Item | Value |
---|---|
geneid | 11316 |
ensemblid | ENSG00000105669.14 |
hgncid | 2234 |
symbol | COPE |
name | COPI coat complex subunit epsilon |
refseq_nuc | NM_007263.4 |
refseq_prot | NP_009194.2 |
ensembl_nuc | ENST00000262812.9 |
ensembl_prot | ENSP00000262812.3 |
mane_status | MANE Select |
chr | chr19 |
start | 18899514 |
end | 18919387 |
strand | - |
ver | v1.2 |
region | chr19:18899514-18919387 |
region5000 | chr19:18894514-18924387 |
regionname0 | COPE_chr19_18899514_18919387 |
regionname5000 | COPE_chr19_18894514_18924387 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 308 | 215 | 19 | 44 | 103 | 13 | 34 | 73 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0002 | 0/0 | 308 | 75 | 36 | 11 | 17 | 1 | 10 | 15 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0003 | 0/0 | 308 | 33 | 33 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0004 | 0/0 | 308 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0005 | 0/0 | 308 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0006 | 0/0 | 308 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0007 | 0/0 | 308 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 927 | 116 | 12 | 17 | 61 | 6 | 19 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0002 | 0/1 | 927 | 93 | 6 | 26 | 39 | 7 | 14 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0003 | 0/0 | 927 | 72 | 36 | 11 | 14 | 1 | 10 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0004 | 0/0 | 927 | 17 | 17 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0005 | 0/0 | 927 | 7 | 7 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0006 | 0/0 | 927 | 4 | 4 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0007 | 0/0 | 927 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0008 | 0/0 | 927 | 3 | 3 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0009 | 0/0 | 927 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0010 | 0/0 | 927 | 2 | 1 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0011 | 0/0 | 927 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0012 | 0/0 | 927 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0013 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0014 | 0/0 | 927 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0015 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0016 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0017 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0018 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
c0019 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 205 | 330 | 94 | 56 | 120 | 14 | 44 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0002 | 1/0 | 6 | 0 | 1 | 4 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 927 | 116 | 12 | 17 | 61 | 6 | 19 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0001c0002 | 0/1 | 927 | 93 | 6 | 26 | 39 | 7 | 14 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0001c0009 | 0/0 | 927 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0001c0010 | 0/0 | 927 | 2 | 1 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0001c0012 | 0/0 | 927 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0002c0003 | 0/0 | 927 | 72 | 36 | 11 | 14 | 1 | 10 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0002c0007 | 0/0 | 927 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0003c0004 | 0/0 | 927 | 17 | 17 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0003c0005 | 0/0 | 927 | 7 | 7 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0003c0008 | 0/0 | 927 | 3 | 3 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0003c0011 | 0/0 | 927 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0003c0016 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0003c0017 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0003c0018 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0003c0019 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0004c0006 | 0/0 | 927 | 4 | 4 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0005c0015 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0006c0013 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 | |
a0007c0014 | 0/0 | 927 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1131 | 116 | 12 | 17 | 61 | 6 | 19 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0001c0002t0001 | 0/1 | 1131 | 93 | 6 | 26 | 39 | 7 | 14 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0001c0009t0001 | 0/0 | 1131 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0001c0010t0001 | 0/0 | 1131 | 2 | 1 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0001c0012t0001 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0002c0003t0001 | 0/0 | 1131 | 72 | 36 | 11 | 14 | 1 | 10 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0002c0007t0001 | 0/0 | 1131 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0003c0004t0001 | 0/0 | 1131 | 17 | 17 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0003c0005t0001 | 0/0 | 1131 | 7 | 7 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0003c0008t0001 | 0/0 | 1131 | 3 | 3 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0003c0011t0001 | 0/0 | 1131 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0003c0016t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0003c0017t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0003c0018t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0003c0019t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0004c0006t0001 | 0/0 | 1131 | 4 | 4 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0005c0015t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0006c0013t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
a0007c0014t0001 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | copy fasta | chr19 | 18894514 | 18924387 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0002 | 1/0 | 6 | 0 | 1 | 4 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0009t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0009t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0009t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0010t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0010t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0001c0012t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0007t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0007t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0002c0007t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0004t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0005t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0005t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0005t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0008t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0008t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0008t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0011t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0011t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0016t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0017t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0018t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0003c0019t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0004c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0004c0006t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0004c0006t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0004c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0005c0015t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0006c0013t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
a0007c0014t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0138 | EUR | GBR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0044 | EUR | GBR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0225 | EUR | GBR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0223 | EUR | FIN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0106 | EUR | FIN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00609 | hp1 | a0002 | c0007 | t0001 | g0137 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00738 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01070 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01081 | hp2 | a0002 | c0003 | t0001 | g0131 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01109 | hp2 | a0002 | c0003 | t0001 | g0193 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01167 | hp2 | a0002 | c0003 | t0001 | g0116 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01169 | hp2 | a0002 | c0003 | t0001 | g0139 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01175 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01346 | hp2 | a0002 | c0003 | t0001 | g0045 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01361 | hp1 | a0002 | c0003 | t0001 | g0149 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01496 | hp2 | a0001 | c0010 | t0001 | g0036 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0246 | EUR | IBS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01891 | hp1 | a0003 | c0004 | t0001 | g0285 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0129 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01928 | hp2 | a0007 | c0014 | t0001 | g0103 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02040 | hp1 | a0002 | c0003 | t0001 | g0068 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02055 | hp1 | a0003 | c0008 | t0001 | g0290 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02055 | hp2 | a0003 | c0005 | t0001 | g0273 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02145 | hp1 | a0002 | c0003 | t0001 | g0255 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02145 | hp2 | a0003 | c0005 | t0001 | g0271 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | CDX | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | CDX | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02257 | hp1 | a0002 | c0003 | t0001 | g0124 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0150 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02258 | hp1 | a0003 | c0004 | t0001 | g0281 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02258 | hp2 | a0002 | c0003 | t0001 | g0156 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02280 | hp1 | a0004 | c0006 | t0001 | g0038 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02280 | hp2 | a0002 | c0003 | t0001 | g0159 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02300 | hp1 | a0002 | c0003 | t0001 | g0194 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02451 | hp1 | a0002 | c0003 | t0001 | g0017 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02451 | hp2 | a0003 | c0004 | t0001 | g0287 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02572 | hp1 | a0003 | c0011 | t0001 | g0288 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02572 | hp2 | a0005 | c0015 | t0001 | g0293 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02602 | hp2 | a0002 | c0003 | t0001 | g0140 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02615 | hp1 | a0002 | c0003 | t0001 | g0146 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02622 | hp1 | a0002 | c0003 | t0001 | g0205 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02622 | hp2 | a0002 | c0003 | t0001 | g0204 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02630 | hp1 | a0003 | c0017 | t0001 | g0277 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0042 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02717 | hp1 | a0002 | c0003 | t0001 | g0130 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02717 | hp2 | a0002 | c0003 | t0001 | g0128 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02723 | hp1 | a0003 | c0005 | t0001 | g0270 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02723 | hp2 | a0003 | c0004 | t0001 | g0018 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02735 | hp2 | a0002 | c0003 | t0001 | g0040 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02809 | hp1 | a0002 | c0003 | t0001 | g0148 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0154 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0203 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02886 | hp1 | a0002 | c0003 | t0001 | g0261 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02886 | hp2 | a0003 | c0004 | t0001 | g0018 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0250 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02896 | hp2 | a0003 | c0004 | t0001 | g0019 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02897 | hp1 | a0003 | c0004 | t0001 | g0019 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02922 | hp1 | a0002 | c0003 | t0001 | g0147 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02922 | hp2 | a0002 | c0003 | t0001 | g0132 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02965 | hp1 | a0003 | c0004 | t0001 | g0274 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02965 | hp2 | a0002 | c0003 | t0001 | g0161 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02970 | hp1 | a0002 | c0003 | t0001 | g0145 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02970 | hp2 | a0003 | c0016 | t0001 | g0289 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0256 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03041 | hp1 | a0003 | c0004 | t0001 | g0278 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03041 | hp2 | a0003 | c0019 | t0001 | g0280 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03098 | hp1 | a0003 | c0004 | t0001 | g0279 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0201 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03130 | hp1 | a0003 | c0005 | t0001 | g0267 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03130 | hp2 | a0002 | c0003 | t0001 | g0202 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03195 | hp1 | a0002 | c0003 | t0001 | g0195 