geneid | 55920 |
---|---|
ensemblid | ENSG00000179051.14 |
hgncid | 30297 |
symbol | RCC2 |
name | regulator of chromosome condensation 2 |
refseq_nuc | NM_018715.4 |
refseq_prot | NP_061185.1 |
ensembl_nuc | ENST00000375436.9 |
ensembl_prot | ENSP00000364585.4 |
mane_status | MANE Select |
chr | chr1 |
start | 17406760 |
end | 17439677 |
strand | - |
ver | v1.2 |
region | chr1:17406760-17439677 |
region5000 | chr1:17401760-17444677 |
regionname0 | RCC2_chr1_17406760_17439677 |
regionname5000 | RCC2_chr1_17401760_17444677 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 522 | 376 | 86 | 73 | 158 | 12 | 45 | 124 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0002 | 0/0 | 522 | 11 | 8 | 3 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0003 | 0/0 | 522 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0004 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0005 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1569 | 261 | 52 | 40 | 131 | 8 | 28 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0002 | 0/0 | 1569 | 108 | 31 | 32 | 25 | 4 | 16 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0003 | 0/0 | 1569 | 10 | 7 | 3 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0004 | 0/0 | 1569 | 3 | 3 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0005 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0006 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0007 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0008 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0009 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0010 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0011 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
c0012 | 0/0 | 1569 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2472 | 128 | 25 | 22 | 61 | 4 | 14 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0002 | 0/0 | 2469 | 84 | 25 | 22 | 24 | 3 | 10 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0003 | 0/0 | 2469 | 56 | 2 | 0 | 49 | 1 | 4 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0004 | 0/0 | 2469 | 47 | 12 | 11 | 14 | 2 | 8 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0005 | 0/0 | 2469 | 15 | 3 | 7 | 0 | 0 | 5 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0006 | 0/0 | 2470 | 8 | 6 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0007 | 0/0 | 2466 | 7 | 2 | 1 | 4 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0008 | 0/0 | 2469 | 6 | 6 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0009 | 0/0 | 2473 | 5 | 3 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0010 | 0/0 | 2468 | 3 | 0 | 1 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0011 | 0/0 | 2469 | 3 | 0 | 2 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0012 | 0/0 | 2468 | 2 | 1 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0013 | 0/0 | 2468 | 2 | 1 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0014 | 0/0 | 2469 | 2 | 0 | 0 | 0 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0015 | 0/0 | 2470 | 2 | 1 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0016 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0017 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0018 | 0/0 | 2471 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0019 | 0/0 | 2471 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0020 | 0/0 | 2468 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0021 | 0/0 | 2462 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0022 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0023 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0024 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0025 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0026 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0027 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0028 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0029 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0030 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0031 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0032 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0033 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0034 | 0/0 | 2469 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
t0035 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0013 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1569 | 261 | 52 | 40 | 131 | 8 | 28 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002 | 0/0 | 1569 | 108 | 31 | 32 | 25 | 4 | 16 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0004 | 0/0 | 1569 | 3 | 3 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0007 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0009 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0011 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0012 | 0/0 | 1569 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0002c0003 | 0/0 | 1569 | 10 | 7 | 3 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0002c0005 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0003c0006 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0004c0010 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0005c0008 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4040 | 125 | 25 | 22 | 59 | 4 | 13 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0003 | 0/0 | 4037 | 54 | 2 | 0 | 48 | 1 | 3 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0004 | 0/0 | 4037 | 40 | 6 | 11 | 13 | 2 | 8 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0006 | 0/0 | 4038 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0007 | 0/0 | 4034 | 7 | 2 | 1 | 4 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0008 | 0/0 | 4037 | 6 | 6 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0009 | 0/0 | 4041 | 5 | 3 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0010 | 0/0 | 4036 | 3 | 0 | 1 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0014 | 0/0 | 4037 | 2 | 0 | 0 | 0 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0016 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0017 | 0/0 | 4036 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0018 | 0/0 | 4039 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0019 | 0/0 | 4039 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0021 | 0/0 | 4030 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0022 | 0/0 | 4040 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0023 | 0/0 | 4040 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0024 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0025 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0026 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0027 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0028 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0029 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0030 | 0/0 | 4040 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0031 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0034 | 0/0 | 4037 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0001t0035 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002t0002 | 0/0 | 4037 | 82 | 25 | 21 | 23 | 3 | 10 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002t0004 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002t0005 | 0/0 | 4037 | 15 | 3 | 7 | 0 | 0 | 5 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002t0011 | 0/0 | 4037 | 3 | 0 | 2 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002t0012 | 0/0 | 4036 | 2 | 1 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002t0013 | 0/0 | 4036 | 2 | 1 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002t0020 | 0/0 | 4036 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002t0032 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0002t0033 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0004t0004 | 0/0 | 4037 | 3 | 3 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0007t0001 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0009t0001 | 0/0 | 4040 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0011t0001 | 0/0 | 4040 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0001c0012t0002 | 0/0 | 4037 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0002c0003t0004 | 0/0 | 4037 | 3 | 3 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0002c0003t0006 | 0/0 | 4038 | 5 | 3 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0002c0003t0015 | 0/0 | 4038 | 2 | 1 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0002c0005t0006 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0003c0006t0003 | 0/0 | 4037 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0004c0010t0003 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
a0005c0008t0002 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | copy fasta | chr1 | 17401760 | 17444677 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0013 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0006g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0009g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0009g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0009g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0010g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0010g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0014g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0014g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0016g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0017g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0018g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0019g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0021g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0022g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0023g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0024g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0025g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0026g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0027g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0028g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0029g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0030g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0031g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0034g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0035g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0001 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0011g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0011g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0011g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0012g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0012g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0013g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0020g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0032g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0033g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0004t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0004t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0004t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0007t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0009t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0011t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0012t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0006g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0006g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0006g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0006g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0015g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0015g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0005t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0003c0006t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0004c0010t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0005c0008t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0244 | EUR | GBR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00140 | hp2 | a0001 | c0002 | t0011 | g0184 | EUR | GBR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00280 | hp1 | a0001 | c0001 | t0024 | g0048 | EUR | FIN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0167 | EUR | FIN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0298 | EUR | FIN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00639 | hp1 | a0001 | c0001 | t0034 | g0214 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0224 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00642 | hp1 | a0001 | c0002 | t0020 | g0338 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0297 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0158 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00738 | hp1 | a0001 | c0002 | t0005 | g0150 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0153 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0299 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01069 | hp2 | a0001 | c0001 | t0009 | g0257 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01070 | hp2 | a0001 | c0002 | t0013 | g0030 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01071 | hp1 | a0001 | c0002 | t0005 | g0028 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0256 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0347 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01081 | hp2 | a0001 | c0002 | t0005 | g0134 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01099 | hp1 | a0002 | c0003 | t0006 | g0324 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01106 | hp1 | a0002 | c0003 | t0006 | g0325 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0300 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0349 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01168 | hp2 | a0001 | c0002 | t0011 | g0209 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01169 | hp2 | a0001 | c0002 | t0011 | g0208 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01175 | hp1 | a0001 | c0002 | t0005 | g0175 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01175 | hp2 | a0001 | c0002 | t0005 | g0174 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01243 | hp2 | a0002 | c0003 | t0015 | g0323 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0156 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0132 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01361 | hp2 | a0001 | c0012 | t0002 | g0314 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01433 | hp2 | a0001 | c0002 | t0005 | g0166 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0311 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0191 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | IBS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0201 | EUR | IBS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01884 | hp2 | a0002 | c0003 | t0006 | g0014 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01891 | hp2 | a0002 | c0003 | t0004 | g0319 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01928 | hp2 | a0001 | c0001 | t0021 | g0115 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01943 | hp1 | a0001 | c0001 | t0019 | g0066 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0216 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0194 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0195 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0217 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0218 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02004 | hp2 | a0001 | c0002 | t0005 | g0157 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0344 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02145 | hp2 | a0002 | c0003 | t0015 | g0320 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | CDX | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CDX | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0343 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0165 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0148 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0198 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02280 | hp1 | a0001 | c0001 | t0017 | g0356 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0193 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0108 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0332 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0357 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0215 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0258 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02622 | hp1 | a0002 | c0003 | t0006 | g0014 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02622 | hp2 | a0001 | c0004 | t0004 | g0328 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0352 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0203 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02683 | hp2 | a0003 | c0006 | t0003 | g0212 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0303 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0333 