Item | Value |
---|---|
geneid | 222546 |
ensemblid | ENSG00000185002.10 |
hgncid | 21478 |
symbol | RFX6 |
name | regulatory factor X6 |
refseq_nuc | NM_173560.4 |
refseq_prot | NP_775831.2 |
ensembl_nuc | ENST00000332958.3 |
ensembl_prot | ENSP00000332208.2 |
mane_status | MANE Select |
chr | chr6 |
start | 116877242 |
end | 116932161 |
strand | + |
ver | v1.2 |
region | chr6:116877242-116932161 |
region5000 | chr6:116872242-116937161 |
regionname0 | RFX6_chr6_116877242_116932161 |
regionname5000 | RFX6_chr6_116872242_116937161 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 928 | 346 | 78 | 53 | 157 | 16 | 40 | 128 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0002 | 0/0 | 928 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0003 | 0/0 | 928 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0004 | 0/0 | 928 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0005 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0006 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0007 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0008 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0009 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0010 | 0/0 | 928 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2787 | 237 | 63 | 43 | 96 | 12 | 21 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0002 | 0/0 | 2787 | 103 | 10 | 10 | 60 | 4 | 19 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0003 | 0/0 | 2787 | 10 | 9 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0004 | 0/0 | 2787 | 5 | 4 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0005 | 0/0 | 2787 | 4 | 0 | 4 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0006 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0007 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0008 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0009 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0010 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0011 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0012 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0013 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0014 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0015 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0016 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
c0017 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 690 | 245 | 71 | 42 | 97 | 12 | 21 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
t0002 | 0/0 | 690 | 121 | 22 | 15 | 61 | 4 | 19 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
t0003 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
t0004 | 0/0 | 690 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
t0005 | 0/0 | 690 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
t0006 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
t0007 | 0/0 | 690 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
t0008 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 14 | 1 | 3 | 8 | 1 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0004 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2787 | 237 | 63 | 43 | 96 | 12 | 21 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0002 | 0/0 | 2787 | 103 | 10 | 10 | 60 | 4 | 19 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0006 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0009 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0010 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0012 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0016 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0002c0003 | 0/0 | 2787 | 10 | 9 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0002c0007 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0003c0004 | 0/0 | 2787 | 5 | 4 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0004c0005 | 0/0 | 2787 | 4 | 0 | 4 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0005c0017 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0006c0011 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0007c0014 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0008c0015 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0009c0013 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0010c0008 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3476 | 235 | 62 | 42 | 96 | 12 | 21 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0001t0007 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0001t0008 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0002t0002 | 0/0 | 3476 | 100 | 9 | 8 | 60 | 4 | 19 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0002t0003 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0002t0004 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0002t0005 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0006t0001 | 0/0 | 3476 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0009t0001 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0010t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0012t0002 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0001c0016t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0002c0003t0002 | 0/0 | 3476 | 9 | 8 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0002c0003t0006 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0002c0007t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0003c0004t0002 | 0/0 | 3476 | 5 | 4 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0004c0005t0002 | 0/0 | 3476 | 4 | 0 | 4 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0005c0017t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0006c0011t0002 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0007c0014t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0008c0015t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0009c0013t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
a0010c0008t0002 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | copy fasta | chr6 | 116872242 | 116937161 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 14 | 1 | 3 | 8 | 1 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0002t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0006t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0006t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0009t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0010t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0012t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0001c0016t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0002c0003t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0002c0003t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0002c0003t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0002c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0002c0003t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0002c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0002c0003t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0002c0007t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0003c0004t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0003c0004t0002g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0003c0004t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0004c0005t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0004c0005t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0004c0005t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0005c0017t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0006c0011t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0007c0014t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0008c0015t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0009c0013t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
a0010c0008t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0251 | EUR | GBR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | FIN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0209 | EUR | FIN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00642 | hp1 | a0010 | c0008 | t0002 | g0015 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG00741 | hp2 | a0002 | c0003 | t0002 | g0074 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01074 | hp1 | a0003 | c0004 | t0002 | g0023 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0049 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0037 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0285 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01258 | hp1 | a0004 | c0005 | t0002 | g0051 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01496 | hp2 | a0001 | c0002 | t0005 | g0047 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0040 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0210 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0284 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG01993 | hp2 | a0004 | c0005 | t0002 | g0019 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0054 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02080 | hp2 | a0006 | c0011 | t0002 | g0213 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02145 | hp2 | a0003 | c0004 | t0002 | g0022 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0184 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02148 | hp2 | a0004 | c0005 | t0002 | g0052 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | CDX | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02273 | hp1 | a0004 | c0005 | t0002 | g0019 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02280 | hp2 | a0003 | c0004 | t0002 | g0048 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02300 | hp1 | a0001 | c0002 | t0004 | g0037 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0212 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0089 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0220 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0183 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02615 | hp1 | a0002 | c0007 | t0001 | g0076 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02647 | hp2 | a0001 | c0012 | t0002 | g0185 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0015 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0180 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02717 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0177 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02818 | hp1 | a0008 | c0015 | t0001 | g0082 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02818 | hp2 | a0001 | c0002 | t0003 | g0088 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02886 | hp2 | a0002 | c0003 | t0002 | g0077 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02895 | hp1 | a0002 | c0003 | t0002 | g0024 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0072 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02897 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02897 | hp2 | a0002 | c0003 | t0002 | g0024 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0247 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0216 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03098 | hp1 | a0002 | c0003 | t0006 | g0078 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0259 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03139 | hp2 | a0001 | c0010 | t0001 | g0252 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03195 | hp2 | a0002 | c0003 | t0002 | g0073 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0238 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03486 | hp1 | a0003 | c0004 | t0002 | g0023 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0224 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03540 | hp1 | a0001 | c0006 | t0001 | g0083 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0169 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0182 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0168 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0240 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0241 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0170 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0246 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0257 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0178 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0249 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18906 | hp1 | a0005 | c0017 | t0001 | g0171 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0173 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18990 | hp2 | a0001 | c0009 | t0001 | g0274 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19030 | hp1 | a0001 | c0006 | t0001 | g0075 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19030 | hp2 | a0007 | c0014 | t0001 | g0117 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19043 | hp2 | a0001 | c0016 | t0001 | g0007 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19059 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19075 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA19240 | hp2 | a0003 | c0004 | t0002 | g0022 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0060 | AFR | ASW | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | TSI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | USA | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | USA | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | USA | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA20300 | hp2 | a0002 | c0003 | t0002 | g0008 | AFR | USA | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
NA21309 | hp2 | a0009 | c0013 | t0001 | g0064 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0271 | REF | REF | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0094 | REF | REF | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116877325
|
C | A | 2 | a0002a0003 | 16 | HG00741.hp2 HG01074.hp1 HG02145.hp2 others(13): Show |
missense_variant | MODERATE | c.50C>A | p.Ala17Glu | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/19 | 84/3476 | 50/2787 | 17/928 | chr6 | 116877325 | ||
chr6:116877337
|
C | A | 1 | a0010 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.62C>A | p.Ser21Tyr | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/19 | 96/3476 | 62/2787 | 21/928 | chr6 | 116877337 | ||
chr6:116918049
|
G | A | 1 | a0004 | 4 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(1): Show |
missense_variant | MODERATE | c.985G>A | p.Val329Ile | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/19 | 1019/3476 | 985/2787 | 329/928 | chr6 | 116918049 | ||
chr6:116920454
|
C | T | 1 | a0002 | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
missense_variant&splice_region_variant | MODERATE | c.1327C>T | p.His443Tyr | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/19 | 1361/3476 | 1327/2787 | 443/928 | chr6 | 116920454 | ||
chr6:116925643
|
C | A | 1 | a0009 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1869C>A | p.Asp623Glu | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/19 | 1903/3476 | 1869/2787 | 623/928 | chr6 | 116925643 | ||
chr6:116927317
|
C | G | 1 | a0005 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2176C>G | p.Arg726Gly | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 2210/3476 | 2176/2787 | 726/928 | chr6 | 116927317 | ||
chr6:116927402
|
C | T | 1 | a0006 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.2261C>T | p.Pro754Leu | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 2295/3476 | 2261/2787 | 754/928 | chr6 | 116927402 | ||
chr6:116928759
|
G | C | 1 | a0007 | 1 | NA19030.hp2 | missense_variant&splice_region_variant | MODERATE | c.2399G>C | p.Gly800Ala | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/19 | 2433/3476 | 2399/2787 | 800/928 | chr6 | 116928759 | ||
chr6:116928913
|
G | T | 1 | a0008 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.2553G>T | p.Gln851His | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/19 | 2587/3476 | 2553/2787 | 851/928 | chr6 | 116928913 | ||
chr6:116932161
|