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03195 | hp2 | a0003 | c0018 | t0001 | g0276 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0189 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03209 | hp2 | a0003 | c0005 | t0001 | g0272 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03225 | hp2 | a0003 | c0004 | t0001 | g0283 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0259 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03453 | hp1 | a0004 | c0006 | t0001 | g0125 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03453 | hp2 | a0002 | c0003 | t0001 | g0197 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03486 | hp2 | a0002 | c0003 | t0001 | g0192 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03516 | hp1 | a0003 | c0008 | t0001 | g0292 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0157 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03540 | hp1 | a0003 | c0004 | t0001 | g0284 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03540 | hp2 | a0003 | c0004 | t0001 | g0264 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03579 | hp1 | a0004 | c0006 | t0001 | g0144 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03579 | hp2 | a0003 | c0004 | t0001 | g0286 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03688 | hp2 | a0002 | c0003 | t0001 | g0123 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0226 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03704 | hp2 | a0002 | c0003 | t0001 | g0039 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0041 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0258 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03927 | hp2 | a0002 | c0003 | t0001 | g0155 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03942 | hp1 | a0002 | c0003 | t0001 | g0253 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04115 | hp2 | a0002 | c0003 | t0001 | g0126 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04184 | hp1 | a0001 | c0012 | t0001 | g0028 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04204 | hp1 | a0002 | c0003 | t0001 | g0199 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0211 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0240 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0236 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18522 | hp1 | a0002 | c0003 | t0001 | g0196 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18522 | hp2 | a0003 | c0005 | t0001 | g0268 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18612 | hp2 | a0001 | c0009 | t0001 | g0296 | EAS | CHB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18906 | hp2 | a0002 | c0003 | t0001 | g0251 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18941 | hp1 | a0002 | c0003 | t0001 | g0133 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18959 | hp1 | a0002 | c0007 | t0001 | g0142 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18964 | hp2 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18969 | hp2 | a0002 | c0003 | t0001 | g0141 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18989 | hp1 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19000 | hp1 | a0002 | c0003 | t0001 | g0127 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19004 | hp1 | a0002 | c0003 | t0001 | g0069 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19004 | hp2 | a0002 | c0007 | t0001 | g0136 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0262 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19043 | hp2 | a0003 | c0004 | t0001 | g0265 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19057 | hp1 | a0002 | c0003 | t0001 | g0071 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19057 | hp2 | a0001 | c0009 | t0001 | g0295 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0151 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19067 | hp1 | a0002 | c0003 | t0001 | g0153 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19068 | hp2 | a0001 | c0009 | t0001 | g0294 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19074 | hp1 | a0002 | c0003 | t0001 | g0134 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19080 | hp1 | a0002 | c0003 | t0001 | g0152 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19240 | hp1 | a0003 | c0004 | t0001 | g0275 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA19240 | hp2 | a0003 | c0004 | t0001 | g0282 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20129 | hp1 | a0002 | c0003 | t0001 | g0017 | AFR | ASW | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ASW | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | TSI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0016 | EUR | TSI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | GIH | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02109 | hp2 | a0003 | c0005 | t0001 | g0269 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02486 | hp1 | a0002 | c0003 | t0001 | g0254 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02486 | hp2 | a0006 | c0013 | t0001 | g0252 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02559 | hp1 | a0003 | c0011 | t0001 | g0266 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG02559 | hp2 | a0003 | c0008 | t0001 | g0291 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03471 | hp1 | a0002 | c0003 | t0001 | g0198 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0190 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
HG06807 | hp2 | a0002 | c0003 | t0001 | g0160 | AFR | USA | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | USA | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA20300 | hp2 | a0001 | c0010 | t0001 | g0143 | AFR | USA | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA21309 | hp1 | a0004 | c0006 | t0001 | g0117 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0222 | REF | REF | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:18899880 | T | C | 1 | a0007 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.872A>G | p.Gln291Arg | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 9/10 | 911/1131 | 872/927 | 291/308 | chr19 | 18899880 | ||
chr19:18899893 | T | G | 1 | a0007 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.859A>C | p.Ile287Leu | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 9/10 | 898/1131 | 859/927 | 287/308 | chr19 | 18899893 | ||
chr19:18907024 | A | G | 1 | a0006 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.379T>C | p.Tyr127His | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 418/1131 | 379/927 | 127/308 | chr19 | 18907024 | ||
chr19:18907053 | G | A | 3 | a0002a0005a0006 | 77 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(74): Show |
missense_variant | MODERATE | c.350C>T | p.Thr117Ile | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 389/1131 | 350/927 | 117/308 | chr19 | 18907053 | ||
chr19:18911007 | C | T | 1 | a0004 | 4 | HG02280.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.254G>A | p.Arg85His | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/10 | 293/1131 | 254/927 | 85/308 | chr19 | 18911007 | ||
chr19:18919311 | G | C | 2 | a0003a0005 | 34 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(31): Show |
missense_variant | MODERATE | c.38C>G | p.Ser13Cys | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/10 | 77/1131 | 38/927 | 13/308 | chr19 | 18919311 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:18900435 | T | C | 9 | a0001c0002a0001c0010a0003c0004others(6): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
synonymous_variant | LOW | c.750A>G | p.Pro250Pro | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/10 | 789/1131 | 750/927 | 250/308 | chr19 | 18900435 | ||
chr19:18904798 | G | A | 1 | a0002c0007 | 3 | HG00609.hp1 NA18959.hp1 NA19004.hp2 |
synonymous_variant | LOW | c.552C>T | p.Leu184Leu | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/10 | 591/1131 | 552/927 | 184/308 | chr19 | 18904798 | ||
chr19:18906968 | G | A | 1 | a0003c0019 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.435C>T | p.Ser145Ser | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 474/1131 | 435/927 | 145/308 | chr19 | 18906968 | ||
chr19:18906986 | C | T | 1 | a0003c0017 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.417G>A | p.Ala139Ala | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 456/1131 | 417/927 | 139/308 | chr19 | 18906986 | ||
chr19:18907016 | G | A | 1 | a0001c0012 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.387C>T | p.His129His | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 426/1131 | 387/927 | 129/308 | chr19 | 18907016 | ||
chr19:18907019 | G | T | 1 | a0006c0013 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.384C>A | p.Leu128Leu | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 423/1131 | 384/927 | 128/308 | chr19 | 18907019 | ||
chr19:18911033 | G | A | 2 | a0003c0008a0003c0016 | 4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.228C>T | p.Ser76Ser | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/10 | 267/1131 | 228/927 | 76/308 | chr19 | 18911033 | ||
chr19:18912987 | C | T | 1 | a0003c0016 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.186G>A | p.Ala62Ala | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/10 | 225/1131 | 186/927 | 62/308 | chr19 | 18912987 | ||
chr19:18913044 | T | C | 8 | a0001c0002a0003c0004a0003c0008others(5): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
splice_region_variant&synonymous_variant | LOW | c.129A>G | p.Leu43Leu | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/10 | 168/1131 | 129/927 | 43/308 | chr19 | 18913044 | ||
chr19:18919319 | G | A | 1 | a0001c0009 | 3 | NA18612.hp2 NA19057.hp2 NA19068.hp2 |
synonymous_variant | LOW | c.30C>T | p.Ser10Ser | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/10 | 69/1131 | 30/927 | 10/308 | chr19 | 18919319 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:18900094 | C | G | 3 | a0002c0007t0001g0136a0002c0007t0001g0137a0002c0007t0001g0142 | 3 | HG00609.hp1 NA18959.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.805-147G>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900094 | ||||||
chr19:18900104 | G | C | 20 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0084others(17): Show | 21 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-157C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900104 | ||||||
chr19:18900117 | TG | T | 3 | a0001c0001t0001g0074a0001c0002t0001g0177a0007c0014t0001g0103 | 3 | HG01928.hp2 HG03491.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.805-171delC | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900117 | ||||||
chr19:18900124 | GC | G | 90 | a0001c0001t0001g0074a0001c0001t0001g0115a0001c0001t0001g0118others(87): Show | 93 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.805-178delG | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900124 | ||||||
chr19:18900139 | G | A | 22 | a0002c0003t0001g0116a0002c0003t0001g0139a0002c0003t0001g0189others(19): Show | 22 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.805-192C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900139 | ||||||
chr19:18900164 | ATGGTGGG others(10): Show |
A | 1 | a0002c0003t0001g0194 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.804+200_804+216del others(17): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900164 | ||||||
chr19:18900575 | G | A | 7 | a0003c0004t0001g0018a0003c0004t0001g0264a0003c0004t0001g0275others(4): Show | 8 | HG02258.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.736-126C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900575 | ||||||
chr19:18900706 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.736-257A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900706 | ||||||
chr19:18900965 | G | C | 205 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(202): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.736-516C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900965 | ||||||
chr19:18900970 | T | C | 13 | a0003c0004t0001g0019a0003c0004t0001g0265a0003c0004t0001g0274others(10): Show | 14 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.736-521A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900970 | ||||||
chr19:18900983 | C | T | 1 | a0001c0009t0001g0294 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.736-534G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900983 | ||||||
chr19:18901056 | T | C | 75 | a0002c0003t0001g0005a0002c0003t0001g0017a0002c0003t0001g0039others(72): Show | 78 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.736-607A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901056 | ||||||
chr19:18901076 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.736-627G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901076 | ||||||
chr19:18901117 | GGGGGACC others(9): Show |
G | 1 | a0002c0003t0001g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.736-684_736-669del others(16): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901117 | ||||||
chr19:18901250 | T | C | 6 | a0002c0003t0001g0116a0002c0003t0001g0139a0002c0003t0001g0203others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.736-801A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901250 | ||||||
chr19:18901413 | C | T | 7 | a0003c0004t0001g0018a0003c0004t0001g0264a0003c0004t0001g0275others(4): Show | 8 | HG02258.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.736-964G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901413 | ||||||
chr19:18901444 | A | G | 4 | a0003c0004t0001g0279a0003c0004t0001g0281a0003c0004t0001g0282others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-995T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901444 | ||||||
chr19:18901498 | AGCAGTAC others(3): Show |