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02735 | hp1 | a0001 | c0002 | t0005 | g0155 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0219 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02738 | hp1 | a0001 | c0002 | t0032 | g0173 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02738 | hp2 | a0001 | c0002 | t0005 | g0171 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02809 | hp1 | a0001 | c0004 | t0004 | g0346 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02818 | hp2 | a0002 | c0003 | t0004 | g0321 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0339 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02886 | hp2 | a0001 | c0001 | t0029 | g0241 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02895 | hp2 | a0001 | c0001 | t0028 | g0285 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0353 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0330 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02965 | hp1 | a0001 | c0002 | t0013 | g0176 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02965 | hp2 | a0002 | c0003 | t0004 | g0318 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02970 | hp2 | a0001 | c0002 | t0005 | g0170 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02976 | hp1 | a0001 | c0002 | t0033 | g0335 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02976 | hp2 | a0001 | c0001 | t0022 | g0069 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03017 | hp1 | a0001 | c0001 | t0035 | g0367 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0152 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0147 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03098 | hp1 | a0002 | c0005 | t0006 | g0326 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03130 | hp2 | a0001 | c0002 | t0005 | g0172 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0317 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0341 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0163 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03209 | hp1 | a0001 | c0004 | t0004 | g0345 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0340 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0189 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0145 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0308 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0151 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03516 | hp2 | a0001 | c0002 | t0012 | g0366 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0207 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0130 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0283 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03710 | hp1 | a0001 | c0002 | t0005 | g0136 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0272 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0168 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03942 | hp1 | a0001 | c0001 | t0014 | g0273 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0302 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04115 | hp1 | a0001 | c0002 | t0005 | g0360 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04115 | hp2 | a0001 | c0001 | t0016 | g0015 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04184 | hp1 | a0001 | c0002 | t0005 | g0169 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04184 | hp2 | a0001 | c0007 | t0001 | g0038 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0160 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0287 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0348 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0342 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0362 | EAS | CHB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18747 | hp1 | a0001 | c0002 | t0012 | g0183 | EAS | CHB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | CHB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0336 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18946 | hp1 | a0001 | c0001 | t0026 | g0305 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18946 | hp2 | a0001 | c0001 | t0023 | g0067 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0361 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18956 | hp1 | a0001 | c0002 | t0004 | g0182 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18962 | hp1 | a0001 | c0001 | t0007 | g0351 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18963 | hp2 | a0001 | c0001 | t0007 | g0312 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18964 | hp1 | a0001 | c0001 | t0030 | g0100 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0365 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18983 | hp2 | a0001 | c0001 | t0007 | g0310 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18994 | hp2 | a0001 | c0011 | t0001 | g0129 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19030 | hp1 | a0001 | c0001 | t0027 | g0327 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0334 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19055 | hp2 | a0001 | c0001 | t0010 | g0253 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19058 | hp1 | a0005 | c0008 | t0002 | g0181 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19079 | hp1 | a0004 | c0010 | t0003 | g0364 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19081 | hp1 | a0001 | c0009 | t0001 | g0058 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19084 | hp1 | a0001 | c0001 | t0025 | g0296 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19087 | hp2 | a0001 | c0001 | t0007 | g0309 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19089 | hp1 | a0001 | c0001 | t0010 | g0230 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19089 | hp2 | a0001 | c0001 | t0018 | g0064 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19240 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0355 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0350 | AFR | ASW | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0329 | AFR | ASW | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0013 | EUR | TSI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0164 | EUR | TSI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | GIH | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20905 | hp2 | a0001 | c0001 | t0014 | g0275 | SAS | GIH | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0154 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0200 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02109 | hp2 | a0001 | c0002 | t0005 | g0029 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02486 | hp2 | a0002 | c0003 | t0006 | g0322 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0331 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03471 | hp1 | a0001 | c0001 | t0031 | g0016 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | USA | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0354 | AFR | USA | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0313 | AFR | USA | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0262 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0337 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0085 | REF | REF | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0128 | REF | REF | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17420785
|
G | C | 1 | a0005 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.788C>G | p.Ala263Gly | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/13 | 929/4040 | 788/1569 | 263/522 | chr1 | 17420785 | ||
chr1:17420786
|
C | G | 1 | a0005 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.787G>C | p.Ala263Pro | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/13 | 928/4040 | 787/1569 | 263/522 | chr1 | 17420786 | ||
chr1:17422289
|
T | C | 1 | a0004 | 1 | NA19079.hp1 | missense_variant&splice_region_variant | MODERATE | c.658A>G | p.Thr220Ala | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/13 | 799/4040 | 658/1569 | 220/522 | chr1 | 17422289 | ||
chr1:17438267
|
A | G | 1 | a0003 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.248T>C | p.Val83Ala | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 389/4040 | 248/1569 | 83/522 | chr1 | 17438267 | ||
chr1:17438292
|
C | T | 1 | a0002 | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
missense_variant | MODERATE | c.223G>A | p.Ala75Thr | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 364/4040 | 223/1569 | 75/522 | chr1 | 17438292 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17413090
|
G | A | 4 | a0001c0002a0001c0012a0002c0005others(1): Show | 111 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(108): Show |
synonymous_variant | LOW | c.1296C>T | p.Ile432Ile | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/13 | 1437/4040 | 1296/1569 | 432/522 | chr1 | 17413090 | ||
chr1:17413550
|
A | G | 1 | a0001c0009 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1194T>C | p.Ala398Ala | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/13 | 1335/4040 | 1194/1569 | 398/522 | chr1 | 17413550 | ||
chr1:17416549
|
C | T | 1 | a0001c0004 | 3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.957G>A | p.Thr319Thr | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/13 | 1098/4040 | 957/1569 | 319/522 | chr1 | 17416549 | ||
chr1:17438266
|
C | T | 1 | a0001c0007 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.249G>A | p.Val83Val | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 390/4040 | 249/1569 | 83/522 | chr1 | 17438266 | ||
chr1:17438278
|
G | A | 1 | a0001c0011 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.237C>T | p.Gly79Gly | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 378/4040 | 237/1569 | 79/522 | chr1 | 17438278 | ||
chr1:17438284
|
C | T | 2 | a0002c0003a0002c0005 | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
synonymous_variant | LOW | c.231G>A | p.Lys77Lys | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 372/4040 | 231/1569 | 77/522 | chr1 | 17438284 | ||
chr1:17438299
|
C | A | 1 | a0001c0012 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.216G>T | p.Pro72Pro | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 357/4040 | 216/1569 | 72/522 | chr1 | 17438299 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17406771
|
ATGT | A | 32 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(29): Show | 247 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*2316_*2318delACA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 2316 | chr1 | 17406771 | |||||
chr1:17406859
|
C | A | 1 | a0001c0001t0022 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2231G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 2231 | chr1 | 17406859 | |||||
chr1:17407035
|
G | A | 2 | a0001c0002t0005a0001c0002t0013 | 17 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2055C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 2055 | chr1 | 17407035 | |||||
chr1:17407068
|
T | G | 32 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(29): Show | 247 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*2022A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 2022 | chr1 | 17407068 | |||||
chr1:17407171
|
G | A | 1 | a0001c0001t0023 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1919C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1919 | chr1 | 17407171 | |||||
chr1:17407193
|
G | A | 1 | a0001c0001t0025 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1897C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1897 | chr1 | 17407193 | |||||
chr1:17407322
|
T | C | 1 | a0001c0001t0019 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1768A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1768 | chr1 | 17407322 | |||||
chr1:17407393
|
G | A | 1 | a0001c0001t0024 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1697C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1697 | chr1 | 17407393 | |||||
chr1:17407500
|
G | A | 6 | a0001c0001t0003a0001c0001t0010a0001c0001t0025others(3): Show | 61 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1590C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1590 | chr1 | 17407500 | |||||
chr1:17407559
|
G | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1531C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1531 | chr1 | 17407559 | |||||
chr1:17407899
|
G | A | 1 | a0001c0002t0020 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1191C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1191 | chr1 | 17407899 | |||||
chr1:17407942
|
C | A | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1148G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1148 | chr1 | 17407942 | |||||
chr1:17407955
|
G | A | 1 | a0001c0001t0028 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1135C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1135 | chr1 | 17407955 | |||||
chr1:17407974
|
C | T | 2 | a0001c0001t0008a0001c0001t0017 | 7 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1116G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1116 | chr1 | 17407974 | |||||
chr1:17408047
|
T | A | 1 | a0001c0001t0029 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1043A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1043 | chr1 | 17408047 | |||||
chr1:17408106
|
GAGTCTCA others(3): Show |
G | 1 | a0001c0001t0021 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*974_*983delTGCTGA others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 974 | chr1 | 17408106 | |||||
chr1:17408131
|
G | A | 1 | a0001c0001t0014 | 2 | HG03942.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*959C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 959 | chr1 | 17408131 | |||||
chr1:17408151
|
G | C | 1 | a0001c0002t0011 | 3 | HG00140.hp2 HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*939C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 939 | chr1 | 17408151 | |||||
chr1:17408437
|
C | T | 1 | a0001c0001t0007 | 7 | HG01496.hp1 HG03486.hp1 NA18962.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*653G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 653 | chr1 | 17408437 | |||||
chr1:17408459
|
G | C | 1 | a0001c0002t0033 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*631C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 631 | chr1 | 17408459 | |||||
chr1:17408467
|
C | T | 1 | a0002c0003t0015 | 2 | HG01243.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*623G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 623 | chr1 | 17408467 | |||||
chr1:17408570
|
GAGA | G | 1 | a0001c0001t0007 | 7 | HG01496.hp1 HG03486.hp1 NA18962.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*517_*519delTCT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 517 | chr1 | 17408570 | |||||
chr1:17408585
|
G | A | 1 | a0001c0001t0030 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*505C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 505 | chr1 | 17408585 | |||||
chr1:17408614
|
T | G | 1 | a0001c0001t0031 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 476 | chr1 | 17408614 | |||||
chr1:17408770
|
G | A | 10 | a0001c0002t0002a0001c0002t0005a0001c0002t0011others(7): Show | 109 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*320C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 320 | chr1 | 17408770 | |||||
chr1:17408789
|
T | TA | 5 | a0001c0001t0006a0001c0001t0009a0002c0003t0006others(2): Show | 15 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*300dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 300 | chr1 | 17408789 | |||||
chr1:17408789
|
TA | T | 7 | a0001c0001t0010a0001c0001t0017a0001c0001t0018others(4): Show | 11 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*300delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 300 | chr1 | 17408789 | |||||
chr1:17408844
|
T | G | 1 | a0001c0001t0034 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 246 | chr1 | 17408844 | |||||
chr1:17439582
|
A | G | 1 | a0001c0001t0016 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/13 | 1068 | chr1 | 17439582 | |||||
chr1:17439634
|
G | A | 1 | a0001c0001t0035 | 1 | HG03017.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-98C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/13 | chr1 | 17439634 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17409202
|
G | T | 6 | a0001c0001t0008g0165a0001c0001t0008g0352a0001c0001t0008g0353others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1465-8C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409202 | ||||||
chr1:17409214
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1465-20A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409214 | ||||||
chr1:17409215
|
T | C | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1465-21A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409215 | ||||||
chr1:17409373
|
G | A | 5 | a0001c0002t0005g0150a0001c0002t0005g0155a0001c0002t0005g0157others(2): Show | 5 | HG00738.hp1 HG01433.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-179C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409373 | ||||||
chr1:17409423