A | G | 1 | a0001 | 1 | HG02300.hp1 | splice_region_variant | LOW | c.*655A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | chr6 | 116932161 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116894005
|
T | C | 1 | a0001c0009 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.585T>C | p.Ile195Ile | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/19 | 619/3476 | 585/2787 | 195/928 | chr6 | 116894005 | ||
chr6:116922097
|
T | C | 7 | a0001c0002a0001c0010a0002c0003others(4): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
synonymous_variant | LOW | c.1383T>C | p.Thr461Thr | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/19 | 1417/3476 | 1383/2787 | 461/928 | chr6 | 116922097 | ||
chr6:116923211
|
T | C | 8 | a0001c0002a0001c0010a0001c0012others(5): Show | 126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
synonymous_variant | LOW | c.1542T>C | p.Asn514Asn | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/19 | 1576/3476 | 1542/2787 | 514/928 | chr6 | 116923211 | ||
chr6:116925556
|
C | T | 7 | a0001c0002a0001c0012a0002c0003others(4): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
synonymous_variant | LOW | c.1782C>T | p.His594His | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/19 | 1816/3476 | 1782/2787 | 594/928 | chr6 | 116925556 | ||
chr6:116927055
|
T | C | 7 | a0001c0002a0001c0012a0002c0003others(4): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
synonymous_variant | LOW | c.1914T>C | p.Gly638Gly | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 1948/3476 | 1914/2787 | 638/928 | chr6 | 116927055 | ||
chr6:116927307
|
C | T | 1 | a0001c0006 | 2 | HG03540.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.2166C>T | p.Thr722Thr | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 2200/3476 | 2166/2787 | 722/928 | chr6 | 116927307 | ||
chr6:116927469
|
C | T | 1 | a0001c0016 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2328C>T | p.Ser776Ser | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 2362/3476 | 2328/2787 | 776/928 | chr6 | 116927469 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116931509
|
C | A | 11 | a0001c0002t0002a0001c0002t0003a0001c0002t0004others(8): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*3C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 3 | chr6 | 116931509 | |||||
chr6:116931596
|
T | G | 10 | a0001c0002t0002a0001c0002t0003a0001c0002t0004others(7): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*90T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 90 | chr6 | 116931596 | |||||
chr6:116931597
|
A | G | 1 | a0002c0003t0006 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 91 | chr6 | 116931597 | |||||
chr6:116931964
|
C | T | 1 | a0001c0002t0005 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*458C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 458 | chr6 | 116931964 | |||||
chr6:116932052
|
T | A | 1 | a0002c0003t0006 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 546 | chr6 | 116932052 | |||||
chr6:116932067
|
C | T | 1 | a0001c0001t0008 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*561C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 561 | chr6 | 116932067 | |||||
chr6:116932096
|
T | C | 1 | a0001c0001t0007 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 590 | chr6 | 116932096 | |||||
chr6:116932128
|
G | C | 1 | a0001c0002t0003 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*622G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 622 | chr6 | 116932128 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116877504
|
T | G | 1 | a0003c0004t0002g0048 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.223+6T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/18 | chr6 | 116877504 | ||||||
chr6:116877535
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.223+37C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/18 | chr6 | 116877535 | ||||||
chr6:116877734
|
A | C | 1 | a0001c0001t0001g0286 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.224-62A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/18 | chr6 | 116877734 | ||||||
chr6:116877991
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.380+39A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116877991 | ||||||
chr6:116878144
|
G | A | 1 | a0001c0001t0007g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.380+192G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878144 | ||||||
chr6:116878228
|
C | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(37): Show | 58 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.380+276C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878228 | ||||||
chr6:116878488
|
C | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.380+536C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878488 | ||||||
chr6:116878627
|
C | G | 109 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(106): Show | 122 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.380+675C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878627 | ||||||
chr6:116878660
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.380+708G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878660 | ||||||
chr6:116878660
|
G | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.380+708G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878660 | ||||||
chr6:116878676
|
G | A | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.380+724G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878676 | ||||||
chr6:116878828
|
TTATTATT others(8): Show |
T | 1 | a0001c0001t0001g0258 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.380+882_380+896del others(15): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 116878828 | |||||
chr6:116878870
|
G | GT | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.380+924dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 116878870 | |||||
chr6:116878900
|
CA | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.380+952delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 116878900 | |||||
chr6:116879271
|
C | A | 109 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(106): Show | 122 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.381-1273C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116879271 | ||||||
chr6:116879535
|
G | A | 17 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 19 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.381-1009G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116879535 | ||||||
chr6:116879607
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(72): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.381-937C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116879607 | ||||||
chr6:116879699
|
T | G | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.381-845T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116879699 | ||||||
chr6:116880175
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.381-369A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116880175 | ||||||
chr6:116880415
|
C | T | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.381-129C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116880415 | ||||||
chr6:116880427
|
A | G | 1 | a0001c0002t0002g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381-117A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116880427 | ||||||
chr6:116880705
|
A | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.504+38A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116880705 | ||||||
chr6:116880822
|
A | C | 17 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 19 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.504+155A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116880822 | ||||||
chr6:116881116
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.504+449C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881116 | ||||||
chr6:116881243
|
G | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.504+576G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881243 | ||||||
chr6:116881297
|
C | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG01993.hp1 NA18981.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.504+630C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881297 | ||||||
chr6:116881312
|
C | A | 106 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(103): Show | 119 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.504+645C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881312 | ||||||
chr6:116881509
|
G | A | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.504+842G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881509 | ||||||
chr6:116881525
|
A | G | 1 | a0001c0010t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.505-842A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881525 | ||||||
chr6:116881534
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0016t0001g0007 | 4 | HG02559.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-833T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881534 | ||||||
chr6:116881859
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.505-508G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881859 | ||||||
chr6:116881906
|
C | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.505-461C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881906 | ||||||
chr6:116882484
|
G | T | 1 | a0001c0001t0001g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.566+56G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882484 | ||||||
chr6:116882513
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.566+85A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882513 | ||||||
chr6:116882569
|
G | GA | 43 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0021others(40): Show | 54 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.566+154dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116882569 | |||||
chr6:116882569
|
G | GAA | 7 | a0001c0002t0002g0050a0001c0002t0002g0054a0001c0006t0001g0075others(4): Show | 9 | HG00741.hp2 HG02055.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.566+153_566+154dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116882569 | |||||
chr6:116882569
|
GA | G | 109 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(106): Show | 122 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.566+154delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116882569 | |||||
chr6:116882648
|
C | A | 17 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 19 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.566+220C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882648 | ||||||
chr6:116882712
|
G | A | 1 | a0001c0002t0002g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566+284G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882712 | ||||||
chr6:116882972
|
TG | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.566+545delG | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882972 | ||||||
chr6:116883166
|
A | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0079others(10): Show | 14 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.566+738A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883166 | ||||||
chr6:116883359
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.566+931T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883359 | ||||||
chr6:116883402
|
C | G | 1 | a0001c0002t0002g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566+974C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883402 | ||||||
chr6:116883538
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.566+1110T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883538 | ||||||
chr6:116883548
|
T | G | 1 | a0001c0001t0001g0016 | 3 | HG01256.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.566+1120T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883548 | ||||||
chr6:116883705
|
A | C | 2 | a0002c0003t0002g0024a0002c0003t0006g0078 | 3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.566+1277A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883705 | ||||||
chr6:116883735
|
G | A | 11 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(8): Show | 16 | HG00741.hp2 HG01074.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.566+1307G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883735 | ||||||
chr6:116884122
|
G | A | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+1694G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116884122 | ||||||
chr6:116884230
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(202): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.566+1802T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116884230 | ||||||
chr6:116884974
|
T | TA | 20 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(17): Show | 26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+2551dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116884974 | |||||
chr6:116885232
|
G | A | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.566+2804G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885232 | ||||||
chr6:116885240
|
G | T | 2 | a0002c0003t0002g0024a0002c0003t0006g0078 | 3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.566+2812G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885240 | ||||||
chr6:116885259
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(17): Show | 26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+2831G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885259 | ||||||
chr6:116885406
|
G | A | 3 | a0001c0002t0002g0169a0001c0002t0002g0170a0001c0002t0002g0257 | 3 | HG03654.hp1 HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.566+2978G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885406 | ||||||
chr6:116885678
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(17): Show | 26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+3250A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885678 | ||||||
chr6:116885720
|
GT | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(17): Show | 26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+3301delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116885720 | |||||
chr6:116885883
|
C | A | 1 | a0001c0001t0001g0262 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.566+3455C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885883 | ||||||
chr6:116886158
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(17): Show | 26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+3730G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886158 | ||||||
chr6:116886374
|
G | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(11): Show | 15 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.566+3946G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886374 | ||||||
chr6:116886482
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.566+4054T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886482 | ||||||
chr6:116886514
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0030others(4): Show | 16 | HG00621.hp2 HG02083.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.566+4086A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886514 | ||||||
chr6:116886519
|
A | G | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.566+4091A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886519 | ||||||
chr6:116886669
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566+4241C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886669 | ||||||
chr6:116886762
|
A | C | 1 | a0001c0002t0002g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566+4334A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886762 | ||||||
chr6:116886771
|
C | CA | 8 | a0001c0001t0001g0172a0001c0002t0002g0050a0001c0002t0002g0053others(5): Show | 9 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.566+4352dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116886771 | |||||
chr6:116886934
|
G | T | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.566+4506G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886934 | ||||||
chr6:116886993
