geneid | 1104 |
---|---|
ensemblid | ENSG00000180198.17 |
hgncid | 1913 |
symbol | RCC1 |
name | regulator of chromosome condensation 1 |
refseq_nuc | NM_001381865.2 |
refseq_prot | NP_001368794.1 |
ensembl_nuc | ENST00000683442.1 |
ensembl_prot | ENSP00000508074.1 |
mane_status | MANE Select |
chr | chr1 |
start | 28506043 |
end | 28538989 |
strand | + |
ver | v1.2 |
region | chr1:28506043-28538989 |
region5000 | chr1:28501043-28543989 |
regionname0 | RCC1_chr1_28506043_28538989 |
regionname5000 | RCC1_chr1_28501043_28543989 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 421 | 294 | 88 | 68 | 84 | 18 | 34 | 62 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1266 | 176 | 40 | 39 | 66 | 8 | 21 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
c0002 | 0/0 | 1266 | 85 | 25 | 23 | 17 | 8 | 12 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
c0003 | 0/0 | 1266 | 26 | 19 | 4 | 0 | 2 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
c0004 | 0/0 | 1266 | 5 | 3 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
c0005 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
c0006 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1286 | 226 | 49 | 49 | 83 | 16 | 27 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0002 | 0/0 | 1286 | 36 | 29 | 5 | 0 | 1 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0003 | 0/0 | 1286 | 10 | 1 | 5 | 0 | 1 | 3 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0004 | 0/0 | 1286 | 7 | 6 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0005 | 0/0 | 1286 | 4 | 0 | 3 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0006 | 0/0 | 1253 | 3 | 0 | 2 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0007 | 0/0 | 1284 | 3 | 2 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0008 | 0/0 | 1286 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0009 | 0/0 | 1286 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0010 | 0/0 | 1286 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0011 | 0/0 | 1286 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
t0012 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1266 | 176 | 40 | 39 | 66 | 8 | 21 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0002 | 0/0 | 1266 | 85 | 25 | 23 | 17 | 8 | 12 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0003 | 0/0 | 1266 | 26 | 19 | 4 | 0 | 2 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0004 | 0/0 | 1266 | 5 | 3 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0005 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0006 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2551 | 155 | 28 | 33 | 66 | 8 | 18 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0001t0002 | 0/0 | 2551 | 5 | 4 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0001t0004 | 0/0 | 2551 | 7 | 6 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0001t0006 | 0/0 | 2518 | 3 | 0 | 2 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0001t0007 | 0/0 | 2549 | 3 | 2 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0001t0008 | 0/0 | 2551 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0001t0009 | 0/0 | 2551 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0001t0011 | 0/0 | 2551 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0002t0001 | 0/0 | 2551 | 63 | 17 | 14 | 16 | 7 | 9 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0002t0002 | 0/0 | 2551 | 6 | 6 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0002t0003 | 0/0 | 2551 | 10 | 1 | 5 | 0 | 1 | 3 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0002t0005 | 0/0 | 2551 | 4 | 0 | 3 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0002t0010 | 0/0 | 2551 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0002t0012 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0003t0001 | 0/0 | 2551 | 2 | 1 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0003t0002 | 0/0 | 2551 | 24 | 18 | 4 | 0 | 1 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0004t0001 | 0/0 | 2551 | 5 | 3 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0005t0002 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
a0001c0006t0001 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | copy fasta | chr1 | 28501043 | 28543989 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0006g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0001t0011g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0010g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0002t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0003t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0005t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
a0001c0006t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0046 | EUR | GBR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00280 | hp1 | a0001 | c0002 | t0003 | g0006 | EUR | FIN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00323 | hp1 | a0001 | c0003 | t0002 | g0266 | EUR | FIN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0050 | EUR | FIN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0214 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01069 | hp2 | a0001 | c0004 | t0001 | g0238 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0239 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01099 | hp2 | a0001 | c0002 | t0005 | g0040 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0264 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01167 | hp1 | a0001 | c0002 | t0003 | g0060 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0234 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01175 | hp1 | a0001 | c0002 | t0003 | g0203 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01192 | hp2 | a0001 | c0002 | t0010 | g0039 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0070 | AMR | PUR | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0036 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0263 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01258 | hp2 | a0001 | c0003 | t0002 | g0265 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0037 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0019 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0180 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0020 | EUR | IBS | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0245 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0219 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0280 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01934 | hp1 | a0001 | c0001 | t0009 | g0099 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0235 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02055 | hp1 | a0001 | c0003 | t0002 | g0247 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0279 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02145 | hp1 | a0001 | c0002 | t0003 | g0038 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02145 | hp2 | a0001 | c0005 | t0002 | g0277 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CDX | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0253 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02258 | hp2 | a0001 | c0003 | t0002 | g0268 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02273 | hp2 | a0001 | c0002 | t0005 | g0065 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02293 | hp2 | a0001 | c0002 | t0005 | g0066 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0058 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0281 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02717 | hp2 | a0001 | c0003 | t0002 | g0272 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02723 | hp2 | a0001 | c0003 | t0002 | g0255 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02738 | hp2 | a0001 | c0001 | t0008 | g0011 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0215 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0274 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0250 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02886 | hp2 | a0001 | c0003 | t0002 | g0276 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02896 | hp1 | a0001 | c0003 | t0002 | g0271 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02922 | hp2 | a0001 | c0003 | t0002 | g0278 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0257 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0252 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03130 | hp1 | a0001 | c0003 | t0002 | g0270 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03139 | hp2 | a0001 | c0003 | t0002 | g0246 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0236 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03486 | hp2 | a0001 | c0003 | t0002 | g0248 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03516 | hp1 | a0001 | c0004 | t0001 | g0240 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | ESN | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03579 | hp1 | a0001 | c0003 | t0002 | g0269 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0242 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03669 | hp2 | a0001 | c0001 | t0011 | g0244 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0034 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0275 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0114 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG04204 | hp2 | a0001 | c0002 | t0003 | g0006 | SAS | STU | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18906 | hp1 | a0001 | c0002 | t0012 | g0251 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18906 | hp2 | a0001 | c0003 | t0002 | g0254 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18999 | hp1 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19030 | hp1 | a0001 | c0003 | t0002 | g0256 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0071 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19066 | hp1 | a0001 | c0006 | t0001 | g0174 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0181 | EUR | TSI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | GIH | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | GIH | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01123 | hp1 | a0001 | c0003 | t0002 | g0267 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0033 | AMR | CLM | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0241 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02559 | hp1 | a0001 | c0003 | t0002 | g0249 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | USA | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA20300 | hp2 | a0001 | c0003 | t0002 | g0273 | AFR | USA | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | LWK | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0145 | REF | REF | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0141 | REF | REF | RCC1_chr1_28501043_28543989 | RCC1 | chr1 | 28501043 | 28543989 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:28507478
|
AAAGCTGG others(1184): Show |
A | 1 | a0001 | 3 | HG01167.hp2 HG01978.hp2 HG03239.hp1 |
splice_acceptor_variant&splice_donor_variant&5_prime_UTR_truncation&exon_loss_variant&splice_region_variant&intron_variant | HIGH | c.-261-595_-228-107d others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 28507478 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:28532305
|
A | C | 1 | a0001c0004 | 5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
synonymous_variant | LOW | c.396A>C | p.Ala132Ala | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/13 | 699/2551 | 396/1266 | 132/421 | chr1 | 28532305 | ||
chr1:28535124
|
G | A | 1 | a0001c0002 | 85 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
synonymous_variant | LOW | c.516G>A | p.Val172Val | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 8/13 | 819/2551 | 516/1266 | 172/421 | chr1 | 28535124 | ||
chr1:28536766
|
C | G | 1 | a0001c0006 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.957C>G | p.Gly319Gly | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/13 | 1260/2551 | 957/1266 | 319/421 | chr1 | 28536766 | ||
chr1:28536775
|
G | A | 1 | a0001c0005 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.966G>A | p.Glu322Glu | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/13 | 1269/2551 | 966/1266 | 322/421 | chr1 | 28536775 | ||
