geneid | 5500 |
---|---|
ensemblid | ENSG00000213639.11 |
hgncid | 9282 |
symbol | PPP1CB |
name | protein phosphatase 1 catalytic subunit beta |
refseq_nuc | NM_002709.3 |
refseq_prot | NP_002700.1 |
ensembl_nuc | ENST00000395366.3 |
ensembl_prot | ENSP00000378769.2 |
mane_status | MANE Select |
chr | chr2 |
start | 28751830 |
end | 28802940 |
strand | + |
ver | v1.2 |
region | chr2:28751830-28802940 |
region5000 | chr2:28746830-28807940 |
regionname0 | PPP1CB_chr2_28751830_28802940 |
regionname5000 | PPP1CB_chr2_28746830_28807940 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 327 | 366 | 86 | 74 | 152 | 18 | 34 | 122 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3934 | 144 | 16 | 32 | 77 | 6 | 13 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0002 | 0/1 | 3932 | 61 | 14 | 19 | 12 | 6 | 9 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0003 | 0/0 | 3932 | 42 | 8 | 5 | 24 | 2 | 3 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0004 | 1/0 | 3933 | 21 | 6 | 6 | 7 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0005 | 0/0 | 3932 | 12 | 0 | 0 | 12 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0006 | 0/0 | 3935 | 10 | 1 | 0 | 4 | 1 | 4 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0007 | 0/0 | 3932 | 9 | 9 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0008 | 0/0 | 3932 | 8 | 6 | 2 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0009 | 0/0 | 3933 | 6 | 0 | 0 | 5 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0010 | 0/0 | 3932 | 5 | 4 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0011 | 0/0 | 3931 | 5 | 0 | 3 | 1 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0012 | 0/0 | 3934 | 5 | 4 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0013 | 0/0 | 3927 | 4 | 4 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0014 | 0/0 | 3933 | 3 | 0 | 1 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0015 | 0/0 | 3931 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0016 | 0/0 | 3934 | 2 | 0 | 0 | 0 | 0 | 2 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0017 | 0/0 | 3934 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0018 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0019 | 0/0 | 3932 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0020 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0021 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0022 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0023 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0024 | 0/0 | 3932 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0025 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0026 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0027 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0028 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0029 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0030 | 0/0 | 3934 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0031 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0032 | 0/0 | 3935 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0033 | 0/0 | 3935 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0034 | 0/0 | 3934 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0035 | 0/0 | 3934 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0036 | 0/0 | 3931 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0037 | 0/0 | 3935 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0038 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0039 | 0/0 | 3931 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0040 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0041 | 0/0 | 3931 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
t0042 | 0/0 | 3932 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 0 | 3 | 2 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0003 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0036 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0294 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 984 | 207 | 37 | 40 | 103 | 8 | 18 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002 | 0/1 | 984 | 159 | 49 | 34 | 49 | 10 | 16 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4917 | 143 | 16 | 32 | 77 | 6 | 12 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0004 | 1/0 | 4916 | 18 | 3 | 6 | 7 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0005 | 0/0 | 4915 | 12 | 0 | 0 | 12 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0006 | 0/0 | 4918 | 10 | 1 | 0 | 4 | 1 | 4 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0012 | 0/0 | 4917 | 5 | 4 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0013 | 0/0 | 4910 | 4 | 4 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0016 | 0/0 | 4917 | 2 | 0 | 0 | 0 | 0 | 2 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0017 | 0/0 | 4917 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0018 | 0/0 | 4915 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0023 | 0/0 | 4917 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0026 | 0/0 | 4915 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0027 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0028 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0029 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0030 | 0/0 | 4917 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0032 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0035 | 0/0 | 4917 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0036 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0001t0038 | 0/0 | 4913 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0001 | 0/0 | 4917 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0002 | 0/1 | 4915 | 61 | 14 | 19 | 12 | 6 | 9 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0003 | 0/0 | 4915 | 42 | 8 | 5 | 24 | 2 | 3 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0004 | 0/0 | 4916 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0007 | 0/0 | 4915 | 9 | 9 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0008 | 0/0 | 4915 | 8 | 6 | 2 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0009 | 0/0 | 4916 | 6 | 0 | 0 | 5 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0010 | 0/0 | 4915 | 5 | 4 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0011 | 0/0 | 4914 | 5 | 0 | 3 | 1 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0014 | 0/0 | 4916 | 3 | 0 | 1 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0015 | 0/0 | 4914 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0019 | 0/0 | 4915 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0020 | 0/0 | 4915 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0021 | 0/0 | 4915 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0022 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0024 | 0/0 | 4915 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0025 | 0/0 | 4915 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0031 | 0/0 | 4917 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0033 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0034 | 0/0 | 4917 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0037 | 0/0 | 4918 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0039 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0040 | 0/0 | 4915 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0041 | 0/0 | 4914 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
a0001c0002t0042 | 0/0 | 4915 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | copy fasta | chr2 | 28746830 | 28807940 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0294 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0004g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0006g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0012g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0012g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0012g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0012g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0013g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0013g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0016g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0016g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0017g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0017g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0018g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0023g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0026g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0027g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0028g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0029g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0030g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0032g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0035g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0036g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0001t0038g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0036 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0004g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0008g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0008g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0009g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0009g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0009g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0010g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0010g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0011g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0011g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0011g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0011g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0011g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0014g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0014g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0014g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0015g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0015g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0019g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0020g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0021g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0022g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0024g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0025g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0031g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0033g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0034g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0037g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0039g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0040g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0041g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
a0001c0002t0042g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0042 | EUR | GBR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0048 | EUR | GBR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0072 | EUR | FIN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0060 | EUR | FIN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | FIN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00438 | hp2 | a0001 | c0002 | t0003 | g0188 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00609 | hp2 | a0001 | c0002 | t0015 | g0186 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0141 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00673 | hp1 | a0001 | c0002 | t0009 | g0063 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00673 | hp2 | a0001 | c0001 | t0005 | g0340 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0144 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00738 | hp1 | a0001 | c0002 | t0019 | g0198 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0071 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0341 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01070 | hp2 | a0001 | c0002 | t0011 | g0035 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01074 | hp1 | a0001 | c0002 | t0008 | g0127 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01074 | hp2 | a0001 | c0002 | t0015 | g0197 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0189 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01099 | hp2 | a0001 | c0002 | t0014 | g0221 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01106 | hp2 | a0001 | c0002 | t0008 | g0168 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01109 | hp1 | a0001 | c0001 | t0030 | g0285 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0277 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01243 | hp2 | a0001 | c0002 | t0010 | g0226 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0133 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01256 | hp1 | a0001 | c0002 | t0011 | g0130 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0274 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0322 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01346 | hp1 | a0001 | c0001 | t0012 | g0272 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01346 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0164 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01433 | hp2 | a0001 | c0002 | t0011 | g0004 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0214 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0229 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0050 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01516 | hp1 | a0001 | c0002 | t0042 | g0001 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01516 | hp2 | a0001 | c0001 | t0006 | g0095 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01517 | hp1 | a0001 | c0002 | t0041 | g0001 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01884 | hp1 | a0001 | c0001 | t0027 | g0309 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01884 | hp2 | a0001 | c0001 | t0013 | g0023 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01891 | hp1 | a0001 | c0002 | t0033 | g0222 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01934 | hp1 | a0001 | c0002 | t0037 | g0346 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01978 | hp1 | a0001 | c0002 | t0003 | g0215 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02027 | hp1 | a0001 | c0002 | t0003 | g0211 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0310 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02258 | hp1 | a0001 | c0002 | t0003 | g0216 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0059 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02280 | hp1 | a0001 | c0002 | t0010 | g0224 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0295 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02451 | hp1 | a0001 | c0002 | t0007 | g0201 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02451 | hp2 | a0001 | c0001 | t0013 | g0002 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02572 | hp2 | a0001 | c0001 | t0023 | g0311 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0172 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0169 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0208 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02630 | hp1 | a0001 | c0001 | t0017 | g0321 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02647 | hp1 | a0001 | c0002 | t0007 | g0220 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02647 | hp2 | a0001 | c0001 | t0017 | g0335 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02723 | hp1 | a0001 | c0002 | t0003 | g0176 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02723 | hp2 | a0001 | c0001 | t0038 | g0022 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0008 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02735 | hp2 | a0001 | c0002 | t0011 | g0057 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02809 | hp1 | a0001 | c0001 | t0012 | g0281 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0150 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02818 | hp2 | a0001 | c0002 | t0008 | g0026 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02922 | hp1 | a0001 | c0002 | t0003 | g0174 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02922 | hp2 | a0001 | c0001 | t0028 | g0013 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0194 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02965 | hp2 | a0001 | c0002 | t0004 | g0343 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02970 | hp1 | a0001 | c0002 | t0022 | g0199 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02970 | hp2 | a0001 | c0002 | t0008 | g0025 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03098 | hp1 | a0001 | c0002 | t0007 | g0200 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03098 | hp2 | a0001 | c0002 | t0008 | g0028 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03130 | hp1 | a0001 | c0002 | t0004 | g0345 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03139 | hp2 | a0001 | c0002 | t0007 | g0219 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03195 | hp1 | a0001 | c0002 | t0007 | g0205 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03195 | hp2 | a0001 | c0001 | t0026 | g0296 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0228 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03225 | hp1 | a0001 | c0001 | t0012 | g0283 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0333 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03453 | hp1 | a0001 | c0002 | t0010 | g0227 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03453 | hp2 | a0001 | c0001 | t0029 | g0273 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03486 | hp1 | a0001 | c0002 | t0008 | g0128 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03486 | hp2 | a0001 | c0002 | t0039 | g0148 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03491 | hp1 | a0001 | c0001 | t0016 | g0119 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03492 | hp2 | a0001 | c0001 | t0016 | g0114 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03540 | hp1 | a0001 | c0002 | t0010 | g0223 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03579 | hp1 | a0001 | c0002 | t0010 | g0225 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03579 | hp2 | a0001 | c0001 | t0012 | g0334 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0137 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0041 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03704 | hp1 | a0001 | c0002 | t0024 | g0049 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0073 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03710 | hp1 | a0001 | c0002 | t0009 | g0165 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03831 | hp1 | a0001 | c0002 | t0003 | g0207 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03831 | hp2 | a0001 | c0001 | t0006 | g0339 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0131 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0166 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0132 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0159 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0238 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0338 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18522 | hp1 | a0001 | c0001 | t0036 | g0020 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18522 | hp2 | a0001 | c0001 | t0013 | g0002 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18906 | hp1 | a0001 | c0002 | t0007 | g0204 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18941 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18942 | hp1 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18943 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18948 | hp2 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18951 | hp1 | a0001 | c0001 | t0032 | g0116 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18954 | hp2 | a0001 | c0002 | t0025 | g0167 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18959 | hp1 | a0001 | c0002 | t0009 | g0070 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0134 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18973 | hp2 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18977 | hp2 | a0001 | c0002 | t0034 | g0046 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18980 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18982 | hp1 | a0001 | c0002 | t0011 | g0052 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18986 | hp2 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18990 | hp2 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18991 | hp2 | a0001 | c0002 | t0014 | g0209 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18993 | hp2 | a0001 | c0002 | t0014 | g0181 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18994 | hp2 | a0001 | c0002 | t0003 | g0212 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19001 | hp1 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19001 | hp2 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19002 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19012 | hp1 | a0001 | c0002 | t0009 | g0138 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0193 | AFR | LWK | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19030 | hp2 | a0001 | c0002 | t0007 | g0203 | AFR | LWK | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19043 | hp1 | a0001 | c0002 | t0031 | g0347 | AFR | LWK | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19043 | hp2 | a0001 | c0002 | t0007 | g0206 | AFR | LWK | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19056 | hp1 | a0001 | c0002 | t0009 | g0062 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19058 | hp2 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19060 | hp1 | a0001 | c0001 | t0035 | g0264 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19060 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19062 | hp1 | a0001 | c0001 | t0018 | g0232 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19065 | hp2 | a0001 | c0002 | t0021 | g0178 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19070 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19075 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19080 | hp1 | a0001 | c0002 | t0020 | g0040 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19080 | hp2 | a0001 | c0001 | t0006 | g0110 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19081 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19083 | hp1 | a0001 | c0002 | t0009 | g0139 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19088 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19090 | hp2 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0190 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ASW | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20129 | hp2 | a0001 | c0002 | t0007 | g0202 | AFR | ASW | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20752 | hp1 | a0001 | c0002 | t0003 | g0218 | EUR | TSI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20805 | hp2 | a0001 | c0002 | t0003 | g0179 | EUR | TSI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | GIH | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02109 | hp1 | a0001 | c0002 | t0008 | g0027 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0149 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG02559 | hp2 | a0001 | c0002 | t0008 | g0024 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0175 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0170 | AFR | USA | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
HG06807 | hp2 | a0001 | c0001 | t0013 | g0002 | AFR | USA | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20300 | hp1 | a0001 | c0002 | t0040 | g0147 | AFR | USA | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
NA20300 | hp2 | a0001 | c0002 | t0004 | g0344 | AFR | USA | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0036 | REF | REF | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0294 | REF | REF | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
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 |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:28778825
|
A | G | 1 | a0001c0002 | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
synonymous_variant | LOW | c.201A>G | p.Gln67Gln | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/8 | 496/4916 | 201/984 | 67/327 | chr2 | 28778825 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:28751922
|
T | C | 1 | a0001c0001t0018 | 1 | NA19062.hp1 | 5_prime_UTR_variant | MODIFIER | c.-203T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/8 | 203 | chr2 | 28751922 | |||||
chr2:28751924
|
C | T | 1 | a0001c0001t0018 | 1 | NA19062.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-201C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/8 | chr2 | 28751924 | ||||||
chr2:28751986
|
C | T | 2 | a0001c0002t0041a0001c0002t0042 | 2 | HG01516.hp1 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-139C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/8 | 139 | chr2 | 28751986 | |||||
chr2:28799389
|
A | G | 2 | a0001c0002t0039a0001c0002t0040 | 2 | HG03486.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*86A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 86 | chr2 | 28799389 | |||||
chr2:28799416
|
TTTAAC | T | 2 | a0001c0001t0013a0001c0001t0038 | 5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*118_*122delCTTAA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 118 | INFO_REALIGN_3_PRIME | chr2 | 28799416 | ||||
chr2:28799983
|
T | A | 1 | a0001c0002t0019 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 680 | chr2 | 28799983 | |||||
chr2:28800093
|
T | C | 9 | a0001c0002t0003a0001c0002t0007a0001c0002t0010others(6): Show | 65 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*790T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 790 | chr2 | 28800093 | |||||
chr2:28800198
|
G | A | 1 | a0001c0001t0023 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*895G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 895 | chr2 | 28800198 | |||||
chr2:28800226
|
C | CT | 15 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(12): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*946dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 947 | INFO_REALIGN_3_PRIME | chr2 | 28800226 | ||||
chr2:28800226
|
C | CTT | 2 | a0001c0001t0006a0001c0002t0037 | 11 | HG01516.hp2 HG01934.hp1 HG03540.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*945_*946dupTT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 947 | INFO_REALIGN_3_PRIME | chr2 | 28800226 | ||||
chr2:28800226
|
CT | C | 13 | a0001c0001t0026a0001c0002t0002a0001c0002t0003others(10): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*946delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 946 | INFO_REALIGN_3_PRIME | chr2 | 28800226 | ||||
chr2:28800226
|
CTT | C | 4 | a0001c0002t0011a0001c0002t0015a0001c0002t0039others(1): Show | 9 | HG00609.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*945_*946delTT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 945 | INFO_REALIGN_3_PRIME | chr2 | 28800226 | ||||
chr2:28800234
|
T | C | 1 | a0001c0002t0024 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*931T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 931 | chr2 | 28800234 | |||||
chr2:28800251
|
AGTT | A | 2 | a0001c0001t0013a0001c0001t0036 | 5 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*955_*957delGTT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 955 | INFO_REALIGN_3_PRIME | chr2 | 28800251 | ||||
chr2:28800270
|
A | G | 1 | a0001c0001t0035 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*967A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 967 | chr2 | 28800270 | |||||
chr2:28800321
|
G | A | 1 | a0001c0002t0025 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1018 | chr2 | 28800321 | |||||
chr2:28800634
|
G | T | 1 | a0001c0002t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1331 | chr2 | 28800634 | |||||
chr2:28800883
|
A | G | 10 | a0001c0002t0002a0001c0002t0009a0001c0002t0011others(7): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1580A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1580 | chr2 | 28800883 | |||||
chr2:28801071
|
G | T | 1 | a0001c0001t0017 | 2 | HG02630.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1768G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1768 | chr2 | 28801071 | |||||
chr2:28801255
|
A | G | 1 | a0001c0002t0021 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1952A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1952 | chr2 | 28801255 | |||||
chr2:28801403
|
A | C | 1 | a0001c0002t0020 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2100A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2100 | chr2 | 28801403 | |||||
chr2:28801432
|
C | CT | 6 | a0001c0001t0013a0001c0001t0030a0001c0001t0032others(3): Show | 9 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2143dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2144 | INFO_REALIGN_3_PRIME | chr2 | 28801432 | ||||
chr2:28801570
|
T | C | 1 | a0001c0002t0021 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2267T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2267 | chr2 | 28801570 | |||||
chr2:28801678
|
A | G | 1 | a0001c0001t0030 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2375 | chr2 | 28801678 | |||||
chr2:28801729
|
A | G | 3 | a0001c0001t0013a0001c0001t0038a0001c0002t0037 | 6 | HG01884.hp2 HG01934.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2426A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2426 | chr2 | 28801729 | |||||
chr2:28801746
|
T | G | 1 | a0001c0001t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2443T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2443 | chr2 | 28801746 | |||||
chr2:28801816
|
A | T | 1 | a0001c0001t0016 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2513A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2513 | chr2 | 28801816 | |||||
chr2:28801997
|
C | T | 1 | a0001c0002t0033 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2694C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2694 | chr2 | 28801997 | |||||
chr2:28802277
|
T | C | 1 | a0001c0002t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2974T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2974 | chr2 | 28802277 | |||||
chr2:28802368
|
G | C | 1 | a0001c0002t0010 | 5 | HG01243.hp2 HG02280.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3065G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3065 | chr2 | 28802368 | |||||
chr2:28802613
|
A | G | 17 | a0001c0002t0002a0001c0002t0003a0001c0002t0008others(14): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*3310A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3310 | chr2 | 28802613 | |||||
chr2:28802668
|
T | C | 1 | a0001c0001t0028 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3365T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3365 | chr2 | 28802668 | |||||
chr2:28802675
|
C | G | 3 | a0001c0001t0012a0001c0001t0017a0001c0001t0029 | 8 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3372C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3372 | chr2 | 28802675 | |||||
chr2:28802852
|
A | G | 1 | a0001c0001t0030 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3549A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3549 | chr2 | 28802852 | |||||
chr2:28802867
|
TAA | T | 2 | a0001c0001t0005a0001c0001t0018 | 13 | HG00544.hp2 HG00673.hp2 HG02027.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3565_*3566delAA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3565 | chr2 | 28802867 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:28752191
|
G | T | 5 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(2): Show | 5 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+15G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752191 | ||||||
chr2:28752241
|
G | C | 236 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(233): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.52+65G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752241 | ||||||
chr2:28752246
|
C | T | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.52+70C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752246 | ||||||
chr2:28752396
|
C | T | 1 | a0001c0002t0002g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52+220C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752396 | ||||||
chr2:28752430
|
G | C | 1 | a0001c0001t0018g0232 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.52+254G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752430 | ||||||
chr2:28752432
|
C | G | 1 | a0001c0001t0018g0232 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.52+256C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752432 | ||||||
chr2:28752458
|
G | A | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.52+282G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752458 | ||||||
chr2:28752540
|
C | G | 1 | a0001c0001t0018g0232 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.52+364C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752540 | ||||||
chr2:28752632
|
A | T | 1 | a0001c0001t0001g0230 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.52+456A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752632 | ||||||
chr2:28752669
|
A | T | 2 | a0001c0002t0002g0228a0001c0002t0002g0229 | 2 | HG01496.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.52+493A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752669 | ||||||
chr2:28752681
|
C | T | 5 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(2): Show | 5 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+505C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752681 | ||||||
chr2:28752787
|
T | A | 1 | a0001c0002t0003g0016 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+611T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752787 | ||||||
chr2:28752824
|
C | G | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.52+648C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752824 | ||||||
chr2:28752875
|
A | G | 1 | a0001c0002t0002g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52+699A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752875 | ||||||
chr2:28752950
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.52+774A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752950 | ||||||
chr2:28753032
|
A | G | 5 | a0001c0002t0010g0223a0001c0002t0010g0224a0001c0002t0010g0225others(2): Show | 5 | HG01243.hp2 HG02280.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+856A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753032 | ||||||
chr2:28753064
|
A | G | 1 | a0001c0002t0003g0016 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+888A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753064 | ||||||
chr2:28753065
|
G | A | 1 | a0001c0002t0003g0016 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+889G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753065 | ||||||
chr2:28753100
|
A | C | 1 | a0001c0001t0004g0341 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52+924A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753100 | ||||||
chr2:28753177
|
A | G | 5 | a0001c0001t0004g0021a0001c0001t0013g0002a0001c0001t0013g0023others(2): Show | 7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+1001A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753177 | ||||||
chr2:28753215
|
T | TC | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.52+1040dupC | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28753215 | |||||
chr2:28753363
|
A | T | 1 | a0001c0002t0003g0016 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+1187A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753363 | ||||||
chr2:28753502
|
T | C | 1 | a0001c0002t0003g0171 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.52+1326T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753502 | ||||||
chr2:28753537
|
A | G | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.52+1361A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753537 | ||||||
chr2:28753945
|
C | T | 1 | a0001c0001t0005g0340 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.52+1769C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753945 | ||||||
chr2:28753948
|
G | C | 5 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0026others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+1772G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753948 | ||||||
chr2:28754031
|
C | T | 2 | a0001c0002t0002g0169a0001c0002t0002g0170 | 2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.52+1855C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754031 | ||||||
chr2:28754099
|
A | C | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+1923A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754099 | ||||||
chr2:28754107
|
T | C | 2 | a0001c0001t0004g0021a0001c0001t0036g0020 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.52+1931T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754107 | ||||||
chr2:28754169
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.52+1993T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754169 | ||||||
chr2:28754196
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.52+2020T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754196 | ||||||
chr2:28754200
|
A | G | 1 | a0001c0002t0008g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.52+2024A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754200 | ||||||
chr2:28754225
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.52+2049G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754225 | ||||||
chr2:28754311
|
G | T | 1 | a0001c0002t0003g0016 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+2135G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754311 | ||||||
chr2:28754338
|
G | A | 1 | a0001c0002t0002g0030 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.52+2162G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754338 | ||||||
chr2:28754345
|
CG | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(123): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.52+2179delG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28754345 | |||||
chr2:28754345
|
CGG | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.52+2178_52+2179del others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28754345 | |||||
chr2:28754350
|
G | C | 1 | a0001c0002t0003g0016 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+2174G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754350 | ||||||
chr2:28754357
|
G | A | 15 | a0001c0002t0007g0200a0001c0002t0007g0201a0001c0002t0007g0202others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.52+2181G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754357 | ||||||
chr2:28754378
|
T | C | 223 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(220): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.52+2202T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754378 | ||||||