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(17): Show | 26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+4565G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886993 | ||||||
chr6:116886995
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.566+4567G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886995 | ||||||
chr6:116887168
|
A | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.566+4740A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887168 | ||||||
chr6:116887191
|
T | G | 1 | a0001c0001t0001g0122 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.566+4763T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887191 | ||||||
chr6:116887295
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | NA18949.hp2 NA18991.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.566+4867T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887295 | ||||||
chr6:116887346
|
G | T | 106 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(103): Show | 119 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.566+4918G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887346 | ||||||
chr6:116887360
|
C | T | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+4932C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887360 | ||||||
chr6:116887558
|
T | C | 1 | a0001c0002t0002g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.566+5130T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887558 | ||||||
chr6:116887763
|
C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(259): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.566+5335C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887763 | ||||||
chr6:116887820
|
C | T | 1 | a0001c0001t0001g0046 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.566+5392C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887820 | ||||||
chr6:116888082
|
A | C | 1 | a0001c0002t0002g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566+5654A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888082 | ||||||
chr6:116888327
|
T | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.567-5660T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888327 | ||||||
chr6:116888346
|
A | G | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-5641A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888346 | ||||||
chr6:116888547
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(73): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.567-5440G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888547 | ||||||
chr6:116888697
|
A | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(17): Show | 26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.567-5290A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888697 | ||||||
chr6:116888889
|
T | C | 106 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(103): Show | 119 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.567-5098T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888889 | ||||||
chr6:116888959
|
G | T | 12 | a0001c0002t0002g0067a0002c0003t0002g0008a0002c0003t0002g0024others(9): Show | 17 | HG00741.hp2 HG01074.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.567-5028G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888959 | ||||||
chr6:116889006
|
G | A | 12 | a0001c0002t0002g0067a0002c0003t0002g0008a0002c0003t0002g0024others(9): Show | 17 | HG00741.hp2 HG01074.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.567-4981G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889006 | ||||||
chr6:116889092
|
A | G | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-4895A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889092 | ||||||
chr6:116889187
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.567-4800A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889187 | ||||||
chr6:116889238
|
T | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(23): Show | 32 | HG00741.hp2 HG01074.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.567-4749T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889238 | ||||||
chr6:116889300
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.567-4687T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889300 | ||||||
chr6:116889336
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 12 | HG01496.hp1 HG02132.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.567-4651G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889336 | ||||||
chr6:116889343
|
T | G | 1 | a0001c0002t0002g0175 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.567-4644T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889343 | ||||||
chr6:116889354
|
G | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(23): Show | 32 | HG00741.hp2 HG01074.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.567-4633G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889354 | ||||||
chr6:116889374
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.567-4613T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889374 | ||||||
chr6:116889443
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(71): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.567-4544A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889443 | ||||||
chr6:116889573
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.567-4414T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889573 | ||||||
chr6:116889676
|
T | C | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-4311T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889676 | ||||||
chr6:116889729
|
C | A | 1 | a0001c0001t0007g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.567-4258C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889729 | ||||||
chr6:116889936
|
G | A | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.567-4051G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889936 | ||||||
chr6:116889945
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.567-4042C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889945 | ||||||
chr6:116890043
|
A | AAG | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.567-3943_567-3942d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116890043 | |||||
chr6:116890399
|
G | T | 1 | a0001c0002t0002g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.567-3588G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890399 | ||||||
chr6:116890547
|
C | T | 1 | a0001c0002t0002g0249 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.567-3440C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890547 | ||||||
chr6:116890553
|
C | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02300.hp2 NA18966.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.567-3434C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890553 | ||||||
chr6:116890646
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.567-3341T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890646 | ||||||
chr6:116890653
|
C | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(73): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.567-3334C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890653 | ||||||
chr6:116890896
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(17): Show | 26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.567-3091G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890896 | ||||||
chr6:116890990
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.567-2997T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890990 | ||||||
chr6:116891017
|
T | C | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.567-2970T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891017 | ||||||
chr6:116891037
|
T | A | 11 | a0001c0002t0002g0047a0001c0002t0002g0177a0001c0002t0002g0178others(8): Show | 11 | HG00735.hp1 HG00741.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.567-2950T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891037 | ||||||
chr6:116891095
|
T | C | 106 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(103): Show | 119 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.567-2892T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891095 | ||||||
chr6:116891321
|
T | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG02258.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.567-2666T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891321 | ||||||
chr6:116891371
|
A | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(23): Show | 32 | HG00741.hp2 HG01074.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.567-2616A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891371 | ||||||
chr6:116891452
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.567-2535T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891452 | ||||||
chr6:116891458
|
A | G | 1 | a0001c0002t0002g0248 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.567-2529A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891458 | ||||||
chr6:116891526
|
A | G | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.567-2461A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891526 | ||||||
chr6:116891756
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.567-2231A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891756 | ||||||
chr6:116891819
|
T | C | 1 | a0001c0001t0001g0043 | 2 | NA18983.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.567-2168T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891819 | ||||||
chr6:116892068
|
T | C | 1 | a0001c0002t0002g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.567-1919T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892068 | ||||||
chr6:116892145
|
T | C | 2 | a0002c0003t0002g0024a0002c0003t0006g0078 | 3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.567-1842T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892145 | ||||||
chr6:116892290
|
G | C | 2 | a0001c0001t0001g0116a0007c0014t0001g0117 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.567-1697G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892290 | ||||||
chr6:116892308
|
T | C | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-1679T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892308 | ||||||
chr6:116892434
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0263a0001c0001t0001g0282 | 5 | HG01891.hp1 HG02486.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.567-1553A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892434 | ||||||
chr6:116892447
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(207): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.567-1540A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892447 | ||||||
chr6:116892451
|
T | C | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.567-1536T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892451 | ||||||
chr6:116892563
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.567-1424G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892563 | ||||||
chr6:116892746
|
G | A | 1 | a0001c0002t0002g0020 | 2 | NA18957.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.567-1241G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892746 | ||||||
chr6:116892832
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(219): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.567-1155C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892832 | ||||||
chr6:116893016
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.567-971T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893016 | ||||||
chr6:116893054
|
G | A | 1 | a0001c0002t0002g0184 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.567-933G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893054 | ||||||
chr6:116893085
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(203): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.567-902A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893085 | ||||||
chr6:116893510
|
T | G | 1 | a0001c0001t0001g0264 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.567-477T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893510 | ||||||
chr6:116893512
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.567-475G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893512 | ||||||
chr6:116893534
|
G | T | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.567-453G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893534 | ||||||
chr6:116893543
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.567-444T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893543 | ||||||
chr6:116893559
|
A | T | 3 | a0002c0003t0002g0024a0002c0003t0002g0077a0002c0003t0006g0078 | 4 | HG02886.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-428A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893559 | ||||||
chr6:116893703
|
A | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.567-284A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893703 | ||||||
chr6:116893741
|
G | A | 1 | a0001c0012t0002g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.567-246G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893741 | ||||||
chr6:116893776
|
A | C | 3 | a0001c0001t0001g0264a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | NA18993.hp2 NA18994.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.567-211A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893776 | ||||||
chr6:116893951
|
T | C | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.567-36T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893951 | ||||||
chr6:116894120
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.644+56T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894120 | ||||||
chr6:116894137
|
G | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0056others(13): Show | 18 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.644+73G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894137 | ||||||
chr6:116894217
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.644+153T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894217 | ||||||
chr6:116894257
|
T | A | 1 | a0001c0002t0002g0127 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.644+193T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894257 | ||||||
chr6:116894464
|
T | G | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.644+400T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894464 | ||||||
chr6:116894496
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.644+432T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894496 | ||||||
chr6:116894508
|
A | G | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.644+444A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894508 | ||||||
chr6:116894647
|
A | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(11): Show | 15 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.645-533A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894647 | ||||||
chr6:116894657
|
T | TGA | 118 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0038others(115): Show | 134 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.645-522_645-521dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 116894657 | |||||
chr6:116894658
|
G | GAA | 10 | a0001c0001t0001g0034a0001c0002t0002g0013a0001c0002t0002g0186others(7): Show | 13 | HG02074.hp1 HG02129.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-521_645-520ins others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 116894658 | |||||
chr6:116894718
|
T | A | 1 | a0001c0001t0001g0017 | 3 | NA18942.hp2 NA18977.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.645-462T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894718 | ||||||
chr6:116894754
|
C | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(11): Show | 15 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.645-426C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894754 | ||||||
chr6:116894962
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.645-218G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894962 | ||||||
chr6:116895238