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1465-229C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409423 | ||||||
chr1:17409424
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1465-230T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409424 | ||||||
chr1:17409464
|
G | T | 9 | a0001c0001t0008g0165a0001c0001t0008g0207a0001c0001t0008g0352others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1465-270C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409464 | ||||||
chr1:17409504
|
C | T | 2 | a0001c0002t0002g0131a0001c0002t0002g0132 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1465-310G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409504 | ||||||
chr1:17409646
|
G | A | 1 | a0001c0001t0003g0254 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1464+328C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409646 | ||||||
chr1:17409866
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1464+108C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409866 | ||||||
chr1:17409935
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0045 | 2 | HG02074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1464+39G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409935 | ||||||
chr1:17409936
|
G | A | 5 | a0001c0001t0001g0056a0001c0001t0001g0094a0001c0001t0001g0109others(2): Show | 5 | HG00280.hp2 HG01943.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.1464+38C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409936 | ||||||
chr1:17410082
|
A | G | 239 | a0001c0001t0001g0050a0001c0001t0003g0018a0001c0001t0003g0032others(236): Show | 249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1387-31T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410082 | ||||||
chr1:17410409
|
G | A | 11 | a0001c0001t0006g0210a0001c0001t0006g0357a0002c0003t0004g0318others(8): Show | 12 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1387-358C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410409 | ||||||
chr1:17410575
|
G | A | 1 | a0001c0001t0004g0304 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1387-524C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410575 | ||||||
chr1:17410582
|
C | T | 1 | a0001c0001t0004g0288 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1387-531G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410582 | ||||||
chr1:17410694
|
C | G | 1 | a0002c0003t0004g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1387-643G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410694 | ||||||
chr1:17410890
|
G | C | 2 | a0001c0002t0012g0366a0001c0002t0020g0338 | 2 | HG00642.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1387-839C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410890 | ||||||
chr1:17410944
|
G | C | 17 | a0001c0002t0002g0010a0001c0002t0002g0153a0001c0002t0002g0154others(14): Show | 18 | HG00741.hp1 HG01081.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1387-893C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410944 | ||||||
chr1:17411125
|
C | A | 1 | a0001c0001t0004g0276 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1386+997G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411125 | ||||||
chr1:17411143
|
G | A | 1 | a0002c0003t0004g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1386+979C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411143 | ||||||
chr1:17411315
|
G | A | 1 | a0001c0002t0002g0347 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1386+807C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411315 | ||||||
chr1:17411580
|
C | CA | 22 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(19): Show | 22 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1386+541dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411580 | ||||||
chr1:17411580
|
CA | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0091others(6): Show | 10 | HG02040.hp2 HG02273.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386+541delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411580 | ||||||
chr1:17411671
|
T | C | 334 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(331): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.1386+451A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411671 | ||||||
chr1:17411803
|
A | G | 1 | a0001c0002t0002g0329 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1386+319T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411803 | ||||||
chr1:17411826
|
CT | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | NA18977.hp1 NA19010.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1386+295delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411826 | ||||||
chr1:17412074
|
AC | A | 109 | a0001c0001t0001g0220a0001c0001t0003g0018a0001c0001t0003g0032others(106): Show | 111 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1386+47delG | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17412074 | ||||||
chr1:17412248
|
C | T | 10 | a0001c0001t0006g0210a0001c0001t0006g0357a0002c0003t0004g0318others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1314-54G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412248 | ||||||
chr1:17412273
|
T | TGTG | 3 | a0002c0003t0006g0324a0002c0003t0015g0320a0002c0003t0015g0323 | 3 | HG01099.hp1 HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1314-82_1314-80dup others(3): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412273 | ||||||
chr1:17412366
|
G | C | 1 | a0001c0001t0031g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1314-172C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412366 | ||||||
chr1:17412412
|
G | C | 9 | a0001c0001t0008g0165a0001c0001t0008g0207a0001c0001t0008g0352others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1314-218C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412412 | ||||||
chr1:17412769
|
C | T | 1 | a0001c0001t0004g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1313+304G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412769 | ||||||
chr1:17412817
|
T | G | 231 | a0001c0001t0001g0050a0001c0001t0001g0220a0001c0001t0003g0018others(228): Show | 241 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1313+256A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412817 | ||||||
chr1:17412863
|
A | G | 1 | a0002c0003t0004g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1313+210T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412863 | ||||||
chr1:17413021
|
C | CA | 8 | a0001c0001t0008g0165a0001c0001t0008g0207a0001c0001t0008g0352others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1313+51dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17413021 | ||||||
chr1:17413023
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0024others(1): Show | 4 | NA18612.hp1 NA18970.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313+50G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17413023 | ||||||
chr1:17413049
|
C | T | 1 | a0001c0001t0027g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1313+24G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17413049 | ||||||
chr1:17413254
|
G | C | 1 | a0001c0002t0002g0349 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1208-76C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413254 | ||||||
chr1:17413318
|
C | T | 9 | a0001c0001t0008g0165a0001c0001t0008g0207a0001c0001t0008g0352others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1208-140G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413318 | ||||||
chr1:17413324
|
T | C | 239 | a0001c0001t0001g0220a0001c0001t0003g0018a0001c0001t0003g0032others(236): Show | 249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1208-146A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413324 | ||||||
chr1:17413379
|
G | C | 1 | a0001c0002t0005g0174 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1207+158C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413379 | ||||||
chr1:17413382
|
C | T | 1 | a0001c0001t0003g0264 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1207+155G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413382 | ||||||
chr1:17413523
|
C | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0065others(1): Show | 4 | HG02523.hp2 NA18946.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207+14G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413523 | ||||||
chr1:17413761
|
A | G | 1 | a0001c0001t0029g0241 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1027-44T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413761 | ||||||
chr1:17413838
|
A | C | 1 | a0001c0002t0002g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1027-121T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413838 | ||||||
chr1:17413854
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1027-137G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413854 | ||||||
chr1:17413855
|
G | A | 1 | a0001c0002t0002g0329 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1027-138C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413855 | ||||||
chr1:17413861
|
G | A | 126 | a0001c0001t0001g0220a0001c0001t0003g0018a0001c0001t0003g0032others(123): Show | 129 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1027-144C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413861 | ||||||
chr1:17413880
|
C | A | 1 | a0001c0001t0004g0278 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1027-163G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413880 | ||||||
chr1:17413882
|
A | C | 1 | a0001c0001t0004g0278 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1027-165T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413882 | ||||||
chr1:17413883
|
C | T | 1 | a0001c0001t0004g0278 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1027-166G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413883 | ||||||
chr1:17414007
|
A | T | 1 | a0001c0001t0003g0233 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1027-290T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414007 | ||||||
chr1:17414033
|
G | A | 2 | a0001c0001t0004g0287a0001c0001t0029g0241 | 2 | HG02886.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1027-316C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414033 | ||||||
chr1:17414168
|
C | A | 1 | a0001c0001t0014g0273 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1027-451G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414168 | ||||||
chr1:17414169
|
C | G | 1 | a0001c0002t0002g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1027-452G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414169 | ||||||
chr1:17414183
|
G | C | 2 | a0001c0001t0004g0304a0001c0001t0004g0315 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1027-466C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414183 | ||||||
chr1:17414224
|
T | G | 10 | a0001c0001t0006g0210a0001c0001t0006g0357a0002c0003t0004g0318others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1027-507A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414224 | ||||||
chr1:17414480
|
A | T | 1 | a0002c0005t0006g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1027-763T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414480 | ||||||
chr1:17414529
|
C | CA | 6 | a0001c0001t0003g0222a0001c0001t0003g0245a0001c0002t0002g0141others(3): Show | 6 | HG02602.hp1 HG02683.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-813dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414529 | ||||||
chr1:17414529
|
CA | C | 8 | a0001c0001t0001g0071a0001c0001t0008g0165a0001c0001t0008g0207others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-813delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414529 | ||||||
chr1:17414536
|
AAAAAACA others(9): Show |
A | 3 | a0001c0004t0004g0328a0001c0004t0004g0345a0001c0004t0004g0346 | 3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1027-835_1027-820d others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414536 | ||||||
chr1:17414537
|
A | C | 1 | a0001c0001t0007g0311 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1027-820T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414537 | ||||||
chr1:17414542
|
C | A | 1 | a0001c0001t0003g0222 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1027-825G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414542 | ||||||
chr1:17414548
|
G | A | 262 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0043others(259): Show | 274 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1027-831C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414548 | ||||||
chr1:17414552
|
C | CA | 19 | a0001c0001t0003g0266a0001c0001t0004g0276a0001c0001t0004g0284others(16): Show | 19 | HG01081.hp2 HG01175.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1027-836dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414552 | ||||||
chr1:17414559
|
A | C | 3 | a0001c0004t0004g0328a0001c0004t0004g0345a0001c0004t0004g0346 | 3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1027-842T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414559 | ||||||
chr1:17414566
|
C | A | 3 | a0001c0004t0004g0328a0001c0004t0004g0345a0001c0004t0004g0346 | 3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1027-849G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414566 | ||||||
chr1:17414569
|
C | CA | 24 | a0001c0001t0001g0043a0001c0001t0001g0126a0001c0001t0001g0316others(21): Show | 24 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1027-853dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414569 | ||||||
chr1:17414570
|
A | C | 1 | a0001c0002t0002g0142 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1027-853T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414570 | ||||||
chr1:17414611
|
C | T | 1 | a0001c0002t0002g0344 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1027-894G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414611 | ||||||
chr1:17414631
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1027-914G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414631 | ||||||
chr1:17414646
|
C | A | 1 | a0001c0001t0016g0015 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1027-929G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414646 | ||||||
chr1:17414647
|
C | T | 1 | a0001c0002t0002g0205 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1027-930G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414647 | ||||||
chr1:17414700
|
C | T | 1 | a0001c0002t0002g0153 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1027-983G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414700 | ||||||
chr1:17414701
|
G | A | 1 | a0001c0002t0011g0184 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1027-984C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414701 | ||||||
chr1:17414745
|
C | A | 1 | a0001c0001t0008g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1027-1028G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414745 | ||||||
chr1:17414791
|
C | CAGCTGAT others(10): Show |
1 | a0001c0001t0004g0276 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1027-1091_1027-107 others(21): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414791 | ||||||
chr1:17415035
|
G | A | 1 | a0001c0002t0002g0191 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1027-1318C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415035 | ||||||
chr1:17415041
|
C | T | 1 | a0001c0001t0004g0278 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1027-1324G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415041 | ||||||
chr1:17415339
|
C | G | 10 | a0001c0001t0006g0210a0001c0001t0006g0357a0002c0003t0004g0318others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1026+1141G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415339 | ||||||
chr1:17415357
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1026+1123C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415357 | ||||||
chr1:17415495
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1026+985C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415495 | ||||||
chr1:17415528
|
T | C | 105 | a0001c0001t0001g0220a0001c0001t0003g0018a0001c0001t0003g0032others(102): Show | 107 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1026+952A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415528 | ||||||
chr1:17415713
|
T | C | 121 | a0001c0001t0001g0220a0001c0001t0003g0018a0001c0001t0003g0032others(118): Show | 124 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1026+767A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415713 | ||||||
chr1:17415714
|
A | C | 2 | a0001c0001t0004g0288a0002c0003t0006g0324 | 2 | HG01099.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1026+766T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415714 | ||||||
chr1:17415717
|
A | C | 1 | a0001c0001t0003g0350 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1026+763T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415717 | ||||||
chr1:17415728
|
T | C | 2 | a0001c0002t0002g0333a0001c0002t0002g0337 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1026+752A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415728 | ||||||