chr2:28754408
|
A | G | 199 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(196): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.52+2232A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754408 | ||||||
chr2:28754443
|
C | T | 4 | a0001c0002t0002g0131a0001c0002t0002g0132a0001c0002t0002g0166others(1): Show | 4 | HG03710.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+2267C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754443 | ||||||
chr2:28754454
|
A | G | 1 | a0001c0002t0002g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.52+2278A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754454 | ||||||
chr2:28754470
|
C | G | 1 | a0001c0002t0003g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.52+2294C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754470 | ||||||
chr2:28754574
|
A | G | 2 | a0001c0002t0002g0129a0001c0002t0011g0130 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.52+2398A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754574 | ||||||
chr2:28754580
|
A | G | 1 | a0001c0002t0003g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.52+2404A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754580 | ||||||
chr2:28754855
|
A | G | 1 | a0001c0002t0019g0198 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.52+2679A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754855 | ||||||
chr2:28754928
|
T | C | 2 | a0001c0002t0002g0037a0001c0002t0002g0038 | 2 | HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.52+2752T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754928 | ||||||
chr2:28755025
|
G | A | 6 | a0001c0001t0004g0018a0001c0001t0004g0021a0001c0001t0013g0002others(3): Show | 8 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+2849G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755025 | ||||||
chr2:28755028
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0337 | 2 | HG01106.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.52+2852C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755028 | ||||||
chr2:28755037
|
G | A | 2 | a0001c0001t0013g0002a0001c0001t0013g0023 | 4 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+2861G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755037 | ||||||
chr2:28755041
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52+2865A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755041 | ||||||
chr2:28755081
|
G | A | 3 | a0001c0002t0003g0172a0001c0002t0003g0218a0001c0002t0014g0221 | 3 | HG01099.hp2 HG02602.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.52+2905G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755081 | ||||||
chr2:28755208
|
C | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.52+3032C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755208 | ||||||
chr2:28755258
|
C | T | 4 | a0001c0002t0002g0131a0001c0002t0002g0132a0001c0002t0002g0166others(1): Show | 4 | HG03710.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+3082C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755258 | ||||||
chr2:28755292
|
G | A | 1 | a0001c0001t0030g0285 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.52+3116G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755292 | ||||||
chr2:28755313
|
T | G | 5 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0026others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+3137T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755313 | ||||||
chr2:28755329
|
C | T | 3 | a0001c0002t0008g0127a0001c0002t0008g0128a0001c0002t0008g0168 | 3 | HG01074.hp1 HG01106.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.52+3153C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755329 | ||||||
chr2:28755532
|
T | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0234a0001c0001t0001g0236others(11): Show | 14 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.52+3356T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755532 | ||||||
chr2:28755613
|
T | G | 5 | a0001c0001t0005g0240a0001c0001t0005g0291a0001c0001t0005g0292others(2): Show | 5 | HG00544.hp2 NA18944.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+3437T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755613 | ||||||
chr2:28755853
|
A | T | 1 | a0001c0002t0003g0016 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+3677A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755853 | ||||||
chr2:28755875
|
T | C | 21 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(18): Show | 21 | HG01243.hp2 HG01891.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+3699T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755875 | ||||||
chr2:28756030
|
A | G | 1 | a0001c0002t0015g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.52+3854A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756030 | ||||||
chr2:28756107
|
T | C | 3 | a0001c0001t0013g0002a0001c0001t0013g0023a0001c0001t0038g0022 | 5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+3931T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756107 | ||||||
chr2:28756210
|
T | C | 3 | a0001c0001t0013g0002a0001c0001t0013g0023a0001c0001t0038g0022 | 5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+4034T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756210 | ||||||
chr2:28756312
|
T | C | 1 | a0001c0002t0003g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.52+4136T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756312 | ||||||
chr2:28756323
|
T | C | 1 | a0001c0002t0002g0039 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.52+4147T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756323 | ||||||
chr2:28756330
|
C | T | 2 | a0001c0002t0002g0228a0001c0002t0002g0229 | 2 | HG01496.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.52+4154C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756330 | ||||||
chr2:28756499
|
T | G | 60 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(57): Show | 64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.52+4323T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756499 | ||||||
chr2:28756578
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.52+4402G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756578 | ||||||
chr2:28756808
|
TA | T | 350 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(347): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.52+4640delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28756808 | |||||
chr2:28756856
|
A | G | 1 | a0001c0001t0012g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52+4680A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756856 | ||||||
chr2:28756970
|
A | G | 2 | a0001c0002t0003g0195a0001c0002t0003g0196 | 2 | NA18942.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.52+4794A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756970 | ||||||
chr2:28757012
|
C | A | 1 | a0001c0001t0001g0286 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.52+4836C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757012 | ||||||
chr2:28757282
|
A | G | 2 | a0001c0002t0008g0127a0001c0002t0008g0128 | 2 | HG01074.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.52+5106A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757282 | ||||||
chr2:28757376
|
A | G | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+5200A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757376 | ||||||
chr2:28757380
|
C | T | 1 | a0001c0002t0003g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.52+5204C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757380 | ||||||
chr2:28757381
|
G | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0241others(18): Show | 23 | HG00280.hp1 HG01106.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.52+5205G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757381 | ||||||
chr2:28757525
|
G | C | 2 | a0001c0002t0003g0218a0001c0002t0014g0221 | 2 | HG01099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.52+5349G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757525 | ||||||
chr2:28757571
|
G | A | 1 | a0001c0002t0002g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.52+5395G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757571 | ||||||
chr2:28757763
|
G | C | 9 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(6): Show | 9 | HG00544.hp1 NA18948.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+5587G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757763 | ||||||
chr2:28757820
|
G | A | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+5644G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757820 | ||||||
chr2:28758034
|
AT | A | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.52+5866delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28758034 | |||||
chr2:28758048
|
A | AT | 6 | a0001c0001t0001g0126a0001c0001t0001g0239a0001c0001t0001g0282others(3): Show | 6 | HG02083.hp1 HG02698.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+5886dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28758048 | |||||
chr2:28758048
|
A | T | 1 | a0001c0002t0003g0016 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+5872A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758048 | ||||||
chr2:28758049
|
T | A | 1 | a0001c0002t0003g0016 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+5873T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758049 | ||||||
chr2:28758322
|
A | G | 1 | a0001c0002t0003g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.52+6146A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758322 | ||||||
chr2:28758355
|
C | G | 1 | a0001c0001t0004g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52+6179C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758355 | ||||||
chr2:28758586
|
A | G | 2 | a0001c0002t0002g0072a0001c0002t0002g0073 | 2 | HG00280.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.52+6410A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758586 | ||||||
chr2:28758610
|
C | T | 15 | a0001c0002t0007g0200a0001c0002t0007g0201a0001c0002t0007g0202others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.52+6434C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758610 | ||||||
chr2:28758650
|
A | C | 1 | a0001c0002t0002g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.52+6474A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758650 | ||||||
chr2:28758663
|
T | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0306 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.52+6487T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758663 | ||||||
chr2:28758755
|
G | A | 1 | a0001c0002t0020g0040 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.52+6579G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758755 | ||||||
chr2:28758788
|
C | G | 1 | a0001c0002t0002g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.52+6612C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758788 | ||||||
chr2:28759117
|
G | A | 131 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(128): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.52+6941G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759117 | ||||||
chr2:28759164
|
A | G | 131 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(128): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.52+6988A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759164 | ||||||
chr2:28759192
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.52+7016G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759192 | ||||||
chr2:28759239
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.52+7063C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759239 | ||||||
chr2:28759350
|
T | C | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.52+7174T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759350 | ||||||
chr2:28759484
|
C | T | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.52+7308C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759484 | ||||||
chr2:28759492
|
C | G | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+7316C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759492 | ||||||
chr2:28759520
|
C | CA | 88 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(85): Show | 91 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.52+7370dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759520 | |||||
chr2:28759520
|
C | CAA | 7 | a0001c0001t0001g0234a0001c0001t0001g0241a0001c0001t0001g0258others(4): Show | 7 | HG01106.hp1 HG02074.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+7369_52+7370dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759520 | |||||
chr2:28759520
|
CAAAAAAA others(3): Show |
C | 145 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(142): Show | 151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+7361_52+7370del others(10): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759520 | |||||
chr2:28759520
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0002t0031g0347a0001c0002t0037g0346 | 2 | HG01934.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52+7359_52+7370del others(12): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759520 | |||||
chr2:28759547
|
G | C | 2 | a0001c0001t0001g0302a0001c0001t0005g0252 | 2 | NA19001.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.52+7371G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759547 | ||||||
chr2:28759557
|
A | G | 3 | a0001c0001t0013g0002a0001c0001t0013g0023a0001c0001t0038g0022 | 5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+7381A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759557 | ||||||
chr2:28759643
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.52+7467G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759643 | ||||||
chr2:28759662
|
G | T | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.52+7486G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759662 | ||||||
chr2:28759684
|
C | T | 1 | a0001c0001t0006g0124 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.52+7508C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759684 | ||||||
chr2:28759713
|
G | A | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+7537G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759713 | ||||||
chr2:28759763
|
G | A | 131 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(128): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.52+7587G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759763 | ||||||
chr2:28759786
|
T | C | 1 | a0001c0001t0004g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52+7610T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759786 | ||||||
chr2:28759862
|
G | A | 1 | a0001c0002t0022g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.52+7686G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759862 | ||||||
chr2:28759882
|
G | C | 1 | a0001c0002t0002g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.52+7706G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759882 | ||||||
chr2:28759948
|
G | GTTAAC | 155 | a0001c0001t0004g0018a0001c0001t0004g0021a0001c0001t0013g0002others(152): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.52+7776_52+7777ins others(5): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759948 | |||||
chr2:28759961
|
C | G | 66 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(63): Show | 70 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.52+7785C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759961 | ||||||
chr2:28760108
|
C | T | 1 | a0001c0001t0004g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52+7932C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760108 | ||||||
chr2:28760300
|
T | C | 131 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(128): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.52+8124T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760300 | ||||||
chr2:28760524
|
A | G | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.52+8348A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760524 | ||||||
chr2:28760605
|
A | G | 1 | a0001c0001t0004g0341 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52+8429A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760605 | ||||||
chr2:28760679
|
A | G | 1 | a0001c0001t0012g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.52+8503A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760679 | ||||||
chr2:28760680
|
A | G | 1 | a0001c0002t0002g0036 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.52+8504A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760680 | ||||||
chr2:28760844
|
G | A | 1 | a0001c0002t0002g0041 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.52+8668G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760844 | ||||||
chr2:28760918
|
C | T | 1 | a0001c0002t0037g0346 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.52+8742C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760918 | ||||||
chr2:28760945
|
G | C | 1 | a0001c0001t0029g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.52+8769G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760945 | ||||||
chr2:28760974
|
C | T | 1 | a0001c0001t0036g0020 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.52+8798C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760974 | ||||||
chr2:28760986
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.52+8810C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760986 | ||||||
chr2:28761043
|
G | A | 1 | a0001c0001t0027g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.52+8867G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761043 | ||||||
chr2:28761125
|
T | C | 188 | a0001c0001t0001g0019a0001c0001t0001g0259a0001c0001t0001g0275others(185): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.52+8949T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761125 | ||||||
chr2:28761189
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52+9013C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761189 | ||||||
chr2:28761387
|
G | T | 5 | a0001c0002t0003g0011a0001c0002t0003g0191a0001c0002t0003g0192others(2): Show | 6 | HG01074.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+9211G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761387 | ||||||
chr2:28761552
|
C | A | 66 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(63): Show | 70 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.52+9376C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761552 | ||||||
chr2:28761634
|
G | C | 1 | a0001c0001t0004g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.52+9458G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761634 | ||||||
chr2:28761716
|
C | A | 6 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(3): Show | 6 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+9540C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761716 | ||||||
chr2:28761831
|
C | T | 9 | a0001c0002t0007g0201a0001c0002t0007g0202a0001c0002t0007g0203others(6): Show | 9 | HG02451.hp1 HG02647.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.52+9655C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761831 | ||||||
chr2:28761864
|
A | G | 4 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+9688A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761864 | ||||||
chr2:28761920
|
G | C | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+9744G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761920 | ||||||
chr2:28762284
|