A | 1 | a0001c0002t0001g0219 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.736-1059_736-1050d others(12): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901498 | ||||||
chr19:18901549 | G | A | 85 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(82): Show | 88 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.736-1100C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901549 | ||||||
chr19:18901682 | A | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0095others(1): Show | 5 | HG00140.hp2 HG01981.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.736-1233T>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901682 | ||||||
chr19:18901796 | G | A | 4 | a0003c0008t0001g0290a0003c0008t0001g0291a0003c0008t0001g0292others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-1347C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901796 | ||||||
chr19:18901806 | G | A | 2 | a0001c0002t0001g0181a0001c0002t0001g0237 | 2 | NA19009.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.736-1357C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901806 | ||||||
chr19:18901841 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.736-1392C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901841 | ||||||
chr19:18901906 | C | T | 4 | a0003c0008t0001g0290a0003c0008t0001g0291a0003c0008t0001g0292others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+1362G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901906 | ||||||
chr19:18902179 | C | CA | 35 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(32): Show | 42 | HG00597.hp2 HG00673.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.735+1088dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | ||||||
chr19:18902179 | C | CAA | 73 | a0001c0001t0001g0090a0001c0001t0001g0115a0001c0001t0001g0118others(70): Show | 76 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.735+1087_735+1088d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | ||||||
chr19:18902179 | C | CAAA | 13 | a0002c0003t0001g0043a0002c0003t0001g0069a0002c0003t0001g0083others(10): Show | 13 | HG00609.hp1 HG01175.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.735+1086_735+1088d others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | ||||||
chr19:18902179 | CA | C | 75 | a0001c0001t0001g0060a0001c0002t0001g0031a0001c0002t0001g0032others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.735+1088delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | ||||||
chr19:18902179 | CAAAA | C | 20 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0263others(17): Show | 21 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.735+1085_735+1088d others(6): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | ||||||
chr19:18902282 | G | A | 7 | a0003c0004t0001g0018a0003c0004t0001g0264a0003c0004t0001g0275others(4): Show | 8 | HG02258.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.735+986C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902282 | ||||||
chr19:18902324 | C | T | 1 | a0002c0003t0001g0135 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.735+944G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902324 | ||||||
chr19:18902391 | G | A | 1 | a0003c0004t0001g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.735+877C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902391 | ||||||
chr19:18902607 | T | G | 21 | a0003c0004t0001g0018a0003c0004t0001g0019a0003c0004t0001g0264others(18): Show | 23 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.735+661A>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902607 | ||||||
chr19:18902664 | CA | C | 186 | a0001c0001t0001g0034a0001c0001t0001g0057a0001c0001t0001g0074others(183): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.735+603delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902664 | ||||||
chr19:18902707 | AAAGGAAG others(11): Show |
A | 1 | a0001c0002t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.735+543_735+560del others(18): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902707 | ||||||
chr19:18902714 | G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0263 | 3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.735+554C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902714 | ||||||
chr19:18902716 | A | AAAGG | 57 | a0001c0002t0001g0169a0001c0002t0001g0176a0001c0002t0001g0182others(54): Show | 59 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.735+548_735+551dup others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | ||||||
chr19:18902716 | A | AAAGGAAG others(6): Show |
37 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0096others(34): Show | 37 | HG00642.hp1 HG00741.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.735+551_735+552ins others(13): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | ||||||
chr19:18902716 | A | AAAGGAAG others(24): Show |
1 | a0001c0002t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.735+551_735+552ins others(31): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | ||||||
chr19:18902716 | A | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0263 | 3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.735+552T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | ||||||
chr19:18902716 | AAAGGAAA others(2): Show |
A | 19 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 23 | HG00597.hp2 HG00673.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.735+543_735+551del others(9): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | ||||||
chr19:18902720 | GA | G | 73 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(70): Show | 74 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.735+547delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902720 | ||||||
chr19:18902721 | A | AAGGAAAG others(10): Show |
2 | a0003c0011t0001g0266a0003c0011t0001g0288 | 2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.735+546_735+547ins others(17): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902721 | ||||||
chr19:18902723 | A | G | 7 | a0002c0003t0001g0005a0002c0003t0001g0039a0002c0003t0001g0040others(4): Show | 9 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+545T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902723 | ||||||
chr19:18902723 | A | T | 1 | a0002c0003t0001g0152 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.735+545T>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902723 | ||||||
chr19:18902725 | G | A | 7 | a0002c0003t0001g0005a0002c0003t0001g0039a0002c0003t0001g0040others(4): Show | 9 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+543C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902725 | ||||||
chr19:18902728 | G | A | 61 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(58): Show | 62 | HG00609.hp1 HG01109.hp2 HG01123.hp2 others(59): Show |
intron_variant | MODIFIER | c.735+540C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902728 | ||||||
chr19:18902728 | G | GGAA | 6 | a0002c0003t0001g0005a0002c0003t0001g0039a0002c0003t0001g0040others(3): Show | 8 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+537_735+539dup others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902728 | ||||||
chr19:18902730 | A | AAGG | 13 | a0002c0003t0001g0043a0002c0003t0001g0129a0003c0004t0001g0019others(10): Show | 14 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.735+537_735+538ins others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902730 | ||||||
chr19:18902730 | A | G | 61 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(58): Show | 62 | HG00609.hp1 HG01109.hp2 HG01123.hp2 others(59): Show |
intron_variant | MODIFIER | c.735+538T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902730 | ||||||
chr19:18902738 | GA | G | 19 | a0001c0001t0001g0115a0001c0010t0001g0143a0002c0003t0001g0005others(16): Show | 21 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.735+529delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902738 | ||||||
chr19:18902741 | A | G | 1 | a0002c0003t0001g0253 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.735+527T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902741 | ||||||
chr19:18902743 | G | A | 1 | a0002c0003t0001g0253 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.735+525C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902743 | ||||||
chr19:18902747 | GA | G | 33 | a0001c0001t0001g0115a0001c0010t0001g0143a0002c0003t0001g0005others(30): Show | 37 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.735+520delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902747 | ||||||
chr19:18902748 | A | AAGG | 53 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(50): Show | 53 | HG00609.hp1 HG01109.hp2 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.735+519_735+520ins others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902748 | ||||||
chr19:18902752 | G | A | 2 | a0002c0003t0001g0043a0002c0003t0001g0129 | 2 | HG01175.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.735+516C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902752 | ||||||
chr19:18902752 | G | GAAGGA | 21 | a0001c0002t0001g0169a0001c0002t0001g0206a0001c0002t0001g0207others(18): Show | 21 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.735+511_735+515dup others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902752 | ||||||
chr19:18902756 | G | GA | 12 | a0001c0002t0001g0016a0001c0002t0001g0105a0001c0002t0001g0111others(9): Show | 13 | HG01167.hp1 HG01175.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.735+511dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902756 | ||||||
chr19:18902756 | G | GAAAGGAA others(3): Show |
1 | a0001c0002t0001g0232 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.735+511_735+512ins others(10): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902756 | ||||||
chr19:18902756 | G | GAAAGGAA others(21): Show |
7 | a0001c0002t0001g0044a0001c0002t0001g0106a0001c0002t0001g0107others(4): Show | 7 | HG00099.hp2 HG00323.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.735+511_735+512ins others(28): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902756 | ||||||
chr19:18902757 | AAGG | A | 7 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0263others(4): Show | 7 | HG00323.hp1 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+508_735+510del others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902757 | ||||||
chr19:18902757 | AAGGAAGG others(9): Show |
A | 1 | a0001c0002t0001g0109 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.735+495_735+510del others(16): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902757 | ||||||
chr19:18902760 | G | A | 2 | a0002c0003t0001g0043a0002c0003t0001g0129 | 2 | HG01175.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.735+508C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902760 | ||||||
chr19:18902763 | G | A | 5 | a0001c0002t0001g0220a0002c0003t0001g0131a0002c0003t0001g0138others(2): Show | 5 | HG00099.hp1 HG01081.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.735+505C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902763 | ||||||
chr19:18902765 | A | G | 1 | a0001c0002t0001g0220 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.735+503T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902765 | ||||||
chr19:18902767 | G | A | 90 | a0001c0001t0001g0115a0001c0002t0001g0016a0001c0002t0001g0031others(87): Show | 94 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.735+501C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | ||||||
chr19:18902767 | G | GGAA | 4 | a0003c0004t0001g0265a0003c0011t0001g0266a0003c0011t0001g0288others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+500_735+501ins others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | ||||||
chr19:18902767 | G | GGAAAGAA others(86): Show |
3 | a0001c0001t0001g0120a0001c0001t0001g0122a0004c0006t0001g0117 | 3 | HG01123.hp2 HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.735+500_735+501ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | ||||||
chr19:18902767 | G | GGAAAGAA others(86): Show |
1 | a0001c0001t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.735+500_735+501ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | ||||||
chr19:18902767 | G | GGAAGGAA others(90): Show |
1 | a0001c0001t0001g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.735+500_735+501ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | ||||||
chr19:18902768 | G | GAAAGAAA others(95): Show |
2 | a0002c0003t0001g0053a0002c0003t0001g0161 | 2 | HG02965.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(102): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(99): Show |
3 | a0002c0003t0001g0068a0002c0003t0001g0124a0002c0003t0001g0147 | 3 | HG02040.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(106): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(70): Show |
1 | a0002c0003t0001g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(77): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(74): Show |
1 | a0002c0003t0001g0126 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(81): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(78): Show |
1 | a0002c0003t0001g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(82): Show |
1 | a0002c0003t0001g0189 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(89): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(86): Show |
20 | a0002c0003t0001g0017a0002c0003t0001g0041a0002c0003t0001g0042others(17): Show | 21 | HG00609.hp1 HG01346.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.735+499_735+500ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(90): Show |
3 | a0002c0003t0001g0190a0002c0003t0001g0205a0002c0007t0001g0142 | 3 | HG02622.hp1 HG03471.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(94): Show |
1 | a0002c0003t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(102): Show |