chr1:17415838
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1026+642C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415838 | ||||||
chr1:17415839
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1026+641A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415839 | ||||||
chr1:17415842
|
G | A | 19 | a0001c0001t0003g0033a0001c0001t0003g0221a0001c0001t0003g0225others(16): Show | 19 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1026+638C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415842 | ||||||
chr1:17415845
|
G | T | 1 | a0001c0001t0004g0270 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1026+635C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415845 | ||||||
chr1:17415864
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0054others(5): Show | 9 | HG01891.hp1 HG02257.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026+616A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415864 | ||||||
chr1:17415967
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1026+513C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415967 | ||||||
chr1:17415999
|
G | A | 1 | a0002c0003t0004g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1026+481C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415999 | ||||||
chr1:17416068
|
CA | C | 6 | a0001c0002t0002g0347a0001c0002t0002g0348a0001c0002t0005g0155others(3): Show | 6 | HG01070.hp2 HG01074.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026+411delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416068 | ||||||
chr1:17416077
|
A | AGG | 4 | a0001c0002t0002g0349a0002c0003t0006g0322a0002c0003t0015g0320others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+402_1026+403i others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416077 | ||||||
chr1:17416078
|
A | AG | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(92): Show | 102 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1026+401dupC | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416078 | ||||||
chr1:17416078
|
A | AGG | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0023others(22): Show | 27 | HG00323.hp2 HG00423.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1026+400_1026+401d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416078 | ||||||
chr1:17416078
|
A | G | 14 | a0001c0001t0001g0109a0001c0001t0006g0210a0001c0001t0006g0357others(11): Show | 15 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1026+402T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416078 | ||||||
chr1:17416078
|
AG | A | 40 | a0001c0001t0003g0228a0001c0001t0003g0229a0001c0001t0003g0234others(37): Show | 41 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1026+401delC | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416078 | ||||||
chr1:17416083
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0359 | 3 | HG02145.hp1 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1026+397C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416083 | ||||||
chr1:17416088
|
G | A | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1026+392C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416088 | ||||||
chr1:17416089
|
G | C | 4 | a0001c0001t0010g0253a0001c0002t0002g0178a0001c0002t0002g0179others(1): Show | 4 | HG02523.hp1 NA19055.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+391C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416089 | ||||||
chr1:17416090
|
C | G | 14 | a0001c0001t0001g0037a0001c0001t0001g0071a0001c0001t0001g0076others(11): Show | 14 | HG01167.hp2 HG02280.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026+390G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416090 | ||||||
chr1:17416117
|
C | T | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1026+363G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416117 | ||||||
chr1:17416118
|
G | A | 1 | a0001c0001t0004g0304 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1026+362C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416118 | ||||||
chr1:17416429
|
C | T | 1 | a0001c0002t0033g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1026+51G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416429 | ||||||
chr1:17416437
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1026+43T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416437 | ||||||
chr1:17416723
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.860-77A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17416723 | ||||||
chr1:17416859
|
C | G | 1 | a0001c0001t0028g0285 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.860-213G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17416859 | ||||||
chr1:17417117
|
T | C | 230 | a0001c0001t0001g0220a0001c0001t0003g0018a0001c0001t0003g0032others(227): Show | 240 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.860-471A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417117 | ||||||
chr1:17417164
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.860-518C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417164 | ||||||
chr1:17417173
|
C | T | 230 | a0001c0001t0001g0220a0001c0001t0003g0018a0001c0001t0003g0032others(227): Show | 240 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.860-527G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417173 | ||||||
chr1:17417240
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.860-594G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417240 | ||||||
chr1:17417307
|
C | G | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.860-661G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417307 | ||||||
chr1:17417358
|
C | G | 13 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0056others(10): Show | 13 | HG00280.hp2 HG01943.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.860-712G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417358 | ||||||
chr1:17417400
|
G | T | 1 | a0001c0001t0003g0294 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.860-754C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417400 | ||||||
chr1:17417692
|
A | C | 1 | a0001c0001t0029g0241 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.860-1046T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417692 | ||||||
chr1:17417733
|
C | T | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.860-1087G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417733 | ||||||
chr1:17417916
|
A | G | 4 | a0001c0001t0003g0234a0001c0001t0003g0244a0001c0001t0003g0350others(1): Show | 4 | HG00099.hp1 HG00639.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-1270T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417916 | ||||||
chr1:17418035
|
A | AT | 113 | a0001c0001t0001g0206a0001c0001t0008g0165a0001c0001t0008g0207others(110): Show | 120 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.860-1390dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418035 | ||||||
chr1:17418040
|
A | G | 113 | a0001c0001t0001g0206a0001c0001t0008g0165a0001c0001t0008g0207others(110): Show | 120 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.860-1394T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418040 | ||||||
chr1:17418159
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.860-1513G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418159 | ||||||
chr1:17418213
|
A | AT | 9 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0043others(6): Show | 9 | HG00323.hp2 HG00423.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.860-1568dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | ||||||
chr1:17418213
|
A | ATT | 31 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0004g0211others(28): Show | 33 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.860-1569_860-1568d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | ||||||
chr1:17418213
|
A | G | 1 | a0001c0002t0002g0179 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.860-1567T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | ||||||
chr1:17418213
|
AT | A | 105 | a0001c0001t0001g0037a0001c0001t0001g0113a0001c0001t0001g0114others(102): Show | 113 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.860-1568delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | ||||||
chr1:17418213
|
ATT | A | 9 | a0001c0002t0002g0141a0001c0002t0002g0331a0001c0002t0002g0332others(6): Show | 9 | HG00738.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.860-1569_860-1568d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | ||||||
chr1:17418269
|
C | T | 1 | a0001c0002t0002g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.860-1623G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418269 | ||||||
chr1:17418323
|
T | C | 1 | a0003c0006t0003g0212 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.860-1677A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418323 | ||||||
chr1:17418356
|
G | A | 240 | a0001c0001t0001g0206a0001c0001t0001g0220a0001c0001t0003g0032others(237): Show | 251 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.860-1710C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418356 | ||||||
chr1:17418390
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.860-1744C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418390 | ||||||
chr1:17418441
|
G | A | 1 | a0001c0001t0004g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.860-1795C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418441 | ||||||
chr1:17418581
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.860-1935G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418581 | ||||||
chr1:17418719
|
G | T | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.859+1995C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418719 | ||||||
chr1:17418741
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.859+1973T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418741 | ||||||
chr1:17418812
|
G | A | 5 | a0001c0002t0002g0145a0001c0002t0002g0146a0001c0002t0002g0147others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.859+1902C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418812 | ||||||
chr1:17418918
|
A | T | 1 | a0005c0008t0002g0181 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.859+1796T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418918 | ||||||
chr1:17419223
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.859+1491C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419223 | ||||||
chr1:17419321
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.859+1393A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419321 | ||||||
chr1:17419353
|
C | T | 1 | a0001c0002t0002g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.859+1361G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419353 | ||||||
chr1:17419537
|
A | C | 10 | a0002c0003t0004g0318a0002c0003t0004g0319a0002c0003t0004g0321others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.859+1177T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419537 | ||||||
chr1:17419580
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.859+1134C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419580 | ||||||
chr1:17419772
|
C | CGGACTGC others(6): Show |
1 | a0001c0002t0002g0329 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.859+941_859+942ins others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419772 | ||||||
chr1:17419777
|
C | T | 108 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(105): Show | 115 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.859+937G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419777 | ||||||
chr1:17419828
|
GTCTCGGG others(35): Show |
G | 1 | a0001c0001t0004g0281 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.859+844_859+885del others(42): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419828 | ||||||
chr1:17419844
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.859+870G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419844 | ||||||
chr1:17419908
|
G | T | 1 | a0001c0002t0002g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.859+806C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419908 | ||||||
chr1:17420028
|
A | G | 1 | a0001c0001t0004g0108 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.859+686T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420028 | ||||||
chr1:17420051
|
G | A | 1 | a0001c0002t0032g0173 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.859+663C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420051 | ||||||
chr1:17420069
|
G | A | 1 | a0002c0003t0006g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.859+645C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420069 | ||||||
chr1:17420086
|
G | A | 3 | a0001c0002t0002g0151a0001c0002t0002g0152a0001c0002t0002g0167 | 3 | HG00323.hp1 HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.859+628C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420086 | ||||||
chr1:17420192
|
T | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0055 | 2 | HG01070.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.859+522A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420192 | ||||||
chr1:17420339
|
A | G | 1 | a0001c0001t0004g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.859+375T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420339 | ||||||
chr1:17420346
|
T | C | 1 | a0001c0001t0007g0312 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.859+368A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420346 | ||||||
chr1:17420580
|
C | T | 1 | a0001c0001t0028g0285 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.859+134G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420580 | ||||||
chr1:17421014
|
C | G | 1 | a0001c0002t0002g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.745-186G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421014 | ||||||
chr1:17421223
|
T | C | 1 | a0001c0001t0003g0231 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.745-395A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421223 | ||||||
chr1:17421230
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.745-402G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421230 | ||||||
chr1:17421231
|
G | A | 1 | a0001c0001t0029g0241 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.745-403C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421231 | ||||||
chr1:17421244
|
C | A | 1 | a0005c0008t0002g0181 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.745-416G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421244 | ||||||
chr1:17421314
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.745-486C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421314 | ||||||
chr1:17421452
|
G | A | 1 | a0001c0001t0003g0232 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.745-624C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421452 | ||||||
chr1:17421472
|
C | A | 1 | a0001c0001t0007g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.745-644G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421472 | ||||||
chr1:17421480
|
C | T | 1 | a0004c0010t0003g0364 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.745-652G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421480 | ||||||
chr1:17421481
|
G | A | 3 | a0001c0001t0004g0013a0001c0001t0004g0213a0001c0001t0004g0280 | 4 | HG02280.hp2 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-653C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421481 | ||||||
chr1:17421496
|
C | G | 2 | a0001c0001t0004g0304a0001c0001t0004g0315 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.745-668G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421496 | ||||||
chr1:17421531
|
A | G | 242 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(239): Show | 253 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.744+672T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421531 | ||||||
chr1:17421692
|
G | A | 5 | a0001c0001t0004g0013a0001c0001t0004g0213a0001c0001t0004g0279others(2): Show | 6 | HG00738.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+511C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421692 | ||||||
chr1:17421774
|
C | T | 1 | a0001c0004t0004g0328 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.744+429G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421774 | ||||||
chr1:17421792
|
G | A | 99 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(96): Show | 106 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.744+411C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421792 | ||||||
chr1:17421931
|
C | A | 242 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(239): Show | 253 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.744+272G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421931 | ||||||
chr1:17421935
|
G | A | 1 | a0001c0002t0002g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.744+268C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421935 | ||||||
chr1:17422019
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.744+184G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17422019 | ||||||
