001c0001t0001g0189others(17): Show | 20 | HG01261.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.664-1377_664-1362d others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTTTTT others(10): Show |
A | 60 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0126others(57): Show | 61 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.664-1378_664-1362d others(19): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTTTTT others(11): Show |
A | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0048others(95): Show | 103 | HG00280.hp1 HG00280.hp2 HG00673.hp1 others(100): Show |
intron_variant | MODIFIER | c.664-1379_664-1362d others(20): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTTTTT others(12): Show |
A | 37 | a0001c0001t0001g0006a0001c0001t0001g0129a0001c0001t0001g0133others(34): Show | 38 | HG00544.hp1 HG00642.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.664-1380_664-1362d others(21): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698351
|
ATTTTTTT others(13): Show |
A | 1 | a0001c0011t0001g0259 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.664-1381_664-1362d others(22): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | |||||
chr20:43698414
|
G | A | 12 | a0001c0017t0002g0123a0002c0007t0001g0110a0002c0007t0003g0105others(9): Show | 13 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.664-1343G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698414 | ||||||
chr20:43698446
|
C | T | 1 | a0002c0004t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.664-1311C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698446 | ||||||
chr20:43698661
|
A | AT | 7 | a0001c0001t0001g0141a0001c0001t0001g0213a0001c0001t0001g0225others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.664-1074dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698661 | |||||
chr20:43698661
|
AT | A | 59 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(56): Show | 61 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.664-1074delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698661 | |||||
chr20:43698661
|
ATTT | A | 21 | a0001c0001t0002g0049a0002c0003t0001g0013a0002c0003t0001g0014others(18): Show | 21 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.664-1076_664-1074d others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698661 | |||||
chr20:43698809
|
C | T | 2 | a0001c0002t0001g0090a0001c0002t0001g0091 | 2 | HG01993.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.664-948C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698809 | ||||||
chr20:43698872
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.664-885G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698872 | ||||||
chr20:43698927
|
T | C | 1 | a0002c0003t0001g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.664-830T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698927 | ||||||
chr20:43699036
|
A | T | 1 | a0001c0001t0002g0049 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.664-721A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699036 | ||||||
chr20:43699080
|
C | G | 1 | a0001c0002t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.664-677C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699080 | ||||||
chr20:43699107
|
C | T | 1 | a0001c0002t0001g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.664-650C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699107 | ||||||
chr20:43699130
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.664-627C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699130 | ||||||
chr20:43699163
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.664-594C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699163 | ||||||
chr20:43699169
|
G | A | 1 | a0002c0004t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.664-588G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699169 | ||||||
chr20:43699205
|
ATTTTG | A | 7 | a0001c0017t0002g0123a0002c0007t0001g0110a0002c0007t0003g0105others(4): Show | 7 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-537_664-533del others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43699205 | |||||
chr20:43699214
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.664-543T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699214 | ||||||
chr20:43699246
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0132a0001c0001t0001g0136others(10): Show | 14 | HG00642.hp2 HG00741.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.664-511A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699246 | ||||||
chr20:43699325
|
C | T | 3 | a0005c0008t0001g0112a0005c0008t0001g0114a0005c0008t0001g0115 | 3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.664-432C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699325 | ||||||
chr20:43699340
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-417C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699340 | ||||||
chr20:43699444
|
T | C | 1 | a0002c0003t0001g0031 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.664-313T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699444 | ||||||
chr20:43699582
|
G | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.664-175G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699582 | ||||||
chr20:43699590
|
G | A | 12 | a0001c0017t0002g0123a0002c0007t0001g0110a0002c0007t0003g0105others(9): Show | 13 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.664-167G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699590 | ||||||
chr20:43700109
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 232 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(229): Show |
intron_variant | MODIFIER | c.951+65A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700109 | ||||||
chr20:43700136
|
C | T | 44 | a0001c0001t0001g0006a0001c0001t0001g0129a0001c0001t0001g0133others(41): Show | 45 | HG00544.hp1 HG00642.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.951+92C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700136 | ||||||
chr20:43700240
|
C | T | 49 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(46): Show | 50 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.951+196C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700240 | ||||||
chr20:43700292
|
G | A | 3 | a0005c0008t0001g0112a0005c0008t0001g0114a0005c0008t0001g0115 | 3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.951+248G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700292 | ||||||
