geneid | 1265 |
---|---|
ensemblid | ENSG00000064666.15 |
hgncid | 2156 |
symbol | CNN2 |
name | calponin 2 |
refseq_nuc | NM_004368.4 |
refseq_prot | NP_004359.1 |
ensembl_nuc | ENST00000263097.9 |
ensembl_prot | ENSP00000263097.2 |
mane_status | MANE Select |
chr | chr19 |
start | 1026608 |
end | 1039065 |
strand | + |
ver | v1.2 |
region | chr19:1026608-1039065 |
region5000 | chr19:1021608-1044065 |
regionname0 | CNN2_chr19_1026608_1039065 |
regionname5000 | CNN2_chr19_1021608_1044065 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 309 | 387 | 97 | 68 | 156 | 14 | 50 | 110 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0002 | 0/0 | 309 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0003 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 930 | 233 | 68 | 25 | 108 | 10 | 22 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0002 | 0/0 | 930 | 46 | 5 | 22 | 5 | 2 | 12 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0003 | 1/1 | 930 | 30 | 16 | 3 | 7 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0004 | 0/0 | 930 | 29 | 0 | 3 | 22 | 1 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0005 | 0/0 | 930 | 20 | 0 | 4 | 11 | 0 | 5 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0006 | 0/0 | 930 | 10 | 0 | 7 | 0 | 1 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0007 | 0/0 | 930 | 5 | 0 | 3 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0008 | 0/0 | 930 | 4 | 4 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0009 | 0/0 | 930 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0010 | 0/0 | 930 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0011 | 0/0 | 930 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0012 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0013 | 0/0 | 930 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0014 | 0/0 | 930 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0015 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0016 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0017 | 0/0 | 930 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
c0018 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1221 | 104 | 17 | 21 | 45 | 8 | 13 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0002 | 0/0 | 1221 | 56 | 1 | 0 | 51 | 0 | 4 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0003 | 1/1 | 1220 | 51 | 9 | 6 | 28 | 1 | 5 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0004 | 0/0 | 1221 | 40 | 4 | 19 | 5 | 2 | 10 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0005 | 0/0 | 1220 | 29 | 19 | 4 | 1 | 2 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0006 | 0/0 | 1220 | 17 | 12 | 3 | 1 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0007 | 0/0 | 1217 | 15 | 0 | 10 | 0 | 1 | 4 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0008 | 0/0 | 1218 | 14 | 0 | 1 | 12 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0009 | 0/0 | 1222 | 10 | 8 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0010 | 0/0 | 1220 | 9 | 9 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0011 | 0/0 | 1221 | 8 | 8 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0012 | 0/0 | 1221 | 4 | 0 | 1 | 0 | 0 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0013 | 0/0 | 1221 | 3 | 1 | 1 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0014 | 0/0 | 1221 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0015 | 0/0 | 1220 | 3 | 1 | 0 | 1 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0016 | 0/0 | 1218 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0017 | 0/0 | 1219 | 2 | 0 | 1 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0018 | 0/0 | 1221 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0019 | 0/0 | 1220 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0020 | 0/0 | 1221 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0021 | 0/0 | 1217 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0022 | 0/0 | 1220 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0023 | 0/0 | 1220 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0024 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0025 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0026 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0027 | 0/0 | 1221 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0028 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0029 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0030 | 0/0 | 1220 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0031 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0032 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0033 | 0/0 | 1220 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
t0034 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 22 | 0 | 5 | 16 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0002 | 0/0 | 15 | 0 | 0 | 14 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0003 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0004 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0005 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0006 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0007 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0008 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0132 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 930 | 233 | 68 | 25 | 108 | 10 | 22 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0002 | 0/0 | 930 | 46 | 5 | 22 | 5 | 2 | 12 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0003 | 1/1 | 930 | 30 | 16 | 3 | 7 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0004 | 0/0 | 930 | 29 | 0 | 3 | 22 | 1 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0005 | 0/0 | 930 | 20 | 0 | 4 | 11 | 0 | 5 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0006 | 0/0 | 930 | 10 | 0 | 7 | 0 | 1 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0007 | 0/0 | 930 | 5 | 0 | 3 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0008 | 0/0 | 930 | 4 | 4 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0009 | 0/0 | 930 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0011 | 0/0 | 930 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0013 | 0/0 | 930 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0014 | 0/0 | 930 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0015 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0016 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0017 | 0/0 | 930 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0018 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0002c0010 | 0/0 | 930 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0003c0012 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2150 | 97 | 17 | 16 | 44 | 8 | 12 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0002 | 0/0 | 2150 | 55 | 1 | 0 | 50 | 0 | 4 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0003 | 0/0 | 2149 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0005 | 0/0 | 2149 | 27 | 18 | 4 | 1 | 2 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0006 | 0/0 | 2149 | 17 | 12 | 3 | 1 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0009 | 0/0 | 2151 | 10 | 8 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0010 | 0/0 | 2149 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0011 | 0/0 | 2150 | 7 | 7 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0014 | 0/0 | 2150 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0015 | 0/0 | 2149 | 3 | 1 | 0 | 1 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0017 | 0/0 | 2148 | 2 | 0 | 1 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0018 | 0/0 | 2150 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0022 | 0/0 | 2149 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0025 | 0/0 | 2150 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0026 | 0/0 | 2150 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0027 | 0/0 | 2150 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0028 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0029 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0030 | 0/0 | 2149 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0001t0034 | 0/0 | 2150 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0002t0004 | 0/0 | 2150 | 38 | 4 | 19 | 5 | 2 | 8 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0002t0012 | 0/0 | 2150 | 4 | 0 | 1 | 0 | 0 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0002t0013 | 0/0 | 2150 | 3 | 1 | 1 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0002t0023 | 0/0 | 2149 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0003t0003 | 1/1 | 2149 | 22 | 9 | 3 | 6 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0003t0010 | 0/0 | 2149 | 6 | 6 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0003t0031 | 0/0 | 2149 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0003t0033 | 0/0 | 2149 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0004t0003 | 0/0 | 2149 | 28 | 0 | 3 | 21 | 1 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0004t0032 | 0/0 | 2149 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0005t0007 | 0/0 | 2146 | 5 | 0 | 3 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0005t0008 | 0/0 | 2147 | 13 | 0 | 1 | 11 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0005t0016 | 0/0 | 2147 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0006t0007 | 0/0 | 2146 | 10 | 0 | 7 | 0 | 1 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0007t0001 | 0/0 | 2150 | 4 | 0 | 3 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0007t0002 | 0/0 | 2150 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0008t0019 | 0/0 | 2149 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0008t0020 | 0/0 | 2150 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0009t0010 | 0/0 | 2149 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0011t0004 | 0/0 | 2150 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0013t0001 | 0/0 | 2150 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0014t0005 | 0/0 | 2149 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0015t0011 | 0/0 | 2150 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0016t0024 | 0/0 | 2150 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0017t0021 | 0/0 | 2146 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0001c0018t0008 | 0/0 | 2147 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0002c0010t0001 | 0/0 | 2150 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
a0003c0012t0005 | 0/0 | 2149 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | copy fasta | chr19 | 1021608 | 1044065 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 0 | 3 | 14 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0006 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0004 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0010g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0011g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0011g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0011g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0014g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0014g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0015g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0017g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0017g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0018g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0018g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0022g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0025g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0026g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0027g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0029g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0030g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0001t0034g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0005 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0012g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0012g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0012g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0012g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0013g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0013g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0002t0023g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0132 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0031g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0003t0033g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0002 | 0/0 | 15 | 0 | 0 | 14 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0004t0032g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0007g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0007g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0007g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0008g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0008g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0008g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0008g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0008g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0016g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0005t0016g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0006t0007g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0006t0007g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0006t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0006t0007g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0006t0007g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0006t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0007t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0007t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0007t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0007t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0008t0019g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0008t0019g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0008t0020g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0008t0020g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0009t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0009t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0011t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0011t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0013t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0014t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0015t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0016t0024g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0017t0021g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0001c0018t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0002c0010t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0002c0010t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
a0003c0012t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | GBR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00140 | hp1 | a0001 | c0006 | t0007 | g0154 | EUR | GBR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0265 | EUR | FIN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0266 | EUR | FIN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00438 | hp2 | a0001 | c0005 | t0008 | g0011 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00609 | hp1 | a0001 | c0005 | t0008 | g0021 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00609 | hp2 | a0001 | c0007 | t0001 | g0032 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00621 | hp1 | a0001 | c0001 | t0028 | g0001 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00639 | hp2 | a0001 | c0002 | t0004 | g0040 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00733 | hp1 | a0001 | c0002 | t0004 | g0075 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00733 | hp2 | a0001 | c0002 | t0004 | g0137 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00735 | hp1 | a0001 | c0006 | t0007 | g0010 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG00735 | hp2 | a0001 | c0002 | t0004 | g0226 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01070 | hp2 | a0001 | c0006 | t0007 | g0146 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01071 | hp1 | a0001 | c0002 | t0004 | g0142 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01071 | hp2 | a0001 | c0006 | t0007 | g0153 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01074 | hp1 | a0001 | c0007 | t0001 | g0135 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01074 | hp2 | a0001 | c0002 | t0004 | g0018 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01081 | hp1 | a0001 | c0002 | t0004 | g0039 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01099 | hp1 | a0001 | c0002 | t0004 | g0252 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01106 | hp1 | a0001 | c0006 | t0007 | g0010 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01106 | hp2 | a0001 | c0003 | t0003 | g0179 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0009 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01167 | hp1 | a0001 | c0001 | t0017 | g0008 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01168 | hp1 | a0001 | c0006 | t0007 | g0010 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01168 | hp2 | a0001 | c0005 | t0007 | g0120 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01169 | hp1 | a0001 | c0006 | t0007 | g0010 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01175 | hp1 | a0001 | c0003 | t0003 | g0031 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01175 | hp2 | a0001 | c0006 | t0007 | g0155 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01192 | hp2 | a0001 | c0003 | t0003 | g0178 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01243 | hp1 | a0001 | c0001 | t0030 | g0253 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01256 | hp1 | a0001 | c0004 | t0003 | g0016 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01257 | hp1 | a0001 | c0005 | t0007 | g0030 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01257 | hp2 | a0001 | c0002 | t0004 | g0206 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01258 | hp1 | a0001 | c0005 | t0007 | g0030 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01258 | hp2 | a0001 | c0004 | t0003 | g0016 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01261 | hp1 | a0001 | c0002 | t0004 | g0209 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01346 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01433 | hp1 | a0001 | c0007 | t0001 | g0032 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01516 | hp1 | a0001 | c0002 | t0004 | g0018 | EUR | IBS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01884 | hp1 | a0001 | c0002 | t0004 | g0040 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0086 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01934 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01934 | hp2 | a0001 | c0005 | t0008 | g0249 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01943 | hp1 | a0001 | c0001 | t0006 | g0052 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01943 | hp2 | a0001 | c0002 | t0013 | g0023 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01952 | hp1 | a0002 | c0010 | t0001 | g0006 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01975 | hp2 | a0001 | c0002 | t0004 | g0224 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0082 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01978 | hp2 | a0001 | c0007 | t0001 | g0157 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01981 | hp1 | a0001 | c0002 | t0004 | g0025 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01981 | hp2 | a0001 | c0002 | t0004 | g0039 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01993 | hp1 | a0001 | c0002 | t0023 | g0005 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02027 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02040 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02055 | hp2 | a0001 | c0008 | t0020 | g0172 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02071 | hp2 | a0001 | c0002 | t0004 | g0095 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02074 | hp1 | a0001 | c0003 | t0003 | g0232 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02083 | hp1 | a0001 | c0005 | t0008 | g0012 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02083 | hp2 | a0001 | c0001 | t0029 | g0136 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02129 | hp2 | a0001 | c0004 | t0003 | g0160 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02132 | hp1 | a0001 | c0005 | t0008 | g0044 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02132 | hp2 | a0001 | c0005 | t0008 | g0021 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02145 | hp1 | a0001 | c0003 | t0010 | g0169 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02148 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02148 | hp2 | a0001 | c0017 | t0021 | g0151 