chr1:17422059
|
A | C | 1 | a0001c0002t0002g0347 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.744+144T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17422059 | ||||||
chr1:17422171
|
A | C | 1 | a0001c0001t0001g0041 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.744+32T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17422171 | ||||||
chr1:17422389
|
T | C | 2 | a0001c0002t0002g0156a0001c0002t0002g0158 | 2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.656-98A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 5/12 | chr1 | 17422389 | ||||||
chr1:17422407
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.656-116C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 5/12 | chr1 | 17422407 | ||||||
chr1:17422635
|
C | A | 2 | a0001c0002t0002g0348a0001c0002t0002g0349 | 2 | HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.655+70G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 5/12 | chr1 | 17422635 | ||||||
chr1:17422963
|
C | CCAA | 365 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(362): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.524-130_524-128dup others(3): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17422963 | ||||||
chr1:17423007
|
C | A | 4 | a0001c0001t0004g0011a0001c0001t0004g0216a0001c0001t0004g0217others(1): Show | 5 | HG01243.hp1 HG01943.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-171G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423007 | ||||||
chr1:17423008
|
G | A | 108 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(105): Show | 115 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.524-172C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423008 | ||||||
chr1:17423061
|
G | A | 3 | a0001c0001t0001g0031a0001c0002t0012g0366a0001c0002t0020g0338 | 3 | HG00423.hp2 HG00642.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.524-225C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423061 | ||||||
chr1:17423081
|
C | T | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.524-245G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423081 | ||||||
chr1:17423139
|
A | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0017others(10): Show | 16 | HG00741.hp2 HG01928.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.524-303T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423139 | ||||||
chr1:17423152
|
C | T | 1 | a0001c0002t0002g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.524-316G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423152 | ||||||
chr1:17423285
|
G | C | 4 | a0001c0001t0009g0012a0001c0001t0009g0256a0001c0001t0009g0257others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-449C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423285 | ||||||
chr1:17423545
|
C | T | 1 | a0001c0002t0033g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.524-709G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423545 | ||||||
chr1:17423548
|
C | A | 2 | a0001c0001t0003g0350a0001c0001t0010g0224 | 2 | HG00639.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.524-712G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423548 | ||||||
chr1:17423682
|
G | A | 1 | a0001c0002t0002g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.524-846C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423682 | ||||||
chr1:17423767
|
G | C | 4 | a0001c0001t0003g0234a0001c0001t0003g0244a0001c0001t0003g0350others(1): Show | 4 | HG00099.hp1 HG00639.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-931C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423767 | ||||||
chr1:17423863
|
T | A | 8 | a0001c0001t0007g0308a0001c0001t0007g0309a0001c0001t0007g0310others(5): Show | 8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.524-1027A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423863 | ||||||
chr1:17424056
|
T | C | 243 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(240): Show | 254 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.524-1220A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424056 | ||||||
chr1:17424056
|
T | G | 1 | a0001c0001t0031g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.524-1220A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424056 | ||||||
chr1:17424077
|
G | A | 8 | a0001c0001t0007g0308a0001c0001t0007g0309a0001c0001t0007g0310others(5): Show | 8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.524-1241C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424077 | ||||||
chr1:17424189
|
G | A | 108 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(105): Show | 115 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.523+1352C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424189 | ||||||
chr1:17424274
|
G | A | 1 | a0001c0001t0007g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.523+1267C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424274 | ||||||
chr1:17424368
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0103a0001c0001t0001g0119 | 3 | HG02809.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.523+1173C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424368 | ||||||
chr1:17424761
|
G | A | 1 | a0001c0002t0002g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.523+780C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424761 | ||||||
chr1:17424875
|
C | T | 2 | a0001c0002t0012g0366a0001c0002t0020g0338 | 2 | HG00642.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.523+666G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424875 | ||||||
chr1:17424967
|
C | G | 2 | a0001c0002t0011g0208a0001c0002t0011g0209 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.523+574G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424967 | ||||||
chr1:17425014
|
G | A | 1 | a0001c0001t0004g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.523+527C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425014 | ||||||
chr1:17425108
|
T | G | 1 | a0001c0001t0016g0015 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.523+433A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425108 | ||||||
chr1:17425137
|
T | C | 1 | a0001c0001t0004g0271 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.523+404A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425137 | ||||||
chr1:17425212
|
G | A | 3 | a0001c0002t0002g0347a0001c0002t0002g0348a0001c0002t0002g0349 | 3 | HG01074.hp2 HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.523+329C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425212 | ||||||
chr1:17425361
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.523+180A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425361 | ||||||
chr1:17425449
|
C | T | 2 | a0001c0002t0002g0192a0001c0002t0002g0195 | 2 | HG01978.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.523+92G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425449 | ||||||
chr1:17425458
|
T | C | 1 | a0001c0002t0002g0347 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.523+83A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425458 | ||||||
chr1:17425467
|
A | C | 4 | a0001c0001t0004g0299a0001c0001t0004g0300a0001c0001t0004g0301others(1): Show | 4 | HG01069.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.523+74T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425467 | ||||||
chr1:17425504
|
A | G | 103 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(100): Show | 110 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.523+37T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425504 | ||||||
chr1:17425716
|
C | G | 1 | a0001c0001t0003g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.380-32G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425716 | ||||||
chr1:17425771
|
C | T | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.380-87G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425771 | ||||||
chr1:17425955
|
C | G | 125 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(122): Show | 133 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.380-271G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425955 | ||||||
chr1:17425992
|
C | T | 3 | a0001c0001t0008g0353a0001c0001t0008g0354a0001c0001t0008g0355 | 3 | HG02897.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.380-308G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425992 | ||||||
chr1:17425995
|
G | A | 2 | a0001c0002t0005g0174a0001c0002t0032g0173 | 2 | HG01175.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.380-311C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425995 | ||||||
chr1:17426011
|
C | T | 1 | a0001c0002t0005g0029 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.380-327G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426011 | ||||||
chr1:17426019
|
C | T | 3 | a0001c0002t0002g0347a0001c0002t0002g0348a0001c0002t0002g0349 | 3 | HG01074.hp2 HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.380-335G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426019 | ||||||
chr1:17426100
|
C | G | 1 | a0001c0001t0003g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.380-416G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426100 | ||||||
chr1:17426102
|
GACCCAGG others(11): Show |
G | 1 | a0001c0001t0003g0033 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.380-436_380-419del others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426102 | ||||||
chr1:17426108
|
G | A | 7 | a0001c0001t0006g0357a0001c0001t0008g0352a0001c0001t0008g0353others(4): Show | 7 | HG02280.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.380-424C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426108 | ||||||
chr1:17426205
|
T | G | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.380-521A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426205 | ||||||
chr1:17426235
|
G | A | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.380-551C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426235 | ||||||
chr1:17426294
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.380-610C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426294 | ||||||
chr1:17426330
|
C | T | 1 | a0001c0002t0002g0168 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.380-646G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426330 | ||||||
chr1:17426377
|
A | C | 243 | a0001c0001t0001g0050a0001c0001t0001g0186a0001c0001t0001g0202others(240): Show | 254 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.380-693T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426377 | ||||||
chr1:17426494
|
G | A | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.380-810C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426494 | ||||||
chr1:17426695
|
T | C | 243 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(240): Show | 254 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.380-1011A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426695 | ||||||
chr1:17426753
|
A | T | 1 | a0001c0001t0007g0351 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.380-1069T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426753 | ||||||
chr1:17426759
|
C | CT | 16 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0034others(13): Show | 16 | HG00423.hp2 HG00735.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.380-1076dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | ||||||
chr1:17426759
|
CT | C | 21 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0084others(18): Show | 21 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.380-1076delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | ||||||
chr1:17426759
|
CTT | C | 85 | a0001c0001t0003g0033a0001c0001t0003g0221a0001c0001t0003g0222others(82): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.380-1077_380-1076d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | ||||||
chr1:17426759
|
CTTT | C | 38 | a0001c0001t0001g0220a0001c0001t0003g0235a0001c0001t0003g0252others(35): Show | 40 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.380-1078_380-1076d others(5): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | ||||||
chr1:17426759
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0002t0002g0163a0001c0002t0002g0361 | 2 | HG03195.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.380-1087_380-1076d others(14): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | ||||||
chr1:17426759
|
CTTTTTTT others(6): Show |
C | 95 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(92): Show | 102 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.380-1088_380-1076d others(15): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | ||||||
chr1:17426759
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0002t0002g0147a0001c0002t0002g0189 | 2 | HG03041.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.380-1089_380-1076d others(16): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | ||||||
chr1:17426763
|
T | C | 1 | a0001c0002t0002g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.380-1079A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426763 | ||||||
chr1:17426766
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0061 | 2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.380-1082A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426766 | ||||||
chr1:17426812
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.380-1128C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426812 | ||||||
chr1:17426844
|
C | A | 100 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(97): Show | 107 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.380-1160G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426844 | ||||||
chr1:17427077
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.380-1393A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427077 | ||||||
chr1:17427143
|
G | A | 117 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(114): Show | 124 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.380-1459C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427143 | ||||||
chr1:17427221
|
G | C | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.380-1537C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427221 | ||||||
chr1:17427253
|
C | T | 106 | a0001c0001t0001g0220a0001c0001t0003g0032a0001c0001t0003g0033others(103): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.380-1569G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427253 | ||||||
chr1:17427328
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.380-1644C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427328 | ||||||
chr1:17427343
|
G | A | 1 | a0001c0001t0004g0215 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.380-1659C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427343 | ||||||
chr1:17427421
|
G | A | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.379+1685C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427421 | ||||||
chr1:17427462
|
T | TTAAAACT others(7): Show |
1 | a0001c0001t0003g0033 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.379+1630_379+1643d others(16): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427462 | ||||||
chr1:17427598
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.379+1508A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427598 | ||||||
chr1:17427618
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.379+1488C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427618 | ||||||
chr1:17427732
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.379+1374G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427732 | ||||||
chr1:17427761
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.379+1345A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427761 | ||||||
chr1:17427883
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.379+1223A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427883 | ||||||
chr1:17427884
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.379+1222C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427884 | ||||||
chr1:17427885
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.379+1221G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427885 | ||||||
chr1:17427894
|
T | A | 1 | a0001c0012t0002g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.379+1212A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427894 | ||||||
chr1:17427972
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | NA19003.hp1 NA19067.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.379+1134C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427972 | ||||||
chr1:17428035
|
T | A | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379+1071A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428035 | ||||||
chr1:17428038
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0358 | 3 | HG00642.hp2 HG01261.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.379+1068C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428038 | ||||||
chr1:17428112
|
T | A | 10 | a0002c0003t0004g0318a0002c0003t0004g0319a0002c0003t0004g0321others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.379+994A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428112 | ||||||