1 | a0002c0003t0001g0253 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(109): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(65): Show |
1 | a0002c0003t0001g0123 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(72): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(77): Show |
4 | a0002c0003t0001g0071a0002c0003t0001g0135a0002c0003t0001g0197others(1): Show | 4 | HG02486.hp2 HG03453.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+499_735+500ins others(84): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(81): Show |
3 | a0002c0003t0001g0148a0002c0003t0001g0151a0002c0003t0001g0153 | 3 | HG02809.hp1 NA19060.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(88): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(85): Show |
1 | a0002c0003t0001g0069 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(92): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(89): Show |
4 | a0002c0003t0001g0127a0002c0003t0001g0133a0002c0003t0001g0141others(1): Show | 4 | HG02818.hp1 NA18941.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+499_735+500ins others(96): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(93): Show |
2 | a0002c0003t0001g0134a0002c0003t0001g0202 | 2 | HG03130.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(100): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(97): Show |
2 | a0002c0003t0001g0193a0002c0003t0001g0254 | 2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(104): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(101): Show |
2 | a0002c0003t0001g0116a0002c0003t0001g0139 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.735+499_735+500ins others(108): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(105): Show |
1 | a0002c0003t0001g0256 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(112): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(113): Show |
1 | a0002c0003t0001g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(120): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(81): Show |
1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(88): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGAAA others(94): Show |
1 | a0002c0003t0001g0152 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(91): Show |
1 | a0002c0003t0001g0005 | 3 | HG00738.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(98): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(74): Show |
2 | a0002c0003t0001g0128a0002c0003t0001g0145 | 2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(81): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(94): Show |
1 | a0002c0003t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(106): Show |
1 | a0002c0003t0001g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(113): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(74): Show |
1 | a0002c0003t0001g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(81): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(78): Show |
1 | a0002c0003t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(86): Show |
2 | a0002c0003t0001g0146a0002c0003t0001g0149 | 2 | HG01361.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(77): Show |
1 | a0002c0003t0001g0132 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(84): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(81): Show |
1 | a0002c0003t0001g0070 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(88): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(60): Show |
1 | a0004c0006t0001g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(67): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(64): Show |
1 | a0002c0003t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(71): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(76): Show |
1 | a0002c0003t0001g0043 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(83): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAAGGAA others(71): Show |
1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(78): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAGGAAA others(99): Show |
1 | a0002c0003t0001g0250 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(106): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAGGAAA others(85): Show |
1 | a0002c0003t0001g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(92): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GAAGGAAG others(85): Show |
1 | a0002c0003t0001g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(92): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GGAAAGAA others(74): Show |
1 | a0002c0003t0001g0131 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(81): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GGAAAGAA others(78): Show |
1 | a0004c0006t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902768 | G | GGAAAGAA others(82): Show |
2 | a0002c0003t0001g0138a0002c0003t0001g0199 | 2 | HG00099.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(89): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | ||||||
chr19:18902769 | G | A | 43 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0263others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.735+499C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902769 | ||||||
chr19:18902771 | A | G | 6 | a0003c0004t0001g0279a0003c0004t0001g0281a0003c0004t0001g0282others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+497T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902771 | ||||||
chr19:18902772 | A | AGAAG | 9 | a0001c0001t0001g0009a0001c0001t0001g0059a0001c0001t0001g0073others(6): Show | 10 | HG01433.hp1 HG02074.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.735+492_735+495dup others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | ||||||
chr19:18902772 | A | G | 117 | a0001c0001t0001g0058a0001c0001t0001g0158a0001c0001t0001g0162others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.735+496T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | ||||||
chr19:18902772 | AGAAG | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 57 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.735+492_735+495del others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | ||||||
chr19:18902772 | AGAAGGAA others(1): Show |
A | 7 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0034others(4): Show | 8 | HG01070.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+488_735+495del others(8): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | ||||||
chr19:18902772 | AGAAGGAA others(5): Show |
A | 3 | a0001c0001t0001g0023a0001c0001t0001g0079a0001c0001t0001g0089 | 3 | HG02523.hp1 HG02602.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.735+484_735+495del others(12): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | ||||||
chr19:18902772 | AGAAGGAA others(9): Show |
A | 7 | a0001c0001t0001g0065a0003c0005t0001g0267a0003c0005t0001g0268others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+480_735+495del others(16): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | ||||||
chr19:18902772 | AGAAGGAA others(13): Show |
A | 1 | a0003c0005t0001g0270 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.735+476_735+495del others(20): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | ||||||
chr19:18902773 | G | A | 6 | a0003c0004t0001g0279a0003c0004t0001g0281a0003c0004t0001g0282others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+495C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902773 | ||||||
chr19:18902773 | G | GA | 8 | a0001c0002t0001g0044a0001c0002t0001g0106a0001c0002t0001g0107others(5): Show | 8 | HG00099.hp2 HG00323.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+494dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902773 | ||||||
chr19:18902775 | A | AAGGAAGG others(26): Show |
3 | a0001c0002t0001g0016a0001c0002t0001g0165a0001c0002t0001g0215 | 4 | HG02132.hp1 HG02155.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+492_735+493ins others(33): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902775 | ||||||
chr19:18902775 | A | AAGGAAGG others(35): Show |
1 | a0001c0002t0001g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.735+492_735+493ins others(42): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902775 | ||||||
chr19:18902776 | G | A | 33 | a0001c0001t0001g0057a0002c0003t0001g0005a0002c0003t0001g0017others(30): Show | 36 | HG00609.hp1 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.735+492C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902776 | ||||||
chr19:18902777 | G | A | 5 | a0001c0002t0001g0016a0001c0002t0001g0105a0001c0002t0001g0111others(2): Show | 6 | HG01167.hp1 HG02132.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.735+491C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902777 | ||||||
chr19:18902778 | AAGGAAGG | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0002t0001g0104others(1): Show | 4 | HG02615.hp2 HG03239.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+483_735+489del others(7): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902778 | ||||||
chr19:18902778 | AAGGAAGG others(8): Show |
A | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.735+475_735+489del others(15): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902778 | ||||||
chr19:18902780 | G | A | 20 | a0002c0003t0001g0017a0002c0003t0001g0069a0002c0003t0001g0070others(17): Show | 21 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.735+488C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902780 | ||||||
chr19:18902781 | G | GA | 6 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0164others(3): Show | 6 | HG00323.hp2 HG01192.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+486dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902781 | ||||||
chr19:18902784 | G | A | 6 | a0002c0003t0001g0123a0002c0003t0001g0126a0002c0003t0001g0128others(3): Show | 6 | HG01891.hp2 HG02602.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+484C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902784 | ||||||
chr19:18902785 | G | A | 1 | a0001c0002t0001g0232 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.735+483C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902785 | ||||||
chr19:18902792 | G | A | 1 | a0001c0010t0001g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.735+476C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902792 | ||||||
chr19:18902801 | G | GAAAGAAA others(75): Show |
2 | a0003c0008t0001g0290a0003c0008t0001g0292 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.735+466_735+467ins others(82): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902801 | ||||||
chr19:18902805 | G | A | 2 | a0003c0008t0001g0290a0003c0008t0001g0292 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.735+463C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902805 | ||||||
chr19:18902805 | G | GAAAGAAA others(83): Show |
1 | a0003c0016t0001g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.735+462_735+463ins others(90): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902805 | ||||||
chr19:18902805 | G | GAAAGAAA others(67): Show |
1 | a0003c0008t0001g0291 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.735+462_735+463ins others(74): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902805 | ||||||
chr19:18902809 | G | A | 4 | a0003c0008t0001g0290a0003c0008t0001g0291a0003c0008t0001g0292others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+459C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902809 | ||||||
chr19:18902809 | G | GA | 20 | a0001c0002t0001g0032a0001c0002t0001g0112a0001c0002t0001g0114others(17): Show | 20 | HG01346.hp1 HG01433.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.735+458dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902809 | ||||||
chr19:18902812 | G | A | 2 | a0002c0003t0001g0138a0002c0003t0001g0199 | 2 | HG00099.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.735+456C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902812 | ||||||
chr19:18902813 | G | A | 4 | a0003c0008t0001g0290a0003c0008t0001g0291a0003c0008t0001g0292others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+455C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902813 | ||||||
chr19:18902813 | G | GA | 11 | a0001c0002t0001g0170a0001c0002t0001g0172a0001c0002t0001g0174others(8): Show | 11 | HG01071.hp2 HG01261.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+454dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902813 | ||||||
chr19:18902813 | G | GAAGAAAG others(40): Show |
2 | a0003c0004t0001g0018a0003c0004t0001g0275 | 3 | HG02723.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.735+454_735+455ins others(47): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902813 | ||||||
chr19:18902816 | G | A | 2 | a0002c0003t0001g0138a0002c0003t0001g0199 | 2 | HG00099.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.735+452C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902816 | ||||||
chr19:18902817 | G | A | 6 | a0003c0004t0001g0018a0003c0004t0001g0275a0003c0008t0001g0290others(3): Show | 7 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+451C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | ||||||
chr19:18902817 | G | GA | 4 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0245others(1): Show | 4 | HG01255.hp1 HG03239.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+450dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | ||||||
chr19:18902817 | G | GAAAGAAA others(38): Show |
1 | a0003c0004t0001g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.735+450_735+451ins others(45): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | ||||||
chr19:18902817 | G | GAAAGCAA others(105): Show |
3 | a0003c0004t0001g0279a0003c0004t0001g0281a0003c0019t0001g0280 | 3 | HG02258.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.735+450_735+451ins others(112): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | ||||||