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02155 | hp1 | a0001 | c0018 | t0008 | g0193 | EAS | CDX | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02155 | hp2 | a0001 | c0004 | t0032 | g0017 | EAS | CDX | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CDX | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02165 | hp2 | a0001 | c0004 | t0003 | g0186 | EAS | CDX | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02257 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0216 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02293 | hp1 | a0001 | c0004 | t0003 | g0149 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02293 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02300 | hp1 | a0002 | c0010 | t0001 | g0001 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02300 | hp2 | a0001 | c0002 | t0012 | g0221 | AMR | PEL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02451 | hp1 | a0001 | c0003 | t0010 | g0190 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02451 | hp2 | a0001 | c0001 | t0025 | g0056 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0171 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02572 | hp2 | a0001 | c0003 | t0010 | g0071 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02602 | hp2 | a0001 | c0002 | t0004 | g0235 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02615 | hp1 | a0001 | c0008 | t0019 | g0173 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0258 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0022 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02647 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02647 | hp2 | a0001 | c0003 | t0003 | g0176 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02683 | hp1 | a0001 | c0004 | t0003 | g0198 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02698 | hp1 | a0001 | c0004 | t0003 | g0002 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02698 | hp2 | a0001 | c0001 | t0027 | g0097 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02717 | hp1 | a0001 | c0008 | t0019 | g0089 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0066 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02723 | hp2 | a0001 | c0001 | t0015 | g0080 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02738 | hp2 | a0001 | c0002 | t0004 | g0237 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02809 | hp2 | a0001 | c0003 | t0010 | g0068 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0175 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02895 | hp1 | a0001 | c0009 | t0010 | g0167 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02895 | hp2 | a0001 | c0001 | t0022 | g0061 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02896 | hp2 | a0003 | c0012 | t0005 | g0065 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02897 | hp1 | a0001 | c0009 | t0010 | g0168 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02965 | hp1 | a0001 | c0003 | t0033 | g0164 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02970 | hp1 | a0001 | c0016 | t0024 | g0094 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02970 | hp2 | a0001 | c0003 | t0010 | g0189 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03017 | hp2 | a0001 | c0002 | t0004 | g0250 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03041 | hp1 | a0001 | c0003 | t0003 | g0177 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03098 | hp1 | a0001 | c0001 | t0010 | g0085 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03130 | hp2 | a0001 | c0003 | t0003 | g0182 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0070 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0191 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03225 | hp1 | a0001 | c0008 | t0020 | g0174 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03225 | hp2 | a0001 | c0015 | t0011 | g0060 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03239 | hp1 | a0001 | c0004 | t0003 | g0195 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03239 | hp2 | a0001 | c0002 | t0012 | g0131 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0022 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03486 | hp1 | a0001 | c0003 | t0003 | g0183 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03486 | hp2 | a0001 | c0003 | t0003 | g0181 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03490 | hp1 | a0001 | c0006 | t0007 | g0033 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03491 | hp1 | a0001 | c0005 | t0007 | g0026 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03491 | hp2 | a0001 | c0001 | t0015 | g0140 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03492 | hp2 | a0001 | c0005 | t0007 | g0026 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03516 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | ESN | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03540 | hp1 | a0001 | c0003 | t0003 | g0185 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0180 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03654 | hp1 | a0001 | c0002 | t0004 | g0045 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0081 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03669 | hp2 | a0001 | c0002 | t0004 | g0236 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03688 | hp1 | a0001 | c0011 | t0004 | g0156 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03688 | hp2 | a0001 | c0002 | t0012 | g0238 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03704 | hp1 | a0001 | c0002 | t0004 | g0046 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03704 | hp2 | a0001 | c0001 | t0017 | g0073 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03710 | hp1 | a0001 | c0003 | t0003 | g0031 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03710 | hp2 | a0001 | c0005 | t0016 | g0218 | SAS | PJL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03834 | hp1 | a0001 | c0006 | t0007 | g0033 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0092 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03927 | hp1 | a0001 | c0005 | t0008 | g0143 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03927 | hp2 | a0001 | c0003 | t0003 | g0130 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03942 | hp1 | a0001 | c0002 | t0004 | g0234 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03942 | hp2 | a0001 | c0011 | t0004 | g0163 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04115 | hp2 | a0001 | c0013 | t0001 | g0054 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04184 | hp2 | a0001 | c0002 | t0013 | g0233 | SAS | BEB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04199 | hp2 | a0001 | c0005 | t0016 | g0213 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04204 | hp1 | a0001 | c0002 | t0012 | g0240 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04204 | hp2 | a0001 | c0002 | t0004 | g0228 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0074 | SAS | STU | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18612 | hp2 | a0001 | c0001 | t0014 | g0003 | EAS | CHB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CHB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18906 | hp1 | a0001 | c0003 | t0010 | g0166 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18944 | hp2 | a0001 | c0005 | t0008 | g0012 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18945 | hp2 | a0001 | c0004 | t0003 | g0148 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18950 | hp1 | a0001 | c0001 | t0009 | g0244 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18951 | hp1 | a0001 | c0005 | t0008 | g0011 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18954 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18960 | hp2 | a0001 | c0004 | t0003 | g0150 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18964 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18966 | hp2 | a0001 | c0005 | t0008 | g0011 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18968 | hp2 | a0001 | c0003 | t0031 | g0013 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18969 | hp2 | a0001 | c0005 | t0008 | g0012 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18971 | hp2 | a0001 | c0005 | t0008 | g0259 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18972 | hp1 | a0001 | c0003 | t0003 | g0104 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18972 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18973 | hp1 | a0001 | c0007 | t0002 | g0152 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18975 | hp1 | a0001 | c0001 | t0018 | g0116 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18979 | hp1 | a0001 | c0004 | t0003 | g0147 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18979 | hp2 | a0001 | c0001 | t0009 | g0041 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18980 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18983 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18990 | hp2 | a0001 | c0002 | t0004 | g0230 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18995 | hp2 | a0001 | c0001 | t0014 | g0051 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19000 | hp1 | a0001 | c0004 | t0003 | g0017 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19004 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19005 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19005 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19009 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19011 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19012 | hp2 | a0001 | c0003 | t0003 | g0112 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0134 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19055 | hp2 | a0001 | c0001 | t0026 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19056 | hp1 | a0001 | c0002 | t0004 | g0223 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19056 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19060 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19065 | hp2 | a0001 | c0002 | t0004 | g0007 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19066 | hp2 | a0001 | c0002 | t0004 | g0215 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19070 | hp2 | a0001 | c0001 | t0018 | g0111 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19079 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19080 | hp1 | a0001 | c0003 | t0003 | g0048 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19081 | hp1 | a0001 | c0004 | t0003 | g0017 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19085 | hp1 | a0001 | c0005 | t0008 | g0162 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19085 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19087 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | YRI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20129 | hp1 | a0001 | c0002 | t0004 | g0076 | AFR | ASW | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20129 | hp2 | a0001 | c0002 | t0013 | g0023 | AFR | ASW | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20805 | hp1 | a0001 | c0004 | t0003 | g0016 | EUR | TSI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0008 | EUR | TSI | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20905 | hp1 | a0001 | c0014 | t0005 | g0072 | SAS | GIH | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01123 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG01123 | hp2 | a0001 | c0002 | t0004 | g0077 | AMR | CLM | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0084 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0262 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02486 | hp2 | a0001 | c0003 | t0003 | g0184 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG02559 | hp2 | a0001 | c0001 | t0034 | g0145 | AFR | ACB | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0058 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0088 | AFR | MSL | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG06807 | hp1 | a0001 | c0001 | t0011 | g0192 | AFR | USA | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | USA | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18955 | hp1 | a0001 | c0001 | t0014 | g0197 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | USA | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA20300 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | USA | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0003 | g0132 | REF | REF | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0003 | g0129 | REF | REF | CNN2_chr19_1021608_1044065 | CNN2 | chr19 | 1021608 | 1044065 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:1032624
|
C | A | 1 | a0003 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.318C>A | p.Phe106Leu | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/7 | 372/2149 | 318/930 | 106/309 | chr19 | 1032624 | ||
chr19:1037635
|
C | T | 1 | a0002 | 2 | HG01952.hp1 HG02300.hp1 |
missense_variant | MODERATE | c.665C>T | p.Thr222Met | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 719/2149 | 665/930 | 222/309 | chr19 | 1037635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:1031115
|
C | G | 1 | a0001c0018 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.108C>G | p.Thr36Thr | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/7 | 162/2149 | 108/930 | 36/309 | chr19 | 1031115 | ||
chr19:1032690
|
G | T | 5 | a0001c0004a0001c0006a0001c0007others(2): Show | 47 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(44): Show |
synonymous_variant | LOW | c.384G>T | p.Ala128Ala | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/7 | 438/2149 | 384/930 | 128/309 | chr19 | 1032690 | ||
chr19:1036153
|
C | T | 1 | a0001c0016 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.414C>T | p.Ser138Ser | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 5/7 | 468/2149 | 414/930 | 138/309 | chr19 | 1036153 | ||
chr19:1036204
|
C | T | 1 | a0001c0015 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.465C>T | p.Asp155Asp | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 5/7 | 519/2149 | 465/930 | 155/309 | chr19 | 1036204 | ||
chr19:1036445
|
G | A | 3 | a0001c0002a0001c0009a0001c0011 | 50 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(47): Show |
synonymous_variant | LOW | c.537G>A | p.Ser179Ser | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 591/2149 | 537/930 | 179/309 | chr19 | 1036445 | ||
chr19:1036457
|
C | G | 4 | a0001c0005a0001c0006a0001c0017others(1): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
synonymous_variant | LOW | c.549C>G | p.Ala183Ala | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 603/2149 | 549/930 | 183/309 | chr19 | 1036457 | ||
chr19:1036469
|
A | G | 4 | a0001c0005a0001c0006a0001c0017others(1): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
synonymous_variant | LOW | c.561A>G | p.Arg187Arg | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 615/2149 | 561/930 | 187/309 | chr19 | 1036469 | ||
chr19:1036544
|
G | A | 1 | a0001c0013 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.636G>A | p.Thr212Thr | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 690/2149 | 636/930 | 212/309 | chr19 | 1036544 | ||
chr19:1036553
|
T | C | 14 | a0001c0001a0001c0002a0001c0005others(11): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
synonymous_variant | LOW | c.645T>C | p.Cys215Cys | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/7 | 699/2149 | 645/930 | 215/309 | chr19 | 1036553 | ||
chr19:1037762
|
G | A | 1 | a0001c0014 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.792G>A | p.Leu264Leu | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 846/2149 | 792/930 | 264/309 | chr19 | 1037762 | ||
chr19:1037810
|
C | T | 1 | a0001c0017 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.840C>T | p.Ala280Ala | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 894/2149 | 840/930 | 280/309 | chr19 | 1037810 | ||
chr19:1037858
|
C | T | 1 | a0001c0008 | 4 | HG02055.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
synonymous_variant | LOW | c.888C>T | p.Val296Val | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 942/2149 | 888/930 | 296/309 | chr19 | 1037858 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:1026618
|
C | G | 1 | a0001c0001t0034 | 1 | HG02559.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/7 | 44 | chr19 | 1026618 | |||||
chr19:1037933
|
G | C | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(33): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*33G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 33 | chr19 | 1037933 | |||||
chr19:1037942
|
G | T | 5 | a0001c0001t0002a0001c0001t0009a0001c0001t0014others(2): Show | 72 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*42G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 42 | chr19 | 1037942 | |||||
chr19:1037965
|
T | C | 1 | a0001c0001t0014 | 3 | NA18612.hp2 NA18955.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*65T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 65 | chr19 | 1037965 | |||||
chr19:1037969
|
C | CT | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(20): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*83dupT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 84 | INFO_REALIGN_3_PRIME | chr19 | 1037969 | ||||
chr19:1037969
|
C | CTT | 3 | a0001c0001t0009a0001c0001t0028a0001c0001t0029 | 12 | HG00621.hp1 HG02083.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*82_*83dupTT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 84 | INFO_REALIGN_3_PRIME | chr19 | 1037969 | ||||
chr19:1037969
|
CTT | C | 3 | a0001c0005t0008a0001c0005t0016a0001c0018t0008 | 16 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*82_*83delTT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 82 | INFO_REALIGN_3_PRIME | chr19 | 1037969 | ||||
chr19:1037969
|
CTTT | C | 3 | a0001c0005t0007a0001c0006t0007a0001c0017t0021 | 16 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*81_*83delTTT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 81 | INFO_REALIGN_3_PRIME | chr19 | 1037969 | ||||
chr19:1037987
|
A | G | 5 | a0001c0002t0004a0001c0002t0012a0001c0002t0013others(2): Show | 48 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*87A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 87 | chr19 | 1037987 | |||||
chr19:1038077
|
T | G | 3 | a0001c0005t0008a0001c0005t0016a0001c0018t0008 | 16 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*177T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 177 | chr19 | 1038077 | |||||
chr19:1038125
|
C | G | 1 | a0001c0001t0027 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 225 | chr19 | 1038125 | |||||
chr19:1038153
|
C | T | 4 | a0001c0001t0010a0001c0003t0010a0001c0003t0033others(1): Show | 10 | HG02145.hp1 HG02451.hp1 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*253C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 253 | chr19 | 1038153 | |||||
chr19:1038154
|
T | C | 1 | a0001c0016t0024 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 254 | chr19 | 1038154 | |||||
chr19:1038179
|
G | T | 2 | a0001c0001t0018a0001c0001t0026 | 3 | NA18975.hp1 NA19055.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*279G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 279 | chr19 | 1038179 | |||||
chr19:1038223
|
C | G | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(33): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*323C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 323 | chr19 | 1038223 | |||||
chr19:1038290
|
A | C | 4 | a0001c0001t0005a0001c0001t0017a0001c0014t0005others(1): Show | 31 | HG00323.hp1 HG01109.hp1 HG01167.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*390A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 390 | chr19 | 1038290 | |||||
chr19:1038291
|
AG | A | 4 | a0001c0001t0005a0001c0001t0017a0001c0014t0005others(1): Show | 31 | HG00323.hp1 HG01109.hp1 HG01167.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*392delG | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 392 | chr19 | 1038291 | |||||
chr19:1038320
|
C | T | 1 | a0001c0001t0029 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*420C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 420 | chr19 | 1038320 | |||||
chr19:1038371
|
C | T | 1 | a0001c0004t0032 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*471C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 471 | chr19 | 1038371 | |||||
chr19:1038372
|
T | G | 1 | a0001c0004t0032 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 472 | chr19 | 1038372 | |||||
chr19:1038378
|
A | G | 1 | a0001c0003t0031 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 478 | chr19 | 1038378 | |||||
chr19:1038446
|
C | T | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(33): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*546C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 546 | chr19 | 1038446 | |||||
chr19:1038572
|