chr1:28537923
|
A | G | 2 | a0001c0003a0001c0005 | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
synonymous_variant | LOW | c.1182A>G | p.Lys394Lys | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 1485/2551 | 1182/1266 | 394/421 | chr1 | 28537923 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:28506070
|
C | T | 1 | a0001c0002t0012 | 1 | NA18906.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-276C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/13 | chr1 | 28506070 | ||||||
chr1:28506074
|
T | G | 5 | a0001c0001t0002a0001c0002t0002a0001c0002t0012others(2): Show | 37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-272T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/13 | chr1 | 28506074 | ||||||
chr1:28506075
|
C | T | 1 | a0001c0001t0011 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-271C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/13 | 23792 | chr1 | 28506075 | |||||
chr1:28516777
|
T | G | 1 | a0001c0001t0004 | 7 | HG00639.hp2 HG02280.hp1 HG03195.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-100T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/13 | 13090 | chr1 | 28516777 | |||||
chr1:28516806
|
A | G | 1 | a0001c0002t0003 | 10 | HG00280.hp1 HG01123.hp2 HG01167.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-71A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/13 | 13061 | chr1 | 28516806 | |||||
chr1:28538104
|
C | A | 1 | a0001c0001t0008 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*97C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 97 | chr1 | 28538104 | |||||
chr1:28538219
|
A | G | 1 | a0001c0002t0005 | 4 | HG01099.hp2 HG02273.hp2 HG02293.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*212A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 212 | chr1 | 28538219 | |||||
chr1:28538665
|
C | T | 1 | a0001c0002t0010 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*658C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 658 | chr1 | 28538665 | |||||
chr1:28538698
|
C | T | 1 | a0001c0001t0009 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*691C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 691 | chr1 | 28538698 | |||||
chr1:28538756
|
GGA | G | 1 | a0001c0001t0007 | 3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*755_*756delAG | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 13/13 | 755 | INFO_REALIGN_3_PRIME | chr1 | 28538756 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:28506175
|
A | G | 37 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(34): Show | 37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-262+91A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506175 | ||||||
chr1:28506185
|
G | A | 37 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(34): Show | 37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-262+101G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506185 | ||||||
chr1:28506201
|
C | CT | 26 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(23): Show | 26 | HG00323.hp1 HG00639.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-262+132dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28506201 | |||||
chr1:28506201
|
CT | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0008g0011others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-262+132delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28506201 | |||||
chr1:28506277
|
C | T | 1 | a0001c0004t0001g0242 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-262+193C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506277 | ||||||
chr1:28506294
|
C | T | 5 | a0001c0004t0001g0238a0001c0004t0001g0239a0001c0004t0001g0240others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-262+210C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506294 | ||||||
chr1:28506331
|
C | T | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-262+247C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506331 | ||||||
chr1:28506411
|
C | A | 62 | a0001c0001t0001g0030a0001c0002t0001g0001a0001c0002t0001g0002others(59): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-262+327C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506411 | ||||||
chr1:28506411
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-262+327C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506411 | ||||||
chr1:28506519
|
C | T | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-262+435C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506519 | ||||||
chr1:28506558
|
A | G | 29 | a0001c0002t0002g0250a0001c0002t0002g0252a0001c0002t0002g0253others(26): Show | 29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-262+474A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506558 | ||||||
chr1:28506651
|
A | G | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-262+567A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506651 | ||||||
chr1:28506660
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-262+576C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506660 | ||||||
chr1:28506708
|
C | G | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-262+624C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506708 | ||||||
chr1:28506777
|
C | T | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-262+693C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506777 | ||||||
chr1:28506849
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-262+765G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506849 | ||||||
chr1:28506919
|
C | T | 1 | a0001c0003t0002g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-262+835C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506919 | ||||||
chr1:28506924
|
A | G | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-262+840A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506924 | ||||||
chr1:28506926
|
G | T | 37 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(34): Show | 37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-262+842G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506926 | ||||||
chr1:28506982
|
G | A | 112 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0072others(109): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.-262+898G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28506982 | ||||||
chr1:28507004
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-262+920C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507004 | ||||||
chr1:28507024
|
CATTTTT | C | 13 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(10): Show | 13 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-262+949_-262+954d others(8): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507024 | |||||
chr1:28507131
|
G | T | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-261-997G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507131 | ||||||
chr1:28507137
|
T | A | 1 | a0001c0002t0001g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-261-991T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507137 | ||||||
chr1:28507137
|
T | G | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-991T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507137 | ||||||
chr1:28507213
|
G | A | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-915G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507213 | ||||||
chr1:28507253
|
C | T | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-875C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507253 | ||||||
chr1:28507258
|
T | C | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-870T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507258 | ||||||
chr1:28507296
|
T | A | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-261-832T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507296 | ||||||
chr1:28507322
|
T | A | 35 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(32): Show | 35 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.-261-806T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507322 | ||||||
chr1:28507339
|
T | C | 1 | a0001c0002t0001g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-261-789T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507339 | ||||||
chr1:28507538
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-261-590A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507538 | ||||||
chr1:28507600
|
C | CT | 30 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.-261-507dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507600 | |||||
chr1:28507600
|
CT | C | 71 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0072others(68): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-261-507delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507600 | |||||
chr1:28507600
|
CTT | C | 28 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0007g0070others(25): Show | 28 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-261-508_-261-507d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507600 | |||||
chr1:28507600
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0078 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-261-518_-261-507d others(14): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507600 | |||||
chr1:28507612
|
T | C | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261-516T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507612 | ||||||
chr1:28507639
|
G | C | 5 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261-489G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507639 | ||||||
chr1:28507642
|
G | T | 62 | a0001c0001t0001g0030a0001c0002t0001g0001a0001c0002t0001g0002others(59): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-261-486G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507642 | ||||||
chr1:28507816
|
A | G | 37 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(34): Show | 37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-261-312A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507816 | ||||||
chr1:28507886
|
G | A | 2 | a0001c0002t0001g0019a0001c0002t0001g0020 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-261-242G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507886 | ||||||
chr1:28507907
|
G | A | 29 | a0001c0002t0002g0250a0001c0002t0002g0252a0001c0002t0002g0253others(26): Show | 29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-261-221G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507907 | ||||||
chr1:28507971
|
AGCTGGAG others(11): Show |
A | 1 | a0001c0001t0001g0010 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-261-149_-261-132d others(20): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 28507971 | |||||
chr1:28507978
|
G | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0091a0001c0001t0001g0092others(16): Show | 20 | HG00438.hp2 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.-261-150G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507978 | ||||||
chr1:28507989
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-261-139C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28507989 | ||||||
chr1:28508074
|
G | A | 17 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(14): Show | 20 | HG00639.hp1 HG01070.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-261-54G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28508074 | ||||||
chr1:28508085
|
T | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG00280.hp2 HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-261-43T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 1/12 | chr1 | 28508085 | ||||||
chr1:28508287
|
T | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0205 | 2 | HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-229+127T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508287 | ||||||
chr1:28508381
|
TAGTC | T | 29 | a0001c0002t0002g0250a0001c0002t0002g0252a0001c0002t0002g0253others(26): Show | 29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-229+224_-229+227d others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 28508381 | |||||
chr1:28508529
|