chr19:18902817 | G | GAAAGCAA others(109): Show |
1 | a0003c0004t0001g0282 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.735+450_735+451ins others(116): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | ||||||
chr19:18902817 | G | GAAGAAAG others(44): Show |
1 | a0003c0004t0001g0264 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.735+450_735+451ins others(51): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | ||||||
chr19:18902820 | G | A | 48 | a0001c0001t0001g0115a0002c0003t0001g0005a0002c0003t0001g0017others(45): Show | 51 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.735+448C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902820 | ||||||
chr19:18902821 | G | A | 12 | a0003c0004t0001g0018a0003c0004t0001g0264a0003c0004t0001g0275others(9): Show | 13 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.735+447C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGAAA others(18): Show |
1 | a0003c0004t0001g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.735+446_735+447ins others(25): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(100): Show |
1 | a0001c0002t0001g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.735+446_735+447ins others(107): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(108): Show |
1 | a0001c0002t0001g0213 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(112): Show |
1 | a0001c0002t0001g0211 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(119): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(104): Show |
1 | a0001c0002t0001g0225 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.735+446_735+447ins others(111): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(108): Show |
2 | a0001c0002t0001g0206a0001c0002t0001g0238 | 2 | HG00609.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.735+446_735+447ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(112): Show |
1 | a0001c0002t0001g0207 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(119): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(140): Show |
1 | a0001c0002t0001g0257 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.735+446_735+447ins others(147): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(104): Show |
2 | a0001c0002t0001g0209a0001c0002t0001g0218 | 2 | HG00408.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.735+446_735+447ins others(111): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(108): Show |
1 | a0001c0002t0001g0234 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(132): Show |
1 | a0001c0002t0001g0247 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(139): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(148): Show |
1 | a0001c0002t0001g0249 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(155): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(112): Show |
2 | a0001c0002t0001g0222a0001c0002t0001g0260 | 2 | HG01978.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.735+446_735+447ins others(119): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(128): Show |
1 | a0001c0002t0001g0258 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(135): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(99): Show |
1 | a0001c0002t0001g0169 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(106): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902821 | G | GAAAGGAA others(111): Show |
1 | a0001c0002t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(118): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | ||||||
chr19:18902824 | G | A | 61 | a0001c0001t0001g0115a0002c0003t0001g0005a0002c0003t0001g0017others(58): Show | 64 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.735+444C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902824 | ||||||
chr19:18902825 | G | A | 31 | a0001c0002t0001g0169a0001c0002t0001g0206a0001c0002t0001g0207others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.735+443C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAAAGA others(33): Show |
9 | a0002c0003t0001g0128a0002c0003t0001g0129a0002c0003t0001g0145others(6): Show | 9 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(40): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAAAGA others(38): Show |
31 | a0002c0003t0001g0017a0002c0003t0001g0041a0002c0003t0001g0042others(28): Show | 32 | HG00609.hp1 HG01346.hp2 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(45): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAAAGA others(43): Show |
2 | a0002c0003t0001g0005a0002c0003t0001g0261 | 4 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(50): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(32): Show |
2 | a0002c0003t0001g0131a0002c0003t0001g0132 | 2 | HG01081.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(39): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(37): Show |
5 | a0002c0003t0001g0195a0002c0003t0001g0197a0002c0003t0001g0198others(2): Show | 5 | HG02896.hp1 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(44): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(42): Show |
1 | a0002c0003t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(49): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(47): Show |
3 | a0002c0003t0001g0193a0002c0003t0001g0202a0002c0003t0001g0203 | 3 | HG01109.hp2 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(54): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(56): Show |
1 | a0002c0003t0001g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(63): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(24): Show |
4 | a0001c0001t0001g0121a0001c0001t0001g0122a0002c0003t0001g0138others(1): Show | 4 | HG00099.hp1 HG02895.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(31): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(41): Show |
1 | a0002c0003t0001g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(48): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(46): Show |
2 | a0002c0003t0001g0040a0002c0003t0001g0068 | 2 | HG02040.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(53): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(51): Show |
5 | a0002c0003t0001g0043a0002c0003t0001g0253a0002c0003t0001g0254others(2): Show | 5 | HG01175.hp1 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(58): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(32): Show |
3 | a0002c0003t0001g0124a0002c0003t0001g0148a0002c0003t0001g0205 | 3 | HG02257.hp1 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(39): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(31): Show |
1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(38): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(36): Show |
1 | a0002c0003t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(43): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(35): Show |
2 | a0004c0006t0001g0125a0004c0006t0001g0144 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(42): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGAAA others(78): Show |
1 | a0003c0004t0001g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGGAA others(100): Show |
1 | a0001c0002t0001g0221 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(107): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGGAA others(104): Show |
1 | a0001c0002t0001g0223 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(111): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGGAA others(108): Show |
2 | a0001c0002t0001g0224a0001c0002t0001g0242 | 2 | HG00642.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGGAA others(116): Show |
1 | a0001c0002t0001g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(123): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGGAA others(91): Show |
1 | a0001c0002t0001g0216 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(98): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAAGGAA others(83): Show |
1 | a0001c0002t0001g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(90): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGAAAG others(59): Show |
1 | a0002c0003t0001g0139 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(66): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(28): Show |
2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG01123.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(35): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(50): Show |
1 | a0002c0003t0001g0194 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(57): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(40): Show |
1 | a0004c0006t0001g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(47): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(108): Show |
1 | a0001c0002t0001g0096 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(128): Show |
1 | a0001c0002t0001g0246 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(135): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(166): Show |
1 | a0001c0002t0001g0177 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(173): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(95): Show |
1 | a0001c0002t0001g0240 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(102): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(91): Show |
1 | a0001c0002t0001g0210 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(98): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(155): Show |
1 | a0001c0002t0001g0175 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(162): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(107): Show |
1 | a0001c0002t0001g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(114): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(99): Show |
1 | a0001c0002t0001g0200 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(106): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAA others(155): Show |
1 | a0001c0002t0001g0032 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(162): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(32): Show |
1 | a0004c0006t0001g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(39): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(49): Show |
1 | a0002c0003t0001g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(56): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(54): Show |
1 | a0002c0003t0001g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(61): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(58): Show |
1 | a0003c0004t0001g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(65): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(87): Show |
1 | a0003c0004t0001g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(94): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(91): Show |
1 | a0001c0002t0001g0236 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(98): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(131): Show |
1 | a0001c0002t0001g0227 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(138): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(95): Show |
1 | a0001c0002t0001g0220 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(102): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(137): Show |
1 | a0001c0002t0001g0262 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(144): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(58): Show |
2 | a0002c0003t0001g0146a0002c0003t0001g0149 | 2 | HG01361.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(65): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(71): Show |
1 | a0003c0004t0001g0283 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(78): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(83): Show |
1 | a0003c0004t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(90): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(111): Show |
1 | a0001c0002t0001g0259 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(118): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(119): Show |
1 | a0001c0002t0001g0241 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(126): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(115): Show |
1 | a0001c0002t0001g0245 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(122): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(79): Show |
1 | a0003c0004t0001g0019 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(86): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(78): Show |
1 | a0003c0018t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(40): Show |
1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(47): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(78): Show |
1 | a0001c0002t0001g0191 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(95): Show |
1 | a0003c0017t0001g0277 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(102): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(79): Show |
1 | a0001c0002t0001g0176 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(86): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(78): Show |
1 | a0001c0002t0001g0031 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(127): Show |
1 | a0001c0002t0001g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(134): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(88): Show |
1 | a0001c0002t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(95): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(82): Show |
3 | a0001c0002t0001g0167a0001c0002t0001g0170a0001c0002t0001g0183 | 3 | HG01261.hp1 HG01993.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(89): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(90): Show |
1 | a0001c0002t0001g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(98): Show |
1 | a0001c0002t0001g0186 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(105): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(86): Show |