C | T | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(27): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*672C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 672 | chr19 | 1038572 | |||||
chr19:1038686
|
G | C | 1 | a0001c0001t0029 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*786G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 786 | chr19 | 1038686 | |||||
chr19:1038687
|
C | G | 1 | a0001c0001t0029 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 787 | chr19 | 1038687 | |||||
chr19:1038745
|
T | G | 1 | a0001c0017t0021 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*845T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 845 | chr19 | 1038745 | |||||
chr19:1038845
|
A | C | 1 | a0001c0002t0013 | 3 | HG01943.hp2 HG04184.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*945A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 945 | chr19 | 1038845 | |||||
chr19:1038850
|
A | G | 1 | a0001c0005t0016 | 2 | HG03710.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 950 | chr19 | 1038850 | |||||
chr19:1038863
|
C | G | 8 | a0001c0002t0012a0001c0005t0007a0001c0005t0008others(5): Show | 38 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*963C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 963 | chr19 | 1038863 | |||||
chr19:1038872
|
C | G | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(33): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*972C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 972 | chr19 | 1038872 | |||||
chr19:1038894
|
C | T | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(33): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*994C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 994 | chr19 | 1038894 | |||||
chr19:1038896
|
C | T | 1 | a0001c0001t0030 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 996 | chr19 | 1038896 | |||||
chr19:1038924
|
C | T | 2 | a0001c0001t0011a0001c0015t0011 | 8 | HG02630.hp2 HG02647.hp1 HG03209.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1024C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1024 | chr19 | 1038924 | |||||
chr19:1038926
|
G | A | 3 | a0001c0001t0010a0001c0003t0010a0001c0009t0010 | 9 | HG02145.hp1 HG02451.hp1 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1026G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1026 | chr19 | 1038926 | |||||
chr19:1038948
|
C | G | 1 | a0001c0001t0026 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1048 | chr19 | 1038948 | |||||
chr19:1038950
|
G | C | 1 | a0001c0001t0026 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1050G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1050 | chr19 | 1038950 | |||||
chr19:1038996
|
A | C | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(37): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*1096A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 7/7 | 1096 | chr19 | 1038996 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:1026845
|
C | G | 11 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 11 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+121C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026845 | ||||||
chr19:1026849
|
C | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0254a0001c0001t0001g0255others(4): Show | 9 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+125C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026849 | ||||||
chr19:1026928
|
G | A | 10 | a0001c0001t0001g0047a0001c0002t0004g0045a0001c0002t0004g0046others(7): Show | 16 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+204G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026928 | ||||||
chr19:1026958
|
T | TC | 81 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0043others(78): Show | 100 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.63+243dupC | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1026958 | |||||
chr19:1026962
|
C | CA | 3 | a0001c0001t0001g0050a0001c0001t0002g0049a0001c0001t0014g0051 | 3 | HG00597.hp2 NA18949.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.63+238_63+239insA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026962 | ||||||
chr19:1026965
|
C | G | 1 | a0001c0001t0006g0019 | 3 | HG03579.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.63+241C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1026965 | ||||||
chr19:1027064
|
G | A | 1 | a0001c0005t0008g0021 | 2 | HG00609.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.63+340G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027064 | ||||||
chr19:1027181
|
G | A | 1 | a0001c0001t0006g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.63+457G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027181 | ||||||
chr19:1027287
|
G | T | 21 | a0001c0001t0001g0047a0001c0001t0001g0260a0001c0001t0001g0261others(18): Show | 27 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.63+563G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027287 | ||||||
chr19:1027344
|
G | T | 11 | a0001c0001t0001g0047a0001c0002t0004g0045a0001c0002t0004g0046others(8): Show | 17 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+620G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027344 | ||||||
chr19:1027372
|
T | A | 1 | a0001c0018t0008g0193 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.63+648T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027372 | ||||||
chr19:1027416
|
C | T | 1 | a0001c0001t0011g0192 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.63+692C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027416 | ||||||
chr19:1027502
|
C | T | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0011g0191others(2): Show | 5 | HG02451.hp1 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+778C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027502 | ||||||
chr19:1027611
|
G | A | 11 | a0001c0001t0001g0047a0001c0002t0004g0045a0001c0002t0004g0046others(8): Show | 17 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+887G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027611 | ||||||
chr19:1027621
|
C | A | 1 | a0001c0001t0030g0253 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.63+897C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027621 | ||||||
chr19:1027641
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0194 | 5 | HG01516.hp2 HG02738.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+917G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027641 | ||||||
chr19:1027741
|
C | T | 1 | a0001c0004t0003g0186 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.63+1017C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027741 | ||||||
chr19:1027798
|
A | C | 79 | a0001c0001t0001g0047a0001c0001t0001g0170a0001c0001t0001g0187others(76): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.63+1074A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027798 | ||||||
chr19:1027873
|
G | C | 1 | a0001c0001t0034g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.63+1149G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027873 | ||||||
chr19:1027905
|
T | C | 1 | a0001c0005t0008g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.63+1181T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1027905 | ||||||
chr19:1028144
|
G | C | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+1420G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028144 | ||||||
chr19:1028150
|
G | A | 27 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0161others(24): Show | 47 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+1426G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028150 | ||||||
chr19:1028298
|
G | T | 1 | a0001c0006t0007g0033 | 2 | HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.63+1574G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028298 | ||||||
chr19:1028383
|
C | T | 1 | a0001c0011t0004g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.63+1659C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028383 | ||||||
chr19:1028404
|
AG | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0194others(1): Show | 6 | HG01516.hp2 HG02559.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+1683delG | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1028404 | |||||
chr19:1028435
|
C | G | 10 | a0001c0001t0001g0047a0001c0002t0004g0045a0001c0002t0004g0046others(7): Show | 15 | HG00438.hp2 HG02083.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+1711C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028435 | ||||||
chr19:1028969
|
G | GTCAGGGG others(33): Show |
1 | a0001c0013t0001g0054 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.64-2063_64-2062ins others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1028969 | |||||
chr19:1028980
|
C | G | 13 | a0001c0001t0001g0047a0001c0001t0001g0144a0001c0003t0003g0013others(10): Show | 19 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-2091C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1028980 | ||||||
chr19:1029023
|
TCCCAAAT others(33): Show |
T | 1 | a0001c0018t0008g0193 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.64-2040_64-2001del others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029023 | |||||
chr19:1029031
|
A | C | 12 | a0001c0001t0001g0047a0001c0001t0001g0144a0001c0003t0003g0013others(9): Show | 18 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-2040A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029031 | ||||||
chr19:1029031
|
AATCCCAG others(471): Show |
A | 5 | a0001c0002t0004g0005a0001c0002t0004g0045a0001c0002t0004g0046others(2): Show | 10 | HG01071.hp1 HG01123.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-1982_64-1505del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029031 | |||||
chr19:1029046
|
CAGCTCAG others(152): Show |
C | 1 | a0001c0001t0009g0141 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.64-1902_64-1744del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029046 | |||||
chr19:1029049
|
C | G | 1 | a0001c0001t0011g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-2022C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029049 | ||||||
chr19:1029101
|
T | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(20): Show | 33 | HG01516.hp2 HG01891.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-1970T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029101 | ||||||
chr19:1029129
|
CTCAGGGG others(431): Show |
C | 26 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0005g0004others(23): Show | 34 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.64-1920_64-1483del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029129 | |||||
chr19:1029169
|
CTCAGGGG others(391): Show |
C | 32 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(29): Show | 43 | HG01516.hp2 HG01891.hp2 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.64-1888_64-1491del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029169 | |||||
chr19:1029176
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.64-1895G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029176 | ||||||
chr19:1029275
|
CAGGCAGG others(192): Show |
C | 9 | a0001c0001t0006g0009a0001c0001t0006g0084a0001c0001t0006g0086others(6): Show | 12 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-1743_64-1545del | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029275 | |||||
chr19:1029331
|
A | C | 1 | a0001c0001t0015g0140 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.64-1740A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029331 | ||||||
chr19:1029340
|
TACCCAAA others(73): Show |
T | 11 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 11 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-1707_64-1628del others(80): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029340 | |||||
chr19:1029364
|
T | TAGCTCAG others(33): Show |
1 | a0001c0005t0008g0249 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-1637_64-1598dup others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029364 | |||||
chr19:1029414
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.64-1657G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029414 | ||||||
chr19:1029474
|
T | C | 132 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0047others(129): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.64-1597T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029474 | ||||||
chr19:1029527
|
C | A | 1 | a0001c0001t0027g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64-1544C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029527 | ||||||
chr19:1029567
|
G | C | 9 | a0001c0001t0006g0009a0001c0001t0006g0084a0001c0001t0006g0086others(6): Show | 12 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-1504G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029567 | ||||||
chr19:1029637
|
C | T | 1 | a0001c0001t0009g0244 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.64-1434C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029637 | ||||||
chr19:1029708
|
C | CT | 68 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(65): Show | 90 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(87): Show |
intron_variant | MODIFIER | c.64-1352dupT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 1029708 | |||||
chr19:1029801
|
G | A | 8 | a0001c0001t0005g0034a0001c0001t0005g0165a0001c0001t0005g0251others(5): Show | 9 | HG02145.hp1 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1270G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029801 | ||||||
chr19:1029831
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.64-1240C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029831 | ||||||
chr19:1029989
|
G | A | 1 | a0001c0001t0014g0197 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64-1082G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029989 | ||||||
chr19:1029993
|
C | T | 58 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(55): Show | 79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-1078C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1029993 | ||||||
chr19:1030015
|
C | T | 58 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(55): Show | 79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-1056C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030015 | ||||||
chr19:1030140
|
G | A | 58 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(55): Show | 79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-931G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030140 | ||||||
chr19:1030163
|
A | C | 49 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(46): Show | 67 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-908A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030163 | ||||||
chr19:1030169
|
C | T | 49 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(46): Show | 67 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-902C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030169 | ||||||
chr19:1030170
|
A | G | 58 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(55): Show | 79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-901A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030170 | ||||||
chr19:1030282
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18973.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.64-789C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030282 | ||||||
chr19:1030304
|
C | T | 1 | a0001c0004t0003g0160 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.64-767C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030304 | ||||||
chr19:1030305
|
G | C | 49 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(46): Show | 67 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-766G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030305 | ||||||
chr19:1030321
|
G | T | 81 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(78): Show | 99 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.64-750G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030321 | ||||||
chr19:1030352
|
C | T | 1 | a0001c0001t0011g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-719C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030352 | ||||||
chr19:1030365
|
A | G | 58 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(55): Show | 79 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-706A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030365 | ||||||
chr19:1030432
|
T | C | 193 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(190): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.64-639T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030432 | ||||||
chr19:1030478
|
G | T | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(48): Show | 69 | HG00733.hp1 HG01109.hp1 HG01123.hp2 others(66): Show |
intron_variant | MODIFIER | c.64-593G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030478 | ||||||
chr19:1030482
|
T | C | 2 | a0001c0001t0002g0042a0001c0001t0009g0042 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.64-589T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030482 | ||||||
chr19:1030487
|
C | G | 2 | a0001c0001t0002g0042a0001c0001t0009g0042 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.64-584C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030487 | ||||||
chr19:1030495
|
G | A | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | NA18980.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.64-576G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030495 | ||||||
chr19:1030550
|
G | C | 37 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(34): Show | 50 | HG01109.hp2 HG01516.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.64-521G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030550 | ||||||
chr19:1030571
|
A | G | 1 | a0001c0002t0004g0252 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.64-500A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030571 | ||||||
chr19:1030593
|
T | C | 1 | a0003c0012t0005g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.64-478T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030593 | ||||||
chr19:1030594
|
C | T | 1 | a0003c0012t0005g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.64-477C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030594 | ||||||
chr19:1030612
|
T | C | 1 | a0001c0011t0004g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-459T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030612 | ||||||
chr19:1030634
|
T | G | 1 | a0001c0001t0002g0202 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.64-437T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030634 | ||||||
chr19:1030651
|
C | G | 200 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(197): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.64-420C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030651 | ||||||
chr19:1030760
|
G | C | 1 | a0001c0001t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-311G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030760 | ||||||
chr19:1030767
|
G | A | 22 | a0001c0001t0005g0004a0001c0001t0005g0008a0001c0001t0005g0066others(19): Show | 30 | HG00733.hp1 HG00733.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.64-304G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030767 | ||||||
chr19:1030788
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.64-283G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030788 | ||||||
chr19:1030794
|
C | T | 1 | a0001c0001t0029g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.64-277C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030794 | ||||||
chr19:1030903
|
A | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0087a0001c0001t0006g0090others(2): Show | 8 | HG01109.hp2 HG01884.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-168A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030903 | ||||||
chr19:1030957
|
G | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(259): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.64-114G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030957 | ||||||
chr19:1030997
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0002g0242 | 3 | NA18955.hp2 NA18964.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.64-74C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1030997 | ||||||
chr19:1031051
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-20C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | chr19 | 1031051 | ||||||
chr19:1031213
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(233): Show | 322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.185+21A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031213 | ||||||
chr19:1031249
|
A | C | 11 | a0001c0001t0006g0175a0001c0003t0003g0176a0001c0003t0003g0177others(8): Show | 11 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.185+57A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031249 | ||||||
chr19:1031286
|
G | A | 1 | a0001c0001t0011g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.185+94G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031286 | ||||||