G | A | 37 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(34): Show | 37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-228-301G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508529 | ||||||
chr1:28508587
|
T | A | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-228-243T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508587 | ||||||
chr1:28508660
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-228-170G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508660 | ||||||
chr1:28508758
|
CAT | C | 37 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(34): Show | 37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-228-69_-228-68del others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 28508758 | |||||
chr1:28508776
|
T | C | 3 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0057 | 3 | HG01109.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-228-54T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 2/12 | chr1 | 28508776 | ||||||
chr1:28508914
|
AT | A | 34 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(31): Show | 34 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-153+20delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28508914 | |||||
chr1:28508915
|
T | A | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+10T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28508915 | ||||||
chr1:28508984
|
A | C | 1 | a0001c0002t0003g0203 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-153+79A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28508984 | ||||||
chr1:28509098
|
C | T | 13 | a0001c0002t0002g0250a0001c0002t0002g0252a0001c0002t0002g0253others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153+193C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509098 | ||||||
chr1:28509148
|
GT | G | 37 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(34): Show | 37 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-153+248delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28509148 | |||||
chr1:28509298
|
C | T | 2 | a0001c0001t0007g0070a0001c0001t0007g0071 | 2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-153+393C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509298 | ||||||
chr1:28509371
|
AGCTGCGA others(10): Show |
A | 1 | a0001c0003t0002g0276 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-153+468_-153+484d others(19): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28509371 | |||||
chr1:28509386
|
C | T | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-153+481C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509386 | ||||||
chr1:28509466
|
C | T | 1 | a0001c0003t0002g0275 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-153+561C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509466 | ||||||
chr1:28509534
|
C | T | 7 | a0001c0001t0001g0111a0001c0001t0001g0200a0001c0001t0001g0201others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153+629C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509534 | ||||||
chr1:28509543
|
T | C | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+638T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509543 | ||||||
chr1:28509596
|
A | G | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+691A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509596 | ||||||
chr1:28509902
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-153+997G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28509902 | ||||||
chr1:28510215
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-153+1310A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510215 | ||||||
chr1:28510277
|
T | C | 1 | a0001c0001t0004g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-153+1372T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510277 | ||||||
chr1:28510288
|
G | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0081a0001c0001t0001g0112others(1): Show | 5 | HG01069.hp1 HG02572.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153+1383G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510288 | ||||||
chr1:28510317
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-153+1412A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510317 | ||||||
chr1:28510500
|
G | A | 50 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(47): Show | 50 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-153+1595G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510500 | ||||||
chr1:28510585
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-153+1680A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510585 | ||||||
chr1:28510614
|
C | G | 1 | a0001c0001t0001g0107 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-153+1709C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510614 | ||||||
chr1:28510651
|
A | G | 1 | a0001c0002t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-153+1746A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510651 | ||||||
chr1:28510703
|
A | T | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+1798A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510703 | ||||||
chr1:28510895
|
A | G | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-153+1990A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510895 | ||||||
chr1:28510924
|
A | T | 114 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0072others(111): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-153+2019A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510924 | ||||||
chr1:28510931
|
T | C | 19 | a0001c0001t0001g0012a0001c0001t0001g0108a0001c0001t0001g0109others(16): Show | 19 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-153+2026T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28510931 | ||||||
chr1:28511011
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-153+2106C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511011 | ||||||
chr1:28511063
|
T | C | 134 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0069others(131): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-153+2158T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511063 | ||||||
chr1:28511077
|
A | T | 7 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(4): Show | 7 | HG00558.hp2 HG00738.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153+2172A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511077 | ||||||
chr1:28511155
|
A | G | 8 | a0001c0003t0002g0269a0001c0003t0002g0270a0001c0003t0002g0271others(5): Show | 8 | HG02717.hp2 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-153+2250A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511155 | ||||||
chr1:28511205
|
C | A | 1 | a0001c0003t0002g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-153+2300C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511205 | ||||||
chr1:28511368
|
A | G | 155 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0030others(152): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-153+2463A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511368 | ||||||
chr1:28511403
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-153+2498G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511403 | ||||||
chr1:28511403
|
GT | G | 52 | a0001c0001t0001g0030a0001c0001t0007g0071a0001c0002t0001g0001others(49): Show | 60 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.-153+2513delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511403 | |||||
chr1:28511403
|
GTT | G | 45 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.-153+2512_-153+251 others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511403 | |||||
chr1:28511405
|
T | G | 5 | a0001c0001t0007g0071a0001c0002t0002g0281a0001c0003t0002g0245others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-153+2500T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511405 | ||||||
chr1:28511406
|
T | G | 45 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.-153+2501T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511406 | ||||||
chr1:28511408
|
T | G | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153+2503T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511408 | ||||||
chr1:28511429
|
C | CT | 50 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(47): Show | 50 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-153+2525dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511429 | |||||
chr1:28511432
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-153+2527G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511432 | ||||||
chr1:28511439
|
C | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0081a0001c0001t0001g0111others(17): Show | 21 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-153+2534C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511439 | ||||||
chr1:28511521
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-153+2616G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511521 | ||||||
chr1:28511667
|
C | CT | 11 | a0001c0001t0001g0105a0001c0001t0001g0119a0001c0002t0001g0056others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-153+2774dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511667 | |||||
chr1:28511686
|
T | A | 17 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(14): Show | 20 | HG00639.hp1 HG01070.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-153+2781T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511686 | ||||||
chr1:28511686
|
T | G | 97 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0072others(94): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-153+2781T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511686 | ||||||
chr1:28511854
|
G | A | 1 | a0001c0003t0002g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-153+2949G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511854 | ||||||
chr1:28511855
|
G | T | 2 | a0001c0001t0001g0090a0001c0001t0004g0089 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-153+2950G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511855 | ||||||
chr1:28511962
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-153+3057C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511962 | ||||||
chr1:28511974
|
TC | T | 12 | a0001c0001t0001g0072a0001c0001t0002g0262a0001c0002t0002g0279others(9): Show | 12 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-153+3071delC | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511974 | |||||
chr1:28511975
|
CCT | C | 37 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(34): Show | 37 | HG00323.hp1 HG01071.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-153+3071_-153+307 others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28511975 | ||||||
chr1:28511976
|
C | CT | 7 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(4): Show | 7 | HG01175.hp1 HG01981.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153+3091dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511976 | |||||
chr1:28511976
|
CT | C | 141 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(138): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.-153+3091delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28511976 | |||||
chr1:28512035
|
C | T | 8 | a0001c0001t0001g0139a0001c0002t0001g0051a0001c0002t0001g0052others(5): Show | 8 | NA18939.hp2 NA18960.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.-153+3130C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512035 | ||||||
chr1:28512036
|
G | A | 48 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(45): Show | 48 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-153+3131G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512036 | ||||||
chr1:28512129
|
G | A | 9 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0015others(6): Show | 11 | HG01070.hp2 HG01109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-153+3224G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512129 | ||||||
chr1:28512178
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-153+3273C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512178 | ||||||
chr1:28512201
|
A | G | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+3296A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512201 | ||||||
chr1:28512221
|
T | TCCACCCG others(37): Show |