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG01071.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.672+31C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116895238 | ||||||
chr6:116895503
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.672+296C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116895503 | ||||||
chr6:116895645
|
T | TAC | 26 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0057others(23): Show | 29 | HG01081.hp2 HG01109.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.672+469_672+470dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | |||||
chr6:116895645
|
T | TACAC | 78 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(75): Show | 87 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.672+467_672+470dup others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | |||||
chr6:116895645
|
T | TACACAC | 17 | a0001c0001t0001g0108a0001c0001t0001g0172a0001c0001t0001g0176others(14): Show | 21 | HG00673.hp1 HG00673.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+465_672+470dup others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | |||||
chr6:116895645
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0002t0002g0194others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+463_672+470dup others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | |||||
chr6:116895645
|
T | TACACACA others(3): Show |
1 | a0001c0002t0002g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.672+461_672+470dup others(10): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | |||||
chr6:116895645
|
TAC | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0081others(18): Show | 28 | HG00099.hp2 HG00642.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.672+469_672+470del others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | |||||
chr6:116895645
|
TACAC | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0066a0001c0001t0001g0068others(5): Show | 9 | HG02559.hp2 HG02886.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.672+467_672+470del others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | |||||
chr6:116895741
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(17): Show | 26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.672+534A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116895741 | ||||||
chr6:116896219
|
C | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0021others(147): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.672+1012C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896219 | ||||||
chr6:116896411
|
A | G | 2 | a0001c0001t0001g0029a0001c0002t0002g0127 | 3 | HG02155.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.672+1204A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896411 | ||||||
chr6:116896582
|
G | A | 1 | a0001c0002t0002g0203 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.672+1375G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896582 | ||||||
chr6:116896597
|
CA | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.672+1392delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116896597 | |||||
chr6:116896602
|
A | T | 1 | a0001c0012t0002g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.672+1395A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896602 | ||||||
chr6:116896627
|
G | C | 1 | a0001c0006t0001g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.672+1420G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896627 | ||||||
chr6:116896707
|
CA | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(227): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.672+1512delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116896707 | |||||
chr6:116896707
|
CAA | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.672+1511_672+1512d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116896707 | |||||
chr6:116896787
|
C | T | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.672+1580C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896787 | ||||||
chr6:116896974
|
G | C | 1 | a0001c0001t0001g0162 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.672+1767G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896974 | ||||||
chr6:116897163
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | NA18972.hp2 NA19078.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.672+1956G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897163 | ||||||
chr6:116897192
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.672+1985G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897192 | ||||||
chr6:116897278
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.672+2071A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897278 | ||||||
chr6:116897316
|
C | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.672+2109C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897316 | ||||||
chr6:116897383
|
C | T | 4 | a0001c0001t0001g0176a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+2176C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897383 | ||||||
chr6:116897405
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672+2198C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897405 | ||||||
chr6:116897449
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672+2242G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897449 | ||||||
chr6:116897459
|
T | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(11): Show | 15 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.672+2252T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897459 | ||||||
chr6:116897479
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.672+2272T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897479 | ||||||
chr6:116897530
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.672+2323T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897530 | ||||||
chr6:116897545
|
G | A | 1 | a0001c0001t0007g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.672+2338G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897545 | ||||||
chr6:116897638
|
C | T | 1 | a0001c0001t0007g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.672+2431C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897638 | ||||||
chr6:116897695
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.672+2488C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897695 | ||||||
chr6:116897730
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.672+2523C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897730 | ||||||
chr6:116897836
|
T | A | 1 | a0001c0002t0002g0205 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.672+2629T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897836 | ||||||
chr6:116897927
|
T | C | 1 | a0001c0001t0007g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.672+2720T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897927 | ||||||
chr6:116898022
|
A | T | 1 | a0001c0002t0002g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.672+2815A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898022 | ||||||
chr6:116898253
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.672+3046T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898253 | ||||||
chr6:116898361
|
A | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0021others(147): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.672+3154A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898361 | ||||||
chr6:116898374
|
G | C | 1 | a0001c0001t0001g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.672+3167G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898374 | ||||||
chr6:116898693
|
A | G | 1 | a0001c0001t0001g0046 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.672+3486A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898693 | ||||||
chr6:116898731
|
A | G | 1 | a0003c0004t0002g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672+3524A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898731 | ||||||
chr6:116898892
|
C | A | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.672+3685C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898892 | ||||||
chr6:116898908
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.672+3701T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898908 | ||||||
chr6:116899090
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.672+3883T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899090 | ||||||
chr6:116899136
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.672+3929G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899136 | ||||||
chr6:116899248
|
T | C | 1 | a0001c0001t0008g0259 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.672+4041T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899248 | ||||||
chr6:116899484
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.672+4277A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899484 | ||||||
chr6:116899494
|
T | G | 1 | a0001c0001t0001g0266 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.672+4287T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899494 | ||||||
chr6:116899506
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.672+4299G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899506 | ||||||
chr6:116899751
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.672+4544T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899751 | ||||||
chr6:116900023
|
C | T | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.672+4816C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900023 | ||||||
chr6:116900079
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.672+4872A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900079 | ||||||
chr6:116900166
|
T | G | 1 | a0001c0002t0002g0186 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.672+4959T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900166 | ||||||
chr6:116900287
|
G | T | 8 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(5): Show | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+5080G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900287 | ||||||
chr6:116900340
|
C | T | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.672+5133C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900340 | ||||||
chr6:116900341
|
G | A | 8 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0120others(5): Show | 8 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.672+5134G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900341 | ||||||
chr6:116900379
|
C | T | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.672+5172C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900379 | ||||||
chr6:116900429
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(19): Show | 26 | HG00741.hp2 HG01884.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.672+5222G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900429 | ||||||
chr6:116900551
|
G | A | 3 | a0001c0002t0002g0206a0001c0002t0002g0207a0001c0002t0002g0208 | 3 | NA19003.hp1 NA19005.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.672+5344G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900551 | ||||||
chr6:116900603
|
A | T | 2 | a0001c0001t0001g0116a0007c0014t0001g0117 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.672+5396A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900603 | ||||||
chr6:116900604
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.672+5397T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900604 | ||||||
chr6:116900904
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.672+5697C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900904 | ||||||
chr6:116900998
|
CTG | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0084a0001c0006t0001g0075others(1): Show | 4 | HG02717.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+5793_672+5794d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116900998 | |||||
chr6:116900999
|
T | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0034others(125): Show | 147 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.672+5792T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900999 | ||||||
chr6:116901066
|
T | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0021others(147): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.672+5859T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901066 | ||||||
chr6:116901115
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.672+5908C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901115 | ||||||
chr6:116901364
|
A | ATTTAGT | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.672+6158_672+6159i others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116901364 | |||||
chr6:116901510
|
A | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02451.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.672+6303A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901510 | ||||||
chr6:116901532
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.672+6325T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901532 | ||||||
chr6:116901690
|
A | G | 1 | a0001c0002t0002g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.672+6483A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901690 | ||||||
chr6:116901710
|
T | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.672+6503T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901710 | ||||||
chr6:116901715
|
C | T | 1 | a0001c0002t0002g0285 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.672+6508C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901715 | ||||||
chr6:116901818
|
AT | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0034others(125): Show | 147 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.672+6614delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116901818 | |||||
chr6:116901828
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0002t0002g0060 | 3 | HG02965.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672+6621T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901828 | ||||||
chr6:116901994
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0002t0002g0060 | 3 | HG02965.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672+6787A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901994 | ||||||
chr6:116902153
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672+6946A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902153 | ||||||
chr6:116902160
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.672+6953G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902160 | ||||||
chr6:116902577
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.672+7370C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902577 | ||||||
chr6:116902631
|
G | A | 1 | a0001c0001t0007g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.672+7424G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902631 | ||||||
chr6:116902659
|
A | T | 1 | a0001c0002t0002g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.672+7452A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902659 | ||||||
chr6:116902806
|
T | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 12 | HG01496.hp1 HG02132.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.672+7599T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902806 | ||||||
chr6:116902986
|
A | G | 5 | a0001c0002t0002g0054a0001c0002t0002g0067a0003c0004t0002g0022others(2): Show | 7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+7779A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902986 | ||||||
chr6:116903014
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.672+7807A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903014 | ||||||
chr6:116903049
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0239 | 3 | HG00738.hp2 HG01261.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.672+7842C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903049 | ||||||
chr6:116903085
|
C | T | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-7850C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903085 | ||||||
chr6:116903140
|