CTAAA | C | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.52+10123_52+10126d others(6): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28762284 | |||||
chr2:28762300
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.52+10124A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762300 | ||||||
chr2:28762353
|
G | A | 6 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(3): Show | 6 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+10177G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762353 | ||||||
chr2:28762549
|
G | A | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.52+10373G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762549 | ||||||
chr2:28762635
|
T | G | 1 | a0001c0002t0003g0171 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.52+10459T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762635 | ||||||
chr2:28762650
|
T | C | 1 | a0001c0001t0004g0087 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.52+10474T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762650 | ||||||
chr2:28762693
|
C | T | 1 | a0001c0001t0038g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.52+10517C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762693 | ||||||
chr2:28762754
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.52+10578A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762754 | ||||||
chr2:28762808
|
C | G | 166 | a0001c0001t0001g0017a0001c0001t0001g0234a0001c0001t0001g0236others(163): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.52+10632C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762808 | ||||||
chr2:28763016
|
C | T | 3 | a0001c0002t0008g0127a0001c0002t0008g0128a0001c0002t0008g0168 | 3 | HG01074.hp1 HG01106.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.52+10840C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763016 | ||||||
chr2:28763451
|
G | GA | 115 | a0001c0001t0001g0151a0001c0001t0001g0259a0001c0001t0001g0275others(112): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.52+11286dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28763451 | |||||
chr2:28763701
|
A | G | 4 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+11525A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763701 | ||||||
chr2:28763702
|
CGTTA | C | 87 | a0001c0001t0036g0020a0001c0002t0002g0001a0001c0002t0002g0004others(84): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.52+11531_52+11534d others(6): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28763702 | |||||
chr2:28763741
|
G | A | 1 | a0001c0002t0002g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.52+11565G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763741 | ||||||
chr2:28763743
|
C | T | 4 | a0001c0001t0001g0278a0001c0001t0001g0313a0001c0001t0001g0328others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+11567C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763743 | ||||||
chr2:28763928
|
A | ACAC | 157 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.52+11753_52+11754i others(5): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28763928 | |||||
chr2:28763944
|
G | A | 6 | a0001c0002t0010g0223a0001c0002t0010g0224a0001c0002t0010g0225others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+11768G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763944 | ||||||
chr2:28763981
|
A | G | 4 | a0001c0001t0012g0283a0001c0002t0004g0343a0001c0002t0004g0344others(1): Show | 4 | HG02965.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+11805A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763981 | ||||||
chr2:28764064
|
T | G | 1 | a0001c0002t0021g0178 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.52+11888T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764064 | ||||||
chr2:28764080
|
G | A | 1 | a0001c0002t0008g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.52+11904G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764080 | ||||||
chr2:28764105
|
A | G | 1 | a0001c0002t0025g0167 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.52+11929A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764105 | ||||||
chr2:28764295
|
CT | C | 6 | a0001c0001t0004g0018a0001c0001t0004g0021a0001c0001t0013g0002others(3): Show | 8 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+12121delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28764295 | |||||
chr2:28764297
|
T | A | 6 | a0001c0001t0004g0018a0001c0001t0004g0021a0001c0001t0013g0002others(3): Show | 8 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+12121T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764297 | ||||||
chr2:28764337
|
A | G | 5 | a0001c0002t0003g0011a0001c0002t0003g0191a0001c0002t0003g0192others(2): Show | 6 | HG01074.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+12161A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764337 | ||||||
chr2:28764384
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0006g0015 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.52+12208C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764384 | ||||||
chr2:28764411
|
G | A | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.52+12235G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764411 | ||||||
chr2:28764459
|
C | CA | 12 | a0001c0001t0004g0018a0001c0001t0004g0021a0001c0001t0013g0002others(9): Show | 15 | HG01074.hp2 HG01346.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+12298dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28764459 | |||||
chr2:28764459
|
CA | C | 20 | a0001c0001t0001g0156a0001c0001t0001g0250a0001c0001t0001g0320others(17): Show | 20 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.52+12298delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28764459 | |||||
chr2:28764569
|
C | G | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-12282C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764569 | ||||||
chr2:28764701
|
G | A | 6 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(3): Show | 6 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-12150G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764701 | ||||||
chr2:28764723
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.53-12128C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764723 | ||||||
chr2:28764814
|
A | G | 1 | a0001c0002t0002g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.53-12037A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764814 | ||||||
chr2:28764824
|
G | C | 2 | a0001c0002t0002g0031a0001c0002t0002g0032 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.53-12027G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764824 | ||||||
chr2:28764826
|
T | C | 2 | a0001c0001t0004g0021a0001c0001t0036g0020 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53-12025T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764826 | ||||||
chr2:28764918
|
C | CA | 126 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(123): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.53-11921dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28764918 | |||||
chr2:28764944
|
G | A | 6 | a0001c0001t0004g0018a0001c0001t0004g0021a0001c0001t0013g0002others(3): Show | 8 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-11907G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764944 | ||||||
chr2:28764982
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.53-11869C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764982 | ||||||
chr2:28765006
|
A | G | 1 | a0001c0002t0002g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.53-11845A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765006 | ||||||
chr2:28765033
|
G | A | 1 | a0001c0002t0002g0039 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.53-11818G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765033 | ||||||
chr2:28765069
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.53-11782A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765069 | ||||||
chr2:28765085
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0006g0238 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.53-11766T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765085 | ||||||
chr2:28765217
|
T | C | 205 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.53-11634T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765217 | ||||||
chr2:28765276
|
A | G | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-11575A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765276 | ||||||
chr2:28765308
|
T | C | 1 | a0001c0002t0002g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.53-11543T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765308 | ||||||
chr2:28766195
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-10656G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766195 | ||||||
chr2:28766281
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.53-10570T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766281 | ||||||
chr2:28766474
|
A | G | 1 | a0001c0002t0007g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.53-10377A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766474 | ||||||
chr2:28766801
|
A | G | 152 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(149): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.53-10050A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766801 | ||||||
chr2:28766824
|
G | A | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-10027G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766824 | ||||||
chr2:28766941
|
C | T | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-9910C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766941 | ||||||
chr2:28766949
|
C | T | 5 | a0001c0002t0010g0223a0001c0002t0010g0224a0001c0002t0010g0225others(2): Show | 5 | HG01243.hp2 HG02280.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-9902C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766949 | ||||||
chr2:28766950
|
G | A | 2 | a0001c0001t0027g0309a0001c0002t0008g0127 | 2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.53-9901G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766950 | ||||||
chr2:28767021
|
C | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.53-9830C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767021 | ||||||
chr2:28767080
|
CA | C | 87 | a0001c0001t0001g0241a0001c0002t0002g0001a0001c0002t0002g0004others(84): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.53-9757delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28767080 | |||||
chr2:28767109
|
A | G | 154 | a0001c0001t0030g0285a0001c0002t0001g0235a0001c0002t0002g0001others(151): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.53-9742A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767109 | ||||||
chr2:28767111
|
A | C | 154 | a0001c0001t0030g0285a0001c0002t0001g0235a0001c0002t0002g0001others(151): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.53-9740A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767111 | ||||||
chr2:28767336
|
C | G | 66 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(63): Show | 70 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.53-9515C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767336 | ||||||
chr2:28767359
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.53-9492G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767359 | ||||||
chr2:28767446
|
AAC | A | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-9401_53-9400del others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28767446 | |||||
chr2:28767524
|
A | T | 22 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0001g0280others(19): Show | 22 | HG00544.hp2 HG00673.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.53-9327A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767524 | ||||||
chr2:28767554
|
C | G | 1 | a0001c0001t0004g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-9297C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767554 | ||||||
chr2:28767652
|
C | A | 1 | a0001c0002t0020g0040 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.53-9199C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767652 | ||||||
chr2:28767668
|
A | G | 5 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0026others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-9183A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767668 | ||||||
chr2:28767702
|
A | T | 1 | a0001c0001t0038g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-9149A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767702 | ||||||
chr2:28767713
|
T | C | 1 | a0001c0002t0003g0179 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.53-9138T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767713 | ||||||
chr2:28767814
|
A | G | 1 | a0001c0002t0003g0179 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.53-9037A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767814 | ||||||
chr2:28767879
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0279a0001c0001t0001g0314others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-8972T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767879 | ||||||
chr2:28767953
|
C | G | 4 | a0001c0002t0002g0030a0001c0002t0002g0037a0001c0002t0002g0038others(1): Show | 4 | HG02257.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-8898C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767953 | ||||||
chr2:28767980
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.53-8871A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767980 | ||||||
chr2:28768188
|
G | A | 2 | a0001c0001t0004g0021a0001c0001t0036g0020 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53-8663G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768188 | ||||||
chr2:28768394
|
C | T | 1 | a0001c0001t0004g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-8457C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768394 | ||||||
chr2:28768405
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0004g0277 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.53-8446A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768405 | ||||||
chr2:28768422
|
T | G | 1 | a0001c0001t0030g0285 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.53-8429T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768422 | ||||||
chr2:28768432
|
A | G | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-8419A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768432 | ||||||
chr2:28768490
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.53-8361C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768490 | ||||||
chr2:28768501
|
G | A | 1 | a0001c0001t0027g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-8350G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768501 | ||||||
chr2:28768661
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.53-8190G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768661 | ||||||
chr2:28768856
|
A | G | 15 | a0001c0002t0007g0200a0001c0002t0007g0201a0001c0002t0007g0202others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.53-7995A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768856 | ||||||
chr2:28769134
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.53-7717A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769134 | ||||||
chr2:28769138
|
T | C | 153 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(150): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.53-7713T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769138 | ||||||
chr2:28769154
|
T | G | 132 | a0001c0001t0001g0019a0001c0002t0002g0001a0001c0002t0002g0004others(129): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.53-7697T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769154 | ||||||
chr2:28769169
|
T | C | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-7682T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769169 | ||||||
chr2:28769248
|
A | G | 1 | a0001c0002t0007g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.53-7603A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769248 | ||||||
chr2:28769255
|
G | A | 1 | a0001c0002t0002g0041 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.53-7596G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769255 | ||||||
chr2:28769298
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.53-7553G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769298 | ||||||
chr2:28769329
|
C | T | 15 | a0001c0002t0007g0200a0001c0002t0007g0201a0001c0002t0007g0202others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.53-7522C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769329 | ||||||
chr2:28769395
|
C | G | 3 | a0001c0001t0013g0002a0001c0001t0013g0023a0001c0001t0038g0022 | 5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-7456C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769395 | ||||||
chr2:28769415
|
T | C | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-7436T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769415 | ||||||
chr2:28769427
|
G | A | 71 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(68): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.53-7424G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769427 | ||||||
chr2:28769539
|
A | G | 153 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(150): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.53-7312A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769539 | ||||||
chr2:28769741
|
C | G | 153 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(150): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.53-7110C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769741 | ||||||
chr2:28769749
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.53-7102A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769749 | ||||||
chr2:28769880
|
A | G | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-6971A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769880 | ||||||
chr2:28770023
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.53-6828C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770023 | ||||||
chr2:28770122
|
G | T | 1 | a0001c0001t0004g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-6729G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770122 | ||||||
chr2:28770148
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.53-6703A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770148 | ||||||
chr2:28770160
|
G | T | 1 | a0001c0002t0001g0235 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.53-6691G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770160 | ||||||
chr2:28770178
|
G | A | 41 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(38): Show | 45 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.53-6673G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770178 | ||||||
chr2:28770239
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-6612G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770239 | ||||||
chr2:28770371
|
A | G | 1 | a0001c0002t0002g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.53-6480A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770371 | ||||||
chr2:28770380
|
AAGG | A | 4 | a0001c0002t0002g0034a0001c0002t0002g0133a0001c0002t0002g0135others(1): Show | 4 | HG01070.hp2 HG01255.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-6470_53-6468del others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770380 | ||||||
chr2:28770381
|
A | AG | 49 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0075others(46): Show | 52 | HG00558.hp1 HG00733.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.53-6460dupG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770381 | |||||