114 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0072others(111): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-153+3321_-153+332 others(48): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28512221 | |||||
chr1:28512282
|
G | A | 48 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(45): Show | 48 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-153+3377G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512282 | ||||||
chr1:28512306
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-153+3401C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512306 | ||||||
chr1:28512419
|
ATGTAAAC others(8): Show |
A | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-153+3516_-153+353 others(19): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28512419 | |||||
chr1:28512915
|
G | C | 109 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0072others(106): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-152-3810G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28512915 | ||||||
chr1:28513169
|
T | C | 9 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0015others(6): Show | 11 | HG01070.hp2 HG01109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-152-3556T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513169 | ||||||
chr1:28513183
|
C | T | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-152-3542C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513183 | ||||||
chr1:28513239
|
G | T | 29 | a0001c0002t0002g0250a0001c0002t0002g0252a0001c0002t0002g0253others(26): Show | 29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-152-3486G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513239 | ||||||
chr1:28513595
|
T | A | 1 | a0001c0002t0003g0058 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-152-3130T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513595 | ||||||
chr1:28513983
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-152-2742A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513983 | ||||||
chr1:28513989
|
C | T | 156 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0030others(153): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-152-2736C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28513989 | ||||||
chr1:28514060
|
T | G | 64 | a0001c0001t0001g0030a0001c0002t0001g0001a0001c0002t0001g0002others(61): Show | 74 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.-152-2665T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514060 | ||||||
chr1:28514156
|
C | CA | 6 | a0001c0001t0001g0079a0001c0001t0001g0121a0001c0002t0001g0051others(3): Show | 6 | HG01109.hp2 HG02074.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.-152-2557dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514156 | |||||
chr1:28514171
|
C | T | 2 | a0001c0002t0001g0041a0001c0002t0001g0042 | 2 | HG01106.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-152-2554C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514171 | ||||||
chr1:28514195
|
T | A | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-152-2530T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514195 | ||||||
chr1:28514233
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-152-2492G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514233 | ||||||
chr1:28514302
|
T | G | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-152-2423T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514302 | ||||||
chr1:28514306
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-152-2419C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514306 | ||||||
chr1:28514385
|
G | C | 1 | a0001c0001t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-152-2340G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514385 | ||||||
chr1:28514405
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-152-2320G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514405 | ||||||
chr1:28514428
|
C | T | 29 | a0001c0002t0002g0250a0001c0002t0002g0252a0001c0002t0002g0253others(26): Show | 29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-152-2297C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514428 | ||||||
chr1:28514449
|
C | CA | 67 | a0001c0001t0001g0030a0001c0001t0001g0105a0001c0001t0001g0230others(64): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-152-2266dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514449 | |||||
chr1:28514449
|
CA | C | 29 | a0001c0002t0002g0250a0001c0002t0002g0252a0001c0002t0002g0253others(26): Show | 29 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-152-2266delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514449 | |||||
chr1:28514460
|
C | A | 2 | a0001c0002t0001g0059a0001c0002t0001g0067 | 2 | HG02300.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-152-2265C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514460 | ||||||
chr1:28514487
|
T | TGTG | 6 | a0001c0001t0004g0208a0001c0001t0004g0216a0001c0001t0004g0217others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-152-2233_-152-223 others(7): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514487 | |||||
chr1:28514704
|
T | C | 1 | a0001c0003t0002g0270 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-152-2021T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514704 | ||||||
chr1:28514732
|
G | T | 7 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053others(4): Show | 7 | NA18939.hp2 NA18960.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-152-1993G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514732 | ||||||
chr1:28514744
|
A | G | 1 | a0001c0002t0001g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-152-1981A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514744 | ||||||
chr1:28514851
|
G | A | 1 | a0001c0005t0002g0277 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-152-1874G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514851 | ||||||
chr1:28514856
|
C | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0182 | 2 | HG02080.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-152-1869C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514856 | ||||||
chr1:28514862
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-152-1863G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514862 | ||||||
chr1:28514870
|
G | A | 1 | a0001c0001t0006g0234 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-152-1855G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28514870 | ||||||
chr1:28514878
|
AAAAT | A | 5 | a0001c0002t0001g0013a0001c0003t0002g0245a0001c0003t0002g0246others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-152-1837_-152-183 others(8): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28514878 | |||||
chr1:28515005
|
C | G | 1 | a0001c0002t0001g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-152-1720C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515005 | ||||||
chr1:28515114
|
CCAAAAAT others(1): Show |
C | 5 | a0001c0004t0001g0238a0001c0004t0001g0239a0001c0004t0001g0240others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-152-1603_-152-159 others(12): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28515114 | |||||
chr1:28515213
|
C | T | 3 | a0001c0002t0005g0018a0001c0002t0005g0040a0001c0002t0005g0065 | 3 | HG01099.hp2 HG02273.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-152-1512C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515213 | ||||||
chr1:28515246
|
C | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0081a0001c0001t0001g0112others(14): Show | 18 | HG00639.hp2 HG01069.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.-152-1479C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515246 | ||||||
chr1:28515521
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-152-1204G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515521 | ||||||
chr1:28515574
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-152-1151G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515574 | ||||||
chr1:28515697
|
A | G | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-152-1028A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515697 | ||||||
chr1:28515828
|
C | T | 67 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(64): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-152-897C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515828 | ||||||
chr1:28515876
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-152-849G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28515876 | ||||||
chr1:28516127
|
G | A | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-152-598G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28516127 | ||||||
chr1:28516137
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-152-588C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28516137 | ||||||
chr1:28516239
|
C | T | 1 | a0001c0003t0002g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-152-486C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | chr1 | 28516239 | ||||||
chr1:28516501
|
CA | C | 100 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0069others(97): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-152-207delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28516501 | |||||
chr1:28516501
|
CAA | C | 32 | a0001c0001t0001g0213a0001c0002t0001g0021a0001c0002t0001g0022others(29): Show | 32 | HG00323.hp1 HG00323.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-152-208_-152-207d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28516501 | |||||
chr1:28516678
|
CA | C | 7 | a0001c0001t0004g0089a0001c0001t0004g0208a0001c0001t0004g0214others(4): Show | 7 | HG00639.hp2 HG02280.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-152-43delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 28516678 | |||||
chr1:28517111
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-10+244G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517111 | ||||||
chr1:28517121
|
C | CA | 6 | a0001c0001t0001g0092a0001c0002t0001g0025a0001c0002t0002g0250others(3): Show | 6 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+267dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28517121 | |||||
chr1:28517128
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-10+261A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517128 | ||||||
chr1:28517198
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-10+331A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517198 | ||||||
chr1:28517249
|
T | C | 7 | a0001c0001t0004g0089a0001c0001t0004g0208a0001c0001t0004g0214others(4): Show | 7 | HG00639.hp2 HG02280.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+382T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517249 | ||||||
chr1:28517369
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-10+502C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517369 | ||||||
chr1:28517543
|
CTTG | C | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+679_-10+681del others(3): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28517543 | |||||
chr1:28517584
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-10+717C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517584 | ||||||
chr1:28517763
|
TG | T | 6 | a0001c0003t0002g0247a0001c0003t0002g0248a0001c0003t0002g0249others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+898delG | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28517763 | |||||
chr1:28517807
|
C | T | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-10+940C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517807 | ||||||
chr1:28517981
|
C | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA19010.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-10+1114C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28517981 | ||||||
chr1:28518080
|
C | G | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-10+1213C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518080 | ||||||
chr1:28518100
|
T | TGGCCAAG others(14): Show |
2 | a0001c0002t0003g0033a0001c0002t0003g0060 | 2 | HG01123.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-10+1257_-10+1277d others(23): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28518100 | |||||
chr1:28518100