2 | a0001c0002t0001g0166a0001c0002t0001g0184 | 2 | HG01981.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(90): Show |
5 | a0001c0002t0001g0114a0001c0002t0001g0171a0001c0002t0001g0178others(2): Show | 5 | HG01361.hp2 NA18954.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(94): Show |
1 | a0001c0002t0001g0112 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(102): Show |
1 | a0001c0002t0001g0173 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(109): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(90): Show |
2 | a0001c0002t0001g0188a0001c0002t0001g0237 | 2 | NA18980.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(94): Show |
2 | a0001c0002t0001g0230a0001c0002t0001g0233 | 2 | HG01109.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(102): Show |
2 | a0001c0002t0001g0172a0001c0002t0001g0179 | 2 | NA18939.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(109): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(114): Show |
1 | a0001c0002t0001g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(121): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(93): Show |
1 | a0001c0002t0001g0181 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(100): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(102): Show |
2 | a0001c0002t0001g0180a0001c0002t0001g0239 | 2 | NA18995.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(109): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(97): Show |
1 | a0001c0002t0001g0235 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(104): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(94): Show |
1 | a0001c0002t0001g0168 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGAAG others(106): Show |
1 | a0001c0002t0001g0219 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(113): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902825 | G | GAAGGGAA others(189): Show |
1 | a0001c0002t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(196): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | ||||||
chr19:18902826 | A | AAAGAAAG others(46): Show |
1 | a0003c0011t0001g0266 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.735+441_735+442ins others(53): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902826 | ||||||
chr19:18902826 | A | AAAGAAAG others(50): Show |
1 | a0003c0011t0001g0288 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735+441_735+442ins others(57): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902826 | ||||||
chr19:18902826 | A | AAGGAAAG others(54): Show |
1 | a0001c0010t0001g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.735+441_735+442ins others(61): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902826 | ||||||
chr19:18902828 | G | GGAAGGAA others(100): Show |
1 | a0001c0002t0001g0187 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.735+439_735+440ins others(107): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902828 | ||||||
chr19:18902830 | A | C | 7 | a0003c0004t0001g0019a0003c0004t0001g0274a0003c0004t0001g0278others(4): Show | 8 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+438T>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902830 | ||||||
chr19:18902836 | T | C | 1 | a0001c0002t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.735+432A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902836 | ||||||
chr19:18902996 | G | A | 10 | a0003c0004t0001g0019a0003c0004t0001g0265a0003c0004t0001g0274others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+272C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902996 | ||||||
chr19:18903439 | C | T | 87 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(84): Show | 90 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.580-16G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903439 | ||||||
chr19:18903452 | G | A | 1 | a0001c0002t0001g0262 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-29C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903452 | ||||||
chr19:18903498 | G | A | 1 | a0003c0011t0001g0266 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.580-75C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903498 | ||||||
chr19:18903565 | A | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0102 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.580-142T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903565 | ||||||
chr19:18903578 | G | GT | 3 | a0001c0010t0001g0143a0003c0011t0001g0266a0003c0011t0001g0288 | 3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.580-156dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903578 | ||||||
chr19:18903613 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.580-190C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903613 | ||||||
chr19:18903841 | C | T | 2 | a0001c0002t0001g0104a0001c0002t0001g0108 | 2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.580-418G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903841 | ||||||
chr19:18903874 | G | A | 1 | a0002c0003t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.580-451C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903874 | ||||||
chr19:18903881 | C | G | 1 | a0001c0002t0001g0218 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.580-458G>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903881 | ||||||
chr19:18903952 | G | A | 74 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0096others(71): Show | 74 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.580-529C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903952 | ||||||
chr19:18904000 | T | C | 75 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0096others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.580-577A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904000 | ||||||
chr19:18904224 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.579+547G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904224 | ||||||
chr19:18904297 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.579+474T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904297 | ||||||
chr19:18904312 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.579+459C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904312 | ||||||
chr19:18904334 | G | A | 3 | a0001c0002t0001g0097a0001c0002t0001g0109a0003c0004t0001g0287 | 3 | HG02109.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.579+437C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904334 | ||||||
chr19:18904682 | C | T | 19 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0084others(16): Show | 20 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.579+89G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904682 | ||||||
chr19:18904736 | C | T | 2 | a0002c0003t0001g0195a0002c0003t0001g0196 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.579+35G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904736 | ||||||
chr19:18905008 | A | ACCTGCCC others(12): Show |
1 | a0002c0003t0001g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.498-157_498-156ins others(19): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905008 | ||||||
chr19:18905026 | C | G | 10 | a0003c0004t0001g0019a0003c0004t0001g0265a0003c0004t0001g0274others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-174G>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905026 | ||||||
chr19:18905026 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.498-174G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905026 | ||||||
chr19:18905093 | A | G | 21 | a0003c0004t0001g0018a0003c0004t0001g0019a0003c0004t0001g0264others(18): Show | 23 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.498-241T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905093 | ||||||
chr19:18905161 | A | G | 1 | a0003c0005t0001g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.498-309T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905161 | ||||||
chr19:18905299 | A | G | 190 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(187): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.497+277T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905299 | ||||||
chr19:18905475 | A | G | 3 | a0004c0006t0001g0038a0004c0006t0001g0125a0004c0006t0001g0144 | 3 | HG02280.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.497+101T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905475 | ||||||
chr19:18905494 | A | AGACGCTC others(8): Show |
1 | a0001c0002t0001g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.497+67_497+81dupAC others(13): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905494 | ||||||
chr19:18905494 | AGACGCTC others(8): Show |
A | 6 | a0003c0004t0001g0279a0003c0004t0001g0281a0003c0004t0001g0282others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+67_497+81delAC others(13): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905494 | ||||||
chr19:18905641 | G | A | 5 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0002t0001g0213others(2): Show | 5 | HG00642.hp2 HG00741.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.444-12C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905641 | ||||||
chr19:18905645 | A | AG | 20 | a0001c0001t0001g0033a0001c0001t0001g0057a0001c0002t0001g0031others(17): Show | 20 | HG00609.hp2 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.444-17dupC | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905645 | ||||||
chr19:18905867 | C | T | 1 | a0003c0018t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.444-238G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905867 | ||||||
chr19:18905892 | T | C | 7 | a0001c0010t0001g0143a0003c0008t0001g0290a0003c0008t0001g0291others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.444-263A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905892 | ||||||
chr19:18905939 | G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0263 | 3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.444-310C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905939 | ||||||
chr19:18905976 | G | A | 74 | a0002c0003t0001g0005a0002c0003t0001g0017a0002c0003t0001g0039others(71): Show | 77 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.444-347C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905976 | ||||||
chr19:18906169 | G | A | 18 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0097others(15): Show | 19 | HG00099.hp2 HG00323.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.444-540C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906169 | ||||||
chr19:18906196 | T | A | 10 | a0003c0004t0001g0019a0003c0004t0001g0265a0003c0004t0001g0274others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.444-567A>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906196 | ||||||
chr19:18906258 | C | T | 2 | a0001c0002t0001g0242a0001c0002t0001g0257 | 2 | HG01123.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.444-629G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906258 | ||||||
chr19:18906528 | C | T | 1 | a0001c0002t0001g0258 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.443+432G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906528 | ||||||
chr19:18906546 | G | A | 1 | a0001c0002t0001g0211 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.443+414C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906546 | ||||||
chr19:18906732 | G | A | 3 | a0001c0002t0001g0247a0001c0002t0001g0248a0001c0002t0001g0249 | 3 | HG00738.hp2 HG01175.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.443+228C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906732 | ||||||
chr19:18906763 | T | C | 212 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.443+197A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906763 | ||||||
chr19:18906852 | C | T | 3 | a0001c0010t0001g0143a0003c0011t0001g0266a0003c0011t0001g0288 | 3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.443+108G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906852 | ||||||
chr19:18906902 | G | A | 7 | a0003c0005t0001g0267a0003c0005t0001g0268a0003c0005t0001g0269others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.443+58C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906902 | ||||||
chr19:18907191 | G | C | 10 | a0003c0004t0001g0019a0003c0004t0001g0265a0003c0004t0001g0274others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.291-79C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907191 | ||||||
chr19:18907442 | C | T | 7 | a0003c0005t0001g0267a0003c0005t0001g0268a0003c0005t0001g0269others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-330G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907442 | ||||||
chr19:18907487 | T | A | 4 | a0003c0008t0001g0290a0003c0008t0001g0291a0003c0008t0001g0292others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-375A>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907487 | ||||||
chr19:18907502 | A | C | 19 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0084others(16): Show | 20 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.291-390T>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907502 | ||||||
chr19:18907549 | G | A | 10 | a0003c0004t0001g0019a0003c0004t0001g0265a0003c0004t0001g0274others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.291-437C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907549 | ||||||
chr19:18907667 | G | A | 7 | a0003c0005t0001g0267a0003c0005t0001g0268a0003c0005t0001g0269others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-555C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907667 | ||||||
chr19:18907675 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.291-563T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907675 | ||||||
chr19:18907762 | G | A | 7 | a0003c0005t0001g0267a0003c0005t0001g0268a0003c0005t0001g0269others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-650C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907762 | ||||||