chr2:28770381
|
A | AGG | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(147): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.53-6461_53-6460dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770381 | |||||
chr2:28770381
|
A | AGGG | 28 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(25): Show | 28 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.53-6462_53-6460dup others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770381 | |||||
chr2:28770381
|
A | G | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-6470A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770381 | ||||||
chr2:28770381
|
AG | A | 65 | a0001c0001t0038g0022a0001c0002t0002g0001a0001c0002t0002g0031others(62): Show | 67 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.53-6460delG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770381 | |||||
chr2:28770382
|
G | A | 1 | a0001c0002t0037g0346 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.53-6469G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770382 | ||||||
chr2:28770392
|
A | G | 7 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0121others(4): Show | 7 | HG00597.hp2 HG01192.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-6459A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770392 | ||||||
chr2:28770464
|
G | GA | 60 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(57): Show | 64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53-6382dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770464 | |||||
chr2:28770627
|
G | C | 1 | a0001c0002t0002g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-6224G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770627 | ||||||
chr2:28770740
|
G | A | 2 | a0001c0002t0008g0024a0001c0002t0008g0025 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.53-6111G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770740 | ||||||
chr2:28770744
|
A | G | 1 | a0001c0002t0002g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.53-6107A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770744 | ||||||
chr2:28770786
|
CA | C | 138 | a0001c0001t0001g0019a0001c0001t0032g0116a0001c0002t0001g0235others(135): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.53-6061delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770786 | |||||
chr2:28770979
|
T | C | 8 | a0001c0001t0001g0076a0001c0002t0002g0045a0001c0002t0009g0062others(5): Show | 8 | HG00673.hp1 NA18959.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-5872T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770979 | ||||||
chr2:28771034
|
C | T | 2 | a0001c0002t0004g0344a0001c0002t0037g0346 | 2 | HG01934.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-5817C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771034 | ||||||
chr2:28771037
|
T | C | 167 | a0001c0001t0001g0019a0001c0001t0004g0018a0001c0001t0004g0021others(164): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.53-5814T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771037 | ||||||
chr2:28771040
|
T | TC | 76 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 79 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.53-5800dupC | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771040 | |||||
chr2:28771040
|
T | TCC | 44 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0082others(41): Show | 44 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.53-5801_53-5800dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771040 | |||||
chr2:28771040
|
TC | T | 16 | a0001c0001t0001g0125a0001c0001t0006g0015a0001c0001t0012g0334others(13): Show | 16 | HG00609.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-5800delC | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771040 | |||||
chr2:28771043
|
C | A | 1 | a0001c0002t0003g0182 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.53-5808C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771043 | ||||||
chr2:28771049
|
C | G | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-5802C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771049 | ||||||
chr2:28771050
|
C | A | 11 | a0001c0002t0002g0047a0001c0002t0002g0048a0001c0002t0002g0064others(8): Show | 11 | HG00140.hp1 HG00558.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-5801C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771050 | ||||||
chr2:28771051
|
C | A | 109 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(106): Show | 114 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.53-5800C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771051 | ||||||
chr2:28771051
|
CA | C | 11 | a0001c0002t0002g0047a0001c0002t0002g0048a0001c0002t0002g0064others(8): Show | 11 | HG00140.hp1 HG00558.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-5799delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771051 | ||||||
chr2:28771052
|
A | C | 110 | a0001c0001t0001g0019a0001c0002t0001g0235a0001c0002t0002g0001others(107): Show | 115 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.53-5799A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771052 | ||||||
chr2:28771053
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-5798C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771053 | ||||||
chr2:28771055
|
C | CT | 27 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0102others(24): Show | 28 | HG00438.hp2 HG00673.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.53-5781dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771055 | |||||
chr2:28771055
|
C | CTT | 10 | a0001c0002t0002g0038a0001c0002t0002g0145a0001c0002t0002g0229others(7): Show | 10 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-5782_53-5781dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771055 | |||||
chr2:28771055
|
C | T | 120 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(117): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.53-5796C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771055 | ||||||
chr2:28771056
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-5795T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771056 | ||||||
chr2:28771109
|
A | G | 45 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(42): Show | 49 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.53-5742A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771109 | ||||||
chr2:28771226
|
G | C | 5 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(2): Show | 5 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-5625G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771226 | ||||||
chr2:28771243
|
G | T | 1 | a0001c0001t0030g0285 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.53-5608G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771243 | ||||||
chr2:28771298
|
A | G | 228 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(225): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.53-5553A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771298 | ||||||
chr2:28771310
|
C | G | 4 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5541C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771310 | ||||||
chr2:28771338
|
A | G | 2 | a0001c0002t0002g0031a0001c0002t0002g0032 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.53-5513A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771338 | ||||||
chr2:28771347
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.53-5504G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771347 | ||||||
chr2:28771416
|
C | CAT | 133 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(130): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.53-5434_53-5433dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771416 | |||||
chr2:28771478
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.53-5373C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771478 | ||||||
chr2:28771604
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0279a0001c0001t0001g0314others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-5247A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771604 | ||||||
chr2:28771671
|
G | T | 65 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(62): Show | 69 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.53-5180G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771671 | ||||||
chr2:28771975
|
C | CA | 68 | a0001c0001t0001g0082a0001c0001t0001g0278a0001c0001t0001g0282others(65): Show | 72 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.53-4861dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771975 | |||||
chr2:28771975
|
CA | C | 89 | a0001c0001t0001g0088a0001c0002t0001g0235a0001c0002t0002g0001others(86): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.53-4861delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771975 | |||||
chr2:28772055
|
G | A | 1 | a0001c0001t0005g0252 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.53-4796G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772055 | ||||||
chr2:28772081
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-4770C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772081 | ||||||
chr2:28772114
|
C | T | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-4737C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772114 | ||||||
chr2:28772115
|
G | A | 5 | a0001c0001t0004g0021a0001c0001t0013g0002a0001c0001t0013g0023others(2): Show | 7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-4736G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772115 | ||||||
chr2:28772190
|
C | T | 2 | a0001c0001t0013g0002a0001c0001t0013g0023 | 4 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-4661C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772190 | ||||||
chr2:28772286
|
G | A | 1 | a0001c0002t0024g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.53-4565G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772286 | ||||||
chr2:28772311
|
A | T | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.53-4540A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772311 | ||||||
chr2:28772360
|
A | G | 87 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(84): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.53-4491A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772360 | ||||||
chr2:28772566
|
C | T | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-4285C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772566 | ||||||
chr2:28772594
|
G | A | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-4257G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772594 | ||||||
chr2:28772657
|
A | C | 60 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(57): Show | 64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53-4194A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772657 | ||||||
chr2:28772680
|
C | T | 4 | a0001c0002t0003g0174a0001c0002t0003g0175a0001c0002t0003g0176others(1): Show | 4 | HG02622.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-4171C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772680 | ||||||
chr2:28772746
|
T | C | 2 | a0001c0002t0002g0129a0001c0002t0011g0130 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.53-4105T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772746 | ||||||
chr2:28772959
|
C | G | 2 | a0001c0001t0016g0114a0001c0001t0016g0119 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53-3892C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772959 | ||||||
chr2:28773083
|
G | A | 4 | a0001c0002t0002g0042a0001c0002t0002g0069a0001c0002t0002g0072others(1): Show | 4 | HG00099.hp1 HG00280.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-3768G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773083 | ||||||
chr2:28773088
|
A | G | 1 | a0001c0002t0037g0346 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.53-3763A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773088 | ||||||
chr2:28773131
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-3720A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773131 | ||||||
chr2:28773159
|
A | G | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-3692A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773159 | ||||||
chr2:28773229
|
T | C | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.53-3622T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773229 | ||||||
chr2:28773429
|
G | A | 205 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.53-3422G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773429 | ||||||
chr2:28773525
|
G | C | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-3326G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773525 | ||||||
chr2:28773589
|
A | G | 2 | a0001c0002t0002g0228a0001c0002t0002g0229 | 2 | HG01496.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.53-3262A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773589 | ||||||
chr2:28773670
|
CT | C | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.53-3174delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28773670 | |||||
chr2:28773703
|
A | T | 1 | a0001c0002t0009g0062 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.53-3148A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773703 | ||||||
chr2:28773757
|
T | C | 1 | a0001c0001t0005g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.53-3094T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773757 | ||||||
chr2:28773795
|
A | G | 1 | a0001c0002t0003g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.53-3056A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773795 | ||||||
chr2:28773802
|
T | C | 1 | a0001c0001t0004g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.53-3049T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773802 | ||||||
chr2:28773964
|
A | G | 4 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0330others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2887A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773964 | ||||||
chr2:28774133
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0006g0015 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-2718G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774133 | ||||||
chr2:28774135
|
G | C | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.53-2716G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774135 | ||||||
chr2:28774143
|
T | C | 1 | a0001c0002t0002g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.53-2708T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774143 | ||||||
chr2:28774262
|
A | G | 4 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2589A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774262 | ||||||
chr2:28774274
|
G | T | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.53-2577G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774274 | ||||||
chr2:28774307
|
A | G | 1 | a0001c0002t0002g0043 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.53-2544A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774307 | ||||||
chr2:28774316
|
A | G | 2 | a0001c0001t0004g0021a0001c0001t0036g0020 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53-2535A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774316 | ||||||
chr2:28774435
|
T | C | 1 | a0001c0002t0002g0050 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.53-2416T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774435 | ||||||
chr2:28774575
|
G | A | 4 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0330others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2276G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774575 | ||||||
chr2:28774674
|
C | T | 4 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2177C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774674 | ||||||
chr2:28774931
|
A | C | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.53-1920A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774931 | ||||||
chr2:28774969
|
C | T | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.53-1882C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774969 | ||||||
chr2:28775070
|
A | G | 60 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(57): Show | 64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53-1781A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775070 | ||||||
chr2:28775211
|
G | C | 152 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(149): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.53-1640G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775211 | ||||||
chr2:28775271
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.53-1580C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775271 | ||||||
chr2:28775322
|
C | T | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.53-1529C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775322 | ||||||
chr2:28775553
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.53-1298C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775553 | ||||||
chr2:28775580
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.53-1271C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775580 | ||||||
chr2:28775765
|
G | A | 1 | a0001c0001t0038g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-1086G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775765 | ||||||
chr2:28775879
|
C | T | 1 | a0001c0002t0014g0221 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.53-972C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775879 | ||||||
chr2:28775880
|
T | G | 1 | a0001c0001t0012g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53-971T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775880 | ||||||
chr2:28775977
|
T | G | 7 | a0001c0002t0002g0149a0001c0002t0002g0169a0001c0002t0002g0170others(4): Show | 7 | HG01496.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-874T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775977 | ||||||
chr2:28776237
|
TTTG | T | 5 | a0001c0001t0004g0021a0001c0001t0013g0002a0001c0001t0013g0023others(2): Show | 7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-605_53-603delGT others(1): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28776237 | |||||
chr2:28776266
|
T | G | 1 | a0001c0002t0002g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.53-585T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776266 | ||||||
chr2:28776269
|
T | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0136 | 2 | HG00558.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.53-582T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776269 | ||||||
chr2:28776292
|
C | T | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.53-559C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776292 | ||||||
chr2:28776318
|
A | C | 1 | a0001c0002t0002g0050 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.53-533A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776318 | ||||||
chr2:28776319
|
A | G | 2 | a0001c0002t0002g0042a0001c0002t0002g0069 | 2 | HG00099.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.53-532A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776319 | ||||||
chr2:28776411
|
G | A | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-440G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776411 | ||||||
chr2:28776419
|
A | G | 343 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(340): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.53-432A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776419 | ||||||
chr2:28776470
|