|
TGGCCAAG others(14): Show |
T | 4 | a0001c0001t0001g0008a0001c0001t0001g0081a0001c0001t0001g0112others(1): Show | 5 | HG01069.hp1 HG02572.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+1257_-10+1277d others(23): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28518100 | |||||
chr1:28518111
|
TCCCCCAG others(21): Show |
T | 1 | a0001c0001t0004g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-10+1248_-10+1275d others(30): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28518111 | |||||
chr1:28518192
|
C | T | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0226others(1): Show | 4 | NA19054.hp1 NA19078.hp2 NA19089.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+1325C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518192 | ||||||
chr1:28518259
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-10+1392C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518259 | ||||||
chr1:28518413
|
C | T | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10+1546C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518413 | ||||||
chr1:28518499
|
GGGGCGCT others(12): Show |
G | 5 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+1640_-10+1658d others(21): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28518499 | |||||
chr1:28518512
|
A | G | 274 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(271): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-10+1645A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518512 | ||||||
chr1:28518525
|
T | C | 120 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(117): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-10+1658T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518525 | ||||||
chr1:28518583
|
C | G | 1 | a0001c0002t0002g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10+1716C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518583 | ||||||
chr1:28518723
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-10+1856G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518723 | ||||||
chr1:28518821
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-10+1954C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518821 | ||||||
chr1:28518914
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10+2047C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518914 | ||||||
chr1:28518937
|
C | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0143 | 2 | HG00673.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-10+2070C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28518937 | ||||||
chr1:28519204
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-10+2337A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519204 | ||||||
chr1:28519301
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-10+2434C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519301 | ||||||
chr1:28519463
|
T | C | 1 | a0001c0002t0001g0052 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-10+2596T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519463 | ||||||
chr1:28519464
|
C | T | 98 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(95): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-10+2597C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519464 | ||||||
chr1:28519551
|
G | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0173a0001c0001t0001g0225others(1): Show | 4 | HG02074.hp1 NA18964.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+2684G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519551 | ||||||
chr1:28519570
|
A | AT | 18 | a0001c0001t0001g0008a0001c0001t0001g0069a0001c0001t0001g0074others(15): Show | 19 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+2716dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28519570 | |||||
chr1:28519598
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-10+2731A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519598 | ||||||
chr1:28519751
|
T | C | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-10+2884T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519751 | ||||||
chr1:28519931
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-10+3064G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28519931 | ||||||
chr1:28520115
|
C | G | 5 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0015others(2): Show | 7 | HG01070.hp2 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+3248C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520115 | ||||||
chr1:28520128
|
A | G | 1 | a0001c0002t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-10+3261A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520128 | ||||||
chr1:28520382
|
G | A | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10+3515G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520382 | ||||||
chr1:28520400
|
G | A | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+3533G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520400 | ||||||
chr1:28520478
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-10+3611T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520478 | ||||||
chr1:28520594
|
G | A | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+3727G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520594 | ||||||
chr1:28520637
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-10+3770G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520637 | ||||||
chr1:28520701
|
G | A | 1 | a0001c0002t0001g0061 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-10+3834G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520701 | ||||||
chr1:28520763
|
C | T | 14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+3896C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520763 | ||||||
chr1:28520800
|
G | A | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10+3933G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520800 | ||||||
chr1:28520989
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-10+4122G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28520989 | ||||||
chr1:28521018
|
G | A | 71 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(68): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-10+4151G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521018 | ||||||
chr1:28521318
|
G | C | 1 | a0001c0001t0011g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-10+4451G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521318 | ||||||
chr1:28521393
|
C | G | 1 | a0001c0002t0010g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-10+4526C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521393 | ||||||
chr1:28521452
|
T | G | 14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+4585T>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521452 | ||||||
chr1:28521499
|
C | CA | 20 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG01109.hp1 HG01243.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+4633dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28521499 | |||||
chr1:28521499
|
C | CAA | 6 | a0001c0001t0002g0258a0001c0002t0002g0281a0001c0004t0001g0238others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+4633_-10+4634i others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28521499 | |||||
chr1:28521499
|
CAGAAAAA others(4): Show |
C | 72 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(69): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.-10+4634_-10+4644d others(13): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28521499 | |||||
chr1:28521501
|
G | A | 48 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(45): Show | 48 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10+4634G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521501 | ||||||
chr1:28521501
|
G | GA | 20 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0078others(17): Show | 20 | HG00673.hp1 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10+4656dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28521501 | |||||
chr1:28521618
|
C | A | 1 | a0001c0001t0001g0145 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-10+4751C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521618 | ||||||
chr1:28521857
|
C | A | 2 | a0001c0002t0001g0003a0001c0002t0001g0023 | 3 | HG03041.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-10+4990C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28521857 | ||||||
chr1:28522076
|
G | T | 71 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(68): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-10+5209G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28522076 | ||||||
chr1:28522763
|
C | T | 14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+5896C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28522763 | ||||||
chr1:28522804
|
A | G | 137 | a0001c0001t0001g0008a0001c0001t0001g0069a0001c0001t0001g0072others(134): Show | 148 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-10+5937A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28522804 | ||||||
chr1:28523027
|
C | CT | 75 | a0001c0001t0001g0010a0001c0001t0001g0069a0001c0001t0001g0072others(72): Show | 86 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-10+6182dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28523027 | |||||
chr1:28523027
|
C | CTT | 12 | a0001c0001t0001g0171a0001c0001t0007g0071a0001c0002t0001g0017others(9): Show | 12 | HG01175.hp2 HG02080.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10+6181_-10+6182d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28523027 | |||||
chr1:28523027
|
CT | C | 11 | a0001c0001t0001g0115a0001c0001t0001g0136a0001c0001t0001g0148others(8): Show | 11 | HG01257.hp2 HG01358.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+6182delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28523027 | |||||
chr1:28523033
|
T | C | 10 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0264others(7): Show | 10 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+6166T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523033 | ||||||
chr1:28523034
|
T | C | 1 | a0001c0003t0002g0263 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10+6167T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523034 | ||||||
chr1:28523116
|
C | T | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+6249C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523116 | ||||||
chr1:28523255
|
A | T | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10+6388A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523255 | ||||||
chr1:28523473
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-9-6385G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523473 | ||||||
chr1:28523615
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9-6243G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523615 | ||||||
chr1:28523972
|
C | T | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9-5886C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28523972 | ||||||
chr1:28524495
|
G | C | 2 | a0001c0001t0004g0089a0001c0001t0004g0214 | 2 | HG00639.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9-5363G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524495 | ||||||
chr1:28524533
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-9-5325G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524533 | ||||||
chr1:28524551
|
C | T | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-9-5307C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524551 | ||||||
chr1:28524617
|
G | T | 1 | a0001c0002t0003g0058 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-9-5241G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524617 | ||||||
chr1:28524626
|
G | C | 2 | a0001c0003t0002g0263a0001c0003t0002g0265 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-9-5232G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524626 | ||||||
chr1:28524801
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-9-5057C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524801 | ||||||
chr1:28524968
|
C | G | 280 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(277): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-9-4890C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28524968 | ||||||