chr1:17428112
|
T | G | 117 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(114): Show | 124 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.379+994A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428112 | ||||||
chr1:17428198
|
A | G | 2 | a0001c0002t0002g0348a0001c0002t0002g0349 | 2 | HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.379+908T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428198 | ||||||
chr1:17428234
|
A | G | 1 | a0001c0009t0001g0058 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.379+872T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428234 | ||||||
chr1:17428271
|
A | C | 244 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(241): Show | 255 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.379+835T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428271 | ||||||
chr1:17428319
|
G | A | 127 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0001g0206others(124): Show | 135 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.379+787C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428319 | ||||||
chr1:17428336
|
C | T | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.379+770G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428336 | ||||||
chr1:17428420
|
CCT | C | 114 | a0001c0001t0001g0220a0001c0001t0003g0032a0001c0001t0003g0033others(111): Show | 117 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.379+684_379+685del others(2): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428420 | ||||||
chr1:17428551
|
C | T | 1 | a0001c0002t0002g0164 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.379+555G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428551 | ||||||
chr1:17428625
|
A | G | 1 | a0001c0001t0031g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.379+481T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428625 | ||||||
chr1:17428919
|
C | A | 6 | a0001c0001t0006g0357a0001c0001t0008g0352a0001c0001t0008g0353others(3): Show | 6 | HG02280.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.379+187G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428919 | ||||||
chr1:17429211
|
G | A | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-12C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429211 | ||||||
chr1:17429304
|
C | T | 1 | a0001c0001t0004g0287 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.286-105G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429304 | ||||||
chr1:17429483
|
A | C | 1 | a0001c0001t0003g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.286-284T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429483 | ||||||
chr1:17429504
|
G | A | 1 | a0001c0002t0002g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.286-305C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429504 | ||||||
chr1:17429522
|
G | A | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-323C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429522 | ||||||
chr1:17429566
|
G | C | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-367C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429566 | ||||||
chr1:17429613
|
C | T | 5 | a0001c0002t0002g0177a0001c0002t0002g0178a0001c0002t0002g0180others(2): Show | 5 | NA18949.hp1 NA19011.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-414G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429613 | ||||||
chr1:17429694
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.286-495G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429694 | ||||||
chr1:17429715
|
T | G | 1 | a0002c0005t0006g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.286-516A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429715 | ||||||
chr1:17429780
|
G | A | 7 | a0001c0002t0002g0331a0001c0002t0002g0332a0001c0002t0002g0339others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.286-581C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429780 | ||||||
chr1:17429843
|
G | T | 1 | a0001c0001t0001g0085 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.286-644C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429843 | ||||||
chr1:17429972
|
G | A | 1 | a0001c0002t0002g0159 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.286-773C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429972 | ||||||
chr1:17430074
|
G | A | 8 | a0001c0001t0007g0308a0001c0001t0007g0309a0001c0001t0007g0310others(5): Show | 8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.286-875C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430074 | ||||||
chr1:17430204
|
T | C | 4 | a0001c0001t0009g0012a0001c0001t0009g0256a0001c0001t0009g0257others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-1005A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430204 | ||||||
chr1:17430488
|
C | CA | 124 | a0001c0001t0001g0050a0001c0001t0001g0149a0001c0001t0001g0186others(121): Show | 131 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.286-1290dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430488 | ||||||
chr1:17430488
|
C | CAA | 13 | a0001c0001t0001g0107a0001c0002t0002g0317a0001c0002t0005g0174others(10): Show | 14 | HG01099.hp1 HG01106.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.286-1291_286-1290d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430488 | ||||||
chr1:17430502
|
A | G | 1 | a0001c0001t0003g0291 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.286-1303T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430502 | ||||||
chr1:17430720
|
G | A | 114 | a0001c0001t0001g0220a0001c0001t0003g0032a0001c0001t0003g0033others(111): Show | 117 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.286-1521C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430720 | ||||||
chr1:17430725
|
T | G | 113 | a0001c0001t0001g0050a0001c0001t0001g0149a0001c0001t0001g0186others(110): Show | 120 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.286-1526A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430725 | ||||||
chr1:17430790
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.286-1591C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430790 | ||||||
chr1:17430970
|
G | A | 2 | a0001c0002t0002g0348a0001c0002t0002g0349 | 2 | HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.286-1771C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430970 | ||||||
chr1:17431025
|
A | G | 1 | a0001c0001t0008g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.286-1826T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431025 | ||||||
chr1:17431095
|
C | T | 1 | a0001c0001t0008g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.286-1896G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431095 | ||||||
chr1:17431103
|
C | T | 6 | a0001c0002t0002g0331a0001c0002t0002g0332a0001c0002t0002g0339others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-1904G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431103 | ||||||
chr1:17431333
|
C | CA | 13 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0055others(10): Show | 14 | HG00099.hp2 HG01070.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.286-2135dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431333 | ||||||
chr1:17431333
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0012t0002g0314 | 3 | HG01361.hp2 HG01496.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.286-2135_286-2134i others(19): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431333 | ||||||
chr1:17431333
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0007g0313 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.286-2135_286-2134i others(20): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431333 | ||||||
chr1:17431333
|
CA | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0017others(11): Show | 17 | HG00423.hp2 HG00741.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.286-2135delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431333 | ||||||
chr1:17431334
|
A | AAAAAAAA others(9): Show |
4 | a0001c0001t0007g0308a0001c0001t0007g0309a0001c0001t0007g0310others(1): Show | 4 | HG03486.hp1 NA18962.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2136_286-2135i others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431334 | ||||||
chr1:17431343
|
A | T | 105 | a0001c0001t0001g0220a0001c0001t0003g0032a0001c0001t0003g0033others(102): Show | 108 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.286-2144T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431343 | ||||||
chr1:17431345
|
A | T | 1 | a0001c0002t0002g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.286-2146T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431345 | ||||||
chr1:17431350
|
A | T | 105 | a0001c0001t0001g0220a0001c0001t0003g0032a0001c0001t0003g0033others(102): Show | 108 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.286-2151T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431350 | ||||||
chr1:17431350
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.286-2162_286-2152d others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431350 | ||||||
chr1:17431355
|
A | AATATATA others(3): Show |
1 | a0001c0002t0002g0336 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.286-2157_286-2156i others(12): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431355 | ||||||
chr1:17431355
|
A | AATATATA others(13): Show |
1 | a0001c0001t0008g0353 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.286-2157_286-2156i others(22): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431355 | ||||||
chr1:17431355
|
A | ATATATAT others(6): Show |
1 | a0001c0002t0002g0334 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.286-2157_286-2156i others(15): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431355 | ||||||
chr1:17431355
|
A | T | 2 | a0001c0001t0031g0016a0001c0002t0002g0262 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.286-2156T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431355 | ||||||
chr1:17431356
|
AAAAATAT | A | 7 | a0002c0003t0004g0319a0002c0003t0006g0014a0002c0003t0006g0322others(4): Show | 8 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.286-2164_286-2158d others(9): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431356 | ||||||
chr1:17431357
|
A | AATATATA others(3): Show |
1 | a0001c0004t0004g0345 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.286-2159_286-2158i others(12): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431357 | ||||||
chr1:17431357
|
A | AATATATA others(33): Show |
1 | a0001c0002t0002g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.286-2159_286-2158i others(42): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431357 | ||||||
chr1:17431357
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0010g0230 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.286-2159_286-2158i others(33): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431357 | ||||||
chr1:17431357
|
A | T | 6 | a0001c0001t0008g0353a0001c0001t0031g0016a0001c0002t0002g0334others(3): Show | 6 | HG02622.hp2 HG02809.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2158T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431357 | ||||||
chr1:17431359
|
A | AAAAAAAA others(14): Show |
1 | a0001c0002t0002g0329 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAAAA others(52): Show |
1 | a0001c0001t0001g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(61): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0008g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(20): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAAAA others(17): Show |
1 | a0001c0002t0002g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(26): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAAAA others(39): Show |
1 | a0001c0002t0002g0152 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(48): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAAAT others(8): Show |
1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(17): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAAAT others(40): Show |
1 | a0001c0002t0002g0151 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(49): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAATA others(3): Show |
1 | a0001c0002t0002g0167 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(12): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAATA others(9): Show |
1 | a0001c0002t0002g0339 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAATA others(15): Show |
1 | a0001c0002t0002g0161 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(24): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAATA others(19): Show |
2 | a0001c0002t0002g0159a0001c0002t0002g0200 | 2 | HG02080.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(28): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAAATA others(39): Show |
1 | a0001c0002t0002g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(48): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0008g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(6): Show |
2 | a0001c0002t0002g0332a0001c0002t0005g0166 | 2 | HG01433.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(15): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(14): Show |
1 | a0001c0001t0008g0352 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(16): Show |
1 | a0001c0002t0002g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(25): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(18): Show |
4 | a0001c0002t0002g0144a0001c0002t0002g0158a0001c0002t0005g0157others(1): Show | 4 | HG00735.hp1 HG02004.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(27): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(20): Show |
2 | a0001c0002t0002g0156a0001c0002t0002g0201 | 2 | HG01255.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(29): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(24): Show |
2 | a0001c0002t0002g0139a0001c0002t0005g0155 | 2 | HG02015.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(33): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(34): Show |
1 | a0001c0002t0002g0141 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(43): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(36): Show |
1 | a0001c0002t0002g0140 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(45): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAAATAT others(44): Show |
1 | a0001c0002t0005g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(53): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(3): Show |
2 | a0001c0002t0002g0135a0001c0002t0002g0347 | 2 | HG01074.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(12): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(5): Show |
3 | a0001c0002t0002g0331a0001c0002t0002g0341a0001c0002t0002g0342 | 3 | HG02559.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(14): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(7): Show |
1 | a0001c0002t0002g0164 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(16): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(9): Show |
2 | a0001c0002t0012g0366a0001c0002t0020g0338 | 2 | HG00642.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(11): Show |
2 | a0001c0002t0002g0148a0001c0002t0002g0343 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(20): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(13): Show |
1 | a0001c0002t0002g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(22): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(15): Show |
1 | a0001c0002t0002g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(24): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(17): Show |
1 | a0001c0002t0002g0333 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(26): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(23): Show |
2 | a0001c0002t0002g0195a0001c0002t0002g0196 | 2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(32): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(25): Show |
2 | a0001c0002t0002g0154a0001c0002t0002g0194 | 2 | HG01123.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(34): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(27): Show |
1 | a0001c0002t0002g0191 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(36): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(29): Show |
1 | a0001c0002t0002g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(38): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAAATATA others(31): Show |
1 | a0001c0002t0002g0153 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(40): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAATATAT others(4): Show |
2 | a0001c0002t0002g0330a0001c0002t0002g0340 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAATATAT others(8): Show |
1 | a0001c0002t0002g0337 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(17): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAATATAT others(10): Show |
1 | a0001c0002t0002g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(19): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAATATAT others(12): Show |