A | G | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.673-7795A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903140 | ||||||
chr6:116903221
|
G | C | 8 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(5): Show | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-7714G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903221 | ||||||
chr6:116903286
|
T | G | 1 | a0001c0002t0002g0187 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.673-7649T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903286 | ||||||
chr6:116903414
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.673-7521T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903414 | ||||||
chr6:116903478
|
A | T | 108 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(105): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.673-7457A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903478 | ||||||
chr6:116903564
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(87): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.673-7371C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903564 | ||||||
chr6:116903598
|
T | C | 1 | a0001c0002t0002g0183 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.673-7337T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903598 | ||||||
chr6:116903657
|
ATATTGTT | A | 7 | a0001c0002t0002g0037a0001c0002t0002g0209a0001c0002t0002g0210others(4): Show | 7 | HG00140.hp1 HG00323.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.673-7273_673-7267d others(9): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116903657 | |||||
chr6:116903699
|
G | C | 2 | a0001c0001t0001g0029a0001c0002t0002g0127 | 3 | HG02155.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.673-7236G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903699 | ||||||
chr6:116903749
|
G | C | 1 | a0001c0002t0002g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.673-7186G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903749 | ||||||
chr6:116903831
|
C | T | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-7104C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903831 | ||||||
chr6:116904180
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.673-6755G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904180 | ||||||
chr6:116904188
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.673-6747T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904188 | ||||||
chr6:116904236
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.673-6699A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904236 | ||||||
chr6:116904249
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.673-6686C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904249 | ||||||
chr6:116904382
|
C | A | 1 | a0001c0001t0001g0017 | 3 | NA18942.hp2 NA18977.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.673-6553C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904382 | ||||||
chr6:116904404
|
A | G | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-6531A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904404 | ||||||
chr6:116904450
|
A | C | 1 | a0002c0007t0001g0076 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.673-6485A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904450 | ||||||
chr6:116904505
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(209): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.673-6430A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904505 | ||||||
chr6:116904947
|
C | T | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-5988C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904947 | ||||||
chr6:116905082
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(87): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.673-5853T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905082 | ||||||
chr6:116905300
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.673-5635T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905300 | ||||||
chr6:116905333
|
T | C | 1 | a0001c0002t0002g0188 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.673-5602T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905333 | ||||||
chr6:116905434
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.673-5501T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905434 | ||||||
chr6:116905437
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.673-5498A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905437 | ||||||
chr6:116905556
|
C | CT | 6 | a0001c0002t0002g0050a0001c0002t0002g0053a0001c0006t0001g0075others(3): Show | 7 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-5364dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116905556 | |||||
chr6:116905556
|
CT | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0115a0001c0001t0001g0166others(2): Show | 7 | HG01256.hp1 HG01433.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-5364delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116905556 | |||||
chr6:116905604
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.673-5331G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905604 | ||||||
chr6:116905646
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.673-5289G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905646 | ||||||
chr6:116905699
|
G | A | 5 | a0001c0002t0002g0054a0001c0002t0002g0067a0003c0004t0002g0022others(2): Show | 7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-5236G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905699 | ||||||
chr6:116905784
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.673-5151T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905784 | ||||||
chr6:116905792
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.673-5143C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905792 | ||||||
chr6:116905911
|
A | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(210): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.673-5024A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905911 | ||||||
chr6:116905952
|
C | CTA | 212 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(209): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.673-4982_673-4981i others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116905952 | |||||
chr6:116906121
|
T | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(59): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.673-4814T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906121 | ||||||
chr6:116906135
|
C | T | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-4800C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906135 | ||||||
chr6:116906187
|
G | A | 15 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0056others(12): Show | 17 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.673-4748G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906187 | ||||||
chr6:116906291
|
A | C | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-4644A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906291 | ||||||
chr6:116906511
|
TA | T | 8 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(5): Show | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-4423delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906511 | ||||||
chr6:116906610
|
T | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0056a0001c0001t0001g0065others(1): Show | 5 | HG00099.hp1 HG01358.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-4325T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906610 | ||||||
chr6:116906691
|
G | T | 2 | a0002c0003t0002g0024a0002c0003t0006g0078 | 3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.673-4244G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906691 | ||||||
chr6:116906743
|
T | TTG | 21 | a0001c0001t0001g0027a0001c0001t0001g0204a0001c0002t0002g0013others(18): Show | 28 | HG00741.hp2 HG01258.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.673-4170_673-4169d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906743 | |||||
chr6:116906743
|
TTG | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(98): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.673-4170_673-4169d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906743 | |||||
chr6:116906858
|
T | TTTG | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-4076_673-4075i others(5): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906858 | |||||
chr6:116906860
|
G | GT | 29 | a0001c0001t0001g0034a0001c0001t0001g0100a0001c0001t0001g0114others(26): Show | 34 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.673-4062dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906860 | |||||
chr6:116906860
|
G | T | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-4075G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906860 | ||||||
chr6:116906860
|
GT | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(71): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.673-4062delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906860 | |||||
chr6:116907080
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0260a0001c0001t0001g0261 | 7 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-3855G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907080 | ||||||
chr6:116907127
|
A | AT | 130 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0038others(127): Show | 147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.673-3801dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116907127 | |||||
chr6:116907178
|
T | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.673-3757T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907178 | ||||||
chr6:116907339
|
T | A | 8 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(5): Show | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-3596T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907339 | ||||||
chr6:116907384
|
C | T | 1 | a0001c0002t0002g0245 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.673-3551C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907384 | ||||||
chr6:116907422
|
G | C | 15 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0056others(12): Show | 17 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.673-3513G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907422 | ||||||
chr6:116907488
|
G | T | 1 | a0001c0002t0002g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.673-3447G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907488 | ||||||
chr6:116907489
|
C | A | 8 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(5): Show | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-3446C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907489 | ||||||
chr6:116907519
|
C | T | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-3416C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907519 | ||||||
chr6:116907644
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.673-3291C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907644 | ||||||
chr6:116907753
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.673-3182A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907753 | ||||||
chr6:116907776
|
T | C | 8 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(5): Show | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-3159T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907776 | ||||||
chr6:116907869
|
AATTTT | A | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-3065_673-3061d others(7): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907869 | ||||||
chr6:116908028
|
C | T | 2 | a0001c0002t0002g0181a0001c0002t0002g0182 | 2 | HG02083.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.673-2907C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908028 | ||||||
chr6:116908092
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(74): Show | 114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.673-2843G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908092 | ||||||
chr6:116908126
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(75): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.673-2809T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908126 | ||||||
chr6:116908430
|
G | C | 130 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0038others(127): Show | 147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.673-2505G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908430 | ||||||
chr6:116908490
|
C | A | 1 | a0001c0001t0001g0005 | 4 | NA18945.hp1 NA18975.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-2445C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908490 | ||||||
chr6:116908580
|
A | C | 1 | a0001c0002t0002g0039 | 2 | NA18975.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.673-2355A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908580 | ||||||
chr6:116908643
|
G | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0038others(132): Show | 153 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.673-2292G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908643 | ||||||
chr6:116908669
|
T | TAC | 11 | a0001c0001t0001g0084a0001c0002t0002g0047a0001c0002t0002g0167others(8): Show | 11 | HG00735.hp1 HG00741.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.673-2248_673-2247d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | |||||
chr6:116908669
|
T | TACAC | 7 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0085others(4): Show | 8 | HG01884.hp2 HG02148.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.673-2250_673-2247d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | |||||
chr6:116908669
|
T | TACACAC | 3 | a0001c0001t0001g0080a0001c0001t0001g0204a0001c0002t0002g0203 | 3 | HG02809.hp1 HG03195.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.673-2252_673-2247d others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | |||||
chr6:116908669
|
TAC | T | 15 | a0001c0001t0001g0021a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.673-2248_673-2247d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | |||||
chr6:116908669
|
TACACACA others(15): Show |
T | 4 | a0002c0003t0002g0008a0002c0003t0002g0072a0002c0003t0002g0073others(1): Show | 6 | HG00741.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-2246_673-2225d others(24): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | |||||
chr6:116908673
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.673-2246_673-2231d others(18): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908673 | |||||
chr6:116908677
|
CACACACA others(5): Show |
C | 8 | a0001c0001t0001g0007a0001c0001t0001g0079a0001c0002t0002g0050others(5): Show | 10 | HG01993.hp2 HG02148.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.673-2246_673-2235d others(14): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908677 | |||||
chr6:116908679
|
CACACACA others(3): Show |
C | 2 | a0001c0001t0001g0070a0001c0002t0002g0183 | 2 | HG02559.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.673-2246_673-2237d others(12): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908679 | |||||
chr6:116908681
|
CACACACA others(1): Show |
C | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0254others(3): Show | 6 | HG01258.hp1 HG01516.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-2246_673-2239d others(10): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908681 | |||||
chr6:116908683
|
CACACAG | C | 18 | a0001c0001t0001g0042a0001c0001t0001g0228a0001c0001t0001g0229others(15): Show | 19 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.673-2246_673-2241d others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908683 | |||||
chr6:116908685
|
CACAG | C | 40 | a0001c0001t0001g0034a0001c0001t0001g0172a0001c0001t0001g0176others(37): Show | 48 | HG00558.hp1 HG00609.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.673-2246_673-2243d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908685 | |||||
chr6:116908687
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.673-2248C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908687 | ||||||
chr6:116908687