chr1:28525040
|
C | A | 5 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4818C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525040 | ||||||
chr1:28525103
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-9-4755C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525103 | ||||||
chr1:28525147
|
T | C | 26 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(23): Show | 26 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-9-4711T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525147 | ||||||
chr1:28525150
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-9-4708A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525150 | ||||||
chr1:28525261
|
C | G | 11 | a0001c0001t0001g0111a0001c0001t0001g0202a0001c0001t0001g0205others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-4597C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525261 | ||||||
chr1:28525588
|
G | A | 1 | a0001c0002t0003g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-9-4270G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525588 | ||||||
chr1:28525680
|
A | C | 1 | a0001c0002t0002g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-9-4178A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525680 | ||||||
chr1:28525726
|
T | C | 5 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4132T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28525726 | ||||||
chr1:28526233
|
C | G | 1 | a0001c0002t0001g0056 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-9-3625C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526233 | ||||||
chr1:28526234
|
G | C | 1 | a0001c0002t0001g0056 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-9-3624G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526234 | ||||||
chr1:28526290
|
AAAAC | A | 3 | a0001c0001t0001g0094a0001c0002t0002g0279a0001c0002t0002g0280 | 3 | HG01891.hp2 HG02055.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-9-3548_-9-3545del others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28526290 | |||||
chr1:28526335
|
T | C | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-9-3523T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526335 | ||||||
chr1:28526393
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-3465C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526393 | ||||||
chr1:28526492
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-9-3366G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526492 | ||||||
chr1:28526757
|
G | A | 2 | a0001c0003t0001g0215a0001c0003t0002g0276 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-9-3101G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526757 | ||||||
chr1:28526828
|
G | C | 119 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(116): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-9-3030G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526828 | ||||||
chr1:28526864
|
T | C | 71 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(68): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-9-2994T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526864 | ||||||
chr1:28526898
|
G | A | 1 | a0001c0002t0001g0056 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-9-2960G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526898 | ||||||
chr1:28526898
|
G | GA | 7 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0103others(4): Show | 7 | HG00438.hp2 HG02559.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-2945dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28526898 | |||||
chr1:28526899
|
A | G | 1 | a0001c0002t0001g0056 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-9-2959A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28526899 | ||||||
chr1:28527033
|
G | C | 3 | a0001c0001t0002g0259a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG01255.hp1 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-9-2825G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527033 | ||||||
chr1:28527069
|
G | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0092a0001c0001t0001g0095others(5): Show | 9 | HG00438.hp2 HG00558.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-2789G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527069 | ||||||
chr1:28527186
|
G | A | 1 | a0001c0002t0003g0034 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9-2672G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527186 | ||||||
chr1:28527266
|
G | A | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9-2592G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527266 | ||||||
chr1:28527347
|
C | G | 71 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(68): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-9-2511C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527347 | ||||||
chr1:28527353
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-9-2505C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527353 | ||||||
chr1:28527401
|
G | A | 1 | a0001c0003t0002g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-9-2457G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527401 | ||||||
chr1:28527712
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-9-2146A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527712 | ||||||
chr1:28527816
|
C | T | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9-2042C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527816 | ||||||
chr1:28527866
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-9-1992G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527866 | ||||||
chr1:28527910
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-9-1948G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28527910 | ||||||
chr1:28528009
|
C | CA | 49 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(46): Show | 49 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-9-1830dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528009 | |||||
chr1:28528009
|
CA | C | 69 | a0001c0001t0001g0136a0001c0001t0001g0169a0001c0002t0001g0001others(66): Show | 78 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.-9-1830delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528009 | |||||
chr1:28528119
|
G | A | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-9-1739G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528119 | ||||||
chr1:28528136
|
A | G | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-9-1722A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528136 | ||||||
chr1:28528194
|
G | A | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9-1664G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528194 | ||||||
chr1:28528248
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-9-1610G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528248 | ||||||
chr1:28528325
|
G | A | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1533G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528325 | ||||||
chr1:28528344
|
T | A | 39 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(36): Show | 45 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.-9-1514T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528344 | ||||||
chr1:28528391
|
G | A | 1 | a0001c0003t0002g0264 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-9-1467G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528391 | ||||||
chr1:28528450
|
A | G | 74 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(71): Show | 84 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-9-1408A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528450 | ||||||
chr1:28528592
|
C | T | 1 | a0001c0002t0001g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9-1266C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528592 | ||||||
chr1:28528691
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-9-1167C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528691 | ||||||
chr1:28528796
|
A | AT | 9 | a0001c0002t0003g0006a0001c0002t0003g0033a0001c0002t0003g0034others(6): Show | 10 | HG00280.hp1 HG01123.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-1054dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528796 | |||||
chr1:28528804
|
T | TTC | 18 | a0001c0001t0001g0078a0001c0003t0002g0245a0001c0003t0002g0246others(15): Show | 18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9-1054_-9-1053ins others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528804 | ||||||
chr1:28528805
|
C | T | 10 | a0001c0002t0001g0077a0001c0003t0001g0180a0001c0003t0001g0215others(7): Show | 10 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-1053C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528805 | ||||||
chr1:28528806
|
C | A | 18 | a0001c0001t0001g0078a0001c0003t0002g0245a0001c0003t0002g0246others(15): Show | 18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9-1052C>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528806 | ||||||
chr1:28528806
|
C | CA | 14 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-1038dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528806 | |||||
chr1:28528806
|
C | CAA | 7 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(4): Show | 7 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-1039_-9-1038dup others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528806 | |||||
chr1:28528806
|
C | CCAA | 9 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0263others(6): Show | 9 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-1052_-9-1051ins others(3): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528806 | ||||||
chr1:28528806
|
CA | C | 60 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(57): Show | 69 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.-9-1038delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528806 | |||||
chr1:28528807
|
A | C | 1 | a0001c0002t0001g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-9-1051A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528807 | ||||||
chr1:28528820
|
A | T | 1 | a0001c0001t0001g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-9-1038A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528820 | ||||||
chr1:28528844
|
C | CT | 100 | a0001c0001t0001g0008a0001c0001t0001g0069a0001c0001t0001g0073others(97): Show | 111 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(108): Show |
intron_variant | MODIFIER | c.-9-994dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528844 | |||||
chr1:28528844
|
C | CTT | 11 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0007g0219others(8): Show | 11 | HG01175.hp1 HG01884.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9-995_-9-994dupTT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528844 | |||||
chr1:28528844
|
CT | C | 11 | a0001c0003t0001g0180a0001c0003t0002g0247a0001c0003t0002g0254others(8): Show | 11 | HG01516.hp2 HG02055.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-994delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28528844 | |||||
chr1:28528870
|
G | C | 74 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(71): Show | 84 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-9-988G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528870 | ||||||
chr1:28528940
|
G | T | 9 | a0001c0001t0001g0072a0001c0001t0007g0070a0001c0001t0007g0071others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9-918G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528940 | ||||||
chr1:28528957
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-9-901G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28528957 | ||||||
chr1:28529037
|
A | AT | 39 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0074others(36): Show | 39 | HG00735.hp1 HG01106.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.-9-804dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529037 | |||||
chr1:28529037
|
AT | A | 16 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(13): Show | 16 | HG01255.hp1 HG02451.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-804delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529037 | |||||
chr1:28529039
|
T | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0105 | 2 | NA19060.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-9-819T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28529039 | ||||||