chr19:1031330
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(105): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.185+138G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031330 | ||||||
chr19:1031338
|
T | TCGGGGG | 13 | a0001c0001t0001g0047a0001c0001t0001g0144a0001c0003t0003g0013others(10): Show | 19 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.185+146_185+147ins others(6): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031338 | ||||||
chr19:1031338
|
T | TG | 5 | a0001c0001t0005g0034a0001c0001t0005g0165a0001c0003t0003g0031others(2): Show | 7 | HG01175.hp1 HG02486.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+148dupG | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031338 | |||||
chr19:1031338
|
T | TGG | 4 | a0001c0001t0001g0170a0001c0001t0005g0251a0001c0003t0010g0169others(1): Show | 4 | HG02145.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+147_185+148dup others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031338 | |||||
chr19:1031338
|
T | TGGGGGGG others(1): Show |
32 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0243others(29): Show | 33 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.185+148_185+149ins others(8): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031338 | |||||
chr19:1031339
|
G | GGGGGGGA | 87 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(84): Show | 124 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.185+148_185+149ins others(7): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031339 | |||||
chr19:1031340
|
G | A | 13 | a0001c0001t0001g0047a0001c0001t0001g0144a0001c0003t0003g0013others(10): Show | 19 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.185+148G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031340 | ||||||
chr19:1031340
|
G | GGGGGGA | 114 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(111): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.185+148_185+149ins others(6): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031340 | ||||||
chr19:1031341
|
C | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(282): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.185+149C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031341 | ||||||
chr19:1031439
|
C | T | 108 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(105): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.185+247C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031439 | ||||||
chr19:1031444
|
A | C | 1 | a0001c0001t0002g0159 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.185+252A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031444 | ||||||
chr19:1031444
|
A | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0247 | 2 | HG02071.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.185+252A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031444 | ||||||
chr19:1031479
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(259): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.185+287T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031479 | ||||||
chr19:1031480
|
G | A | 22 | a0001c0001t0005g0004a0001c0001t0005g0008a0001c0001t0005g0066others(19): Show | 30 | HG00733.hp1 HG00733.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.185+288G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031480 | ||||||
chr19:1031490
|
G | A | 2 | a0001c0006t0007g0146a0001c0006t0007g0153 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.185+298G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031490 | ||||||
chr19:1031539
|
G | A | 1 | a0001c0001t0006g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.185+347G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031539 | ||||||
chr19:1031551
|
C | T | 108 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(105): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.185+359C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031551 | ||||||
chr19:1031564
|
C | CA | 30 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0099others(27): Show | 42 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.185+398dupA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | |||||
chr19:1031564
|
C | CAA | 7 | a0001c0001t0005g0066a0001c0001t0005g0067a0001c0001t0005g0082others(4): Show | 7 | HG00733.hp2 HG01978.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+397_185+398dup others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | |||||
chr19:1031564
|
CA | C | 32 | a0001c0001t0001g0047a0001c0001t0001g0121a0001c0001t0001g0122others(29): Show | 38 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.185+398delA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | |||||
chr19:1031564
|
CAAAAAAA | C | 36 | a0001c0001t0002g0196a0001c0001t0002g0204a0001c0001t0005g0034others(33): Show | 60 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.185+392_185+398del others(7): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | |||||
chr19:1031564
|
CAAAAAAA others(1): Show |
C | 79 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(76): Show | 97 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.185+391_185+398del others(8): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1031564 | |||||
chr19:1031601
|
C | T | 1 | a0001c0007t0002g0152 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.185+409C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031601 | ||||||
chr19:1031622
|
T | C | 1 | a0001c0004t0003g0148 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.185+430T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031622 | ||||||
chr19:1031638
|
G | A | 1 | a0001c0001t0005g0063 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.185+446G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031638 | ||||||
chr19:1031659
|
A | G | 154 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0047others(151): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.185+467A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031659 | ||||||
chr19:1031670
|
A | G | 1 | a0001c0001t0011g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.185+478A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031670 | ||||||
chr19:1031683
|
C | T | 1 | a0001c0005t0007g0030 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.185+491C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031683 | ||||||
chr19:1031813
|
G | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(258): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.186-579G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1031813 | ||||||
chr19:1032004
|
C | T | 3 | a0001c0008t0019g0173a0001c0008t0020g0172a0001c0008t0020g0174 | 3 | HG02055.hp2 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.186-388C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032004 | ||||||
chr19:1032010
|
A | C | 1 | a0003c0012t0005g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.186-382A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032010 | ||||||
chr19:1032030
|
C | G | 1 | a0001c0005t0007g0030 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.186-362C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032030 | ||||||
chr19:1032101
|
A | G | 1 | a0001c0001t0011g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.186-291A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032101 | ||||||
chr19:1032121
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0002g0091a0001c0001t0002g0199others(2): Show | 5 | NA18954.hp2 NA18967.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-271G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032121 | ||||||
chr19:1032155
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.186-237A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032155 | ||||||
chr19:1032159
|
C | T | 1 | a0001c0001t0002g0225 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.186-233C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032159 | ||||||
chr19:1032229
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(80): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.186-163C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032229 | ||||||
chr19:1032234
|
C | CA | 29 | a0001c0001t0001g0098a0001c0001t0001g0101a0001c0001t0001g0102others(26): Show | 30 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.186-141dupA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1032234 | |||||
chr19:1032234
|
C | CAA | 24 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0005g0004others(21): Show | 32 | HG00733.hp1 HG00733.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.186-142_186-141dup others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1032234 | |||||
chr19:1032234
|
CA | C | 12 | a0001c0001t0001g0062a0001c0001t0001g0123a0001c0001t0002g0203others(9): Show | 15 | HG01109.hp2 HG01168.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.186-141delA | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1032234 | |||||
chr19:1032241
|
A | C | 1 | a0001c0001t0011g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.186-151A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032241 | ||||||
chr19:1032251
|
A | AG | 22 | a0001c0004t0003g0002a0001c0004t0003g0017a0001c0004t0003g0147others(19): Show | 42 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.186-140dupG | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 1032251 | |||||
chr19:1032251
|
A | G | 1 | a0001c0017t0021g0151 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.186-141A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032251 | ||||||
chr19:1032324
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.186-68C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032324 | ||||||
chr19:1032335
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186-57G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032335 | ||||||
chr19:1032336
|
G | T | 1 | a0001c0001t0002g0203 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.186-56G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032336 | ||||||
chr19:1032344
|
C | A | 1 | a0003c0012t0005g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.186-48C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032344 | ||||||
chr19:1032370
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(226): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.186-22C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032370 | ||||||
chr19:1032371
|
G | A | 1 | a0001c0001t0011g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.186-21G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 2/6 | chr19 | 1032371 | ||||||
chr19:1032475
|
G | T | 11 | a0001c0001t0005g0008a0001c0001t0005g0067a0001c0001t0005g0074others(8): Show | 13 | HG00733.hp1 HG00733.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.252+17G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 3/6 | chr19 | 1032475 | ||||||
chr19:1032703
|
C | T | 85 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(82): Show | 103 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
splice_region_variant&intron_variant | LOW | c.390+7C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032703 | ||||||
chr19:1032741
|
G | C | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0034g0145others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+45G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032741 | ||||||
chr19:1032757
|
C | T | 91 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(88): Show | 109 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.390+61C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032757 | ||||||
chr19:1032779
|
TTC | T | 25 | a0001c0004t0003g0002a0001c0004t0003g0016a0001c0004t0003g0017others(22): Show | 47 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.390+85_390+86delCT | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1032779 | |||||
chr19:1032863
|
C | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0118a0001c0001t0001g0245 | 3 | NA18947.hp1 NA18956.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.390+167C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032863 | ||||||
chr19:1032872
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(274): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.390+176A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032872 | ||||||
chr19:1032875
|
T | G | 1 | a0003c0012t0005g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.390+179T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032875 | ||||||
chr19:1032882
|
G | A | 1 | a0001c0001t0006g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.390+186G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032882 | ||||||
chr19:1032941
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG00597.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.390+245G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1032941 | ||||||
chr19:1033191
|
G | A | 12 | a0001c0001t0001g0047a0001c0003t0003g0013a0001c0003t0003g0048others(9): Show | 18 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.390+495G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033191 | ||||||
chr19:1033244
|
G | A | 1 | a0001c0001t0030g0253 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.390+548G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033244 | ||||||
chr19:1033355
|
T | C | 1 | a0001c0002t0004g0206 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.390+659T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033355 | ||||||
chr19:1033361
|
A | T | 106 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(103): Show | 128 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.390+665A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033361 | ||||||
chr19:1033379
|
G | T | 2 | a0001c0001t0011g0134a0001c0001t0011g0191 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.390+683G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033379 | ||||||
chr19:1033411
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(91): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.390+715G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033411 | ||||||
chr19:1033463
|
T | C | 2 | a0001c0001t0002g0207a0001c0002t0004g0223 | 2 | HG03831.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.390+767T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033463 | ||||||
chr19:1033560
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(100): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.390+864G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033560 | ||||||
chr19:1033586
|
T | C | 1 | a0001c0003t0003g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.390+890T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033586 | ||||||
chr19:1033625
|
A | T | 1 | a0001c0003t0003g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.390+929A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033625 | ||||||
chr19:1033638
|
G | A | 1 | a0001c0002t0004g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.390+942G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033638 | ||||||
chr19:1033655
|
A | ACG | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+959_390+960ins others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033655 | ||||||
chr19:1033655
|
AGTGTCTG others(29): Show |
A | 101 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(98): Show | 126 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.390+1011_390+1046d others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033655 | |||||
chr19:1033655
|
AGTGTCTG others(379): Show |
A | 7 | a0001c0001t0006g0009a0001c0001t0006g0084a0001c0001t0006g0087others(4): Show | 9 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1029_390+1414d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033655 | |||||
chr19:1033655
|
AGTGTCTG others(1223): Show |
A | 20 | a0001c0003t0003g0013a0001c0003t0031g0013a0001c0004t0003g0002others(17): Show | 41 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+993_391-1212de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033655 | |||||
chr19:1033655
|
AGTGTCTG others(1293): Show |
A | 1 | a0001c0007t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.390+993_391-1142de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033655 | |||||
chr19:1033657
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+961T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033657 | ||||||
chr19:1033671
|
CGGGAGCG others(1433): Show |
C | 1 | a0001c0001t0002g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.390+1011_391-984de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033671 | |||||
chr19:1033672
|
G | C | 9 | a0001c0001t0001g0047a0001c0005t0008g0011a0001c0005t0008g0012others(6): Show | 14 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.390+976G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033672 | ||||||
chr19:1033674
|
G | C | 3 | a0001c0001t0006g0019a0001c0001t0022g0061a0001c0001t0025g0056 | 5 | HG02451.hp2 HG02895.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+978G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033674 | ||||||
chr19:1033678
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.390+982G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033678 | ||||||
chr19:1033679
|
TGGGTGGG others(1224): Show |
T | 1 | a0001c0003t0003g0048 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.390+986_391-1218de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033679 | |||||
chr19:1033686
|
GAC | G | 4 | a0001c0004t0003g0147a0001c0004t0003g0149a0001c0004t0003g0150others(1): Show | 4 | HG02293.hp1 HG03688.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+993_390+994del others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033686 | |||||
chr19:1033688
|
CACGGTGT others(203): Show |
C | 3 | a0001c0001t0006g0052a0001c0001t0022g0061a0001c0001t0025g0056 | 3 | HG01943.hp1 HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.390+1084_390+1293d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033688 | |||||
chr19:1033691
|
GGTGTCTG others(449): Show |
G | 1 | a0001c0001t0001g0047 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.390+996_390+1451de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033691 | ||||||
chr19:1033692
|
G | T | 9 | a0001c0001t0001g0219a0001c0001t0002g0208a0001c0001t0002g0229others(6): Show | 9 | HG01099.hp2 HG01975.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+996G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033692 | ||||||
chr19:1033693
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+997T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033693 | ||||||
chr19:1033707
|
C | G | 13 | a0001c0001t0001g0219a0001c0001t0002g0208a0001c0001t0002g0229others(10): Show | 16 | HG01099.hp2 HG01123.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.390+1011C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033707 | ||||||
chr19:1033707
|
CGGGAGCG others(99): Show |
C | 4 | a0001c0001t0006g0009a0001c0001t0006g0086a0001c0001t0006g0090others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1029_390+1134d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033707 | |||||
chr19:1033710
|
GAGCGTGG others(1151): Show |
G | 1 | a0001c0004t0003g0149 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.390+1047_391-1230d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033710 | |||||
chr19:1033716
|
GGGTGGGA others(1220): Show |
G | 1 | a0001c0004t0003g0147 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.390+1023_391-1185d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033716 | |||||
chr19:1033722
|
GAC | G | 11 | a0001c0001t0001g0219a0001c0001t0002g0208a0001c0001t0002g0229others(8): Show | 11 | HG01099.hp2 HG01123.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.390+1029_390+1030d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033722 | |||||
chr19:1033724
|
CACGGTGT others(237): Show |
C | 1 | a0001c0002t0013g0023 | 2 | HG01943.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.390+1047_390+1290d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033724 | |||||
chr19:1033728
|
G | T | 70 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(67): Show | 88 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.390+1032G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033728 | ||||||
chr19:1033729
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1033T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033729 | ||||||
chr19:1033743
|
G | C | 23 | a0001c0001t0001g0219a0001c0001t0002g0208a0001c0001t0002g0229others(20): Show | 25 | HG01099.hp2 HG01106.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.390+1047G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033743 | ||||||
chr19:1033743
|
GGGGAGCG others(133): Show |
G | 65 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(62): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.390+1187_390+1326d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033743 | |||||