A | G | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.53-381A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776470 | ||||||
chr2:28777077
|
A | G | 2 | a0001c0002t0002g0068a0001c0002t0002g0144 | 2 | HG00735.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.184+95A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777077 | ||||||
chr2:28777127
|
CTT | C | 4 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+146_184+147del others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777127 | ||||||
chr2:28777269
|
G | A | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.184+287G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777269 | ||||||
chr2:28777309
|
G | A | 1 | a0001c0002t0003g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.184+327G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777309 | ||||||
chr2:28777312
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.184+330A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777312 | ||||||
chr2:28777421
|
C | T | 83 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(80): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.184+439C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777421 | ||||||
chr2:28777652
|
T | G | 6 | a0001c0001t0004g0295a0001c0001t0026g0296a0001c0002t0004g0343others(3): Show | 6 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+670T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777652 | ||||||
chr2:28777792
|
A | G | 8 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0026others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+810A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777792 | ||||||
chr2:28777874
|
G | A | 15 | a0001c0002t0007g0200a0001c0002t0007g0201a0001c0002t0007g0202others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.184+892G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777874 | ||||||
chr2:28777924
|
G | A | 4 | a0001c0001t0001g0278a0001c0001t0001g0313a0001c0001t0001g0328others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-885G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777924 | ||||||
chr2:28778596
|
G | T | 1 | a0001c0001t0027g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.185-213G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28778596 | ||||||
chr2:28778649
|
C | T | 2 | a0001c0002t0002g0072a0001c0002t0002g0073 | 2 | HG00280.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.185-160C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28778649 | ||||||
chr2:28778665
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.185-144C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28778665 | ||||||
chr2:28779125
|
A | C | 4 | a0001c0002t0002g0042a0001c0002t0002g0069a0001c0002t0002g0072others(1): Show | 4 | HG00099.hp1 HG00280.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+86A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779125 | ||||||
chr2:28779295
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.415+256A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779295 | ||||||
chr2:28779346
|
T | G | 6 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(3): Show | 6 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+307T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779346 | ||||||
chr2:28779367
|
G | T | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.415+328G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779367 | ||||||
chr2:28779635
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.415+596A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779635 | ||||||
chr2:28779834
|
A | G | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.415+795A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779834 | ||||||
chr2:28779838
|
G | T | 1 | a0001c0001t0004g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.415+799G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779838 | ||||||
chr2:28780034
|
A | G | 2 | a0001c0001t0001g0278a0001c0002t0001g0235 | 2 | HG02615.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.415+995A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780034 | ||||||
chr2:28780052
|
CTTTCTTT | C | 8 | a0001c0001t0012g0272a0001c0001t0012g0281a0001c0001t0012g0283others(5): Show | 8 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1029_415+1035d others(9): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780052 | |||||
chr2:28780084
|
C | CT | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 92 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.415+1066dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | |||||
chr2:28780084
|
C | CTT | 6 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0136others(3): Show | 6 | HG01109.hp2 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+1065_415+1066d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | |||||
chr2:28780084
|
CT | C | 11 | a0001c0001t0001g0246a0001c0001t0001g0250a0001c0001t0001g0256others(8): Show | 11 | HG01515.hp2 HG01928.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.415+1066delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | |||||
chr2:28780084
|
CTTTTTTT others(3): Show |
C | 65 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(62): Show | 69 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.415+1057_415+1066d others(12): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | |||||
chr2:28780084
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0035g0264 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.415+1056_415+1066d others(13): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | |||||
chr2:28780087
|
T | TC | 3 | a0001c0002t0002g0061a0001c0002t0002g0069a0001c0002t0002g0164 | 3 | HG01069.hp1 HG01361.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.415+1048_415+1049i others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780087 | ||||||
chr2:28780088
|
T | C | 83 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(80): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.415+1049T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780088 | ||||||
chr2:28780089
|
T | C | 2 | a0001c0002t0002g0050a0001c0002t0002g0146 | 2 | HG01515.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.415+1050T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780089 | ||||||
chr2:28780174
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0118 | 2 | NA18959.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.415+1135C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780174 | ||||||
chr2:28780348
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.415+1309C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780348 | ||||||
chr2:28780487
|
A | T | 1 | a0001c0002t0003g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.416-1251A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780487 | ||||||
chr2:28780585
|
G | A | 29 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0031others(26): Show | 31 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.416-1153G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780585 | ||||||
chr2:28780598
|
TG | T | 4 | a0001c0002t0003g0174a0001c0002t0003g0175a0001c0002t0003g0176others(1): Show | 4 | HG02622.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-1136delG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780598 | |||||
chr2:28780601
|
G | T | 4 | a0001c0002t0003g0174a0001c0002t0003g0175a0001c0002t0003g0176others(1): Show | 4 | HG02622.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-1137G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780601 | ||||||
chr2:28780712
|
G | A | 1 | a0001c0002t0002g0056 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.416-1026G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780712 | ||||||
chr2:28780847
|
A | G | 1 | a0001c0001t0005g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.416-891A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780847 | ||||||
chr2:28780892
|
T | C | 64 | a0001c0001t0001g0006a0001c0001t0001g0111a0001c0001t0001g0115others(61): Show | 69 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.416-846T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780892 | ||||||
chr2:28780921
|
CTAGT | C | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.416-814_416-811del others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780921 | |||||
chr2:28781071
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0111a0001c0001t0001g0115others(2): Show | 6 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-667C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781071 | ||||||
chr2:28781154
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.416-584G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781154 | ||||||
chr2:28781180
|
C | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.416-558C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781180 | ||||||
chr2:28781302
|
G | C | 1 | a0001c0001t0005g0340 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.416-436G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781302 | ||||||
chr2:28781348
|
A | G | 2 | a0001c0001t0004g0021a0001c0001t0036g0020 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.416-390A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781348 | ||||||
chr2:28781433
|
T | C | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.416-305T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781433 | ||||||
chr2:28781583
|
G | A | 1 | a0001c0001t0030g0285 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.416-155G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781583 | ||||||
chr2:28781718
|
T | A | 1 | a0001c0002t0007g0201 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.416-20T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781718 | ||||||
chr2:28781721
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.416-17A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781721 | ||||||
chr2:28782032
|
T | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0279a0001c0001t0001g0314others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.520+190T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782032 | ||||||
chr2:28782057
|
G | A | 350 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(347): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.520+215G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782057 | ||||||
chr2:28782061
|
T | A | 1 | a0001c0002t0003g0211 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.520+219T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782061 | ||||||
chr2:28782360
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.520+518G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782360 | ||||||
chr2:28782479
|
T | C | 5 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(2): Show | 5 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.520+637T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782479 | ||||||
chr2:28782491
|
T | A | 15 | a0001c0002t0007g0200a0001c0002t0007g0201a0001c0002t0007g0202others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.520+649T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782491 | ||||||
chr2:28782624
|
A | C | 5 | a0001c0002t0002g0045a0001c0002t0009g0070a0001c0002t0009g0138others(2): Show | 5 | NA18959.hp1 NA18977.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.520+782A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782624 | ||||||
chr2:28782650
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.520+808G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782650 | ||||||
chr2:28782665
|
G | A | 15 | a0001c0002t0007g0200a0001c0002t0007g0201a0001c0002t0007g0202others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.520+823G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782665 | ||||||
chr2:28782734
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.520+892C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782734 | ||||||
chr2:28782736
|
G | A | 161 | a0001c0001t0001g0019a0001c0001t0004g0018a0001c0001t0004g0021others(158): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.520+894G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782736 | ||||||
chr2:28783004
|
C | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.521-903C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783004 | ||||||
chr2:28783496
|
G | A | 2 | a0001c0001t0004g0021a0001c0001t0036g0020 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.521-411G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783496 | ||||||
chr2:28783572
|
A | G | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.521-335A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783572 | ||||||
chr2:28783629
|
C | A | 1 | a0001c0001t0030g0285 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.521-278C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783629 | ||||||
chr2:28783650
|
G | A | 20 | a0001c0001t0001g0259a0001c0001t0001g0275a0001c0001t0001g0276others(17): Show | 20 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.521-257G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783650 | ||||||
chr2:28783714
|
G | A | 3 | a0001c0002t0008g0026a0001c0002t0008g0027a0001c0002t0008g0028 | 3 | HG02109.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.521-193G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783714 | ||||||
chr2:28783725
|
G | C | 153 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(150): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.521-182G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783725 | ||||||
chr2:28783757
|
G | GA | 65 | a0001c0002t0001g0235a0001c0002t0003g0008a0001c0002t0003g0009others(62): Show | 69 | HG00438.hp2 HG00609.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.521-138dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 28783757 | |||||
chr2:28784096
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.592+118C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784096 | ||||||
chr2:28784117
|
C | T | 5 | a0001c0001t0004g0021a0001c0001t0013g0002a0001c0001t0013g0023others(2): Show | 7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+139C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784117 | ||||||
chr2:28784168
|
C | T | 5 | a0001c0001t0004g0021a0001c0001t0013g0002a0001c0001t0013g0023others(2): Show | 7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+190C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784168 | ||||||
chr2:28784169
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.592+191G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784169 | ||||||
chr2:28784402
|
C | T | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.592+424C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784402 | ||||||
chr2:28784472
|
C | T | 4 | a0001c0002t0002g0042a0001c0002t0002g0069a0001c0002t0002g0072others(1): Show | 4 | HG00099.hp1 HG00280.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+494C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784472 | ||||||
chr2:28784483
|
T | C | 153 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(150): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.592+505T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784483 | ||||||
chr2:28784509
|
C | T | 15 | a0001c0002t0007g0200a0001c0002t0007g0201a0001c0002t0007g0202others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.592+531C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784509 | ||||||
chr2:28784709
|
G | A | 9 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(6): Show | 11 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.592+731G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784709 | ||||||
chr2:28784779
|
G | A | 1 | a0001c0002t0002g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.592+801G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784779 | ||||||
chr2:28784917
|
C | CA | 98 | a0001c0001t0001g0233a0001c0001t0001g0259a0001c0001t0001g0275others(95): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.592+956dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784917 | |||||
chr2:28784917
|
C | CAA | 13 | a0001c0001t0001g0019a0001c0001t0013g0023a0001c0002t0002g0033others(10): Show | 13 | HG00733.hp2 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+955_592+956dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784917 | |||||
chr2:28784917
|
C | CAAA | 46 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(43): Show | 50 | HG00438.hp2 HG00558.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.592+954_592+956dup others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784917 | |||||
chr2:28784917
|
C | CAAAA | 13 | a0001c0002t0003g0175a0001c0002t0003g0193a0001c0002t0003g0195others(10): Show | 13 | HG01243.hp2 HG01978.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.592+953_592+956dup others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784917 | |||||
chr2:28784930
|
A | G | 2 | a0001c0002t0001g0235a0001c0002t0008g0028 | 2 | HG03098.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.592+952A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784930 | ||||||
chr2:28784942
|
GA | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.592+967delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784942 | |||||
chr2:28784989
|
C | G | 87 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(84): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.592+1011C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784989 | ||||||
chr2:28785065
|
C | CT | 64 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0085others(61): Show | 64 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.592+1115dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTT | 15 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0113others(12): Show | 15 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.592+1114_592+1115d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0008g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.592+1106_592+1115d others(12): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0019a0001c0002t0002g0045a0001c0002t0002g0069others(4): Show | 7 | HG00673.hp1 HG02145.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+1105_592+1115d others(13): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(5): Show |
4 | a0001c0002t0002g0228a0001c0002t0002g0229a0001c0002t0009g0139others(1): Show | 4 | HG01496.hp2 HG03209.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+1104_592+1115d others(14): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(6): Show |
3 | a0001c0002t0002g0072a0001c0002t0008g0128a0001c0002t0009g0138 | 3 | HG00280.hp2 HG03486.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.592+1103_592+1115d others(15): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0008g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.592+1102_592+1115d others(16): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(8): Show |
3 | a0001c0002t0002g0039a0001c0002t0002g0142a0001c0002t0008g0025 | 3 | HG02572.hp1 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.592+1101_592+1115d others(17): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(9): Show |
5 | a0001c0002t0002g0131a0001c0002t0002g0166a0001c0002t0008g0027others(2): Show | 5 | HG02109.hp1 HG03098.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1100_592+1115d others(18): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(10): Show |
4 | a0001c0002t0002g0051a0001c0002t0002g0068a0001c0002t0002g0140others(1): Show | 4 | HG01081.hp2 NA18955.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+1099_592+1115d others(19): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(11): Show |