chr20:43700453
|
G | A | 17 | a0002c0003t0001g0017a0002c0003t0001g0018a0002c0003t0001g0019others(14): Show | 17 | HG02083.hp2 HG03491.hp2 HG03492.hp2 others(14): Show |
intron_variant | MODIFIER | c.951+409G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700453 | ||||||
chr20:43700594
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.951+550C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700594 | ||||||
chr20:43700719
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.951+675G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700719 | ||||||
chr20:43700803
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.951+759A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700803 | ||||||
chr20:43700979
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.951+935C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700979 | ||||||
chr20:43701082
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.951+1038C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701082 | ||||||
chr20:43701159
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 146 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.951+1115C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701159 | ||||||
chr20:43701283
|
TTC | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0062others(26): Show | 31 | HG00280.hp2 HG00673.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.952-1205_952-1204d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43701283 | |||||
chr20:43701297
|
A | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.952-1193A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701297 | ||||||
chr20:43701305
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.952-1185G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701305 | ||||||
chr20:43701324
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.952-1166A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701324 | ||||||
chr20:43701430
|
A | G | 1 | a0001c0002t0001g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.952-1060A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701430 | ||||||
chr20:43701628
|
AG | A | 3 | a0005c0008t0001g0112a0005c0008t0001g0114a0005c0008t0001g0115 | 3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.952-861delG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701628 | ||||||
chr20:43701718
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.952-772C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701718 | ||||||
chr20:43701936
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.952-554T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701936 | ||||||
chr20:43701991
|
G | T | 2 | a0002c0004t0001g0083a0002c0004t0001g0086 | 2 | NA18939.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.952-499G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701991 | ||||||
chr20:43702300
|
T | C | 24 | a0002c0003t0001g0212a0002c0004t0001g0010a0002c0004t0001g0040others(21): Show | 24 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.952-190T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43702300 | ||||||
chr20:43702344
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.952-146G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43702344 | ||||||
chr20:43702413
|
A | C | 3 | a0005c0008t0001g0112a0005c0008t0001g0114a0005c0008t0001g0115 | 3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.952-77A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43702413 | ||||||
chr20:43702906
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG01433.hp2 | splice_region_variant&intron_variant | LOW | c.1365+3G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43702906 | ||||||
chr20:43702931
|
T | C | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1365+28T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43702931 | ||||||
chr20:43702937
|
C | G | 1 | a0001c0002t0001g0068 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1365+34C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43702937 | ||||||
chr20:43703206
|
C | T | 68 | a0002c0003t0001g0002a0002c0003t0001g0013a0002c0003t0001g0014others(65): Show | 69 | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1365+303C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703206 | ||||||
chr20:43703249
|
CA | C | 26 | a0002c0003t0001g0212a0002c0004t0001g0010a0002c0004t0001g0011others(23): Show | 26 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.1365+349delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43703249 | |||||
chr20:43703254
|
A | G | 18 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(15): Show | 18 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1365+351A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703254 | ||||||
chr20:43703310
|
C | T | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(1): Show | 4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+407C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703310 | ||||||
chr20:43703414
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1365+511C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703414 | ||||||
chr20:43703414
|
C | G | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1365+511C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703414 | ||||||
chr20:43703442
|
G | T | 24 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(21): Show | 25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.1365+539G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703442 | ||||||
chr20:43703446
|
C | A | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+543C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703446 | ||||||
chr20:43703700
|
C | T | 4 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0065others(1): Show | 4 | HG01978.hp2 HG02056.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+797C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703700 | ||||||
chr20:43703814
|
CCA | C | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(1): Show | 4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+914_1365+915d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43703814 | |||||
chr20:43703913
|
G | A | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365+1010G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703913 | ||||||
chr20:43704070