chr19:1033743
|
GGGGAGCG others(377): Show |
G | 8 | a0001c0005t0008g0011a0001c0005t0008g0012a0001c0005t0008g0021others(5): Show | 13 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.390+1065_390+1448d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033743 | |||||
chr19:1033743
|
GGGGAGCG others(447): Show |
G | 1 | a0001c0001t0002g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.390+1065_390+1518d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033743 | |||||
chr19:1033746
|
GAGCGTGG others(483): Show |
G | 2 | a0001c0001t0005g0008a0001c0002t0004g0077 | 2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.390+1065_390+1554d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033746 | |||||
chr19:1033758
|
G | GAC | 13 | a0001c0001t0009g0220a0001c0002t0004g0250a0001c0002t0012g0240others(10): Show | 13 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.390+1063_390+1064d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033758 | |||||
chr19:1033758
|
G | GACACCGT others(65): Show |
6 | a0001c0001t0001g0219a0001c0001t0002g0208a0001c0001t0002g0229others(3): Show | 6 | HG01099.hp2 HG01975.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1064_390+1065i others(74): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033758 | |||||
chr19:1033758
|
GACGGTGT others(555): Show |
G | 1 | a0001c0011t0004g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.390+1117_390+1678d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033758 | |||||
chr19:1033761
|
G | C | 3 | a0001c0001t0009g0220a0001c0002t0004g0250a0001c0002t0012g0240 | 3 | HG03017.hp2 HG03516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1065G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033761 | ||||||
chr19:1033763
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1067T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033763 | ||||||
chr19:1033774
|
GACCGGGA others(1291): Show |
G | 2 | a0001c0001t0001g0057a0001c0001t0005g0063 | 2 | HG02965.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.390+1135_391-1002d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033774 | |||||
chr19:1033777
|
C | G | 3 | a0001c0001t0009g0220a0001c0002t0004g0250a0001c0002t0012g0240 | 3 | HG03017.hp2 HG03516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1081C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033777 | ||||||
chr19:1033780
|
G | C | 3 | a0001c0001t0001g0227a0001c0001t0006g0019a0001c0001t0006g0092 | 5 | HG03579.hp2 HG03834.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+1084G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033780 | ||||||
chr19:1033780
|
G | GAGCGTGG others(63): Show |
6 | a0001c0001t0001g0219a0001c0001t0002g0208a0001c0001t0002g0229others(3): Show | 6 | HG01099.hp2 HG01975.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1117_390+1186d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033780 | |||||
chr19:1033780
|
GAGCGTGG others(203): Show |
G | 1 | a0001c0001t0001g0264 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.390+1154_390+1363d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033780 | |||||
chr19:1033780
|
GAGCGTGG others(765): Show |
G | 1 | a0001c0003t0003g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.390+1187_391-1476d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033780 | |||||
chr19:1033795
|
ACG | A | 3 | a0001c0001t0009g0220a0001c0002t0004g0250a0001c0002t0012g0240 | 3 | HG03017.hp2 HG03516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1100_390+1101d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033795 | ||||||
chr19:1033797
|
G | C | 99 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0050others(96): Show | 124 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.390+1101G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033797 | ||||||
chr19:1033799
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1103T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033799 | ||||||
chr19:1033813
|
G | C | 15 | a0001c0001t0006g0019a0001c0001t0009g0220a0001c0002t0004g0250others(12): Show | 17 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.390+1117G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033813 | ||||||
chr19:1033813
|
GGGGAGCG others(449): Show |
G | 9 | a0001c0001t0001g0050a0001c0001t0005g0008a0001c0001t0005g0067others(6): Show | 10 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.390+1154_390+1609d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033813 | |||||
chr19:1033814
|
G | A | 3 | a0001c0001t0009g0220a0001c0002t0004g0250a0001c0002t0012g0240 | 3 | HG03017.hp2 HG03516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1118G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033814 | ||||||
chr19:1033828
|
G | GAC | 13 | a0001c0001t0009g0220a0001c0002t0004g0250a0001c0002t0012g0240others(10): Show | 13 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.390+1133_390+1134d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033828 | |||||
chr19:1033828
|
GACGGTGT others(1117): Show |
G | 1 | a0001c0001t0006g0019 | 3 | HG03579.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.390+1154_391-1157d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033828 | |||||
chr19:1033831
|
G | A | 90 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0187others(87): Show | 114 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.390+1135G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033831 | ||||||
chr19:1033833
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1137T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033833 | ||||||
chr19:1033848
|
G | A | 68 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0241others(65): Show | 86 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.390+1152G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033848 | ||||||
chr19:1033850
|
C | G | 108 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0187others(105): Show | 132 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.390+1154C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033850 | ||||||
chr19:1033864
|
CACGGTGT others(27): Show |
C | 86 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0187others(83): Show | 110 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.390+1205_390+1238d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033864 | |||||
chr19:1033864
|
CACGGTGT others(519): Show |
C | 2 | a0001c0002t0004g0075a0001c0002t0004g0076 | 2 | HG00733.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.390+1205_391-1704d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033864 | |||||
chr19:1033864
|
CACGGTGT others(1291): Show |
C | 1 | a0001c0004t0003g0150 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.390+1187_391-950de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033864 | |||||
chr19:1033868
|
G | T | 4 | a0001c0001t0006g0009a0001c0001t0006g0086a0001c0001t0006g0090others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1172G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033868 | ||||||
chr19:1033869
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1173T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033869 | ||||||
chr19:1033883
|
C | G | 24 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0099others(21): Show | 25 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.390+1187C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033883 | ||||||
chr19:1033886
|
G | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0099a0001c0001t0001g0101others(10): Show | 14 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.390+1190G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033886 | ||||||
chr19:1033886
|
G | T | 1 | a0001c0001t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+1190G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033886 | ||||||
chr19:1033887
|
AGCGTGGG others(236): Show |
A | 1 | a0001c0001t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+1192_390+1434d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033887 | ||||||
chr19:1033898
|
G | GAC | 9 | a0001c0003t0003g0176a0001c0003t0003g0178a0001c0003t0003g0179others(6): Show | 9 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1203_390+1204d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033898 | |||||
chr19:1033898
|
G | GACACGGC others(103): Show |
1 | a0001c0003t0003g0177 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.390+1204_390+1205i others(112): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033898 | |||||
chr19:1033898
|
GACGGTGT others(169): Show |
G | 3 | a0001c0001t0001g0053a0001c0001t0001g0144a0001c0001t0001g0194 | 3 | HG00099.hp2 HG01516.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.390+1239_390+1414d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033898 | |||||
chr19:1033903
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1207T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033903 | ||||||
chr19:1033908
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390+1212G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033908 | ||||||
chr19:1033917
|
C | G | 5 | a0001c0001t0011g0134a0001c0001t0011g0191a0001c0001t0022g0061others(2): Show | 5 | HG02451.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+1221C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033917 | ||||||
chr19:1033920
|
G | C | 25 | a0001c0001t0001g0170a0001c0001t0001g0219a0001c0001t0001g0227others(22): Show | 26 | HG01099.hp2 HG01243.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.390+1224G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033920 | ||||||
chr19:1033934
|
CACGGTGT others(97): Show |
C | 1 | a0001c0001t0001g0109 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.390+1257_390+1360d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033934 | |||||
chr19:1033937
|
GGTGTCTG others(203): Show |
G | 2 | a0001c0001t0001g0117a0001c0001t0002g0161 | 2 | HG02080.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.390+1242_390+1451d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033937 | ||||||
chr19:1033938
|
GTGTCTGG others(203): Show |
G | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0246others(1): Show | 4 | HG00639.hp1 HG00642.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1257_390+1466d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033938 | |||||
chr19:1033939
|
T | C | 12 | a0001c0001t0001g0108a0001c0003t0003g0176a0001c0003t0003g0177others(9): Show | 12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.390+1243T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033939 | ||||||
chr19:1033953
|
G | C | 5 | a0001c0001t0001g0260a0001c0001t0022g0061a0001c0001t0025g0056others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+1257G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033953 | ||||||
chr19:1033953
|
GGGGAGCG others(167): Show |
G | 4 | a0001c0001t0006g0009a0001c0001t0006g0086a0001c0001t0006g0090others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1275_390+1448d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033953 | |||||
chr19:1033956
|
GAGCGTGG others(273): Show |
G | 3 | a0001c0008t0019g0173a0001c0008t0020g0172a0001c0008t0020g0174 | 3 | HG02055.hp2 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.390+1275_390+1554d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033956 | |||||
chr19:1033968
|
G | GAC | 9 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(6): Show | 9 | HG01106.hp2 HG01192.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1273_390+1274d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033968 | |||||
chr19:1033968
|
G | GACACGGC others(31): Show |
1 | a0001c0003t0003g0184 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.390+1274_390+1275i others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1033968 | |||||
chr19:1033970
|
CGGTGTCT others(1009): Show |
C | 2 | a0001c0001t0001g0108a0001c0005t0007g0120 | 2 | HG01168.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.390+1275_391-1144d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033970 | ||||||
chr19:1033973
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1277T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033973 | ||||||
chr19:1033982
|
T | A | 1 | a0003c0012t0005g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.390+1286T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033982 | ||||||
chr19:1033987
|
C | G | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1291C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033987 | ||||||
chr19:1033990
|
C | G | 30 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0260others(27): Show | 36 | HG01106.hp2 HG01192.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.390+1294C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033990 | ||||||
chr19:1033992
|
G | A | 1 | a0001c0001t0030g0253 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.390+1296G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1033992 | ||||||
chr19:1034008
|
G | T | 2 | a0001c0001t0001g0260a0001c0005t0008g0259 | 2 | HG04199.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.390+1312G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034008 | ||||||
chr19:1034009
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1313T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034009 | ||||||
chr19:1034023
|
G | C | 7 | a0001c0001t0001g0260a0001c0001t0009g0220a0001c0001t0022g0061others(4): Show | 7 | HG02451.hp2 HG02895.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+1327G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034023 | ||||||
chr19:1034026
|
G | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(50): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.390+1330G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034026 | ||||||
chr19:1034038
|
G | GAC | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1343_390+1344d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034038 | |||||
chr19:1034038
|
GACGGTGT others(275): Show |
G | 15 | a0001c0001t0002g0007a0001c0001t0009g0007a0001c0001t0009g0141others(12): Show | 19 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.390+1451_391-1702d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034038 | |||||
chr19:1034040
|
C | T | 1 | a0001c0002t0012g0240 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.390+1344C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034040 | ||||||
chr19:1034043
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1347T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034043 | ||||||
chr19:1034057
|
C | G | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1361C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034057 | ||||||
chr19:1034060
|
G | C | 77 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0187others(74): Show | 97 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.390+1364G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034060 | ||||||
chr19:1034064
|
G | A | 10 | a0001c0001t0001g0170a0001c0001t0005g0034a0001c0001t0005g0165others(7): Show | 11 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.390+1368G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034064 | ||||||
chr19:1034074
|
CACGGTGT others(27): Show |
C | 1 | a0001c0001t0011g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.390+1415_390+1448d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034074 | |||||
chr19:1034077
|
G | A | 9 | a0001c0001t0001g0170a0001c0001t0005g0034a0001c0001t0005g0165others(6): Show | 10 | HG02486.hp1 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.390+1381G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034077 | ||||||
chr19:1034079
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1383T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034079 | ||||||
chr19:1034093
|
C | G | 16 | a0001c0001t0001g0260a0001c0001t0009g0220a0001c0002t0004g0250others(13): Show | 16 | HG01106.hp2 HG01192.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.390+1397C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034093 | ||||||
chr19:1034093
|
CGGGAGCG others(345): Show |
C | 4 | a0001c0001t0014g0051a0001c0002t0004g0039a0001c0002t0004g0040others(1): Show | 6 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1434_391-1649d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034093 | |||||
chr19:1034095
|
G | T | 2 | a0001c0001t0001g0260a0001c0005t0008g0259 | 2 | HG04199.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.390+1399G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034095 | ||||||
chr19:1034096
|
G | A | 2 | a0001c0001t0001g0260a0001c0005t0008g0259 | 2 | HG04199.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.390+1400G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034096 | ||||||
chr19:1034096
|
GAGCGTGG others(133): Show |
G | 2 | a0001c0001t0022g0061a0001c0001t0025g0056 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.390+1415_390+1554d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034096 | |||||
chr19:1034108
|
G | GAC | 10 | a0001c0001t0011g0134a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1413_390+1414d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034108 | |||||
chr19:1034108
|
GACGGTGT others(205): Show |
G | 15 | a0001c0001t0001g0188a0001c0001t0002g0038a0001c0001t0002g0049others(12): Show | 16 | HG00597.hp2 HG02056.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.390+1451_390+1662d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034108 | |||||
chr19:1034110
|
CGGTGTCT others(61): Show |
C | 3 | a0001c0001t0001g0260a0001c0003t0003g0176a0001c0003t0003g0181 | 3 | HG02647.hp2 HG03486.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.390+1415_390+1482d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034110 | ||||||
chr19:1034113
|
T | C | 8 | a0001c0003t0003g0177a0001c0003t0003g0178a0001c0003t0003g0179others(5): Show | 8 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+1417T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034113 | ||||||
chr19:1034127
|
C | G | 9 | a0001c0001t0011g0134a0001c0003t0003g0177a0001c0003t0003g0178others(6): Show | 9 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1431C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034127 | ||||||
chr19:1034128
|
G | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0086a0001c0001t0006g0090 | 3 | HG01109.hp2 HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.390+1432G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034128 | ||||||
chr19:1034129
|
G | T | 4 | a0001c0001t0006g0009a0001c0001t0006g0086a0001c0001t0006g0090others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1433G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034129 | ||||||
chr19:1034130
|
G | A | 4 | a0001c0001t0006g0009a0001c0001t0006g0086a0001c0001t0006g0090others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1434G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034130 | ||||||
chr19:1034130
|
G | C | 54 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0187others(51): Show | 71 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.390+1434G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034130 | ||||||
chr19:1034134
|
G | A | 1 | a0001c0003t0010g0169 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.390+1438G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034134 | ||||||
chr19:1034144
|
CACATTGT others(27): Show |
C | 2 | a0001c0003t0003g0180a0001c0003t0003g0182 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.390+1451_390+1484d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034144 | |||||
chr19:1034147
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(174): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.390+1451A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034147 | ||||||
chr19:1034148
|
T | G | 70 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0055others(67): Show | 87 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.390+1452T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034148 | ||||||
chr19:1034149
|
T | C | 6 | a0001c0003t0003g0177a0001c0003t0003g0178a0001c0003t0003g0179others(3): Show | 6 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+1453T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034149 | ||||||
chr19:1034163
|
C | G | 62 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0047others(59): Show | 79 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.390+1467C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034163 | ||||||
chr19:1034178
|
G | GAC | 8 | a0001c0001t0011g0134a0001c0003t0003g0177a0001c0003t0003g0178others(5): Show | 8 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+1483_390+1484d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034178 | |||||
chr19:1034183
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1487T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034183 | ||||||