3 | a0001c0002t0002g0053a0001c0002t0002g0065a0001c0002t0002g0144 | 3 | HG00735.hp2 NA18953.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.592+1098_592+1115d others(20): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(12): Show |
2 | a0001c0002t0002g0145a0001c0002t0020g0040 | 2 | NA19000.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.592+1097_592+1115d others(21): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(13): Show |
1 | a0001c0002t0002g0054 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.592+1096_592+1115d others(22): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(14): Show |
2 | a0001c0002t0002g0050a0001c0002t0002g0071 | 2 | HG00738.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.592+1095_592+1115d others(23): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(15): Show |
2 | a0001c0002t0002g0043a0001c0002t0002g0146 | 2 | NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.592+1094_592+1115d others(24): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(16): Show |
2 | a0001c0002t0002g0064a0001c0002t0011g0130 | 2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.592+1093_592+1115d others(25): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(17): Show |
3 | a0001c0002t0002g0059a0001c0002t0002g0129a0001c0002t0008g0026 | 3 | HG01258.hp1 HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.592+1092_592+1115d others(26): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(18): Show |
2 | a0001c0002t0002g0137a0001c0002t0002g0169 | 2 | HG02615.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.592+1091_592+1115d others(27): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(19): Show |
3 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0060 | 3 | HG00323.hp1 HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.592+1090_592+1115d others(28): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(20): Show |
1 | a0001c0002t0002g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.592+1089_592+1115d others(29): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(22): Show |
1 | a0001c0002t0002g0041 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(31): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(23): Show |
1 | a0001c0002t0002g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.592+1115_592+1116i others(32): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(26): Show |
3 | a0001c0002t0002g0031a0001c0002t0002g0032a0001c0002t0002g0067 | 3 | HG01069.hp2 HG01071.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.592+1115_592+1116i others(35): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0004g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(37): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(29): Show |
3 | a0001c0002t0002g0036a0001c0002t0002g0055a0001c0002t0002g0164 | 3 | HG01361.hp1 NA19088.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.592+1115_592+1116i others(38): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(30): Show |
1 | a0001c0002t0002g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(39): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(32): Show |
1 | a0001c0002t0024g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(41): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(33): Show |
1 | a0001c0002t0002g0132 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.592+1115_592+1116i others(42): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(35): Show |
2 | a0001c0002t0002g0030a0001c0002t0002g0066 | 2 | HG03130.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.592+1115_592+1116i others(44): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(38): Show |
1 | a0001c0002t0008g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(47): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
C | CTTTTTTT others(42): Show |
1 | a0001c0002t0002g0033 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.592+1115_592+1116i others(51): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
CT | C | 36 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0299others(33): Show | 38 | HG00558.hp2 HG01074.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.592+1115delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
CTT | C | 6 | a0001c0002t0002g0044a0001c0002t0002g0047a0001c0002t0002g0135others(3): Show | 6 | HG01175.hp2 HG02145.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+1114_592+1115d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0004g0018a0001c0002t0002g0141 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.592+1106_592+1115d others(12): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0001g0017a0001c0001t0013g0002a0001c0001t0013g0023others(4): Show | 9 | HG00099.hp2 HG01884.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.592+1105_592+1115d others(13): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785065
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.592+1098_592+1115d others(20): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | |||||
chr2:28785220
|
G | A | 1 | a0001c0002t0003g0216 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.592+1242G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785220 | ||||||
chr2:28785223
|
C | T | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.592+1245C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785223 | ||||||
chr2:28785309
|
T | C | 162 | a0001c0001t0001g0019a0001c0001t0004g0018a0001c0001t0004g0021others(159): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.592+1331T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785309 | ||||||
chr2:28785354
|
G | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0074others(18): Show | 21 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.592+1376G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785354 | ||||||
chr2:28785451
|
G | T | 1 | a0001c0001t0038g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.592+1473G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785451 | ||||||
chr2:28785534
|
T | C | 1 | a0001c0001t0030g0285 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.592+1556T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785534 | ||||||
chr2:28785559
|
T | A | 92 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(89): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.592+1581T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785559 | ||||||
chr2:28785657
|
A | AT | 7 | a0001c0001t0001g0161a0001c0002t0001g0235a0001c0002t0003g0008others(4): Show | 8 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.592+1690dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785657 | |||||
chr2:28785668
|
T | A | 55 | a0001c0002t0003g0009a0001c0002t0003g0010a0001c0002t0003g0011others(52): Show | 58 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.592+1690T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785668 | ||||||
chr2:28785693
|
C | T | 2 | a0001c0002t0003g0215a0001c0002t0037g0346 | 2 | HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.592+1715C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785693 | ||||||
chr2:28785801
|
CCT | C | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.592+1828_592+1829d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785801 | |||||
chr2:28786132
|
A | C | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.592+2154A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786132 | ||||||
chr2:28786183
|
G | A | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.592+2205G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786183 | ||||||
chr2:28786223
|
C | A | 91 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(88): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.592+2245C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786223 | ||||||
chr2:28786314
|
A | G | 40 | a0001c0002t0003g0009a0001c0002t0003g0010a0001c0002t0003g0011others(37): Show | 43 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.592+2336A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786314 | ||||||
chr2:28786554
|
T | C | 1 | a0001c0001t0001g0267 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.593-2104T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786554 | ||||||
chr2:28786769
|
C | T | 5 | a0001c0001t0001g0262a0001c0001t0001g0265a0001c0001t0001g0266others(2): Show | 5 | NA18940.hp1 NA18951.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1889C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786769 | ||||||
chr2:28786774
|
C | CA | 27 | a0001c0001t0001g0259a0001c0001t0001g0325a0001c0001t0001g0326others(24): Show | 27 | HG01243.hp2 HG01934.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.593-1863dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | |||||
chr2:28786774
|
C | CAAA | 28 | a0001c0002t0003g0009a0001c0002t0003g0010a0001c0002t0003g0011others(25): Show | 31 | HG00438.hp2 HG00609.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.593-1865_593-1863d others(5): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | |||||
chr2:28786774
|
C | CAAAA | 18 | a0001c0001t0001g0088a0001c0001t0001g0236a0001c0001t0001g0244others(15): Show | 18 | HG00558.hp2 HG01169.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.593-1866_593-1863d others(6): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | |||||
chr2:28786774
|
C | CAAAAA | 114 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.593-1867_593-1863d others(7): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | |||||
chr2:28786774
|
C | CAAAAAA | 28 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0086others(25): Show | 28 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1868_593-1863d others(8): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | |||||
chr2:28786774
|
CA | C | 8 | a0001c0001t0001g0161a0001c0001t0006g0124a0001c0002t0002g0041others(5): Show | 8 | HG00099.hp1 HG00280.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.593-1863delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | |||||
chr2:28786774
|
CAA | C | 85 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(82): Show | 88 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.593-1864_593-1863d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | |||||
chr2:28786797
|
A | G | 1 | a0001c0002t0011g0035 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.593-1861A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786797 | ||||||
chr2:28786934
|
A | G | 1 | a0001c0002t0008g0027 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.593-1724A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786934 | ||||||
chr2:28786974
|
A | T | 153 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(150): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.593-1684A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786974 | ||||||
chr2:28787157
|
C | T | 3 | a0001c0001t0013g0002a0001c0001t0013g0023a0001c0001t0038g0022 | 5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1501C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787157 | ||||||
chr2:28787188
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.593-1470G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787188 | ||||||
chr2:28787200
|
T | C | 153 | a0001c0002t0001g0235a0001c0002t0002g0001a0001c0002t0002g0004others(150): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.593-1458T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787200 | ||||||
chr2:28787226
|
G | A | 2 | a0001c0002t0002g0129a0001c0002t0011g0130 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.593-1432G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787226 | ||||||
chr2:28787230
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.593-1428C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787230 | ||||||
chr2:28787320
|
G | A | 1 | a0001c0002t0002g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.593-1338G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787320 | ||||||
chr2:28787351
|
C | G | 5 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(2): Show | 5 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1307C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787351 | ||||||
chr2:28787445
|
C | T | 1 | a0001c0002t0002g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.593-1213C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787445 | ||||||
chr2:28787473
|
G | A | 152 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(149): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.593-1185G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787473 | ||||||
chr2:28787487
|
C | T | 1 | a0001c0001t0038g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.593-1171C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787487 | ||||||
chr2:28787516
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.593-1142C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787516 | ||||||
chr2:28787651
|
A | G | 87 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(84): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.593-1007A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787651 | ||||||
chr2:28787709
|
A | G | 2 | a0001c0002t0039g0148a0001c0002t0040g0147 | 2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.593-949A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787709 | ||||||
chr2:28787711
|
G | A | 1 | a0001c0001t0006g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.593-947G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787711 | ||||||
chr2:28787825
|
T | C | 1 | a0001c0001t0004g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.593-833T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787825 | ||||||
chr2:28787844
|
A | G | 8 | a0001c0001t0012g0272a0001c0001t0012g0281a0001c0001t0012g0283others(5): Show | 8 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.593-814A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787844 | ||||||
chr2:28787951
|
A | G | 1 | a0001c0002t0002g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.593-707A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787951 | ||||||
chr2:28787960
|
A | G | 55 | a0001c0002t0003g0009a0001c0002t0003g0010a0001c0002t0003g0011others(52): Show | 58 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.593-698A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787960 | ||||||
chr2:28787989
|
A | T | 2 | a0001c0002t0003g0195a0001c0002t0003g0196 | 2 | NA18942.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.593-669A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787989 | ||||||
chr2:28788022
|
T | C | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.593-636T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788022 | ||||||
chr2:28788072
|
C | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0102 | 2 | NA18974.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.593-586C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788072 | ||||||
chr2:28788221
|
G | A | 55 | a0001c0002t0003g0009a0001c0002t0003g0010a0001c0002t0003g0011others(52): Show | 58 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.593-437G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788221 | ||||||
chr2:28788275
|
GAAA | G | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.593-382_593-380del others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788275 | ||||||
chr2:28788404
|
T | C | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-254T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788404 | ||||||
chr2:28788471
|
TTGTA | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.593-184_593-181del others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28788471 | |||||
chr2:28788869
|
G | A | 1 | a0001c0002t0002g0045 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.744+60G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788869 | ||||||
chr2:28788914
|
A | G | 1 | a0001c0001t0004g0079 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.744+105A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788914 | ||||||
chr2:28788922
|
A | G | 1 | a0001c0001t0004g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.744+113A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788922 | ||||||
chr2:28788980
|
C | T | 2 | a0001c0001t0004g0021a0001c0001t0036g0020 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.744+171C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788980 | ||||||
chr2:28788985
|
G | A | 1 | a0001c0002t0002g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.744+176G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788985 | ||||||
chr2:28788987
|
A | G | 1 | a0001c0001t0001g0331 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.744+178A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788987 | ||||||
chr2:28789031
|
A | C | 1 | a0001c0002t0002g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.744+222A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789031 | ||||||
chr2:28789179
|
T | C | 1 | a0001c0002t0003g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.744+370T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789179 | ||||||
chr2:28789335
|
C | T | 5 | a0001c0002t0003g0008a0001c0002t0003g0189a0001c0002t0003g0214others(2): Show | 6 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+526C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789335 | ||||||
chr2:28789400
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.744+591G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789400 | ||||||
chr2:28789510
|
A | G | 1 | a0001c0002t0034g0046 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.744+701A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789510 | ||||||
chr2:28789565
|
T | G | 6 | a0001c0002t0003g0008a0001c0002t0003g0189a0001c0002t0003g0214others(3): Show | 7 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+756T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789565 | ||||||
chr2:28789588
|
T | C | 5 | a0001c0002t0003g0008a0001c0002t0003g0189a0001c0002t0003g0214others(2): Show | 6 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+779T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789588 | ||||||
chr2:28789593
|
A | AT | 11 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0112others(8): Show | 11 | HG00544.hp1 HG00621.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.744+807dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28789593 | |||||
chr2:28789593
|
AT | A | 93 | a0001c0001t0001g0019a0001c0001t0001g0244a0001c0001t0001g0265others(90): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.744+807delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28789593 | |||||
chr2:28789593
|
ATTTTT | A | 55 | a0001c0002t0003g0009a0001c0002t0003g0010a0001c0002t0003g0011others(52): Show | 58 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.744+803_744+807del others(5): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28789593 | |||||
chr2:28789619
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.744+810G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789619 | ||||||
chr2:28789708
|
T | C | 160 | a0001c0001t0001g0019a0001c0001t0004g0018a0001c0001t0004g0021others(157): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.744+899T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789708 | ||||||
chr2:28789711
|