|
G | C | 1 | a0009c0012t0001g0245 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1366-1149G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704070 | ||||||
chr20:43704112
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1366-1107C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704112 | ||||||
chr20:43704142
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.1366-1077C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704142 | ||||||
chr20:43704222
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0062others(4): Show | 9 | HG00673.hp2 HG02071.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366-997G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704222 | ||||||
chr20:43704380
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1366-839G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704380 | ||||||
chr20:43704519
|
G | A | 1 | a0001c0002t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1366-700G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704519 | ||||||
chr20:43704610
|
G | C | 1 | a0002c0007t0003g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1366-609G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704610 | ||||||
chr20:43704611
|
C | G | 22 | a0002c0003t0001g0212a0002c0004t0001g0011a0002c0004t0001g0012others(19): Show | 22 | HG01081.hp1 HG02056.hp1 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.1366-608C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704611 | ||||||
chr20:43704653
|
C | G | 26 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0017t0002g0123others(23): Show | 27 | HG00741.hp2 HG01167.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1366-566C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704653 | ||||||
chr20:43704785
|
A | C | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0017t0002g0123 | 3 | HG02723.hp2 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1366-434A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704785 | ||||||
chr20:43704827
|
C | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0247 | 3 | HG01884.hp2 HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1366-392C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704827 | ||||||
chr20:43705036
|
C | G | 15 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(12): Show | 15 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366-183C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43705036 | ||||||
chr20:43705426
|
G | A | 1 | a0001c0001t0004g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1505+68G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705426 | ||||||
chr20:43705530
|
G | A | 73 | a0001c0017t0002g0123a0002c0003t0001g0002a0002c0003t0001g0017others(70): Show | 75 | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.1505+172G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705530 | ||||||
chr20:43705567
|
T | G | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+209T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705567 | ||||||
chr20:43705576
|
T | G | 6 | a0001c0017t0002g0123a0004c0006t0002g0004a0004c0006t0002g0100others(3): Show | 7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1505+218T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705576 | ||||||
chr20:43705672
|
A | ATATT | 25 | a0001c0001t0001g0043a0001c0001t0001g0137a0001c0001t0001g0150others(22): Show | 25 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1505+356_1505+359d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | |||||
chr20:43705672
|
A | ATATTTAT others(1): Show |
9 | a0001c0001t0001g0042a0001c0001t0001g0183a0001c0001t0001g0210others(6): Show | 9 | HG01261.hp2 HG01361.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1505+352_1505+359d others(10): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | |||||
chr20:43705672
|
A | ATATTTAT others(5): Show |
3 | a0001c0001t0001g0165a0001c0017t0002g0123a0003c0005t0001g0116 | 3 | HG01167.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1505+348_1505+359d others(14): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | |||||
chr20:43705672
|
ATATT | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0087a0001c0001t0001g0219others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1505+356_1505+359d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | |||||
chr20:43705672
|
ATATTTAT others(1): Show |
A | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+352_1505+359d others(10): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | |||||
chr20:43705672
|
ATATTTAT others(13): Show |
A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1505+340_1505+359d others(22): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | |||||
chr20:43705815
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1505+457C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705815 | ||||||
chr20:43705826
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1505+468G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705826 | ||||||
chr20:43705857
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1505+499C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705857 | ||||||
chr20:43705938
|
G | C | 4 | a0002c0007t0001g0110a0005c0008t0001g0112a0005c0008t0001g0114others(1): Show | 4 | HG02486.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1505+580G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705938 | ||||||
chr20:43706003
|
A | G | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1505+645A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706003 | ||||||
chr20:43706193
|
C | T | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1505+835C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706193 | ||||||
chr20:43706269
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0087 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1505+911A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706269 | ||||||
chr20:43706402
|
G | A | 4 | a0002c0007t0001g0110a0005c0008t0001g0112a0005c0008t0001g0114others(1): Show | 4 | HG02486.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1505+1044G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706402 | ||||||
chr20:43706462
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1505+1104A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706462 | ||||||
chr20:43706707
|