chr19:1034197
|
C | G | 11 | a0001c0001t0011g0134a0001c0003t0003g0176a0001c0003t0003g0177others(8): Show | 11 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.390+1501C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034197 | ||||||
chr19:1034200
|
G | C | 52 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0187others(49): Show | 69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.390+1504G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034200 | ||||||
chr19:1034200
|
GAGCGTGG others(29): Show |
G | 2 | a0001c0001t0009g0220a0001c0003t0010g0169 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.390+1537_390+1572d others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034200 | |||||
chr19:1034204
|
G | A | 3 | a0001c0001t0006g0009a0001c0001t0006g0086a0001c0001t0006g0090 | 3 | HG01109.hp2 HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.390+1508G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034204 | ||||||
chr19:1034204
|
GTGGGTGG others(625): Show |
G | 1 | a0001c0002t0004g0046 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.390+1661_391-1142d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034204 | |||||
chr19:1034212
|
GAC | G | 3 | a0001c0001t0001g0260a0001c0001t0011g0134a0001c0005t0008g0259 | 3 | HG04199.hp1 NA18971.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.390+1519_390+1520d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034212 | |||||
chr19:1034217
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.390+1521G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034217 | ||||||
chr19:1034219
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1523T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034219 | ||||||
chr19:1034233
|
G | C | 3 | a0001c0001t0001g0260a0001c0001t0011g0134a0001c0005t0008g0259 | 3 | HG04199.hp1 NA18971.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.390+1537G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034233 | ||||||
chr19:1034234
|
G | C | 7 | a0001c0001t0006g0009a0001c0001t0006g0084a0001c0001t0006g0087others(4): Show | 9 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1538G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034234 | ||||||
chr19:1034235
|
T | G | 74 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0047others(71): Show | 91 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.390+1539T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034235 | ||||||
chr19:1034236
|
A | AGCGTGGG others(26): Show |
2 | a0001c0002t0004g0250a0001c0002t0012g0240 | 2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.390+1540_390+1541i others(35): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034236 | ||||||
chr19:1034236
|
A | C | 1 | a0001c0001t0011g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.390+1540A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034236 | ||||||
chr19:1034236
|
A | G | 71 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0047others(68): Show | 88 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.390+1540A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034236 | ||||||
chr19:1034240
|
G | A | 2 | a0001c0001t0002g0208a0001c0001t0002g0229 | 2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.390+1544G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034240 | ||||||
chr19:1034248
|
GAC | G | 53 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0187others(50): Show | 70 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.390+1555_390+1556d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034248 | |||||
chr19:1034253
|
G | C | 2 | a0001c0001t0005g0008a0001c0002t0004g0077 | 2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.390+1557G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034253 | ||||||
chr19:1034254
|
G | T | 4 | a0001c0001t0009g0220a0001c0002t0004g0250a0001c0002t0012g0240others(1): Show | 4 | HG02145.hp1 HG03017.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1558G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034254 | ||||||
chr19:1034255
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1559T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034255 | ||||||
chr19:1034266
|
GACCGGGA others(799): Show |
G | 1 | a0001c0001t0002g0110 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.390+1591_391-1038d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034266 | |||||
chr19:1034269
|
C | CGGGAGCG others(27): Show |
1 | a0001c0007t0001g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.390+1606_390+1607i others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034269 | |||||
chr19:1034269
|
C | G | 19 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0005g0008others(16): Show | 19 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.390+1573C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034269 | ||||||
chr19:1034269
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.390+1573C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034269 | ||||||
chr19:1034272
|
G | C | 1 | a0001c0001t0011g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.390+1576G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034272 | ||||||
chr19:1034275
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0144a0001c0001t0001g0194 | 3 | HG00099.hp2 HG01516.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.390+1579C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034275 | ||||||
chr19:1034276
|
G | A | 1 | a0001c0003t0010g0169 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.390+1580G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034276 | ||||||
chr19:1034276
|
GTGGGTGG others(553): Show |
G | 1 | a0001c0001t0002g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.390+1591_391-1284d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034276 | |||||
chr19:1034284
|
G | GAC | 65 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0047others(62): Show | 82 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.390+1589_390+1590d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034284 | |||||
chr19:1034284
|
GACGGTGT others(29): Show |
G | 2 | a0001c0001t0001g0144a0001c0001t0001g0264 | 2 | HG00099.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.390+1661_390+1696d others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034284 | |||||
chr19:1034284
|
GACGGTGT others(801): Show |
G | 2 | a0001c0001t0001g0020a0001c0001t0005g0256 | 4 | HG02258.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1607_391-1020d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034284 | |||||
chr19:1034286
|
CGGTGTCT others(693): Show |
C | 1 | a0001c0001t0011g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.390+1591_391-1144d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034286 | ||||||
chr19:1034287
|
G | A | 10 | a0001c0001t0001g0050a0001c0001t0005g0008a0001c0001t0005g0067others(7): Show | 12 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.390+1591G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034287 | ||||||
chr19:1034289
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1593T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034289 | ||||||
chr19:1034300
|
GACCGGGA others(765): Show |
G | 16 | a0001c0001t0001g0119a0001c0001t0002g0103a0001c0001t0002g0115others(13): Show | 23 | HG00438.hp2 HG00609.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.390+1643_391-1020d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034300 | |||||
chr19:1034303
|
C | G | 18 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0005g0257others(15): Show | 18 | HG01106.hp2 HG01109.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.390+1607C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034303 | ||||||
chr19:1034303
|
CGGGAGCG others(871): Show |
C | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.390+1678_391-879de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034303 | |||||
chr19:1034304
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0009g0216 | 2 | HG02280.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.390+1608G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034304 | ||||||
chr19:1034304
|
G | GGGAGCGT others(97): Show |
2 | a0001c0001t0001g0219a0001c0002t0004g0224 | 2 | HG01099.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.390+1624_390+1625i others(106): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034304 | |||||
chr19:1034306
|
G | C | 4 | a0001c0001t0011g0134a0001c0008t0019g0173a0001c0008t0020g0172others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1610G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034306 | ||||||
chr19:1034310
|
G | A | 7 | a0001c0001t0006g0009a0001c0001t0006g0084a0001c0001t0006g0087others(4): Show | 9 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1614G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034310 | ||||||
chr19:1034318
|
GAC | G | 55 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0187others(52): Show | 72 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.390+1625_390+1626d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034318 | |||||
chr19:1034322
|
C | T | 1 | a0001c0001t0018g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.390+1626C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034322 | ||||||
chr19:1034325
|
T | C | 11 | a0001c0001t0005g0257a0001c0003t0003g0176a0001c0003t0003g0177others(8): Show | 11 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.390+1629T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034325 | ||||||
chr19:1034339
|
C | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(98): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.390+1643C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034339 | ||||||
chr19:1034341
|
G | T | 4 | a0001c0001t0009g0220a0001c0002t0004g0250a0001c0002t0012g0240others(1): Show | 4 | HG02145.hp1 HG03017.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1645G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034341 | ||||||
chr19:1034342
|
G | A | 4 | a0001c0001t0009g0220a0001c0002t0004g0250a0001c0002t0012g0240others(1): Show | 4 | HG02145.hp1 HG03017.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1646G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034342 | ||||||
chr19:1034342
|
G | C | 31 | a0001c0001t0001g0188a0001c0001t0002g0007a0001c0001t0002g0038others(28): Show | 36 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.390+1646G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034342 | ||||||
chr19:1034342
|
GAGCGTGG others(273): Show |
G | 1 | a0001c0001t0001g0043 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.390+1679_391-1476d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034342 | |||||
chr19:1034354
|
GAC | G | 15 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0194others(12): Show | 17 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.390+1661_390+1662d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034354 | |||||
chr19:1034356
|
CACGGTGT others(799): Show |
C | 1 | a0001c0001t0005g0257 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.390+1679_391-950de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034356 | |||||
chr19:1034359
|
G | CGTGTCTG others(99): Show |
1 | a0001c0002t0004g0236 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.390+1662_390+1663i others(108): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034359 | ||||||
chr19:1034360
|
G | T | 52 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0187others(49): Show | 69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.390+1664G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034360 | ||||||
chr19:1034361
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1665T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034361 | ||||||
chr19:1034375
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(121): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.390+1679C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034375 | ||||||
chr19:1034378
|
G | C | 1 | a0001c0001t0011g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.390+1682G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034378 | ||||||
chr19:1034390
|
G | GAC | 24 | a0001c0001t0001g0014a0001c0001t0001g0227a0001c0001t0002g0208others(21): Show | 26 | HG01106.hp2 HG01109.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.390+1695_390+1696d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034390 | |||||
chr19:1034390
|
GACGGTGT others(695): Show |
G | 1 | a0001c0001t0015g0140 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.390+1713_391-1020d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034390 | |||||
chr19:1034390
|
GACGGTGT others(801): Show |
G | 49 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(46): Show | 76 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.391-1686_391-879de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034390 | |||||
chr19:1034392
|
C | T | 2 | a0001c0002t0012g0221a0001c0002t0012g0238 | 2 | HG02300.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.390+1696C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034392 | ||||||
chr19:1034392
|
CGGTGTCT others(131): Show |
C | 10 | a0001c0001t0001g0053a0001c0001t0001g0194a0001c0001t0001g0261others(7): Show | 10 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1697_391-1600d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034392 | ||||||
chr19:1034392
|
CGGTGTCT others(587): Show |
C | 1 | a0001c0001t0001g0047 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.390+1697_391-1144d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034392 | ||||||
chr19:1034392
|
CGGTGTCT others(657): Show |
C | 1 | a0001c0001t0001g0024 | 2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.390+1697_391-1074d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034392 | ||||||
chr19:1034395
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+1699T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034395 | ||||||
chr19:1034406
|
GACCGGGA others(659): Show |
G | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.391-1667_391-1002d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034406 | |||||
chr19:1034409
|
C | G | 44 | a0001c0001t0001g0014a0001c0001t0001g0102a0001c0001t0001g0127others(41): Show | 50 | HG01106.hp2 HG01109.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.390+1713C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034409 | ||||||
chr19:1034412
|
G | C | 37 | a0001c0001t0001g0050a0001c0001t0001g0188a0001c0001t0001g0219others(34): Show | 42 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.390+1716G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034412 | ||||||
chr19:1034426
|
CACGGTGT others(167): Show |
C | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.391-1685_391-1512d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034426 | |||||
chr19:1034431
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1699T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034431 | ||||||
chr19:1034442
|
GACGGGGA others(623): Show |
G | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.391-1685_391-1056d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034442 | |||||
chr19:1034443
|
ACGGGGAG others(28): Show |
A | 1 | a0003c0012t0005g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.391-1683_391-1649d others(37): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034443 | |||||
chr19:1034445
|
G | C | 5 | a0001c0001t0001g0144a0001c0001t0011g0134a0001c0003t0003g0176others(2): Show | 5 | HG00099.hp2 HG01192.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-1685G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034445 | ||||||
chr19:1034445
|
GGGGAGCG others(27): Show |
G | 48 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0241others(45): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.391-1682_391-1649d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034445 | |||||
chr19:1034445
|
GGGGAGCG others(167): Show |
G | 1 | a0001c0001t0001g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.391-1682_391-1509d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034445 | |||||
chr19:1034445
|
GGGGAGCG others(483): Show |
G | 4 | a0001c0001t0006g0009a0001c0001t0006g0086a0001c0001t0006g0090others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-1667_391-1178d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034445 | |||||
chr19:1034447
|
G | T | 2 | a0001c0001t0002g0203a0001c0014t0005g0072 | 2 | NA18956.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.391-1683G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034447 | ||||||
chr19:1034448
|
G | A | 2 | a0001c0001t0002g0203a0001c0014t0005g0072 | 2 | NA18956.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.391-1682G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034448 | ||||||
chr19:1034448
|
GAGCGTGG others(97): Show |
G | 1 | a0001c0001t0001g0264 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.391-1667_391-1564d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034448 | |||||
chr19:1034448
|
GAGCGTGG others(167): Show |
G | 1 | a0001c0003t0010g0169 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.391-1667_391-1494d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034448 | |||||
chr19:1034448
|
GAGCGTGG others(413): Show |
G | 3 | a0001c0001t0005g0034a0001c0001t0009g0220a0001c0003t0010g0071 | 3 | HG02572.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.391-1667_391-1248d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034448 | |||||
chr19:1034452
|
GTGGGTGG others(377): Show |
G | 5 | a0001c0001t0006g0009a0001c0001t0006g0084a0001c0001t0006g0087others(2): Show | 7 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.391-1667_391-1284d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034452 | |||||
chr19:1034460
|
G | GAC | 23 | a0001c0001t0001g0260a0001c0001t0002g0203a0001c0001t0002g0208others(20): Show | 23 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.391-1669_391-1668d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034460 | |||||
chr19:1034462
|
C | T | 1 | a0001c0008t0019g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.391-1668C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034462 | ||||||
chr19:1034462
|
CGGTGTCT others(341): Show |
C | 5 | a0001c0001t0001g0170a0001c0001t0005g0034a0001c0001t0005g0165others(2): Show | 5 | HG02486.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-1667_391-1320d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034462 | ||||||
chr19:1034462
|
CGGTGTCT others(517): Show |
C | 5 | a0001c0001t0001g0227a0001c0001t0006g0092a0001c0001t0022g0061others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-1667_391-1144d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034462 | ||||||
chr19:1034465
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1665T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034465 | ||||||
chr19:1034476
|
GACCGGCA others(589): Show |
G | 4 | a0001c0008t0019g0173a0001c0008t0020g0172a0001c0008t0020g0174others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-1648_391-1053d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034476 | |||||
chr19:1034479
|
C | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0260a0001c0001t0002g0208others(13): Show | 18 | HG02895.hp1 HG02897.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.391-1651C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034479 | ||||||
chr19:1034479
|
C | T | 4 | a0001c0001t0001g0188a0001c0001t0034g0145a0001c0003t0010g0189others(1): Show | 4 | HG02451.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-1651C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034479 | ||||||
chr19:1034481
|
G | T | 48 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0241others(45): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.391-1649G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034481 | ||||||
chr19:1034482
|
C | A | 48 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0241others(45): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.391-1648C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034482 | ||||||
chr19:1034482
|
C | G | 43 | a0001c0001t0001g0014a0001c0001t0001g0144a0001c0001t0001g0188others(40): Show | 46 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.391-1648C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034482 | ||||||
chr19:1034482
|
C | T | 1 | a0003c0012t0005g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.391-1648C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034482 | ||||||
chr19:1034494
|
GAC | G | 3 | a0001c0001t0002g0203a0001c0001t0011g0134a0001c0014t0005g0072 | 3 | NA18956.hp2 NA19043.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.391-1633_391-1632d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034494 | |||||
chr19:1034495
|