|
CAG | C | 19 | a0001c0001t0001g0071a0001c0001t0001g0202a0001c0001t0001g0234others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.673-2246_673-2245d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908687 | |||||
chr6:116908689
|
G | C | 40 | a0001c0001t0001g0038a0001c0001t0001g0055a0001c0001t0001g0080others(37): Show | 45 | HG00673.hp2 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.673-2246G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908689 | ||||||
chr6:116908689
|
G | GAC | 15 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0096others(12): Show | 22 | HG00733.hp1 HG01074.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.673-2220_673-2219d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908689 | |||||
chr6:116908689
|
GACAC | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(44): Show | 72 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.673-2222_673-2219d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908689 | |||||
chr6:116908689
|
GACACAC | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 39 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.673-2224_673-2219d others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908689 | |||||
chr6:116908691
|
C | G | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-2244C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908691 | ||||||
chr6:116908695
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.673-2240C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908695 | ||||||
chr6:116908699
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.673-2236C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908699 | ||||||
chr6:116908719
|
G | A | 1 | a0001c0002t0002g0235 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.673-2216G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908719 | ||||||
chr6:116908793
|
T | C | 4 | a0002c0003t0002g0008a0002c0003t0002g0072a0002c0003t0002g0073others(1): Show | 6 | HG00741.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-2142T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908793 | ||||||
chr6:116908795
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0038others(132): Show | 153 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.673-2140A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908795 | ||||||
chr6:116908797
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.673-2138A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908797 | ||||||
chr6:116908902
|
C | T | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-2033C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908902 | ||||||
chr6:116908935
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.673-2000T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908935 | ||||||
chr6:116909176
|
G | C | 130 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0038others(127): Show | 147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.673-1759G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116909176 | ||||||
chr6:116909197
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.673-1738T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116909197 | ||||||
chr6:116909558
|
T | A | 130 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0038others(127): Show | 147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.673-1377T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116909558 | ||||||
chr6:116909630
|
TA | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(74): Show | 114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.673-1299delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909630 | |||||
chr6:116909735
|
C | CT | 74 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0026others(71): Show | 91 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.673-1171dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909735
|
C | CTT | 10 | a0001c0001t0001g0227a0001c0002t0002g0173a0001c0002t0002g0190others(7): Show | 10 | HG00609.hp2 HG02129.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.673-1172_673-1171d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909735
|
C | CTTTTTTT others(3): Show |
4 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(1): Show | 7 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.673-1180_673-1171d others(12): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909735
|
C | CTTTTTTT others(4): Show |
1 | a0002c0003t0002g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.673-1181_673-1171d others(13): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909735
|
C | CTTTTTTT others(5): Show |
1 | a0002c0003t0006g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.673-1182_673-1171d others(14): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909735
|
CT | C | 52 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0070others(49): Show | 56 | HG00323.hp1 HG00639.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.673-1171delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909735
|
CTT | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 14 | HG00733.hp2 HG01884.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.673-1172_673-1171d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909735
|
CTTT | C | 6 | a0001c0001t0001g0071a0001c0001t0001g0084a0001c0001t0001g0087others(3): Show | 6 | HG02717.hp2 HG02818.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-1173_673-1171d others(5): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909735
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0099 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.673-1180_673-1171d others(12): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909735
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0010t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.673-1184_673-1171d others(16): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | |||||
chr6:116909770
|
G | A | 3 | a0001c0001t0001g0110a0002c0003t0002g0024a0002c0003t0006g0078 | 4 | HG02132.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-1165G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116909770 | ||||||
chr6:116910018
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.673-917A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910018 | ||||||
chr6:116910453
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(73): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.673-482A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910453 | ||||||
chr6:116910461
|
T | G | 1 | a0001c0001t0001g0034 | 2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.673-474T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910461 | ||||||
chr6:116910513
|
C | T | 5 | a0001c0002t0002g0054a0001c0002t0002g0067a0003c0004t0002g0022others(2): Show | 7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-422C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910513 | ||||||
chr6:116910514
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.673-421G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910514 | ||||||
chr6:116910706
|
T | C | 1 | a0001c0002t0002g0170 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.673-229T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910706 | ||||||
chr6:116910932
|
T | C | 2 | a0002c0003t0002g0024a0002c0003t0006g0078 | 3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.673-3T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910932 | ||||||
chr6:116911103
|
G | T | 1 | a0001c0002t0002g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.780+61G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116911103 | ||||||
chr6:116911519
|
C | T | 8 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0111others(5): Show | 8 | HG03688.hp1 HG04184.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+477C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116911519 | ||||||
chr6:116911671
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.780+629G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116911671 | ||||||
chr6:116911691
|
G | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 33 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.780+649G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116911691 | ||||||
chr6:116912031
|
C | T | 1 | a0001c0002t0002g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.780+989C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912031 | ||||||
chr6:116912045
|
C | A | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.780+1003C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912045 | ||||||
chr6:116912262
|
C | T | 2 | a0001c0001t0001g0172a0005c0017t0001g0171 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.780+1220C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912262 | ||||||
chr6:116912309
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG02074.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.780+1267G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912309 | ||||||
chr6:116912336
|
C | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(209): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.780+1294C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912336 | ||||||
chr6:116912343
|
G | GA | 16 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(13): Show | 17 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.780+1311dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 116912343 | |||||
chr6:116912481
|
C | T | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+1439C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912481 | ||||||
chr6:116912510
|
T | C | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.780+1468T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912510 | ||||||
chr6:116912722
|
C | A | 1 | a0001c0001t0001g0046 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.780+1680C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912722 | ||||||
chr6:116912847
|
G | GGT | 130 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0038others(127): Show | 147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.780+1806_780+1807d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 116912847 | |||||
chr6:116913207
|
GC | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(73): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.780+2167delC | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 116913207 | |||||
chr6:116913250
|
C | T | 2 | a0001c0002t0002g0212a0001c0002t0002g0238 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.780+2208C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913250 | ||||||
chr6:116913354
|
G | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0038others(132): Show | 153 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.780+2312G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913354 | ||||||
chr6:116913383
|
G | A | 4 | a0002c0003t0002g0008a0002c0003t0002g0072a0002c0003t0002g0073others(1): Show | 6 | HG00741.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+2341G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913383 | ||||||
chr6:116913463
|
C | G | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.780+2421C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913463 | ||||||
chr6:116913489
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG02258.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+2447G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913489 | ||||||
chr6:116913548
|
T | A | 3 | a0001c0002t0002g0041a0001c0002t0002g0201a0001c0002t0002g0237 | 4 | NA18956.hp2 NA18957.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-2460T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913548 | ||||||
chr6:116913548
|
T | C | 107 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0038others(104): Show | 120 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.781-2460T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913548 | ||||||
chr6:116913557
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.781-2451T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913557 | ||||||
chr6:116913620
|
G | A | 1 | a0001c0002t0002g0127 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.781-2388G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913620 | ||||||
chr6:116913680
|
A | C | 5 | a0001c0002t0002g0054a0001c0002t0002g0067a0003c0004t0002g0022others(2): Show | 7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-2328A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913680 | ||||||
chr6:116913799
|
G | T | 2 | a0001c0002t0002g0181a0001c0002t0002g0182 | 2 | HG02083.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.781-2209G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913799 | ||||||
chr6:116913870
|
G | T | 1 | a0001c0002t0002g0194 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.781-2138G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913870 | ||||||
chr6:116914094
|
T | C | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.781-1914T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914094 | ||||||
chr6:116914115
|
C | G | 1 | a0001c0002t0002g0127 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.781-1893C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914115 | ||||||
chr6:116914133
|
C | A | 5 | a0001c0002t0002g0054a0001c0002t0002g0067a0003c0004t0002g0022others(2): Show | 7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-1875C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914133 | ||||||
chr6:116914493
|
G | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0034others(134): Show | 156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.781-1515G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914493 | ||||||
chr6:116914595
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.781-1413T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914595 | ||||||
chr6:116914684
|
C | A | 1 | a0001c0002t0002g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.781-1324C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914684 | ||||||
chr6:116914757
|
C | A | 2 | a0001c0002t0002g0215a0006c0011t0002g0213 | 2 | HG02080.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.781-1251C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914757 | ||||||
chr6:116914933
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0002t0002g0060 | 3 | HG02965.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.781-1075T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914933 | ||||||
chr6:116915214
|
A | G | 19 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0055others(16): Show | 25 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.781-794A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915214 | ||||||
chr6:116915384
|
T | G | 4 | a0002c0003t0002g0008a0002c0003t0002g0072a0002c0003t0002g0073others(1): Show | 6 | HG00741.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-624T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915384 | ||||||
chr6:116915412
|
A | T | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.781-596A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915412 | ||||||
chr6:116915482
|
G | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.781-526G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915482 | ||||||
chr6:116915523
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-485T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915523 | ||||||
chr6:116915545
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.781-463A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915545 | ||||||
chr6:116915659
|
T | G | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-349T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915659 | ||||||
chr6:116915690
|
T | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0034others(134): Show | 156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.781-318T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915690 | ||||||
chr6:116915760