A | C | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0202others(4): Show | 7 | HG00738.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1505+1349A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706707 | ||||||
chr20:43706716
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0197 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1505+1358_1505+135 others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706716 | ||||||
chr20:43706717
|
A | AGTGTTTT others(5): Show |
1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1505+1359_1505+136 others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | AGTTT | 7 | a0003c0005t0001g0116a0003c0005t0001g0117a0003c0005t0001g0118others(4): Show | 7 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(8): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | AGTTTT | 23 | a0002c0004t0001g0011a0002c0004t0001g0040a0002c0004t0001g0044others(20): Show | 23 | HG01081.hp1 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(9): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | AGTTTTT | 6 | a0002c0003t0001g0212a0002c0004t0001g0010a0002c0004t0001g0012others(3): Show | 6 | HG02615.hp2 HG02738.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(10): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | AGTTTTTT others(5): Show |
1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1505+1359_1505+136 others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | AGTTTTTT others(3): Show |
3 | a0002c0003t0001g0013a0002c0003t0001g0015a0002c0003t0001g0016 | 3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(14): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | AGTTTTTT others(4): Show |
6 | a0002c0003t0001g0014a0002c0003t0001g0022a0002c0003t0001g0028others(3): Show | 6 | HG02717.hp2 NA18952.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | AGTTTTTT others(5): Show |
13 | a0002c0003t0001g0017a0002c0003t0001g0018a0002c0003t0001g0019others(10): Show | 13 | HG01361.hp2 HG02083.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | AGTTTTTT others(6): Show |
9 | a0002c0003t0001g0002a0002c0003t0001g0021a0002c0003t0001g0027others(6): Show | 10 | HG01081.hp2 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(17): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | AGTTTTTT others(7): Show |
2 | a0002c0003t0001g0036a0002c0003t0001g0039 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | ATTTT | 8 | a0001c0001t0001g0128a0001c0001t0001g0161a0001c0001t0001g0174others(5): Show | 8 | HG02027.hp1 NA18612.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(8): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0229 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1505+1359_1505+136 others(14): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | ATTTTTTT others(4): Show |
19 | a0001c0001t0001g0133a0001c0001t0001g0151a0001c0001t0001g0180others(16): Show | 19 | HG00738.hp2 HG01099.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | ATTTTTTT others(5): Show |
77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 81 | HG00280.hp2 HG00544.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | ATTTTTTT others(6): Show |
27 | a0001c0001t0001g0007a0001c0001t0001g0124a0001c0001t0001g0129others(24): Show | 28 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(17): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | ATTTTTTT others(7): Show |
6 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0001g0156others(3): Show | 6 | HG00738.hp1 HG01261.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706717
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1505+1359A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | ||||||
chr20:43706718
|
A | AAGTTTTT others(3): Show |
2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1505+1360_1505+136 others(14): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706718 | ||||||
chr20:43706718
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1505+1360_1505+136 others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706718 | ||||||
chr20:43706718
|
A | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 217 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.1505+1360A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706718 | ||||||
chr20:43706719
|
G | GTTTTTTT others(6): Show |
3 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0102 | 4 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1505+1363_1505+137 others(17): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43706719 | |||||
chr20:43706719
|
G | GTTTTTTT others(7): Show |
3 | a0004c0006t0002g0101a0004c0006t0002g0103a0005c0008t0001g0115 | 3 | HG01243.hp1 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1505+1362_1505+137 others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43706719 | |||||
chr20:43706719
|
G | GTTTTTTT others(8): Show |
1 | a0002c0007t0001g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1505+1375_1505+137 others(19): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43706719 | |||||
chr20:43706719
|
G | GTTTTTTT others(9): Show |
2 | a0005c0008t0001g0112a0005c0008t0001g0114 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1505+1375_1505+137 others(20): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43706719 | |||||
chr20:43706719
|
G | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 220 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.1505+1361G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706719 | ||||||
chr20:43706743
|
T | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0177a0001c0001t0001g0185others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1505+1385T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706743 | ||||||
chr20:43706904
|
C | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0160 | 2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1505+1546C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706904 | ||||||
chr20:43706916
|
G | A | 5 | a0002c0007t0003g0105a0002c0007t0003g0106a0002c0007t0003g0107others(2): Show | 5 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1505+1558G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706916 | ||||||
chr20:43706925
|
A | C | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1505+1567A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706925 | ||||||
chr20:43707040