A | T | 1 | a0001c0002t0004g0206 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.391-1635A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034495 | ||||||
chr19:1034501
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1629T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034501 | ||||||
chr19:1034515
|
C | G | 36 | a0001c0001t0001g0014a0001c0001t0001g0144a0001c0001t0001g0260others(33): Show | 44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.391-1615C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034515 | ||||||
chr19:1034518
|
GAGCGTGG others(27): Show |
G | 1 | a0001c0001t0001g0144 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.391-1597_391-1564d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034518 | |||||
chr19:1034530
|
G | GAC | 22 | a0001c0001t0001g0014a0001c0001t0002g0203a0001c0001t0002g0208others(19): Show | 24 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.391-1599_391-1598d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034530 | |||||
chr19:1034534
|
G | T | 1 | a0001c0001t0011g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.391-1596G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034534 | ||||||
chr19:1034535
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1595T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034535 | ||||||
chr19:1034549
|
C | G | 23 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0194others(20): Show | 25 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.391-1581C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034549 | ||||||
chr19:1034550
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.391-1580G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034550 | ||||||
chr19:1034552
|
C | G | 114 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(111): Show | 138 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.391-1578C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034552 | ||||||
chr19:1034570
|
G | T | 16 | a0001c0001t0001g0188a0001c0001t0002g0038a0001c0001t0002g0049others(13): Show | 17 | HG00597.hp2 HG02056.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.391-1560G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034570 | ||||||
chr19:1034571
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1559T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034571 | ||||||
chr19:1034585
|
G | C | 41 | a0001c0001t0001g0188a0001c0001t0002g0007a0001c0001t0002g0038others(38): Show | 46 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.391-1545G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034585 | ||||||
chr19:1034588
|
GAGCGTGG others(27): Show |
G | 3 | a0001c0001t0001g0055a0001c0001t0001g0260a0001c0008t0019g0089 | 3 | HG02717.hp1 HG04199.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-1527_391-1494d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034588 | |||||
chr19:1034600
|
G | GAC | 66 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0241others(63): Show | 83 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.391-1529_391-1528d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034600 | |||||
chr19:1034600
|
G | GACACGGT others(31): Show |
2 | a0001c0001t0002g0208a0001c0001t0002g0229 | 2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.391-1528_391-1527i others(40): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034600 | |||||
chr19:1034602
|
CGGTGTCT others(307): Show |
C | 2 | a0001c0009t0010g0167a0001c0009t0010g0168 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.391-1527_391-1214d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034602 | ||||||
chr19:1034603
|
G | C | 1 | a0001c0001t0002g0203 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.391-1527G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034603 | ||||||
chr19:1034605
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1525T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034605 | ||||||
chr19:1034615
|
A | G | 1 | a0001c0005t0016g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1515A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034615 | ||||||
chr19:1034619
|
C | G | 71 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(68): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.391-1511C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034619 | ||||||
chr19:1034619
|
C | T | 3 | a0001c0002t0004g0075a0001c0002t0004g0076a0001c0002t0004g0077 | 3 | HG00733.hp1 HG01123.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-1511C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034619 | ||||||
chr19:1034620
|
G | A | 1 | a0001c0002t0004g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.391-1510G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034620 | ||||||
chr19:1034621
|
G | T | 2 | a0001c0001t0001g0187a0001c0001t0011g0134 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.391-1509G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034621 | ||||||
chr19:1034622
|
C | A | 2 | a0001c0001t0001g0187a0001c0001t0011g0134 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.391-1508C>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034622 | ||||||
chr19:1034622
|
C | G | 117 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(114): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.391-1508C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034622 | ||||||
chr19:1034634
|
GAC | G | 3 | a0001c0001t0009g0133a0001c0002t0012g0240a0001c0003t0010g0166 | 3 | HG03130.hp1 HG04204.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.391-1493_391-1492d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034634 | |||||
chr19:1034640
|
G | T | 15 | a0001c0001t0002g0007a0001c0001t0009g0007a0001c0001t0009g0141others(12): Show | 19 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.391-1490G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034640 | ||||||
chr19:1034641
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1489T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034641 | ||||||
chr19:1034651
|
A | G | 1 | a0001c0005t0016g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1479A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034651 | ||||||
chr19:1034655
|
G | C | 35 | a0001c0001t0001g0055a0001c0001t0001g0187a0001c0001t0002g0007others(32): Show | 41 | HG00639.hp2 HG00735.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.391-1475G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034655 | ||||||
chr19:1034655
|
GGGGAGCG others(27): Show |
G | 9 | a0001c0001t0001g0188a0001c0001t0002g0207a0001c0001t0009g0042others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1457_391-1424d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034655 | |||||
chr19:1034657
|
G | T | 7 | a0001c0001t0002g0038a0001c0001t0002g0049a0001c0001t0002g0096others(4): Show | 8 | HG00597.hp2 HG02056.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-1473G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034657 | ||||||
chr19:1034658
|
G | A | 7 | a0001c0001t0002g0038a0001c0001t0002g0049a0001c0001t0002g0096others(4): Show | 8 | HG00597.hp2 HG02056.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-1472G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034658 | ||||||
chr19:1034658
|
G | C | 2 | a0001c0001t0001g0127a0001c0003t0003g0104 | 2 | NA18972.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.391-1472G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034658 | ||||||
chr19:1034670
|
G | GAC | 72 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(69): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.391-1459_391-1458d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034670 | |||||
chr19:1034672
|
CGGTGTCT others(61): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.391-1457_391-1390d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034672 | ||||||
chr19:1034672
|
CGGTGTCT others(131): Show |
C | 13 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0204others(10): Show | 22 | HG00423.hp1 HG00621.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.391-1457_391-1320d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034672 | ||||||
chr19:1034675
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1455T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034675 | ||||||
chr19:1034685
|
A | G | 1 | a0001c0005t0016g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1445A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034685 | ||||||
chr19:1034689
|
C | G | 57 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(54): Show | 65 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.391-1441C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034689 | ||||||
chr19:1034691
|
G | T | 9 | a0001c0001t0001g0188a0001c0001t0002g0207a0001c0001t0009g0042others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1439G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034691 | ||||||
chr19:1034692
|
G | A | 9 | a0001c0001t0001g0188a0001c0001t0002g0207a0001c0001t0009g0042others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1438G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034692 | ||||||
chr19:1034692
|
G | C | 2 | a0001c0001t0001g0055a0001c0008t0019g0089 | 2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-1438G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034692 | ||||||
chr19:1034704
|
GAC | G | 7 | a0001c0001t0002g0038a0001c0001t0002g0049a0001c0001t0002g0096others(4): Show | 8 | HG00597.hp2 HG02056.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-1423_391-1422d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034704 | |||||
chr19:1034706
|
C | CGGTGTCT others(61): Show |
1 | a0001c0001t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1424_391-1423i others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034706 | ||||||
chr19:1034709
|
GGTGTCTG others(63): Show |
G | 1 | a0001c0001t0001g0043 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.391-1420_391-1351d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034709 | ||||||
chr19:1034710
|
G | T | 5 | a0001c0001t0009g0088a0001c0001t0014g0051a0001c0002t0004g0039others(2): Show | 7 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.391-1420G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034710 | ||||||
chr19:1034711
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1419T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034711 | ||||||
chr19:1034721
|
A | G | 1 | a0001c0005t0016g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1409A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034721 | ||||||
chr19:1034723
|
AC | A | 14 | a0001c0001t0002g0007a0001c0001t0009g0007a0001c0001t0009g0141others(11): Show | 18 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.391-1405delC | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034723 | |||||
chr19:1034725
|
C | G | 66 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(63): Show | 74 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.391-1405C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034725 | ||||||
chr19:1034727
|
G | T | 1 | a0001c0002t0004g0230 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.391-1403G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034727 | ||||||
chr19:1034728
|
G | A | 1 | a0001c0002t0004g0230 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.391-1402G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034728 | ||||||
chr19:1034728
|
G | C | 1 | a0001c0001t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1402G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034728 | ||||||
chr19:1034728
|
G | T | 14 | a0001c0001t0002g0007a0001c0001t0009g0007a0001c0001t0009g0141others(11): Show | 18 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.391-1402G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034728 | ||||||
chr19:1034729
|
AGCGTGGG others(26): Show |
A | 14 | a0001c0001t0002g0007a0001c0001t0009g0007a0001c0001t0009g0141others(11): Show | 18 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.391-1400_391-1368d others(35): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034729 | ||||||
chr19:1034732
|
GTGGGTGG others(97): Show |
G | 18 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0241others(15): Show | 18 | HG00408.hp2 HG00544.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.391-1387_391-1284d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034732 | |||||
chr19:1034740
|
G | GAC | 32 | a0001c0001t0001g0014a0001c0001t0001g0187a0001c0001t0001g0260others(29): Show | 35 | HG00544.hp2 HG00597.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.391-1389_391-1388d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034740 | |||||
chr19:1034740
|
G | GACACGGT others(65): Show |
2 | a0001c0001t0002g0208a0001c0001t0002g0229 | 2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.391-1388_391-1387i others(74): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034740 | |||||
chr19:1034740
|
GACGGTGT others(205): Show |
G | 2 | a0001c0001t0001g0055a0001c0008t0019g0089 | 2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-1353_391-1142d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034740 | |||||
chr19:1034742
|
CGGTGTCT others(61): Show |
C | 14 | a0001c0001t0002g0003a0001c0001t0002g0041a0001c0001t0002g0093others(11): Show | 19 | HG00423.hp2 HG01243.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.391-1387_391-1320d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034742 | ||||||
chr19:1034742
|
CGGTGTCT others(167): Show |
C | 2 | a0001c0001t0002g0096a0001c0014t0005g0072 | 2 | HG02056.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.391-1387_391-1214d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034742 | ||||||
chr19:1034744
|
GTGTCTGG others(29): Show |
G | 1 | a0001c0001t0001g0260 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.391-1353_391-1318d others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034744 | |||||
chr19:1034745
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1385T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034745 | ||||||
chr19:1034759
|
C | G | 42 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0144others(39): Show | 45 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.391-1371C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034759 | ||||||
chr19:1034761
|
G | T | 1 | a0001c0002t0004g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.391-1369G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034761 | ||||||
chr19:1034762
|
G | A | 1 | a0001c0002t0004g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.391-1368G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034762 | ||||||
chr19:1034762
|
G | GAGCGTGG others(29): Show |
1 | a0001c0001t0009g0088 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-1352_391-1351i others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034762 | |||||
chr19:1034766
|
GTGGGTGG others(63): Show |
G | 5 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0267others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-1351_391-1282d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034766 | |||||
chr19:1034775
|
A | T | 2 | a0001c0002t0004g0018a0001c0002t0004g0237 | 4 | HG01074.hp2 HG01516.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-1355A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034775 | ||||||
chr19:1034776
|
CACATTGT others(27): Show |
C | 9 | a0001c0001t0001g0144a0001c0001t0001g0194a0001c0001t0001g0261others(6): Show | 9 | HG00099.hp2 HG01192.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1351_391-1318d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034776 | |||||
chr19:1034779
|
A | G | 79 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0053others(76): Show | 90 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.391-1351A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034779 | ||||||
chr19:1034780
|
T | G | 62 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0187others(59): Show | 71 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.391-1350T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034780 | ||||||
chr19:1034781
|
T | C | 9 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0179others(6): Show | 9 | HG01106.hp2 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1349T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034781 | ||||||
chr19:1034795
|
C | G | 40 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0188others(37): Show | 45 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.391-1335C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034795 | ||||||
chr19:1034797
|
G | T | 4 | a0001c0001t0014g0051a0001c0002t0004g0039a0001c0002t0004g0040others(1): Show | 6 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-1333G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034797 | ||||||
chr19:1034798
|
G | A | 4 | a0001c0001t0014g0051a0001c0002t0004g0039a0001c0002t0004g0040others(1): Show | 6 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-1332G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034798 | ||||||
chr19:1034810
|
G | GAC | 38 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0038others(35): Show | 41 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.391-1319_391-1318d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034810 | |||||
chr19:1034810
|
G | GACGGTGT others(29): Show |
1 | a0001c0001t0002g0208 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.391-1302_391-1301i others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034810 | |||||
chr19:1034812
|
CGGTGTCT others(97): Show |
C | 1 | a0001c0001t0005g0265 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.391-1317_391-1214d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034812 | ||||||
chr19:1034815
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1315T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034815 | ||||||
chr19:1034829
|
C | G | 73 | a0001c0001t0001g0053a0001c0001t0001g0144a0001c0001t0001g0170others(70): Show | 90 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.391-1301C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034829 | ||||||
chr19:1034836
|
A | G | 129 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0050others(126): Show | 166 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.391-1294A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034836 | ||||||
chr19:1034844
|
GAC | G | 5 | a0001c0001t0014g0051a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 7 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.391-1283_391-1282d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034844 | |||||
chr19:1034851
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1279T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034851 | ||||||
chr19:1034861
|
A | G | 1 | a0001c0005t0016g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1269A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034861 | ||||||
chr19:1034865
|
G | C | 7 | a0001c0001t0001g0260a0001c0001t0002g0229a0001c0001t0014g0051others(4): Show | 9 | HG00639.hp2 HG01081.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.391-1265G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034865 | ||||||
chr19:1034865
|
G | GGGGAGCG others(27): Show |
1 | a0001c0001t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1264_391-1263i others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034865 | |||||
chr19:1034865
|
GGTAAGCG others(63): Show |
G | 1 | a0001c0001t0001g0014 | 3 | HG03490.hp2 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.391-1263_391-1194d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034865 | |||||
chr19:1034867
|
T | G | 125 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0053others(122): Show | 151 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.391-1263T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034867 | ||||||
chr19:1034868
|
A | C | 1 | a0001c0001t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1262A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034868 | ||||||
chr19:1034868
|
A | G | 125 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0053others(122): Show | 151 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.391-1262A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034868 | ||||||
chr19:1034882
|
CACGGTGT others(27): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.391-1211_391-1178d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034882 | |||||
chr19:1034887
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1243T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034887 | ||||||
chr19:1034897
|
A | G | 1 | a0001c0005t0016g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1233A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034897 | ||||||
chr19:1034901
|
C | G | 126 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0144others(123): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.391-1229C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034901 | ||||||