chr19:18907788 | G | T | 1 | a0001c0002t0001g0216 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.291-676C>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907788 | ||||||
chr19:18907805 | C | T | 74 | a0002c0003t0001g0005a0002c0003t0001g0017a0002c0003t0001g0039others(71): Show | 77 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.291-693G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907805 | ||||||
chr19:18907925 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.291-813G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907925 | ||||||
chr19:18908015 | G | A | 3 | a0001c0010t0001g0143a0003c0011t0001g0266a0003c0011t0001g0288 | 3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.291-903C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908015 | ||||||
chr19:18908025 | G | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0263 | 3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.291-913C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908025 | ||||||
chr19:18908034 | A | C | 3 | a0002c0003t0001g0154a0002c0003t0001g0189a0002c0003t0001g0190 | 3 | HG02809.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.291-922T>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908034 | ||||||
chr19:18908057 | A | G | 76 | a0001c0001t0001g0047a0001c0002t0001g0031a0001c0002t0001g0032others(73): Show | 76 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.291-945T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908057 | ||||||
chr19:18908112 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.291-1000C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908112 | ||||||
chr19:18908153 | C | T | 12 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0105others(9): Show | 13 | HG00099.hp2 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.291-1041G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908153 | ||||||
chr19:18908208 | C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0263 | 3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.291-1096G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908208 | ||||||
chr19:18908521 | C | CTCTT | 206 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(203): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.291-1410_291-1409i others(6): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908521 | ||||||
chr19:18908579 | C | T | 3 | a0001c0010t0001g0143a0003c0011t0001g0266a0003c0011t0001g0288 | 3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.291-1467G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908579 | ||||||
chr19:18908602 | C | T | 3 | a0002c0003t0001g0123a0002c0003t0001g0126a0002c0003t0001g0140 | 3 | HG02602.hp2 HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.291-1490G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908602 | ||||||
chr19:18908666 | G | A | 3 | a0003c0004t0001g0018a0003c0004t0001g0264a0003c0004t0001g0275 | 4 | HG02723.hp2 HG02886.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-1554C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908666 | ||||||
chr19:18908932 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.291-1820T>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908932 | ||||||
chr19:18908991 | G | A | 9 | a0002c0003t0001g0005a0002c0003t0001g0039a0002c0003t0001g0040others(6): Show | 11 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.291-1879C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908991 | ||||||
chr19:18909051 | G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01123.hp2 HG02895.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+1920C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909051 | ||||||
chr19:18909060 | T | G | 10 | a0003c0004t0001g0019a0003c0004t0001g0265a0003c0004t0001g0274others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+1911A>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909060 | ||||||
chr19:18909075 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.290+1896C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909075 | ||||||
chr19:18909143 | T | G | 10 | a0003c0004t0001g0019a0003c0004t0001g0265a0003c0004t0001g0274others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+1828A>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909143 | ||||||
chr19:18909360 | G | A | 1 | a0002c0003t0001g0250 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.290+1611C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909360 | ||||||
chr19:18909485 | T | C | 1 | a0001c0002t0001g0031 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.290+1486A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909485 | ||||||
chr19:18909519 | CT | C | 188 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0078others(185): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.290+1451delA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909519 | ||||||
chr19:18909519 | CTT | C | 12 | a0001c0002t0001g0179a0002c0003t0001g0083a0002c0003t0001g0116others(9): Show | 13 | HG01167.hp2 HG02630.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.290+1450_290+1451d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909519 | ||||||
chr19:18909647 | T | C | 75 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0096others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.290+1324A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909647 | ||||||
chr19:18909746 | C | T | 1 | a0001c0002t0001g0215 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.290+1225G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909746 | ||||||
chr19:18909906 | G | A | 4 | a0003c0004t0001g0279a0003c0004t0001g0281a0003c0004t0001g0282others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+1065C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909906 | ||||||
chr19:18909934 | T | C | 2 | a0003c0008t0001g0290a0003c0008t0001g0292 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.290+1037A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909934 | ||||||
chr19:18909935 | A | G | 9 | a0002c0003t0001g0116a0002c0003t0001g0139a0002c0003t0001g0193others(6): Show | 9 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.290+1036T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909935 | ||||||
chr19:18910193 | T | C | 75 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0096others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.290+778A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910193 | ||||||
chr19:18910201 | C | T | 79 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(76): Show | 82 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.290+770G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910201 | ||||||
chr19:18910263 | C | A | 1 | a0002c0003t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.290+708G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910263 | ||||||
chr19:18910268 | C | G | 1 | a0002c0003t0001g0250 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.290+703G>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910268 | ||||||
chr19:18910303 | G | A | 7 | a0003c0004t0001g0019a0003c0004t0001g0274a0003c0004t0001g0278others(4): Show | 8 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.290+668C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910303 | ||||||
chr19:18910366 | G | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | NA18944.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.290+605C>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910366 | ||||||
chr19:18910415 | G | A | 3 | a0001c0010t0001g0143a0003c0011t0001g0266a0003c0011t0001g0288 | 3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.290+556C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910415 | ||||||
chr19:18910585 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.290+386A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910585 | ||||||
chr19:18910631 | C | T | 5 | a0001c0010t0001g0143a0003c0005t0001g0267a0003c0005t0001g0271others(2): Show | 5 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+340G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910631 | ||||||
chr19:18910645 | T | C | 67 | a0002c0003t0001g0017a0002c0003t0001g0053a0002c0003t0001g0068others(64): Show | 68 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.290+326A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910645 | ||||||
chr19:18910676 | G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0101 | 2 | HG00558.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.290+295C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910676 | ||||||
chr19:18910855 | C | A | 1 | a0001c0002t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.290+116G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910855 | ||||||
chr19:18910877 | G | A | 1 | a0003c0004t0001g0281 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.290+94C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910877 | ||||||
chr19:18910904 | G | A | 1 | a0003c0008t0001g0291 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.290+67C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910904 | ||||||
chr19:18911161 | T | C | 205 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(202): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.190-90A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911161 | ||||||
chr19:18911198 | C | A | 75 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0096others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.190-127G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911198 | ||||||
chr19:18911236 | G | A | 25 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0097others(22): Show | 27 | HG00099.hp2 HG00323.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.190-165C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911236 | ||||||
chr19:18911382 | A | G | 1 | a0003c0004t0001g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.190-311T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911382 | ||||||
chr19:18911395 | T | C | 36 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0084others(33): Show | 39 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.190-324A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911395 | ||||||
chr19:18911447 | C | T | 1 | a0001c0002t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.190-376G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911447 | ||||||
chr19:18911555 | ATTTT | A | 74 | a0002c0003t0001g0005a0002c0003t0001g0017a0002c0003t0001g0039others(71): Show | 77 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.190-488_190-485del others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911555 | ||||||
chr19:18911709 | G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0263 | 3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.190-638C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911709 | ||||||
chr19:18911851 | C | CT | 17 | a0001c0001t0001g0021a0001c0001t0001g0056a0001c0001t0001g0076others(14): Show | 17 | HG01928.hp1 HG01928.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.190-781dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911851 | ||||||
chr19:18911851 | CT | C | 6 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 6 | HG01123.hp2 HG02895.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-781delA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911851 | ||||||
chr19:18912135 | C | A | 1 | a0002c0003t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.189+849G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912135 | ||||||
chr19:18912309 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189+675A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912309 | ||||||
chr19:18912461 | G | GA | 41 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0084others(38): Show | 44 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.189+522dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912461 | ||||||
chr19:18912629 | C | T | 4 | a0003c0008t0001g0290a0003c0008t0001g0291a0003c0008t0001g0292others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+355G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912629 | ||||||
chr19:18912717 | C | T | 87 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(84): Show | 90 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.189+267G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912717 | ||||||
chr19:18912738 | C | CA | 11 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0049others(8): Show | 11 | HG02055.hp2 HG02293.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.189+245dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912738 | ||||||
chr19:18912738 | CA | C | 184 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0115others(181): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.189+245delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912738 | ||||||
chr19:18912764 | A | G | 19 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0084others(16): Show | 20 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.189+220T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912764 | ||||||
chr19:18913072 | C | T | 4 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0002t0001g0213others(1): Show | 4 | HG00642.hp2 HG00741.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-26G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913072 | ||||||
chr19:18913228 | C | T | 2 | a0002c0003t0001g0039a0002c0003t0001g0040 | 2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.127-182G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913228 | ||||||
chr19:18913232 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127-186C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913232 | ||||||