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(187): Show | 196 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.1505+1682C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707040 | ||||||
chr20:43707181
|
G | GT | 7 | a0002c0003t0001g0002a0002c0003t0001g0027a0002c0003t0001g0033others(4): Show | 8 | HG01081.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1505+1837dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43707181 | |||||
chr20:43707181
|
GT | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0087a0001c0001t0001g0104others(38): Show | 42 | HG00544.hp1 HG00642.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1505+1837delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43707181 | |||||
chr20:43707194
|
T | A | 1 | a0002c0004t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1505+1836T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707194 | ||||||
chr20:43707195
|
T | A | 35 | a0001c0001t0001g0189a0001c0001t0001g0190a0002c0003t0001g0013others(32): Show | 36 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1505+1837T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707195 | ||||||
chr20:43707196
|
A | T | 25 | a0001c0001t0001g0176a0002c0003t0001g0017a0002c0003t0001g0018others(22): Show | 25 | HG01361.hp2 HG02083.hp2 HG02615.hp1 others(22): Show |
intron_variant | MODIFIER | c.1505+1838A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707196 | ||||||
chr20:43707197
|
A | T | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1505+1839A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707197 | ||||||
chr20:43707263
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1505+1905C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707263 | ||||||
chr20:43707565
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 145 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1505+2207C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707565 | ||||||
chr20:43707640
|
C | T | 72 | a0001c0017t0002g0123a0002c0003t0001g0002a0002c0003t0001g0013others(69): Show | 73 | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.1505+2282C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707640 | ||||||
chr20:43707768
|
T | C | 1 | a0002c0004t0001g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1506-2195T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707768 | ||||||
chr20:43707898
|
G | A | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-2065G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707898 | ||||||
chr20:43707959
|
T | C | 1 | a0001c0002t0001g0059 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1506-2004T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707959 | ||||||
chr20:43708044
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 145 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1506-1919C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708044 | ||||||
chr20:43708314
|
A | G | 1 | a0007c0016t0003g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1506-1649A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708314 | ||||||
chr20:43708317
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1506-1646C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708317 | ||||||
chr20:43708377
|
G | A | 6 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0044others(3): Show | 6 | NA18946.hp2 NA18963.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506-1586G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708377 | ||||||
chr20:43708388
|
C | A | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-1575C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708388 | ||||||
chr20:43708434
|
C | CT | 4 | a0001c0001t0001g0124a0001c0001t0001g0185a0001c0001t0001g0197others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-1521dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43708434 | |||||
chr20:43708495
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1506-1468G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708495 | ||||||
chr20:43708783
|
G | A | 4 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0214others(1): Show | 4 | NA18965.hp2 NA18990.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506-1180G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708783 | ||||||
chr20:43708847
|
C | G | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0253others(1): Show | 4 | HG01891.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-1116C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708847 | ||||||
chr20:43708919
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG02083.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1506-1044C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708919 | ||||||
chr20:43708947
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1506-1016G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708947 | ||||||
chr20:43708976
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1506-987G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708976 | ||||||
chr20:43708991
|
A | G | 5 | a0002c0007t0003g0105a0002c0007t0003g0106a0002c0007t0003g0107others(2): Show | 5 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506-972A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708991 | ||||||
chr20:43709126
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1506-837C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709126 | ||||||
chr20:43709134
|
AG | A | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-827delG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43709134 | |||||
chr20:43709235
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 145 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1506-728C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709235 | ||||||
chr20:43709297
|
A | C | 2 | a0001c0002t0001g0056a0001c0013t0001g0052 | 2 | NA18612.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1506-666A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709297 | ||||||
chr20:43709503
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1506-460T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709503 | ||||||
chr20:43709504
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1506-459C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709504 | ||||||
chr20:43709648
|
C | A | 5 | a0002c0007t0003g0105a0002c0007t0003g0106a0002c0007t0003g0107others(2): Show | 5 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506-315C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709648 | ||||||