chr19:1034904
|
G | C | 1 | a0001c0001t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1226G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034904 | ||||||
chr19:1034916
|
G | GAC | 115 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0170others(112): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.391-1213_391-1212d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034916 | |||||
chr19:1034916
|
G | GACACGGC others(103): Show |
1 | a0001c0003t0003g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.391-1212_391-1211i others(112): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034916 | |||||
chr19:1034916
|
G | GACACGGT others(65): Show |
1 | a0001c0001t0002g0229 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.391-1212_391-1211i others(74): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034916 | |||||
chr19:1034917
|
A | C | 1 | a0001c0003t0003g0048 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.391-1213A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034917 | ||||||
chr19:1034918
|
CGGTGTCT others(61): Show |
C | 4 | a0001c0001t0001g0144a0001c0001t0001g0194a0001c0001t0001g0268others(1): Show | 4 | HG00099.hp2 HG02135.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-1211_391-1144d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034918 | ||||||
chr19:1034918
|
CGGTGTCT others(131): Show |
C | 1 | a0001c0001t0001g0043 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.391-1211_391-1074d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034918 | ||||||
chr19:1034921
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1209T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034921 | ||||||
chr19:1034931
|
A | G | 1 | a0001c0005t0016g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-1199A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034931 | ||||||
chr19:1034932
|
GACCGGGA others(133): Show |
G | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.391-1159_391-1020d others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034932 | |||||
chr19:1034935
|
C | G | 125 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0053others(122): Show | 152 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.391-1195C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034935 | ||||||
chr19:1034950
|
GAC | G | 3 | a0001c0002t0012g0240a0001c0003t0003g0232a0001c0005t0016g0213 | 3 | HG02074.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.391-1177_391-1176d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034950 | |||||
chr19:1034952
|
CACGGTGT others(27): Show |
C | 6 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0267others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-1141_391-1108d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034952 | |||||
chr19:1034957
|
T | C | 10 | a0001c0003t0003g0176a0001c0003t0003g0177a0001c0003t0003g0178others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-1173T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034957 | ||||||
chr19:1034971
|
C | G | 140 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(137): Show | 172 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.391-1159C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034971 | ||||||
chr19:1034986
|
G | GAC | 102 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0053others(99): Show | 123 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.391-1143_391-1142d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | |||||
chr19:1034986
|
G | GACACGGT others(67): Show |
1 | a0001c0001t0001g0219 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.391-1142_391-1141i others(76): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | |||||
chr19:1034986
|
G | GACACGGT others(103): Show |
2 | a0001c0002t0004g0224a0001c0002t0004g0236 | 2 | HG01975.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.391-1142_391-1141i others(112): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | |||||
chr19:1034986
|
G | GACACGGT others(65): Show |
1 | a0001c0001t0002g0208 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.391-1142_391-1141i others(74): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | |||||
chr19:1034986
|
G | GACGGTGT others(29): Show |
1 | a0001c0001t0002g0229 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.391-1126_391-1125i others(38): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1034986 | |||||
chr19:1034988
|
CGGTGTCT others(61): Show |
C | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.391-1141_391-1074d others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034988 | ||||||
chr19:1034988
|
CGGTGTCT others(167): Show |
C | 2 | a0001c0001t0002g0107a0001c0003t0003g0104 | 2 | HG02129.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.391-1141_391-968de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034988 | ||||||
chr19:1034991
|
T | C | 12 | a0001c0001t0001g0108a0001c0003t0003g0176a0001c0003t0003g0177others(9): Show | 12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-1139T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1034991 | ||||||
chr19:1035002
|
GACCGGGA others(63): Show |
G | 33 | a0001c0001t0001g0170a0001c0001t0001g0187a0001c0001t0002g0003others(30): Show | 38 | HG00423.hp2 HG00544.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.391-1089_391-1020d others(72): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035002 | |||||
chr19:1035005
|
C | G | 130 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(127): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.391-1125C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035005 | ||||||
chr19:1035026
|
G | T | 1 | a0001c0001t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1104G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035026 | ||||||
chr19:1035027
|
T | C | 12 | a0001c0001t0001g0108a0001c0003t0003g0176a0001c0003t0003g0177others(9): Show | 12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-1103T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035027 | ||||||
chr19:1035038
|
GACCGGGA others(27): Show |
G | 6 | a0001c0001t0005g0067a0001c0001t0005g0074a0001c0001t0017g0073others(3): Show | 6 | HG00733.hp1 HG00733.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-1071_391-1038d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035038 | |||||
chr19:1035041
|
C | G | 123 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0037others(120): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.391-1089C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035041 | ||||||
chr19:1035056
|
G | GAC | 27 | a0001c0001t0001g0108a0001c0001t0002g0210a0001c0001t0002g0211others(24): Show | 30 | HG00423.hp1 HG01081.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.391-1073_391-1072d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035056 | |||||
chr19:1035058
|
C | T | 1 | a0001c0008t0019g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-1072C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035058 | ||||||
chr19:1035058
|
CGGTGTCT others(97): Show |
C | 1 | a0001c0001t0005g0079 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.391-1071_391-968de others(1): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035058 | ||||||
chr19:1035061
|
T | C | 12 | a0001c0001t0001g0108a0001c0003t0003g0176a0001c0003t0003g0177others(9): Show | 12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-1069T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035061 | ||||||
chr19:1035072
|
T | G | 154 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0035others(151): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.391-1058T>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035072 | ||||||
chr19:1035075
|
C | G | 36 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0050others(33): Show | 41 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-1055C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035075 | ||||||
chr19:1035090
|
GAC | G | 4 | a0001c0001t0001g0043a0001c0002t0004g0039a0001c0002t0004g0235others(1): Show | 6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-1037_391-1036d others(4): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035090 | |||||
chr19:1035092
|
C | CACGGTGT others(27): Show |
1 | a0001c0002t0004g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.391-1035_391-1002d others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035092 | |||||
chr19:1035097
|
T | C | 12 | a0001c0001t0001g0108a0001c0003t0003g0176a0001c0003t0003g0177others(9): Show | 12 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-1033T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035097 | ||||||
chr19:1035111
|
G | C | 1 | a0001c0005t0008g0259 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.391-1019G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035111 | ||||||
chr19:1035113
|
G | T | 1 | a0001c0001t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1017G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035113 | ||||||
chr19:1035114
|
G | A | 1 | a0001c0001t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-1016G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035114 | ||||||
chr19:1035118
|
G | A | 1 | a0001c0001t0006g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.391-1012G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035118 | ||||||
chr19:1035126
|
GACACGGT others(65): Show |
G | 1 | a0001c0005t0016g0213 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.391-1001_391-930de others(73): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035126 | |||||
chr19:1035132
|
G | T | 1 | a0001c0001t0002g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.391-998G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035132 | ||||||
chr19:1035133
|
T | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0108a0001c0001t0005g0256others(11): Show | 16 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.391-997T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035133 | ||||||
chr19:1035147
|
G | C | 2 | a0001c0001t0009g0133a0001c0002t0004g0077 | 2 | HG01123.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.391-983G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035147 | ||||||
chr19:1035162
|
G | GAC | 17 | a0001c0001t0001g0020a0001c0001t0001g0050a0001c0001t0001g0108others(14): Show | 19 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.391-967_391-966dup others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035162 | |||||
chr19:1035164
|
C | T | 1 | a0001c0004t0003g0149 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.391-966C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035164 | ||||||
chr19:1035167
|
T | C | 15 | a0001c0001t0001g0020a0001c0001t0001g0108a0001c0001t0005g0256others(12): Show | 17 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.391-963T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035167 | ||||||
chr19:1035181
|
G | A | 1 | a0001c0002t0012g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.391-949G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035181 | ||||||
chr19:1035181
|
G | C | 3 | a0001c0001t0002g0222a0001c0001t0009g0133a0001c0003t0010g0166 | 3 | HG02135.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.391-949G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035181 | ||||||
chr19:1035181
|
GGGGAGCG others(29): Show |
G | 4 | a0001c0002t0004g0250a0001c0006t0007g0146a0001c0006t0007g0153others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-914_391-879del others(36): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035181 | |||||
chr19:1035196
|
GAC | G | 6 | a0001c0001t0001g0050a0001c0001t0002g0103a0001c0001t0002g0107others(3): Show | 6 | HG01123.hp2 HG02129.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-931_391-930del others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035196 | |||||
chr19:1035198
|
C | CACGGTGT others(63): Show |
2 | a0001c0001t0009g0133a0001c0003t0010g0166 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.391-914_391-913ins others(70): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 1035198 | |||||
chr19:1035203
|
T | C | 15 | a0001c0001t0001g0020a0001c0001t0001g0108a0001c0001t0005g0256others(12): Show | 17 | HG01106.hp2 HG01168.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.391-927T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035203 | ||||||
chr19:1035216
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.391-914C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035216 | ||||||
chr19:1035217
|
C | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(50): Show | 80 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.391-913C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035217 | ||||||
chr19:1035251
|
A | G | 1 | a0003c0012t0005g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.391-879A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035251 | ||||||
chr19:1035253
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(131): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.391-877T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035253 | ||||||
chr19:1035451
|
C | T | 35 | a0001c0001t0001g0101a0001c0001t0001g0114a0001c0001t0001g0119others(32): Show | 40 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-679C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035451 | ||||||
chr19:1035456
|
A | C | 46 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0057others(43): Show | 57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.391-674A>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035456 | ||||||
chr19:1035493
|
G | A | 1 | a0001c0006t0007g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.391-637G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035493 | ||||||
chr19:1035500
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.391-630G>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035500 | ||||||
chr19:1035540
|
G | A | 1 | a0001c0003t0003g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.391-590G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035540 | ||||||
chr19:1035541
|
A | G | 1 | a0001c0003t0003g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.391-589A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035541 | ||||||
chr19:1035610
|
A | T | 1 | a0001c0001t0002g0159 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.391-520A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035610 | ||||||
chr19:1035651
|
G | A | 7 | a0001c0003t0010g0071a0001c0003t0010g0166a0001c0003t0010g0189others(4): Show | 7 | HG02451.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.391-479G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035651 | ||||||
chr19:1035709
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.391-421G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035709 | ||||||
chr19:1035711
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.391-419C>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035711 | ||||||
chr19:1035796
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.391-334C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035796 | ||||||
chr19:1035806
|
T | C | 4 | a0001c0008t0019g0089a0001c0008t0019g0173a0001c0008t0020g0172others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-324T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035806 | ||||||
chr19:1035814
|
T | C | 1 | a0001c0002t0004g0223 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.391-316T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035814 | ||||||
chr19:1035846
|
T | A | 1 | a0001c0003t0003g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.391-284T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035846 | ||||||
chr19:1035887
|
A | T | 1 | a0001c0001t0001g0027 | 2 | NA18990.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.391-243A>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035887 | ||||||
chr19:1035960
|
G | A | 18 | a0001c0003t0003g0013a0001c0003t0003g0048a0001c0003t0003g0070others(15): Show | 34 | HG02027.hp2 HG02040.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.391-170G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1035960 | ||||||
chr19:1036018
|
C | T | 1 | a0001c0002t0004g0095 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.391-112C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1036018 | ||||||
chr19:1036019
|
G | A | 127 | a0001c0001t0001g0035a0001c0001t0001g0170a0001c0001t0001g0187others(124): Show | 161 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.391-111G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1036019 | ||||||
chr19:1036032
|
G | T | 1 | a0001c0015t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.391-98G>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 4/6 | chr19 | 1036032 | ||||||
chr19:1036315
|
A | G | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.507+69A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 5/6 | chr19 | 1036315 | ||||||
chr19:1036575
|
C | T | 18 | a0001c0003t0003g0013a0001c0003t0003g0048a0001c0003t0003g0070others(15): Show | 34 | HG02027.hp2 HG02040.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.654+13C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036575 | ||||||
chr19:1036576
|
G | A | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+14G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036576 | ||||||
chr19:1036621
|
C | T | 1 | a0001c0001t0030g0253 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.654+59C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036621 | ||||||
chr19:1036632
|
T | C | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+70T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036632 | ||||||
chr19:1036651
|
T | C | 1 | a0001c0001t0011g0022 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.654+89T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036651 | ||||||
chr19:1036664
|
AGTCTCAG others(41): Show |
A | 1 | a0001c0001t0011g0022 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.654+108_654+155del others(48): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 1036664 | |||||
chr19:1036692
|
C | T | 10 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(7): Show | 16 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.654+130C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036692 | ||||||
chr19:1036705
|
C | T | 10 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(7): Show | 16 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.654+143C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036705 | ||||||
chr19:1036719
|
G | A | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+157G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036719 | ||||||
chr19:1036736
|
CTG | C | 8 | a0001c0001t0006g0009a0001c0001t0006g0019a0001c0001t0006g0084others(5): Show | 13 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.654+176_654+177del others(2): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 1036736 | |||||
chr19:1036794
|
T | A | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+232T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036794 | ||||||
chr19:1036838
|
T | A | 1 | a0001c0001t0002g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.654+276T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036838 | ||||||
chr19:1036914
|
C | T | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.654+352C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1036914 | ||||||
chr19:1037070
|
C | T | 1 | a0001c0001t0006g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.654+508C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037070 | ||||||
chr19:1037089
|
C | T | 18 | a0001c0003t0003g0013a0001c0003t0003g0048a0001c0003t0003g0070others(15): Show | 34 | HG02027.hp2 HG02040.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.654+527C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037089 | ||||||
chr19:1037109
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(238): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.655-516T>C | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037109 | ||||||
chr19:1037171
|
T | A | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-454T>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037171 | ||||||
chr19:1037552
|
G | A | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-73G>A | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037552 | ||||||
chr19:1037564
|
A | G | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-61A>G | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037564 | ||||||
chr19:1037585
|
C | T | 21 | a0001c0005t0007g0026a0001c0005t0007g0030a0001c0005t0007g0120others(18): Show | 32 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-40C>T | CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 6/6 | chr19 | 1037585 |