chr1:28529163
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-695G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28529163 | ||||||
chr1:28529182
|
C | CT | 59 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(56): Show | 59 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.-9-655dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529182 | |||||
chr1:28529182
|
C | CTT | 63 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0111others(60): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-9-656_-9-655dupTT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529182 | |||||
chr1:28529182
|
C | CTTT | 15 | a0001c0002t0001g0017a0001c0002t0001g0031a0001c0002t0001g0032others(12): Show | 15 | HG02148.hp1 HG02257.hp2 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-657_-9-655dupTT others(1): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529182 | |||||
chr1:28529373
|
G | A | 2 | a0001c0003t0001g0215a0001c0003t0002g0276 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-9-485G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | chr1 | 28529373 | ||||||
chr1:28529697
|
CTG | C | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9-158_-9-157delTG | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 28529697 | |||||
chr1:28530157
|
C | CA | 14 | a0001c0001t0001g0093a0001c0001t0001g0134a0001c0001t0001g0171others(11): Show | 14 | HG00558.hp2 HG00738.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.73+237dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28530157 | |||||
chr1:28530157
|
CA | C | 54 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0069others(51): Show | 55 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.73+237delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28530157 | |||||
chr1:28530157
|
CAA | C | 72 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(69): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.73+236_73+237delAA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28530157 | |||||
chr1:28530161
|
A | C | 71 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(68): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.73+222A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530161 | ||||||
chr1:28530163
|
A | C | 71 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(68): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.73+224A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530163 | ||||||
chr1:28530165
|
A | C | 71 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(68): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.73+226A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530165 | ||||||
chr1:28530167
|
A | C | 48 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(45): Show | 55 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.73+228A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530167 | ||||||
chr1:28530404
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.73+465G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530404 | ||||||
chr1:28530624
|
G | A | 1 | a0001c0002t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.73+685G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530624 | ||||||
chr1:28530630
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73+691G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530630 | ||||||
chr1:28530635
|
G | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0165 | 3 | NA18995.hp1 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.73+696G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530635 | ||||||
chr1:28530786
|
C | T | 2 | a0001c0003t0001g0215a0001c0003t0002g0276 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.73+847C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530786 | ||||||
chr1:28530824
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.73+885G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530824 | ||||||
chr1:28530839
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.73+900C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530839 | ||||||
chr1:28530840
|
G | A | 1 | a0001c0003t0002g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.73+901G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530840 | ||||||
chr1:28530884
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.74-919G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28530884 | ||||||
chr1:28531144
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0227 | 2 | HG00597.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.74-659G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531144 | ||||||
chr1:28531154
|
G | A | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.74-649G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531154 | ||||||
chr1:28531160
|
C | T | 2 | a0001c0003t0001g0215a0001c0003t0002g0276 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.74-643C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531160 | ||||||
chr1:28531234
|
C | T | 7 | a0001c0003t0001g0180a0001c0003t0002g0263a0001c0003t0002g0264others(4): Show | 7 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-569C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531234 | ||||||
chr1:28531259
|
C | CT | 9 | a0001c0001t0001g0069a0001c0002t0002g0280a0001c0003t0002g0247others(6): Show | 9 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.74-539dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28531259 | |||||
chr1:28531259
|
C | CTT | 3 | a0001c0002t0001g0019a0001c0002t0002g0279a0001c0003t0002g0268 | 3 | HG01516.hp1 HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.74-540_74-539dupTT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28531259 | |||||
chr1:28531259
|
C | CTTT | 45 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(42): Show | 52 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.74-541_74-539dupTT others(1): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28531259 | |||||
chr1:28531259
|
C | CTTTT | 14 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0026others(11): Show | 15 | HG00741.hp1 HG01106.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.74-542_74-539dupTT others(2): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 28531259 | |||||
chr1:28531264
|
TC | T | 14 | a0001c0001t0001g0072a0001c0001t0007g0070a0001c0001t0007g0219others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.74-538delC | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531264 | ||||||
chr1:28531265
|
C | T | 107 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(104): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.74-538C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531265 | ||||||
chr1:28531270
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.74-533T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531270 | ||||||
chr1:28531361
|
G | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.74-442G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531361 | ||||||
chr1:28531457
|
C | G | 72 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(69): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.74-346C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531457 | ||||||
chr1:28531631
|
G | A | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.74-172G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531631 | ||||||
chr1:28531632
|
AGAGGTAC others(3): Show |
A | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.74-170_74-161delGA others(8): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 5/12 | chr1 | 28531632 | ||||||
chr1:28532796
|
T | TTTG | 3 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | HG02970.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.441+467_441+469dup others(3): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28532796 | |||||
chr1:28532796
|
TTTG | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0172a0001c0001t0001g0205 | 3 | HG02572.hp1 HG02723.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.441+467_441+469del others(3): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28532796 | |||||
chr1:28532926
|
C | T | 1 | a0001c0003t0002g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.441+576C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28532926 | ||||||
chr1:28532958
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.441+608G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28532958 | ||||||
chr1:28533078
|
T | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0202a0001c0001t0001g0205others(1): Show | 4 | HG00735.hp1 HG00741.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+728T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533078 | ||||||
chr1:28533196
|
G | T | 1 | a0001c0003t0002g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.441+846G>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533196 | ||||||
chr1:28533197
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0233 | 2 | HG03927.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.441+847C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533197 | ||||||
chr1:28533254
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0202a0001c0001t0001g0205others(1): Show | 4 | HG00735.hp1 HG00741.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+904G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533254 | ||||||
chr1:28533276
|
A | C | 2 | a0001c0002t0002g0279a0001c0002t0002g0280 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.441+926A>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533276 | ||||||
chr1:28533399
|
A | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG02970.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+1049A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533399 | ||||||
chr1:28533427
|
C | T | 8 | a0001c0003t0001g0180a0001c0003t0002g0263a0001c0003t0002g0264others(5): Show | 8 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+1077C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533427 | ||||||
chr1:28533428
|
G | A | 2 | a0001c0001t0001g0148a0001c0002t0001g0243 | 2 | HG00639.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.441+1078G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533428 | ||||||
chr1:28533447
|
G | C | 3 | a0001c0003t0001g0215a0001c0003t0002g0269a0001c0003t0002g0276 | 3 | HG02809.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.441+1097G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533447 | ||||||
chr1:28533702
|
G | A | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-1348G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533702 | ||||||
chr1:28533718
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.442-1332C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533718 | ||||||
chr1:28533719
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.442-1331G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533719 | ||||||
chr1:28533758
|
G | A | 1 | a0001c0003t0002g0275 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.442-1292G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533758 | ||||||
chr1:28533770
|
C | CA | 33 | a0001c0001t0001g0008a0001c0001t0001g0081a0001c0001t0001g0091others(30): Show | 34 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.442-1255dupA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | |||||
chr1:28533770
|
CA | C | 30 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0187others(27): Show | 30 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.442-1255delA | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | |||||
chr1:28533770
|
CAA | C | 9 | a0001c0002t0001g0029a0001c0002t0001g0047a0001c0002t0001g0052others(6): Show | 9 | HG00639.hp1 HG00741.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-1256_442-1255d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | |||||
chr1:28533770
|
CAAA | C | 73 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(70): Show | 83 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.442-1257_442-1255d others(5): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | |||||
chr1:28533770