chr20:43710078
|
G | A | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605+16G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710078 | ||||||
chr20:43710415
|
C | A | 1 | a0001c0017t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1605+353C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710415 | ||||||
chr20:43710551
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1605+489T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710551 | ||||||
chr20:43710671
|
G | T | 1 | a0002c0007t0003g0105 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1605+609G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710671 | ||||||
chr20:43710878
|
G | A | 1 | a0002c0004t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1606-610G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710878 | ||||||
chr20:43710963
|
T | G | 1 | a0001c0002t0001g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1606-525T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710963 | ||||||
chr20:43711053
|
C | T | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1606-435C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711053 | ||||||
chr20:43711142
|
G | A | 1 | a0001c0011t0001g0259 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1606-346G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711142 | ||||||
chr20:43711149
|
T | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1606-339T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711149 | ||||||
chr20:43711185
|
C | A | 1 | a0001c0001t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1606-303C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711185 | ||||||
chr20:43711233
|
G | T | 1 | a0001c0002t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1606-255G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711233 | ||||||
chr20:43711254
|
G | A | 24 | a0002c0003t0001g0002a0002c0003t0001g0017a0002c0003t0001g0018others(21): Show | 25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.1606-234G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711254 | ||||||
chr20:43711314
|
C | G | 1 | a0003c0005t0001g0116 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1606-174C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711314 | ||||||
chr20:43711416
|
TG | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0247 | 3 | HG01884.hp2 HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1606-70delG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43711416 | |||||
chr20:43711474
|
G | A | 6 | a0001c0017t0002g0123a0004c0006t0002g0004a0004c0006t0002g0100others(3): Show | 7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1606-14G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711474 | ||||||
chr20:43711773
|
A | G | 1 | a0001c0002t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1719+172A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43711773 | ||||||
chr20:43711886
|
C | T | 1 | a0002c0004t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1719+285C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43711886 | ||||||
chr20:43711923
|
G | T | 4 | a0002c0007t0003g0106a0002c0007t0003g0107a0002c0007t0003g0108others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1719+322G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43711923 | ||||||
chr20:43711993
|
G | A | 1 | a0002c0007t0003g0105 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1719+392G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43711993 | ||||||
chr20:43712022
|
G | A | 26 | a0002c0003t0001g0212a0002c0004t0001g0010a0002c0004t0001g0011others(23): Show | 26 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.1719+421G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712022 | ||||||
chr20:43712044
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 145 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1719+443G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712044 | ||||||
chr20:43712344
|
G | A | 5 | a0002c0007t0003g0105a0002c0007t0003g0106a0002c0007t0003g0107others(2): Show | 5 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720-658G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712344 | ||||||
chr20:43712376
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1720-626G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712376 | ||||||
chr20:43712712
|
G | A | 5 | a0004c0006t0002g0004a0004c0006t0002g0100a0004c0006t0002g0101others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720-290G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712712 | ||||||
chr20:43712790
|
A | C | 1 | a0002c0004t0001g0097 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1720-212A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712790 | ||||||
chr20:43712924
|
A | G | 23 | a0002c0003t0001g0212a0002c0004t0001g0040a0002c0004t0001g0041others(20): Show | 23 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.1720-78A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712924 | ||||||
chr20:43713260
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1824+154G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713260 | ||||||
chr20:43713309
|
C | T | 5 | a0001c0002t0001g0091a0002c0003t0001g0013a0002c0003t0001g0014others(2): Show | 5 | HG02300.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1824+203C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713309 | ||||||
chr20:43713310
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1824+204G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713310 | ||||||
chr20:43713312
|
G | A | 6 | a0002c0007t0003g0105a0002c0007t0003g0106a0002c0007t0003g0107others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1824+206G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713312 | ||||||
chr20:43713338
|
A | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0214others(1): Show | 4 | NA18965.hp2 NA18990.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1824+232A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713338 | ||||||
chr20:43713352
|
C | T | 16 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(13): Show | 17 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1824+246C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713352 | ||||||
chr20:43713391
|