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.781-248G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915760 | ||||||
chr6:116915769
|
T | C | 2 | a0002c0003t0002g0024a0002c0003t0006g0078 | 3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.781-239T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915769 | ||||||
chr6:116916361
|
G | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0034others(134): Show | 156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.972+47G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916361 | ||||||
chr6:116916403
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.972+89A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916403 | ||||||
chr6:116916421
|
T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.972+107T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916421 | ||||||
chr6:116916524
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.972+210A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916524 | ||||||
chr6:116916564
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0002t0002g0060 | 3 | HG02965.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.972+250C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916564 | ||||||
chr6:116916663
|
T | C | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+349T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916663 | ||||||
chr6:116916735
|
C | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.972+421C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916735 | ||||||
chr6:116916770
|
A | T | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+456A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916770 | ||||||
chr6:116916791
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.972+477G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916791 | ||||||
chr6:116917158
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.972+844A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917158 | ||||||
chr6:116917317
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(212): Show | 271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.973-720G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917317 | ||||||
chr6:116917338
|
G | GT | 18 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0081others(15): Show | 22 | HG00323.hp1 HG00741.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.973-684dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917338 | |||||
chr6:116917338
|
G | GTT | 7 | a0001c0001t0001g0071a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG02717.hp2 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-685_973-684dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917338 | |||||
chr6:116917338
|
GT | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0029others(120): Show | 142 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.973-684delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917338 | |||||
chr6:116917343
|
T | TTG | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.973-693_973-692ins others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917343 | |||||
chr6:116917371
|
G | A | 8 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(5): Show | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.973-666G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917371 | ||||||
chr6:116917505
|
A | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.973-532A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917505 | ||||||
chr6:116917763
|
T | G | 1 | a0001c0001t0001g0046 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.973-274T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917763 | ||||||
chr6:116917861
|
ACACT | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0056a0001c0001t0001g0065others(1): Show | 5 | HG00099.hp1 HG01358.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.973-172_973-169del others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917861 | |||||
chr6:116917923
|
A | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 7 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-114A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917923 | ||||||
chr6:116917978
|
T | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0034others(134): Show | 156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.973-59T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917978 | ||||||
chr6:116918001
|
T | TAAAG | 8 | a0002c0003t0002g0008a0002c0003t0002g0024a0002c0003t0002g0072others(5): Show | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.973-34_973-31dupAA others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116918001 | |||||
chr6:116918177
|
C | A | 1 | a0001c0012t0002g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1022+91C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918177 | ||||||
chr6:116918301
|
C | T | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1022+215C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918301 | ||||||
chr6:116918336
|
T | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0034others(134): Show | 156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.1022+250T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918336 | ||||||
chr6:116918518
|
A | T | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1022+432A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918518 | ||||||
chr6:116918558
|
CA | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0056others(31): Show | 38 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1022+484delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 116918558 | |||||
chr6:116918588
|
C | A | 1 | a0001c0001t0001g0133 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1022+502C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918588 | ||||||
chr6:116918600
|
G | GA | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1022+524dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 116918600 | |||||
chr6:116918600
|
G | GAA | 109 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0042others(106): Show | 125 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1022+523_1022+524d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 116918600 | |||||
chr6:116918646
|
T | C | 2 | a0001c0002t0002g0169a0001c0002t0002g0170 | 2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1023-491T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918646 | ||||||
chr6:116919103
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1023-34C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116919103 | ||||||
chr6:116919322
|
A | T | 1 | a0001c0002t0002g0127 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1182+26A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919322 | ||||||
chr6:116919427
|
C | T | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182+131C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919427 | ||||||
chr6:116919430
|
G | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0034others(134): Show | 156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.1182+134G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919430 | ||||||
chr6:116919494
|
G | C | 1 | a0001c0002t0002g0175 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1182+198G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919494 | ||||||
chr6:116919562
|
TAAG | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(75): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1182+270_1182+272d others(5): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 116919562 | |||||
chr6:116919737
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1182+441A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919737 | ||||||
chr6:116919817
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(212): Show | 271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1183-493T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919817 | ||||||
chr6:116919856
|
A | G | 3 | a0001c0001t0001g0084a0001c0006t0001g0075a0001c0006t0001g0083 | 3 | HG02717.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1183-454A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919856 | ||||||
chr6:116919879
|
G | C | 1 | a0001c0001t0001g0059 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1183-431G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919879 | ||||||
chr6:116920041
|
T | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1183-269T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116920041 | ||||||
chr6:116920114
|
A | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0283 | 2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1183-196A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116920114 | ||||||
chr6:116920510
|
C | T | 2 | a0001c0001t0001g0116a0007c0014t0001g0117 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1327+56C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920510 | ||||||
chr6:116920584
|
C | CCTGA | 19 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(16): Show | 21 | HG01258.hp1 HG01884.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+131_1327+132i others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 116920584 | |||||
chr6:116920587
|
A | T | 19 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0071others(16): Show | 21 | HG01258.hp1 HG01884.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+133A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920587 | ||||||
chr6:116920609
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1327+155C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920609 | ||||||
chr6:116920772
|
T | C | 5 | a0001c0002t0002g0197a0001c0002t0002g0242a0001c0002t0002g0243others(2): Show | 5 | HG00673.hp1 NA19000.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1327+318T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920772 | ||||||
chr6:116920858
|
T | C | 121 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0038others(118): Show | 136 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.1327+404T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920858 | ||||||
chr6:116921093
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1327+639T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921093 | ||||||
chr6:116921138
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0202a0001c0001t0001g0260others(29): Show | 38 | HG00673.hp2 HG01243.hp2 HG02080.hp2 others(35): Show |
intron_variant | MODIFIER | c.1327+684A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921138 | ||||||
chr6:116921301
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1328-741C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921301 | ||||||
chr6:116921389
|
A | G | 1 | a0006c0011t0002g0213 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1328-653A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921389 | ||||||
chr6:116921501
|
A | G | 1 | a0001c0002t0003g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1328-541A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921501 | ||||||
chr6:116921523
|
T | C | 1 | a0004c0005t0002g0052 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1328-519T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921523 | ||||||
chr6:116921550
|
A | G | 1 | a0001c0002t0002g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1328-492A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921550 | ||||||
chr6:116921591
|
G | A | 2 | a0001c0002t0002g0206a0001c0002t0002g0208 | 2 | NA19003.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1328-451G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921591 | ||||||
chr6:116921619
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0231 | 2 | HG00639.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1328-423G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921619 | ||||||
chr6:116921655
|
AT | A | 125 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0033others(122): Show | 147 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.1328-372delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 116921655 | |||||
chr6:116921693
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1328-349C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921693 | ||||||
chr6:116921694
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1328-348G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921694 | ||||||
chr6:116921857
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1328-185G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921857 | ||||||
chr6:116921911
|
A | T | 1 | a0001c0012t0002g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1328-131A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921911 | ||||||
chr6:116922018
|
C | CTT | 6 | a0001c0002t0002g0050a0001c0002t0002g0053a0001c0002t0003g0088others(3): Show | 7 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1328-11_1328-10dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 116922018 | |||||
chr6:116922032
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG01106.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1328-10T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116922032 | ||||||
chr6:116922236
|
AG | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0056others(13): Show | 17 | HG00099.hp1 HG01109.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1437+89delG | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 116922236 | |||||
chr6:116922288
|
G | A | 4 | a0002c0003t0002g0008a0002c0003t0002g0072a0002c0003t0002g0074others(1): Show | 7 | HG00741.hp2 HG02145.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1437+137G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922288 | ||||||
chr6:116922554
|
G | C | 2 | a0002c0003t0002g0024a0002c0003t0006g0078 | 3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1437+403G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922554 | ||||||
chr6:116922788
|
T | C | 1 | a0001c0002t0002g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1438-319T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922788 | ||||||
chr6:116922798
|
A | G | 1 | a0001c0001t0001g0011 | 3 | NA18947.hp2 NA18952.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1438-309A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922798 | ||||||
chr6:116922944
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1438-163G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922944 | ||||||
chr6:116923047
|
G | A | 1 | a0001c0002t0002g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1438-60G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116923047 | ||||||
chr6:116923319
|
C | A | 1 | a0001c0012t0002g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1555+95C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923319 | ||||||
chr6:116923391
|
C | T | 1 | a0001c0006t0001g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1555+167C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923391 | ||||||
chr6:116923425
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1555+201T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923425 | ||||||
chr6:116923475
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1555+251C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923475 | ||||||
chr6:116923513
|
T | C | 109 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(106): Show | 126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1555+289T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923513 | ||||||
chr6:116923693
|
A | G | 109 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(106): Show | 126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1555+469A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923693 | ||||||
chr6:116923734
|
G | C | 109 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(106): Show | 126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1555+510G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923734 | ||||||
chr6:116923838
|
T | C | 109 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(106): Show | 126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1555+614T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923838 | ||||||