G | C | 6 | a0001c0001t0012g0272a0001c0001t0012g0281a0001c0001t0012g0334others(3): Show | 6 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+902G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789711 | ||||||
chr2:28789791
|
G | T | 5 | a0001c0002t0003g0008a0001c0002t0003g0189a0001c0002t0003g0214others(2): Show | 6 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+982G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789791 | ||||||
chr2:28789909
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.744+1100T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789909 | ||||||
chr2:28789957
|
C | A | 2 | a0001c0001t0001g0234a0001c0001t0006g0238 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.744+1148C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789957 | ||||||
chr2:28789998
|
TG | T | 6 | a0001c0002t0003g0008a0001c0002t0003g0189a0001c0002t0003g0214others(3): Show | 7 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+1191delG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28789998 | |||||
chr2:28790139
|
A | G | 66 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(63): Show | 70 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.744+1330A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790139 | ||||||
chr2:28790368
|
C | G | 3 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345 | 3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.744+1559C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790368 | ||||||
chr2:28790411
|
C | T | 5 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(2): Show | 5 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+1602C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790411 | ||||||
chr2:28790525
|
A | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0074others(19): Show | 22 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.744+1716A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790525 | ||||||
chr2:28790546
|
G | C | 60 | a0001c0002t0003g0009a0001c0002t0003g0010a0001c0002t0003g0011others(57): Show | 63 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.744+1737G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790546 | ||||||
chr2:28790741
|
A | G | 4 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0330others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+1932A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790741 | ||||||
chr2:28790911
|
A | G | 1 | a0001c0002t0003g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.744+2102A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790911 | ||||||
chr2:28791177
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.744+2368C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791177 | ||||||
chr2:28791325
|
G | T | 349 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(346): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.744+2516G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791325 | ||||||
chr2:28791328
|
G | T | 2 | a0001c0002t0033g0222a0001c0002t0037g0346 | 2 | HG01891.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.744+2519G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791328 | ||||||
chr2:28791354
|
A | G | 1 | a0001c0002t0002g0141 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.745-2509A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791354 | ||||||
chr2:28791386
|
A | G | 1 | a0001c0001t0030g0285 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.745-2477A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791386 | ||||||
chr2:28791487
|
G | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0113a0001c0001t0001g0162 | 3 | HG02698.hp1 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.745-2376G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791487 | ||||||
chr2:28791593
|
G | C | 1 | a0001c0002t0002g0038 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.745-2270G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791593 | ||||||
chr2:28791606
|
G | A | 1 | a0001c0001t0030g0285 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.745-2257G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791606 | ||||||
chr2:28791880
|
C | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.745-1983C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791880 | ||||||
chr2:28792079
|
G | T | 4 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1784G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792079 | ||||||
chr2:28792167
|
C | A | 3 | a0001c0001t0013g0002a0001c0001t0013g0023a0001c0001t0038g0022 | 5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1696C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792167 | ||||||
chr2:28792255
|
G | A | 1 | a0001c0002t0009g0138 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.745-1608G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792255 | ||||||
chr2:28792288
|
C | T | 1 | a0001c0002t0007g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.745-1575C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792288 | ||||||
chr2:28792294
|
C | T | 1 | a0001c0001t0006g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.745-1569C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792294 | ||||||
chr2:28792371
|
A | G | 1 | a0001c0001t0001g0259 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.745-1492A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792371 | ||||||
chr2:28792508
|
C | T | 2 | a0001c0001t0004g0021a0001c0001t0036g0020 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.745-1355C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792508 | ||||||
chr2:28792647
|
A | G | 2 | a0001c0001t0013g0002a0001c0001t0013g0023 | 4 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-1216A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792647 | ||||||
chr2:28792648
|
T | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(54): Show | 59 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.745-1215T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792648 | ||||||
chr2:28792685
|
G | A | 4 | a0001c0002t0002g0034a0001c0002t0002g0133a0001c0002t0002g0135others(1): Show | 4 | HG01070.hp2 HG01255.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-1178G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792685 | ||||||
chr2:28792798
|
T | C | 1 | a0001c0001t0030g0285 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.745-1065T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792798 | ||||||
chr2:28792832
|
A | G | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-1031A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792832 | ||||||
chr2:28793079
|
G | A | 2 | a0001c0001t0005g0291a0001c0001t0005g0293 | 2 | NA18963.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.745-784G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793079 | ||||||
chr2:28793116
|
G | C | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.745-747G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793116 | ||||||
chr2:28793153
|
C | T | 78 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(75): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.745-710C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793153 | ||||||
chr2:28793237
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.745-626C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793237 | ||||||
chr2:28793367
|
A | C | 60 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(57): Show | 64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.745-496A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793367 | ||||||
chr2:28793396
|
TTGTC | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.745-464_745-461del others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28793396 | |||||
chr2:28793616
|
T | A | 3 | a0001c0002t0003g0190a0001c0002t0003g0193a0001c0002t0003g0216 | 3 | HG02258.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.745-247T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793616 | ||||||
chr2:28794083
|
G | T | 6 | a0001c0001t0001g0258a0001c0001t0001g0263a0001c0001t0001g0308others(3): Show | 6 | HG00438.hp1 HG00597.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+86G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794083 | ||||||
chr2:28794123
|
C | T | 8 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0026others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+126C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794123 | ||||||
chr2:28794418
|
C | T | 4 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+421C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794418 | ||||||
chr2:28794419
|
G | A | 15 | a0001c0002t0007g0200a0001c0002t0007g0201a0001c0002t0007g0202others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.879+422G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794419 | ||||||
chr2:28794492
|
C | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.879+495C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794492 | ||||||
chr2:28794608
|
G | A | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(83): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.879+611G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794608 | ||||||
chr2:28794615
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.879+618C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794615 | ||||||
chr2:28794692
|
A | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0153a0001c0001t0001g0155others(9): Show | 14 | HG00438.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+695A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794692 | ||||||
chr2:28794776
|
A | T | 8 | a0001c0001t0012g0272a0001c0001t0012g0281a0001c0001t0012g0283others(5): Show | 8 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.879+779A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794776 | ||||||
chr2:28794815
|
G | T | 1 | a0001c0001t0004g0096 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.879+818G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794815 | ||||||
chr2:28794881
|
T | G | 343 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(340): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.879+884T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794881 | ||||||
chr2:28795004
|
C | T | 60 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(57): Show | 64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.879+1007C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795004 | ||||||
chr2:28795025
|
A | G | 2 | a0001c0001t0013g0002a0001c0001t0013g0023 | 4 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+1028A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795025 | ||||||
chr2:28795176
|
T | G | 4 | a0001c0002t0004g0343a0001c0002t0004g0344a0001c0002t0004g0345others(1): Show | 4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+1179T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795176 | ||||||
chr2:28795237
|
A | T | 2 | a0001c0002t0002g0169a0001c0002t0002g0170 | 2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+1240A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795237 | ||||||
chr2:28795293
|
G | A | 2 | a0001c0001t0001g0302a0001c0001t0005g0252 | 2 | NA19001.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.879+1296G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795293 | ||||||
chr2:28795403
|
T | C | 2 | a0001c0002t0002g0228a0001c0002t0002g0229 | 2 | HG01496.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.879+1406T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795403 | ||||||
chr2:28795483
|
A | G | 3 | a0001c0001t0004g0018a0001c0002t0002g0047a0001c0002t0002g0058 | 3 | HG01257.hp2 HG02055.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.879+1486A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795483 | ||||||
chr2:28795581
|
A | G | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.879+1584A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795581 | ||||||
chr2:28795860
|
T | G | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.879+1863T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795860 | ||||||
chr2:28796023
|
T | C | 152 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(149): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.879+2026T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796023 | ||||||
chr2:28796056
|
C | T | 1 | a0001c0001t0005g0293 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.879+2059C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796056 | ||||||
chr2:28796060
|
T | C | 5 | a0001c0001t0004g0021a0001c0001t0013g0002a0001c0001t0013g0023others(2): Show | 7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+2063T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796060 | ||||||
chr2:28796074
|
G | A | 1 | a0001c0002t0002g0048 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.879+2077G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796074 | ||||||
chr2:28796172
|
A | G | 1 | a0001c0002t0022g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.879+2175A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796172 | ||||||
chr2:28796190
|
TA | T | 152 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(149): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.879+2195delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 28796190 | |||||
chr2:28796270
|
C | T | 1 | a0001c0002t0037g0346 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.879+2273C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796270 | ||||||
chr2:28796385
|
A | G | 1 | a0001c0002t0003g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.879+2388A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796385 | ||||||
chr2:28796514
|
G | T | 3 | a0001c0001t0013g0002a0001c0001t0013g0023a0001c0001t0038g0022 | 5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+2517G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796514 | ||||||
chr2:28796518
|
T | A | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.879+2521T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796518 | ||||||
chr2:28796700
|
T | C | 1 | a0001c0002t0007g0201 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.880-2499T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796700 | ||||||
chr2:28796723
|
A | G | 1 | a0001c0002t0003g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.880-2476A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796723 | ||||||
chr2:28796775
|
T | C | 1 | a0001c0002t0003g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.880-2424T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796775 | ||||||
chr2:28796854
|
A | C | 1 | a0001c0001t0004g0341 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.880-2345A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796854 | ||||||
chr2:28797120
|
C | A | 1 | a0001c0001t0012g0333 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.880-2079C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797120 | ||||||
chr2:28797127
|
T | C | 4 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0330others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-2072T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797127 | ||||||
chr2:28797136
|
T | G | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.880-2063T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797136 | ||||||
chr2:28797186
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.880-2013C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797186 | ||||||
chr2:28797187
|
G | A | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.880-2012G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797187 | ||||||
chr2:28797305
|
C | T | 1 | a0001c0002t0033g0222 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.880-1894C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797305 | ||||||
chr2:28797413
|
A | G | 18 | a0001c0002t0002g0042a0001c0002t0002g0044a0001c0002t0002g0045others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.880-1786A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797413 | ||||||
chr2:28797436
|
A | C | 6 | a0001c0001t0001g0258a0001c0001t0001g0263a0001c0001t0001g0308others(3): Show | 6 | HG00438.hp1 HG00597.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-1763A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797436 | ||||||
chr2:28797494
|
C | G | 67 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010others(64): Show | 71 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.880-1705C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797494 | ||||||
chr2:28797514
|
A | G | 1 | a0001c0002t0010g0227 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.880-1685A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797514 | ||||||
chr2:28797725
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.880-1474T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797725 | ||||||
chr2:28797892
|
A | G | 5 | a0001c0001t0005g0240a0001c0001t0005g0291a0001c0001t0005g0292others(2): Show | 5 | HG00544.hp2 NA18944.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-1307A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797892 | ||||||
chr2:28797931
|
C | T | 1 | a0001c0002t0025g0167 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.880-1268C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797931 | ||||||
chr2:28798292
|
C | G | 1 | a0001c0002t0002g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.880-907C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798292 | ||||||
chr2:28798365
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0160 | 2 | NA18942.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.880-834A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798365 | ||||||
chr2:28798645
|
GAC | G | 151 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(148): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.880-550_880-549del others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 28798645 | |||||
chr2:28798664
|
G | T | 4 | a0001c0002t0003g0174a0001c0002t0003g0175a0001c0002t0003g0176others(1): Show | 4 | HG02622.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-535G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798664 | ||||||
chr2:28798789
|
A | C | 1 | a0001c0001t0004g0092 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.880-410A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798789 | ||||||
chr2:28798844
|
G | A | 1 | a0001c0001t0006g0124 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.880-355G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798844 | ||||||
chr2:28798948
|
CA | C | 151 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0030others(148): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.880-246delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 28798948 | |||||
chr2:28798971
|
A | G | 12 | a0001c0001t0001g0241a0001c0001t0001g0244a0001c0001t0001g0247others(9): Show | 12 | HG01928.hp1 HG01934.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.880-228A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798971 | ||||||
chr2:28798980
|
A | T | 1 | a0001c0002t0031g0347 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.880-219A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798980 | ||||||
chr2:28799143
|
T | G | 8 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0026others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-56T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28799143 | ||||||
chr2:28799195
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.880-4T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28799195 |