C | CT | 12 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(9): Show | 12 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1824+298dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43713391 | |||||
chr20:43713413
|
A | G | 22 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0051others(19): Show | 23 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1824+307A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713413 | ||||||
chr20:43713421
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0151a0001c0001t0001g0164 | 3 | HG01346.hp2 HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1824+315C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713421 | ||||||
chr20:43713481
|
G | A | 1 | a0003c0005t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1824+375G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713481 | ||||||
chr20:43713549
|
G | A | 6 | a0001c0017t0002g0123a0004c0006t0002g0004a0004c0006t0002g0100others(3): Show | 7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1824+443G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713549 | ||||||
chr20:43713607
|
G | A | 6 | a0002c0007t0003g0105a0002c0007t0003g0106a0002c0007t0003g0107others(3): Show | 6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1824+501G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713607 | ||||||
chr20:43713676
|
C | T | 26 | a0002c0003t0001g0212a0002c0004t0001g0010a0002c0004t0001g0011others(23): Show | 26 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.1824+570C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713676 | ||||||
chr20:43713748
|
T | G | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1824+642T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713748 | ||||||
chr20:43713780
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1824+674G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713780 | ||||||
chr20:43713942
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1824+836T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713942 | ||||||
chr20:43714036
|
G | T | 1 | a0001c0001t0001g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1824+930G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714036 | ||||||
chr20:43714081
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 230 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(227): Show |
intron_variant | MODIFIER | c.1824+975C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714081 | ||||||
chr20:43714142
|
A | C | 1 | a0001c0001t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1825-992A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714142 | ||||||
chr20:43714281
|
G | T | 15 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(12): Show | 15 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1825-853G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714281 | ||||||
chr20:43714387
|
C | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.1825-747C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714387 | ||||||
chr20:43714421
|
C | T | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1825-713C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714421 | ||||||
chr20:43714471
|
C | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 210 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.1825-663C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714471 | ||||||
chr20:43714495
|
G | A | 7 | a0001c0001t0001g0206a0001c0017t0002g0123a0004c0006t0002g0004others(4): Show | 8 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-639G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714495 | ||||||
chr20:43714512
|
A | G | 4 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0262others(1): Show | 6 | HG01255.hp2 HG01496.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825-622A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714512 | ||||||
chr20:43714581
|
A | AT | 9 | a0001c0001t0001g0043a0001c0001t0001g0087a0001c0001t0001g0206others(6): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825-541dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43714581 | |||||
chr20:43714730
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 210 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.1825-404G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714730 | ||||||
chr20:43714793
|
G | T | 1 | a0001c0002t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1825-341G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714793 | ||||||
chr20:43714871
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1825-263C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714871 | ||||||
chr20:43714957
|
A | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0247 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1825-177A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714957 | ||||||
chr20:43715045
|
G | A | 5 | a0003c0005t0001g0116a0003c0005t0001g0118a0003c0005t0001g0119others(2): Show | 5 | HG00741.hp2 HG01167.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825-89G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43715045 | ||||||
chr20:43715067
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1825-67G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43715067 | ||||||
chr20:43715376
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1974+93C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715376 | ||||||
chr20:43715489
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1974+206T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715489 | ||||||
chr20:43715507
|
C | G | 1 | a0002c0004t0001g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1974+224C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715507 | ||||||
chr20:43715724
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1975-235G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715724 | ||||||
chr20:43715754
|
G | T | 1 | a0003c0005t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1975-205G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715754 | ||||||
chr20:43715791
|
C | T | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975-168C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715791 | ||||||
chr20:43715865
|
G | A | 4 | a0002c0007t0003g0106a0002c0007t0003g0107a0002c0007t0003g0108others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975-94G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715865 |