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0012g0251 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.442-1264_442-1255d others(12): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533770 | |||||
chr1:28533771
|
A | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0182 | 2 | HG02080.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.442-1279A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533771 | ||||||
chr1:28533840
|
CTTTTCTT others(24): Show |
C | 2 | a0001c0001t0001g0075a0001c0001t0001g0196 | 2 | HG03471.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.442-1205_442-1175d others(33): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533840 | |||||
chr1:28533840
|
CTTTTCTT others(25): Show |
C | 4 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG02970.hp1 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-1205_442-1174d others(34): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533840 | |||||
chr1:28533840
|
CTTTTCTT others(26): Show |
C | 5 | a0001c0004t0001g0238a0001c0004t0001g0239a0001c0004t0001g0240others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-1205_442-1173d others(35): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533840 | |||||
chr1:28533840
|
CTTTTCTT others(27): Show |
C | 4 | a0001c0001t0001g0072a0001c0001t0007g0070a0001c0001t0007g0071others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1205_442-1172d others(36): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533840 | |||||
chr1:28533845
|
C | CT | 8 | a0001c0001t0001g0171a0001c0001t0001g0188a0001c0001t0001g0205others(5): Show | 8 | HG00140.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-1155dupT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
C | CTT | 7 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0087others(4): Show | 7 | HG02280.hp2 HG02559.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1156_442-1155d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
C | CTTTT | 7 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0155others(4): Show | 7 | HG00438.hp1 HG00735.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1158_442-1155d others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0133 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.442-1165_442-1155d others(13): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.442-1167_442-1155d others(15): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.442-1205C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533845 | ||||||
chr1:28533845
|
CT | C | 16 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0121others(13): Show | 16 | HG00738.hp2 HG01167.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1155delT | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTT | C | 10 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0001g0110others(7): Show | 10 | HG00099.hp1 HG00099.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-1156_442-1155d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTT | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0104others(9): Show | 12 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-1157_442-1155d others(5): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTT | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0113a0001c0001t0001g0125others(5): Show | 8 | HG00558.hp2 HG00639.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-1158_442-1155d others(6): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTT | C | 6 | a0001c0001t0001g0081a0001c0001t0001g0112a0001c0001t0001g0144others(3): Show | 6 | HG02572.hp1 HG02572.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1159_442-1155d others(7): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0132a0001c0001t0001g0199 | 2 | HG04199.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.442-1164_442-1155d others(12): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0176a0001c0001t0001g0184 | 2 | HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.442-1165_442-1155d others(13): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0161a0001c0001t0001g0207 | 2 | HG01081.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.442-1167_442-1155d others(15): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0206 | 3 | HG01258.hp1 HG03491.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.442-1168_442-1155d others(16): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0149others(2): Show | 5 | HG00673.hp1 HG01081.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1169_442-1155d others(17): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0096a0001c0001t0001g0151a0001c0001t0001g0162others(1): Show | 4 | HG03491.hp2 NA18959.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1170_442-1155d others(18): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0103 | 3 | HG00438.hp2 HG02165.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.442-1171_442-1155d others(19): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(11): Show |
C | 4 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0128others(1): Show | 5 | HG00558.hp1 HG02155.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1172_442-1155d others(20): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0094a0001c0001t0001g0127 | 2 | NA18612.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.442-1173_442-1155d others(21): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(13): Show |
C | 7 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0156others(4): Show | 7 | HG03831.hp2 NA18939.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-1174_442-1155d others(22): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(15): Show |
C | 6 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0002g0254others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1176_442-1155d others(24): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(16): Show |
C | 8 | a0001c0003t0002g0248a0001c0003t0002g0255a0001c0003t0002g0257others(5): Show | 8 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-1177_442-1155d others(25): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(17): Show |
C | 14 | a0001c0001t0001g0120a0001c0003t0001g0180a0001c0003t0001g0215others(11): Show | 14 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-1178_442-1155d others(26): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(18): Show |
C | 3 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0198 | 3 | HG04204.hp1 NA18947.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.442-1179_442-1155d others(27): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(19): Show |
C | 2 | a0001c0001t0001g0124a0001c0001t0001g0221 | 2 | HG01106.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.442-1180_442-1155d others(28): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(20): Show |
C | 2 | a0001c0001t0001g0182a0001c0002t0002g0281 | 2 | HG02080.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.442-1181_442-1155d others(29): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(21): Show |
C | 3 | a0001c0001t0001g0101a0001c0001t0004g0208a0001c0001t0004g0217 | 3 | HG02280.hp1 HG02300.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.442-1182_442-1155d others(30): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(25): Show |
C | 7 | a0001c0001t0004g0220a0001c0002t0001g0017a0001c0002t0001g0021others(4): Show | 7 | HG01109.hp2 HG02717.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1186_442-1155d others(34): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(26): Show |
C | 70 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(67): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.442-1187_442-1155d others(35): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533845
|
CTTTTTTT others(27): Show |
C | 1 | a0001c0002t0001g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.442-1188_442-1155d others(36): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533845 | |||||
chr1:28533850
|
T | C | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.442-1200T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533850 | ||||||
chr1:28533874
|
T | C | 1 | a0001c0003t0002g0275 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.442-1176T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28533874 | ||||||
chr1:28533900
|
CAG | C | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-1147_442-1146d others(4): Show |
RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 28533900 | |||||
chr1:28534066
|
C | T | 1 | a0001c0002t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.442-984C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534066 | ||||||
chr1:28534201
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.442-849G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534201 | ||||||
chr1:28534243
|
C | T | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-807C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534243 | ||||||
chr1:28534295
|
C | G | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-755C>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534295 | ||||||
chr1:28534342
|
G | A | 46 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(43): Show | 46 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-708G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534342 | ||||||
chr1:28534422
|
C | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0069a0001c0001t0001g0072others(31): Show | 35 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.442-628C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534422 | ||||||
chr1:28534475
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.442-575C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28534475 | ||||||
chr1:28535004
|
G | A | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-46G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 7/12 | chr1 | 28535004 | ||||||
chr1:28535681
|
G | A | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.662-190G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 9/12 | chr1 | 28535681 | ||||||
chr1:28536089
|
A | G | 5 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+63A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 10/12 | chr1 | 28536089 | ||||||
chr1:28536248
|
G | A | 1 | a0001c0002t0001g0052 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.818-14G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 10/12 | chr1 | 28536248 | ||||||
chr1:28536563
|
A | G | 74 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(71): Show | 84 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.937+182A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 11/12 | chr1 | 28536563 | ||||||
chr1:28536997
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1090+98C>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28536997 | ||||||
chr1:28537024
|
G | A | 7 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0097others(4): Show | 7 | HG01261.hp2 HG01433.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1090+125G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537024 | ||||||
chr1:28537136
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1090+237G>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537136 | ||||||
chr1:28537305
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1090+406T>C | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537305 | ||||||
chr1:28537318
|
A | G | 15 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1090+419A>G | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537318 | ||||||
chr1:28537535
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1091-297A>T | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537535 | ||||||
chr1:28537608
|
G | A | 72 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(69): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1091-224G>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537608 | ||||||
chr1:28537651
|
T | A | 27 | a0001c0003t0001g0180a0001c0003t0001g0215a0001c0003t0002g0245others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1091-181T>A | RCC1 | ENSG00000180198.17 | transcript | ENST00000683442.1 | protein_coding | 12/12 | chr1 | 28537651 |