2 | a0001c0001t0006g0357a0001c0001t0017g0356 | 2 | HG02280.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(21): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAATATAT others(14): Show |
1 | a0001c0001t0008g0355 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAATATAT others(16): Show |
1 | a0001c0001t0008g0354 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(25): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAATATAT others(24): Show |
1 | a0001c0002t0002g0143 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(33): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AAATATAT others(28): Show |
1 | a0001c0002t0002g0142 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(37): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AATATATA others(7): Show |
1 | a0001c0002t0002g0344 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.286-2174_286-2161d others(16): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AATATATA others(11): Show |
1 | a0001c0002t0002g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.286-2178_286-2161d others(20): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | AATATATA others(23): Show |
2 | a0001c0002t0002g0192a0001c0002t0002g0193 | 2 | HG02004.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(32): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAA others(18): Show |
1 | a0001c0001t0003g0259 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(27): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAA others(20): Show |
1 | a0001c0001t0004g0287 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(29): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAA others(36): Show |
1 | a0001c0001t0014g0275 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(45): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAA others(42): Show |
1 | a0001c0001t0014g0273 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(51): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAA others(26): Show |
4 | a0001c0001t0003g0242a0001c0001t0003g0244a0001c0001t0003g0307others(1): Show | 4 | HG00099.hp1 HG02040.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(35): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAA others(28): Show |
1 | a0001c0001t0004g0282 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(37): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAA others(36): Show |
1 | a0001c0001t0003g0363 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(45): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(4): Show |
3 | a0001c0001t0001g0220a0001c0001t0004g0211a0001c0001t0004g0219 | 3 | HG02735.hp2 HG03710.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(6): Show |
1 | a0001c0001t0003g0365 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(15): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(8): Show |
4 | a0001c0001t0003g0260a0001c0001t0003g0261a0001c0001t0003g0295others(1): Show | 4 | HG02895.hp2 NA19005.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(17): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(10): Show |
3 | a0001c0001t0003g0266a0001c0001t0004g0215a0001c0001t0004g0302 | 3 | HG02602.hp2 HG03942.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(19): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(12): Show |
1 | a0001c0001t0004g0284 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(21): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(14): Show |
3 | a0001c0001t0009g0012a0001c0001t0009g0258a0001c0001t0034g0214 | 4 | HG00639.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(16): Show |
3 | a0001c0001t0004g0011a0001c0001t0004g0217a0001c0001t0004g0283 | 4 | HG01243.hp1 HG01978.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(25): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(18): Show |
9 | a0001c0001t0003g0254a0001c0001t0003g0255a0001c0001t0003g0293others(6): Show | 9 | HG00438.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(27): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(20): Show |
8 | a0001c0001t0003g0223a0001c0001t0003g0249a0001c0001t0003g0250others(5): Show | 8 | HG02165.hp1 NA18940.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(29): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(22): Show |
6 | a0001c0001t0003g0033a0001c0001t0003g0245a0001c0001t0003g0246others(3): Show | 6 | HG00558.hp1 HG00609.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(31): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(24): Show |
5 | a0001c0001t0003g0239a0001c0001t0003g0240a0001c0001t0004g0013others(2): Show | 6 | HG02886.hp2 HG03486.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(33): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(26): Show |
7 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(4): Show | 7 | HG00673.hp2 HG02071.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(35): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(28): Show |
12 | a0001c0001t0003g0233a0001c0001t0003g0234a0001c0001t0003g0235others(9): Show | 12 | HG00423.hp1 HG00738.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(37): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(30): Show |
4 | a0001c0001t0003g0221a0001c0001t0003g0231a0001c0001t0003g0232others(1): Show | 4 | NA18949.hp2 NA18952.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(39): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(32): Show |
5 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0227others(2): Show | 5 | HG02132.hp2 NA18747.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(41): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(34): Show |
4 | a0001c0001t0003g0362a0001c0001t0004g0274a0001c0001t0004g0298others(1): Show | 4 | HG00323.hp2 HG00639.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(43): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(36): Show |
2 | a0001c0001t0004g0213a0003c0006t0003g0212 | 2 | HG02647.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(45): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(38): Show |
3 | a0001c0001t0003g0032a0001c0001t0003g0350a0001c0001t0004g0272 | 3 | HG03831.hp2 NA19082.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(47): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(40): Show |
4 | a0001c0001t0004g0269a0001c0001t0004g0270a0001c0001t0004g0271others(1): Show | 4 | HG00558.hp2 HG02040.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(49): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAAAAT others(62): Show |
1 | a0001c0001t0004g0297 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(71): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAATAT others(14): Show |
2 | a0001c0001t0009g0256a0001c0001t0009g0257 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAAATAT others(20): Show |
1 | a0001c0001t0003g0222 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(29): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATAT | 6 | a0001c0001t0007g0309a0001c0001t0007g0310a0001c0001t0007g0311others(3): Show | 6 | HG01496.hp1 NA18962.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(5): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0033g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(17): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
A | T | 9 | a0001c0001t0008g0353a0001c0001t0010g0230a0001c0001t0031g0016others(6): Show | 9 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-2160T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431359
|
AAT | A | 37 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0044others(34): Show | 43 | HG00140.hp2 HG01071.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.286-2162_286-2161d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | ||||||
chr1:17431360
|
AT | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(54): Show | 65 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.286-2162delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431360 | ||||||
chr1:17431361
|
T | A | 18 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0062others(15): Show | 18 | HG01123.hp2 HG02148.hp1 HG02300.hp1 others(15): Show |
intron_variant | MODIFIER | c.286-2162A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431361 | ||||||
chr1:17431363
|
T | A | 24 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0002t0002g0001others(21): Show | 30 | HG00140.hp2 HG01071.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.286-2164A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431363 | ||||||
chr1:17431365
|
T | A | 2 | a0001c0002t0002g0203a0001c0002t0002g0204 | 2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.286-2166A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431365 | ||||||
chr1:17431367
|
T | A | 2 | a0001c0001t0003g0264a0001c0002t0002g0204 | 2 | HG00438.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.286-2168A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431367 | ||||||
chr1:17431369
|
T | A | 1 | a0001c0001t0003g0264 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.286-2170A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431369 | ||||||
chr1:17431424
|
T | C | 1 | a0001c0001t0004g0287 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.286-2225A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431424 | ||||||
chr1:17431441
|
C | T | 106 | a0001c0001t0001g0220a0001c0001t0003g0032a0001c0001t0003g0033others(103): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.286-2242G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431441 | ||||||
chr1:17431491
|
C | A | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-2292G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431491 | ||||||
chr1:17431499
|
C | CA | 22 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0051others(19): Show | 22 | HG01099.hp2 HG01106.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.286-2301dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | ||||||
chr1:17431499
|
C | CAA | 98 | a0001c0001t0001g0050a0001c0001t0001g0149a0001c0001t0001g0186others(95): Show | 105 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.286-2302_286-2301d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | ||||||
chr1:17431499
|
C | CAAA | 8 | a0001c0002t0002g0147a0001c0002t0002g0148a0001c0002t0002g0200others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.286-2303_286-2301d others(5): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | ||||||
chr1:17431499
|
CA | C | 20 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(17): Show | 20 | HG01070.hp1 HG01361.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.286-2301delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | ||||||
chr1:17431499
|
CAA | C | 103 | a0001c0001t0001g0220a0001c0001t0003g0032a0001c0001t0003g0033others(100): Show | 106 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.286-2302_286-2301d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | ||||||
chr1:17431553
|
A | G | 5 | a0001c0002t0002g0145a0001c0002t0002g0146a0001c0002t0002g0147others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-2354T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431553 | ||||||
chr1:17431579
|
T | C | 1 | a0001c0001t0027g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286-2380A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431579 | ||||||
chr1:17431582
|
G | C | 2 | a0001c0002t0002g0131a0001c0002t0002g0132 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.286-2383C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431582 | ||||||
chr1:17431694
|
T | A | 8 | a0001c0001t0007g0308a0001c0001t0007g0309a0001c0001t0007g0310others(5): Show | 8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.286-2495A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431694 | ||||||
chr1:17431700
|
C | T | 1 | a0001c0001t0003g0290 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.286-2501G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431700 | ||||||
chr1:17432132
|
C | T | 1 | a0001c0002t0002g0329 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.286-2933G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432132 | ||||||
chr1:17432164
|
T | C | 35 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0004g0211others(32): Show | 37 | HG00323.hp2 HG00558.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.286-2965A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432164 | ||||||
chr1:17432296
|
T | C | 1 | a0001c0001t0004g0289 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.286-3097A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432296 | ||||||
chr1:17432324
|
C | T | 1 | a0001c0001t0003g0295 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.286-3125G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432324 | ||||||
chr1:17432577
|
C | T | 5 | a0001c0002t0002g0145a0001c0002t0002g0146a0001c0002t0002g0147others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-3378G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432577 | ||||||
chr1:17432717
|
T | C | 1 | a0001c0002t0002g0347 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.286-3518A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432717 | ||||||
chr1:17432749
|
T | C | 246 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0149others(243): Show | 257 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.286-3550A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432749 | ||||||
chr1:17432850
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.286-3651G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432850 | ||||||
chr1:17432851
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | NA19003.hp1 NA19067.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-3652C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432851 | ||||||
chr1:17432858
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.286-3659A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432858 | ||||||
chr1:17432890
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.286-3691C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432890 | ||||||
chr1:17432907
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.286-3708C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432907 | ||||||
chr1:17432959
|
AAAAAAG | A | 20 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0002t0002g0001others(17): Show | 26 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.286-3766_286-3761d others(8): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432959 | ||||||
chr1:17432991
|
T | A | 3 | a0001c0001t0003g0033a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG00423.hp1 NA19086.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.286-3792A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432991 | ||||||
chr1:17433021
|
T | C | 3 | a0001c0002t0002g0130a0001c0002t0002g0131a0001c0002t0002g0132 | 3 | HG01256.hp1 HG01258.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.286-3822A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433021 | ||||||
chr1:17433040
|
A | G | 3 | a0001c0004t0004g0328a0001c0004t0004g0345a0001c0004t0004g0346 | 3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.286-3841T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433040 | ||||||
chr1:17433397
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.286-4198C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433397 | ||||||
chr1:17433398
|
C | G | 10 | a0002c0003t0004g0318a0002c0003t0004g0319a0002c0003t0004g0321others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-4199G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433398 | ||||||
chr1:17433423
|
C | T | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-4224G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433423 | ||||||
chr1:17433449
|
T | C | 1 | a0001c0001t0006g0210 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.286-4250A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433449 | ||||||
chr1:17433485
|
C | T | 1 | a0001c0001t0027g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286-4286G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433485 | ||||||
chr1:17433519
|
G | GT | 5 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(2): Show | 5 | HG02559.hp1 HG04204.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-4321dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433519 | ||||||
chr1:17433524
|
T | G | 1 | a0001c0002t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.286-4325A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433524 | ||||||
chr1:17433525
|
T | G | 1 | a0001c0002t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.286-4326A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433525 | ||||||
chr1:17433526
|
T | A | 1 | a0001c0002t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.286-4327A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433526 | ||||||
chr1:17433527
|
G | C | 1 | a0001c0002t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.286-4328C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433527 | ||||||
chr1:17433549