chr6:116924064
|
A | G | 8 | a0001c0001t0001g0042a0001c0001t0001g0228a0001c0001t0001g0229others(5): Show | 9 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1556-605A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116924064 | ||||||
chr6:116924226
|
T | C | 109 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(106): Show | 126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1556-443T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116924226 | ||||||
chr6:116924354
|
C | T | 1 | a0001c0002t0002g0020 | 2 | NA18957.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1556-315C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116924354 | ||||||
chr6:116924850
|
A | G | 4 | a0001c0001t0001g0176a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+59A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116924850 | ||||||
chr6:116924895
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA18949.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1678+104T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116924895 | ||||||
chr6:116925035
|
T | C | 1 | a0001c0002t0002g0189 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1678+244T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116925035 | ||||||
chr6:116925145
|
A | C | 1 | a0001c0002t0002g0224 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1679-308A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116925145 | ||||||
chr6:116925266
|
A | C | 109 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(106): Show | 126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1679-187A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116925266 | ||||||
chr6:116925413
|
G | GA | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1679-34dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr6 | 116925413 | |||||
chr6:116925897
|
ATTAG | A | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1885+242_1885+245d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 116925897 | |||||
chr6:116925936
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0260 | 6 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1885+277A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116925936 | ||||||
chr6:116926034
|
G | C | 1 | a0001c0002t0002g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1885+375G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926034 | ||||||
chr6:116926095
|
G | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1885+436G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926095 | ||||||
chr6:116926132
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1885+473C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926132 | ||||||
chr6:116926251
|
A | G | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1885+592A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926251 | ||||||
chr6:116926388
|
T | A | 1 | a0007c0014t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1886-639T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926388 | ||||||
chr6:116926529
|
A | G | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1886-498A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926529 | ||||||
chr6:116926552
|
C | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1886-475C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926552 | ||||||
chr6:116926743
|
C | T | 1 | a0002c0003t0006g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1886-284C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926743 | ||||||
chr6:116926744
|
A | C | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1886-283A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926744 | ||||||
chr6:116927547
|
T | C | 1 | a0001c0002t0002g0257 | 1 | HG04199.hp2 | splice_region_variant&intron_variant | LOW | c.2398+8T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927547 | ||||||
chr6:116927556
|
G | T | 1 | a0005c0017t0001g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2398+17G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927556 | ||||||
chr6:116927583
|
A | G | 10 | a0001c0001t0001g0071a0001c0001t0001g0119a0001c0001t0001g0128others(7): Show | 13 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2398+44A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927583 | ||||||
chr6:116927743
|
C | CT | 4 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0156others(1): Show | 8 | HG00621.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2398+223dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | |||||
chr6:116927743
|
C | CTTTT | 83 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(80): Show | 96 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.2398+220_2398+223d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | |||||
chr6:116927743
|
C | CTTTTT | 13 | a0001c0002t0002g0060a0001c0002t0002g0150a0001c0002t0002g0167others(10): Show | 13 | HG01516.hp2 HG02056.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.2398+219_2398+223d others(7): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | |||||
chr6:116927743
|
C | CTTTTTTT others(2): Show |
3 | a0002c0003t0002g0008a0002c0003t0002g0077a0003c0004t0002g0022 | 6 | HG02145.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2398+215_2398+223d others(11): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | |||||
chr6:116927743
|
C | CTTTTTTT others(3): Show |
2 | a0001c0002t0002g0054a0002c0003t0002g0074 | 2 | HG00741.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2398+214_2398+223d others(12): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | |||||
chr6:116927743
|
C | CTTTTTTT others(6): Show |
3 | a0001c0002t0002g0050a0004c0005t0002g0019a0004c0005t0002g0052 | 4 | HG01993.hp2 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.2398+211_2398+223d others(15): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | |||||
chr6:116927743
|
C | CTTTTTTT others(7): Show |
2 | a0001c0002t0002g0053a0004c0005t0002g0051 | 2 | HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2398+210_2398+223d others(16): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | |||||
chr6:116927743
|
CT | C | 8 | a0001c0001t0001g0071a0001c0001t0001g0106a0001c0001t0001g0111others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2398+223delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | |||||
chr6:116927769
|
A | G | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2398+230A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927769 | ||||||
chr6:116927796
|
G | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2398+257G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927796 | ||||||
chr6:116927810
|
C | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0030others(4): Show | 16 | HG00621.hp2 HG02083.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.2398+271C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927810 | ||||||
chr6:116928038
|
A | C | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2398+499A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928038 | ||||||
chr6:116928045
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2398+506C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928045 | ||||||
chr6:116928080
|
T | TA | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2398+555dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116928080 | |||||
chr6:116928161
|
A | G | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399-598A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928161 | ||||||
chr6:116928221
|
A | C | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-538A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928221 | ||||||
chr6:116928260
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2399-499G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928260 | ||||||
chr6:116928395
|
C | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-364C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928395 | ||||||
chr6:116928411
|
C | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-348C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928411 | ||||||
chr6:116928462
|
T | C | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-297T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928462 | ||||||
chr6:116928522
|
A | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2399-237A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928522 | ||||||
chr6:116928684
|
A | G | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-75A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928684 | ||||||
chr6:116929010
|
G | C | 1 | a0007c0014t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2611+39G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929010 | ||||||
chr6:116929017
|
A | C | 1 | a0002c0003t0006g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2611+46A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929017 | ||||||
chr6:116929019
|
C | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2611+48C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929019 | ||||||
chr6:116929031
|
A | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0063 | 3 | HG02257.hp2 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2611+60A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929031 | ||||||
chr6:116929139
|
G | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0228a0001c0001t0001g0229others(5): Show | 9 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2611+168G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929139 | ||||||
chr6:116929223
|
G | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 7 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2611+252G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929223 | ||||||
chr6:116929224
|
G | A | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2611+253G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929224 | ||||||
chr6:116929296
|
A | G | 5 | a0001c0002t0002g0050a0001c0002t0002g0053a0004c0005t0002g0019others(2): Show | 6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.2611+325A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929296 | ||||||
chr6:116929352
|
G | C | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2611+381G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929352 | ||||||
chr6:116929407
|
A | T | 2 | a0001c0002t0002g0218a0001c0002t0002g0250 | 2 | NA18951.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2611+436A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929407 | ||||||
chr6:116929414
|
A | AC | 3 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG01106.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2611+444dupC | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr6 | 116929414 | |||||
chr6:116929544
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0172 | 3 | HG02572.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2611+573G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929544 | ||||||
chr6:116929956
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2611+985A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929956 | ||||||
chr6:116929996
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0172 | 3 | HG02572.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2611+1025T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929996 | ||||||
chr6:116930027
|
G | T | 1 | a0001c0002t0002g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2611+1056G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930027 | ||||||
chr6:116930088
|
C | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2611+1117C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930088 | ||||||
chr6:116930113
|
G | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0228a0001c0001t0001g0229others(5): Show | 9 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2611+1142G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930113 | ||||||
chr6:116930113
|
G | T | 1 | a0005c0017t0001g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2611+1142G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930113 | ||||||
chr6:116930138
|
A | C | 1 | a0002c0003t0006g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2611+1167A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930138 | ||||||
chr6:116930280
|
TAGAC | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-1047_2612-104 others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr6 | 116930280 | |||||
chr6:116930332
|
A | G | 107 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(104): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.2612-999A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930332 | ||||||
chr6:116930363
|
AT | A | 96 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(93): Show | 109 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.2612-964delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr6 | 116930363 | |||||
chr6:116930500
|
C | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-831C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930500 | ||||||
chr6:116930554
|
A | G | 1 | a0002c0003t0006g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2612-777A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930554 | ||||||
chr6:116930565
|
G | A | 2 | a0001c0002t0002g0218a0001c0002t0002g0250 | 2 | NA18951.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2612-766G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930565 | ||||||
chr6:116930707
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0134a0001c0001t0001g0139others(5): Show | 11 | NA18962.hp1 NA18972.hp2 NA18981.hp2 others(8): Show |
intron_variant | MODIFIER | c.2612-624C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930707 | ||||||
chr6:116930724
|
A | G | 107 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(104): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.2612-607A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930724 | ||||||
chr6:116930725
|
T | G | 1 | a0002c0003t0006g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2612-606T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930725 | ||||||
chr6:116930792
|
G | C | 2 | a0001c0002t0002g0221a0001c0002t0002g0222 | 2 | NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2612-539G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930792 | ||||||
chr6:116930826
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2612-505C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930826 | ||||||
chr6:116930928
|
T | C | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-403T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930928 | ||||||
chr6:116930973
|
G | A | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-358G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930973 | ||||||
chr6:116931034
|
C | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-297C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931034 | ||||||
chr6:116931035
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2612-296C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931035 | ||||||
chr6:116931084
|
C | T | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-247C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931084 | ||||||
chr6:116931085
|
G | A | 1 | a0005c0017t0001g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2612-246G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931085 | ||||||
chr6:116931178
|
A | G | 108 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(105): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-153A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931178 | ||||||
chr6:116931224
|
T | A | 1 | a0001c0001t0007g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2612-107T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931224 | ||||||
chr6:116931235
|
T | G | 1 | a0002c0003t0006g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2612-96T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931235 |