chr19:18913254 | C | T | 2 | a0001c0002t0001g0209a0001c0002t0001g0210 | 2 | NA18998.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.127-208G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913254 | ||||||
chr19:18913305 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.127-259C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913305 | ||||||
chr19:18913357 | G | A | 1 | a0002c0003t0001g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-311C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913357 | ||||||
chr19:18913534 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.127-488C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913534 | ||||||
chr19:18913581 | C | A | 1 | a0001c0002t0001g0241 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-535G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913581 | ||||||
chr19:18913611 | A | G | 228 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(225): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.127-565T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913611 | ||||||
chr19:18913613 | C | T | 1 | a0002c0003t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.127-567G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913613 | ||||||
chr19:18913616 | T | TC | 228 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(225): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.127-571dupG | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913616 | ||||||
chr19:18913872 | A | T | 1 | a0001c0002t0001g0163 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.127-826T>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913872 | ||||||
chr19:18914163 | C | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0158a0001c0001t0001g0162others(1): Show | 4 | HG00323.hp1 HG02615.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1117G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914163 | ||||||
chr19:18914306 | G | A | 7 | a0003c0005t0001g0267a0003c0005t0001g0268a0003c0005t0001g0269others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-1260C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914306 | ||||||
chr19:18914409 | C | T | 1 | a0002c0003t0001g0053 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.127-1363G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914409 | ||||||
chr19:18914472 | T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 13 | HG00280.hp1 HG01099.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-1426A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914472 | ||||||
chr19:18914605 | C | A | 1 | a0001c0002t0001g0260 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.127-1559G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914605 | ||||||
chr19:18914755 | C | CT | 35 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0047others(32): Show | 39 | HG00597.hp1 HG00597.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.127-1710dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914755 | ||||||
chr19:18914755 | CT | C | 10 | a0001c0001t0001g0035a0001c0001t0001g0073a0001c0001t0001g0074others(7): Show | 10 | HG01168.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-1710delA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914755 | ||||||
chr19:18914775 | T | G | 1 | a0002c0007t0001g0142 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.127-1729A>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914775 | ||||||
chr19:18914840 | T | C | 1 | a0002c0003t0001g0253 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.127-1794A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914840 | ||||||
chr19:18914903 | T | C | 4 | a0003c0008t0001g0290a0003c0008t0001g0291a0003c0008t0001g0292others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1857A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914903 | ||||||
chr19:18914941 | T | C | 3 | a0001c0010t0001g0143a0002c0003t0001g0124a0003c0011t0001g0288 | 3 | HG02257.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.127-1895A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914941 | ||||||
chr19:18915015 | C | T | 1 | a0001c0002t0001g0232 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.127-1969G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915015 | ||||||
chr19:18915167 | C | T | 3 | a0004c0006t0001g0038a0004c0006t0001g0125a0004c0006t0001g0144 | 3 | HG02280.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.127-2121G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915167 | ||||||
chr19:18915278 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.127-2232C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915278 | ||||||
chr19:18915350 | G | C | 1 | a0001c0002t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.127-2304C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915350 | ||||||
chr19:18915683 | T | C | 5 | a0002c0003t0001g0017a0002c0003t0001g0156a0002c0003t0001g0160others(2): Show | 6 | HG02258.hp2 HG02451.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-2637A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915683 | ||||||
chr19:18915981 | C | T | 2 | a0001c0002t0001g0206a0001c0002t0001g0207 | 2 | HG00609.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.127-2935G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915981 | ||||||
chr19:18916042 | A | G | 27 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(24): Show | 28 | HG00323.hp1 HG00323.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-2996T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916042 | ||||||
chr19:18916093 | G | A | 1 | a0003c0004t0001g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-3047C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916093 | ||||||
chr19:18916190 | C | CA | 4 | a0003c0008t0001g0290a0003c0008t0001g0291a0003c0008t0001g0292others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+3032dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916190 | ||||||
chr19:18916352 | C | CA | 11 | a0001c0001t0001g0162a0003c0004t0001g0265a0003c0004t0001g0283others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+2870dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916352 | ||||||
chr19:18916403 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+2820G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916403 | ||||||
chr19:18916422 | G | A | 1 | a0001c0002t0001g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.126+2801C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916422 | ||||||
chr19:18916876 | G | A | 1 | a0001c0010t0001g0036 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.126+2347C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916876 | ||||||
chr19:18916944 | C | CA | 32 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(29): Show | 38 | HG00558.hp2 HG01169.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.126+2278dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | ||||||
chr19:18916944 | C | CAA | 22 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0002t0001g0016others(19): Show | 23 | HG00323.hp2 HG01099.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+2277_126+2278d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | ||||||
chr19:18916944 | C | CAAA | 8 | a0001c0001t0001g0110a0001c0002t0001g0111a0002c0003t0001g0204others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+2276_126+2278d others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | ||||||
chr19:18916944 | CA | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0090others(81): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.126+2278delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | ||||||
chr19:18916944 | CAA | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0047others(7): Show | 13 | HG01168.hp2 HG01515.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+2277_126+2278d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | ||||||
chr19:18917071 | C | A | 1 | a0001c0002t0001g0262 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.126+2152G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917071 | ||||||
chr19:18917114 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.126+2109G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917114 | ||||||
chr19:18917139 | A | G | 1 | a0002c0003t0001g0123 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.126+2084T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917139 | ||||||
chr19:18917195 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.126+2028C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917195 | ||||||
chr19:18917233 | CTTTTTTT others(2): Show |
C | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 14 | HG00597.hp2 HG01168.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+1981_126+1989d others(11): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917233 | ||||||
chr19:18917237 | T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | NA18944.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.126+1986A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917237 | ||||||
chr19:18917241 | C | CT | 9 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01123.hp2 HG01167.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+1981dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917241 | ||||||
chr19:18917241 | C | CTTT | 64 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0002t0001g0031others(61): Show | 64 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.126+1979_126+1981d others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917241 | ||||||
chr19:18917241 | CT | C | 41 | a0001c0001t0001g0082a0001c0001t0001g0098a0001c0001t0001g0099others(38): Show | 42 | HG00323.hp1 HG00323.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.126+1981delA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917241 | ||||||
chr19:18917245 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.126+1978A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917245 | ||||||
chr19:18917246 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.126+1977A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917246 | ||||||
chr19:18917504 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126+1719C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917504 | ||||||
chr19:18917832 | C | T | 16 | a0003c0004t0001g0018a0003c0004t0001g0019a0003c0004t0001g0264others(13): Show | 18 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.126+1391G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917832 | ||||||
chr19:18917947 | T | C | 1 | a0004c0006t0001g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126+1276A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917947 | ||||||
chr19:18918187 | C | CA | 68 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0030others(65): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.126+1035dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918187 | ||||||
chr19:18918187 | C | CAA | 45 | a0001c0002t0001g0031a0001c0002t0001g0166a0001c0002t0001g0167others(42): Show | 45 | HG01109.hp2 HG01261.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.126+1034_126+1035d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918187 | ||||||
chr19:18918187 | C | CAAA | 54 | a0001c0001t0001g0208a0001c0002t0001g0032a0001c0002t0001g0206others(51): Show | 54 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.126+1033_126+1035d others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918187 | ||||||
chr19:18918187 | C | CAAAA | 6 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(3): Show | 6 | HG01123.hp1 HG01978.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+1032_126+1035d others(6): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918187 | ||||||
chr19:18918203 | AG | A | 13 | a0003c0004t0001g0019a0003c0004t0001g0274a0003c0004t0001g0275others(10): Show | 14 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+1019delC | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918203 | ||||||
chr19:18918204 | G | A | 191 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.126+1019C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918204 | ||||||
chr19:18918348 | TAA | T | 8 | a0001c0002t0001g0044a0002c0003t0001g0005a0002c0003t0001g0039others(5): Show | 10 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+873_126+874del others(2): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918348 | ||||||
chr19:18918542 | A | G | 1 | a0004c0006t0001g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126+681T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918542 | ||||||
chr19:18918557 | C | T | 2 | a0003c0004t0001g0018a0003c0004t0001g0264 | 3 | HG02723.hp2 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.126+666G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918557 | ||||||
chr19:18918631 | G | A | 1 | a0005c0015t0001g0293 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.126+592C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918631 | ||||||
chr19:18918734 | G | GT | 6 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(3): Show | 8 | HG01070.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+488dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918734 | ||||||
chr19:18918983 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.126+240A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918983 | ||||||
chr19:18919124 | G | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(11): Show | 16 | HG00280.hp1 HG01099.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.126+99C>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18919124 | ||||||
chr19:18919125 | A | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(11): Show | 16 | HG00280.hp1 HG01099.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.126+98T>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18919125 |