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.286-4350G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433549 | ||||||
chr1:17433602
|
A | G | 101 | a0001c0001t0001g0050a0001c0001t0001g0149a0001c0001t0001g0186others(98): Show | 108 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.286-4403T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433602 | ||||||
chr1:17433662
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.286-4463G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433662 | ||||||
chr1:17433833
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.285+4397G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433833 | ||||||
chr1:17433836
|
G | T | 1 | a0001c0002t0002g0330 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285+4394C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433836 | ||||||
chr1:17433837
|
GAGGTA | G | 6 | a0001c0002t0002g0139a0001c0002t0002g0140a0001c0002t0002g0141others(3): Show | 6 | HG02015.hp2 HG02080.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+4388_285+4392d others(7): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433837 | ||||||
chr1:17433843
|
A | T | 6 | a0001c0002t0002g0139a0001c0002t0002g0140a0001c0002t0002g0141others(3): Show | 6 | HG02015.hp2 HG02080.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+4387T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433843 | ||||||
chr1:17433844
|
G | C | 6 | a0001c0002t0002g0139a0001c0002t0002g0140a0001c0002t0002g0141others(3): Show | 6 | HG02015.hp2 HG02080.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+4386C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433844 | ||||||
chr1:17433845
|
A | T | 6 | a0001c0002t0002g0139a0001c0002t0002g0140a0001c0002t0002g0141others(3): Show | 6 | HG02015.hp2 HG02080.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+4385T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433845 | ||||||
chr1:17433848
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+4382G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433848 | ||||||
chr1:17433936
|
T | C | 38 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0004g0211others(35): Show | 40 | HG00323.hp2 HG00558.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.285+4294A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433936 | ||||||
chr1:17434417
|
C | G | 1 | a0001c0001t0031g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.285+3813G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434417 | ||||||
chr1:17434564
|
A | C | 1 | a0001c0001t0024g0048 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.285+3666T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434564 | ||||||
chr1:17434614
|
C | A | 7 | a0001c0001t0007g0309a0001c0001t0007g0310a0001c0001t0007g0311others(4): Show | 7 | HG01361.hp2 HG01496.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+3616G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434614 | ||||||
chr1:17434647
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+3583C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434647 | ||||||
chr1:17434839
|
G | A | 18 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(15): Show | 19 | HG00438.hp2 HG01081.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.285+3391C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434839 | ||||||
chr1:17434876
|
G | A | 1 | a0001c0001t0003g0295 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.285+3354C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434876 | ||||||
chr1:17435070
|
T | C | 1 | a0001c0001t0001g0316 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.285+3160A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17435070 | ||||||
chr1:17435206
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.285+3024G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17435206 | ||||||
chr1:17435800
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.285+2430G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17435800 | ||||||
chr1:17435918
|
CA | C | 124 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0149others(121): Show | 132 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.285+2311delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17435918 | ||||||
chr1:17436085
|
T | C | 10 | a0002c0003t0004g0318a0002c0003t0004g0319a0002c0003t0004g0321others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+2145A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436085 | ||||||
chr1:17436170
|
A | C | 1 | a0001c0002t0002g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.285+2060T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436170 | ||||||
chr1:17436174
|
G | A | 1 | a0001c0001t0025g0296 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.285+2056C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436174 | ||||||
chr1:17436239
|
G | A | 6 | a0001c0001t0004g0297a0001c0001t0004g0298a0001c0001t0004g0299others(3): Show | 6 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+1991C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436239 | ||||||
chr1:17436320
|
A | G | 2 | a0001c0001t0004g0304a0001c0001t0004g0315 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.285+1910T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436320 | ||||||
chr1:17436364
|
T | C | 2 | a0001c0002t0002g0348a0001c0002t0002g0349 | 2 | HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.285+1866A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436364 | ||||||
chr1:17436397
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0004g0303 | 2 | HG02698.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.285+1833C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436397 | ||||||
chr1:17436440
|
G | A | 1 | a0001c0001t0008g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+1790C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436440 | ||||||
chr1:17436635
|
C | A | 2 | a0001c0002t0002g0135a0001c0002t0002g0317 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.285+1595G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436635 | ||||||
chr1:17436732
|
C | A | 1 | a0002c0005t0006g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285+1498G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436732 | ||||||
chr1:17436816
|
A | G | 245 | a0001c0001t0001g0045a0001c0001t0001g0149a0001c0001t0001g0186others(242): Show | 256 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.285+1414T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436816 | ||||||
chr1:17436934
|
G | A | 1 | a0001c0001t0027g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285+1296C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436934 | ||||||
chr1:17436976
|
A | G | 1 | a0001c0002t0002g0329 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.285+1254T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436976 | ||||||
chr1:17437007
|
C | T | 1 | a0001c0002t0002g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.285+1223G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437007 | ||||||
chr1:17437021
|
A | G | 245 | a0001c0001t0001g0045a0001c0001t0001g0149a0001c0001t0001g0186others(242): Show | 256 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.285+1209T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437021 | ||||||
chr1:17437070
|
G | C | 128 | a0001c0001t0001g0149a0001c0001t0001g0186a0001c0001t0001g0202others(125): Show | 136 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.285+1160C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437070 | ||||||
chr1:17437508
|
G | T | 1 | a0001c0001t0027g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285+722C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437508 | ||||||
chr1:17437557
|
G | C | 2 | a0001c0002t0011g0208a0001c0002t0011g0209 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.285+673C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437557 | ||||||
chr1:17437579
|
C | G | 4 | a0001c0001t0004g0011a0001c0001t0004g0216a0001c0001t0004g0217others(1): Show | 5 | HG01243.hp1 HG01943.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+651G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437579 | ||||||
chr1:17437580
|
G | A | 1 | a0002c0005t0006g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285+650C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437580 | ||||||
chr1:17437601
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.285+629G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437601 | ||||||
chr1:17437637
|
G | A | 8 | a0001c0001t0007g0308a0001c0001t0007g0309a0001c0001t0007g0310others(5): Show | 8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+593C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437637 | ||||||
chr1:17437647
|
C | G | 2 | a0001c0001t0004g0215a0001c0001t0034g0214 | 2 | HG00639.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.285+583G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437647 | ||||||
chr1:17437673
|
A | AGCATGCG others(72): Show |
1 | a0001c0002t0002g0361 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.285+556_285+557ins others(79): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437673 | ||||||
chr1:17437673
|
A | AGCATGCG others(73): Show |
1 | a0001c0001t0026g0305 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.285+556_285+557ins others(80): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437673 | ||||||
chr1:17437673
|
A | AGCATGCG others(71): Show |
361 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(358): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.285+556_285+557ins others(78): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437673 | ||||||
chr1:17437673
|
A | AGCATGCG others(71): Show |
2 | a0002c0003t0004g0318a0002c0003t0004g0319 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.285+556_285+557ins others(78): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437673 | ||||||
chr1:17437673
|
A | AGCATGCG others(71): Show |
1 | a0001c0001t0001g0042 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.285+556_285+557ins others(78): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437673 | ||||||
chr1:17437745
|
C | T | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.285+485G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437745 | ||||||
chr1:17437753
|
ACGGCCGC others(14): Show |
A | 1 | a0001c0001t0003g0306 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.285+456_285+476del others(21): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437753 | ||||||
chr1:17437754
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.285+476G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437754 | ||||||
chr1:17437765
|
C | G | 1 | a0001c0001t0004g0213 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.285+465G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437765 | ||||||
chr1:17437765
|
C | T | 1 | a0001c0004t0004g0328 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285+465G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437765 | ||||||
chr1:17437851
|
C | G | 1 | a0001c0001t0027g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285+379G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437851 | ||||||
chr1:17437882
|
C | A | 1 | a0001c0001t0003g0307 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.285+348G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437882 | ||||||
chr1:17437912
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.285+318T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437912 | ||||||
chr1:17437928
|
C | T | 1 | a0001c0002t0005g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.285+302G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437928 | ||||||
chr1:17437976
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.285+254G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437976 | ||||||
chr1:17437985
|
C | A | 1 | a0001c0001t0001g0316 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.285+245G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437985 | ||||||
chr1:17438008
|
G | T | 1 | a0001c0001t0001g0039 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.285+222C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17438008 | ||||||
chr1:17438044
|
C | T | 1 | a0001c0002t0002g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285+186G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17438044 | ||||||
chr1:17438110
|
C | T | 1 | a0001c0002t0005g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.285+120G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17438110 | ||||||
chr1:17438131
|
G | A | 116 | a0001c0001t0001g0149a0001c0001t0001g0186a0001c0001t0001g0202others(113): Show | 123 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.285+99C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17438131 | ||||||
chr1:17438582
|
G | T | 1 | a0001c0001t0004g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-8-60C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438582 | ||||||
chr1:17438603
|
C | T | 1 | a0001c0002t0002g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-8-81G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438603 | ||||||
chr1:17438641
|
G | A | 8 | a0001c0001t0007g0308a0001c0001t0007g0309a0001c0001t0007g0310others(5): Show | 8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-119C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438641 | ||||||
chr1:17438644
|
G | A | 1 | a0001c0001t0004g0315 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8-122C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438644 | ||||||
chr1:17438767
|
G | T | 3 | a0001c0002t0005g0028a0001c0002t0005g0029a0001c0002t0013g0030 | 3 | HG01070.hp2 HG01071.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-8-245C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438767 | ||||||
chr1:17438817
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-8-295T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438817 | ||||||
chr1:17438873
|
C | T | 3 | a0001c0002t0002g0130a0001c0002t0002g0131a0001c0002t0002g0132 | 3 | HG01256.hp1 HG01258.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-8-351G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438873 | ||||||
chr1:17438988
|
T | C | 245 | a0001c0001t0001g0133a0001c0001t0001g0149a0001c0001t0001g0186others(242): Show | 256 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.-8-466A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438988 | ||||||
chr1:17439009
|
G | C | 245 | a0001c0001t0001g0133a0001c0001t0001g0149a0001c0001t0001g0186others(242): Show | 256 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.-8-487C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439009 | ||||||
chr1:17439049
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9+496A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439049 | ||||||
chr1:17439100
|
G | C | 1 | a0001c0001t0006g0210 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-9+445C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439100 | ||||||
chr1:17439136
|
G | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-9+409C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439136 | ||||||
chr1:17439184
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-9+361G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439184 | ||||||
chr1:17439260
|
C | T | 116 | a0001c0001t0001g0220a0001c0001t0003g0032a0001c0001t0003g0033others(113): Show | 119 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.-9+285G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439260 | ||||||
chr1:17439307
|
G | C | 1 | a0001c0001t0003g0350 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+238C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439307 | ||||||
chr1:17439330
|
C | CT | 17 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0017others(14): Show | 20 | HG00140.hp1 HG00423.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+214dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439330 | ||||||
chr1:17439330
|
CT | C | 150 | a0001c0001t0001g0220a0001c0001t0001g0316a0001c0001t0003g0221others(147): Show | 154 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-9+214delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439330 | ||||||
chr1:17439330
|
CTT | C | 7 | a0001c0001t0006g0357a0001c0001t0007g0351a0001c0001t0008g0352others(4): Show | 7 | HG02280.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+213_-9+214delAA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439330 | ||||||
chr1:17439484
|
G | GA | 9 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0003g0362others(6): Show | 9 | HG02145.hp1 HG03516.hp2 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+60dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439484 | ||||||
chr1:17439488
|
A | G | 1 | a0001c0001t0035g0367 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-9+57T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439488 | ||||||
chr1:17439539
|
C | T | 1 | a0001c0001t0031g0016 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.-9+6G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439539 |