geneid | 9025 |
---|---|
ensemblid | ENSG00000112130.17 |
hgncid | 10071 |
symbol | RNF8 |
name | ring finger protein 8 |
refseq_nuc | NM_003958.4 |
refseq_prot | NP_003949.1 |
ensembl_nuc | ENST00000373479.9 |
ensembl_prot | ENSP00000362578.4 |
mane_status | MANE Select |
chr | chr6 |
start | 37353983 |
end | 37394734 |
strand | + |
ver | v1.2 |
region | chr6:37353983-37394734 |
region5000 | chr6:37348983-37399734 |
regionname0 | RNF8_chr6_37353983_37394734 |
regionname5000 | RNF8_chr6_37348983_37399734 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 485 | 324 | 98 | 58 | 130 | 8 | 28 | 104 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1458 | 206 | 58 | 30 | 98 | 5 | 14 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
c0002 | 1/0 | 1458 | 113 | 38 | 25 | 32 | 3 | 14 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
c0003 | 0/0 | 1458 | 3 | 0 | 3 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
c0004 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
c0005 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 4159 | 143 | 8 | 36 | 69 | 6 | 22 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0002 | 0/0 | 4159 | 49 | 13 | 8 | 25 | 0 | 3 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0003 | 0/0 | 4159 | 28 | 9 | 0 | 19 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0004 | 0/0 | 4159 | 23 | 21 | 2 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0005 | 0/0 | 4159 | 16 | 15 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0006 | 0/0 | 4159 | 12 | 1 | 7 | 2 | 1 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0007 | 0/0 | 4159 | 11 | 3 | 3 | 5 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0008 | 0/0 | 4159 | 10 | 9 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0009 | 0/0 | 4159 | 5 | 5 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0010 | 0/0 | 4159 | 4 | 0 | 0 | 2 | 1 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0011 | 0/0 | 4159 | 3 | 0 | 0 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0012 | 0/0 | 4159 | 3 | 3 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0013 | 0/0 | 4159 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0014 | 0/0 | 4159 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0015 | 0/0 | 4159 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0016 | 0/0 | 4159 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0017 | 0/0 | 4159 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0018 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0019 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0020 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0021 | 0/0 | 4159 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0022 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0023 | 0/0 | 4159 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
t0024 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 14 | 0 | 7 | 6 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0002 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0003 | 1/0 | 5 | 1 | 1 | 1 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0005 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0007 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0008 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1458 | 206 | 58 | 30 | 98 | 5 | 14 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0002 | 1/0 | 1458 | 113 | 38 | 25 | 32 | 3 | 14 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0003 | 0/0 | 1458 | 3 | 0 | 3 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0004 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0005 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5616 | 95 | 3 | 17 | 60 | 3 | 11 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0002 | 0/0 | 5616 | 8 | 4 | 1 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0003 | 0/0 | 5616 | 28 | 9 | 0 | 19 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0004 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0005 | 0/0 | 5616 | 16 | 15 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0006 | 0/0 | 5616 | 12 | 1 | 7 | 2 | 1 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0007 | 0/0 | 5616 | 11 | 3 | 3 | 5 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0008 | 0/0 | 5616 | 10 | 9 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0009 | 0/0 | 5616 | 5 | 5 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0010 | 0/0 | 5616 | 4 | 0 | 0 | 2 | 1 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0011 | 0/0 | 5616 | 3 | 0 | 0 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0014 | 0/0 | 5616 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0015 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0016 | 0/0 | 5616 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0017 | 0/0 | 5616 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0018 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0019 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0020 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0021 | 0/0 | 5616 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0022 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0001t0024 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0002t0001 | 1/0 | 5616 | 45 | 5 | 16 | 9 | 3 | 11 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0002t0002 | 0/0 | 5616 | 41 | 9 | 7 | 22 | 0 | 3 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0002t0004 | 0/0 | 5616 | 20 | 18 | 2 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0002t0012 | 0/0 | 5616 | 3 | 3 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0002t0013 | 0/0 | 5616 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0002t0015 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0002t0023 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0003t0001 | 0/0 | 5616 | 3 | 0 | 3 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0004t0004 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
a0001c0005t0004 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | copy fasta | chr6 | 37348983 | 37399734 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 14 | 0 | 7 | 6 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0007 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0006g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0007g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0007g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0011g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0014g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0014g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0015g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0016g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0016g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0017g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0017g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0018g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0019g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0020g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0021g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0022g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0001t0024g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0003 | 1/0 | 4 | 1 | 0 | 1 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0005 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0008 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0012g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0012g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0015g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0002t0023g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0003t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0003t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0004t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
a0001c0005t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0006 | g0065 | EUR | FIN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0023 | EUR | FIN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00323 | hp1 | a0001 | c0001 | t0010 | g0110 | EUR | FIN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00438 | hp1 | a0001 | c0001 | t0010 | g0122 | EAS | CHS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0097 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00741 | hp1 | a0001 | c0002 | t0004 | g0177 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0043 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0254 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0020 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01169 | hp1 | a0001 | c0001 | t0007 | g0020 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01243 | hp2 | a0001 | c0002 | t0004 | g0181 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0096 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0228 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01361 | hp1 | a0001 | c0001 | t0008 | g0148 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0009 | EUR | IBS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01884 | hp1 | a0001 | c0002 | t0004 | g0174 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01884 | hp2 | a0001 | c0002 | t0012 | g0026 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01891 | hp1 | a0001 | c0002 | t0004 | g0223 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0227 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0156 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0165 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02074 | hp1 | a0001 | c0002 | t0023 | g0195 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02080 | hp2 | a0001 | c0001 | t0010 | g0125 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02145 | hp1 | a0001 | c0002 | t0004 | g0206 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0024 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0150 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02258 | hp1 | a0001 | c0001 | t0019 | g0160 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02523 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0187 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0146 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0151 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0179 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02647 | hp1 | a0001 | c0002 | t0004 | g0190 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0152 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02723 | hp2 | a0001 | c0002 | t0004 | g0012 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0158 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02818 | hp2 | a0001 | c0001 | t0024 | g0176 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0161 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0250 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0185 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0186 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0155 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02976 | hp2 | a0001 | c0001 | t0020 | g0159 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03041 | hp2 | a0001 | c0002 | t0004 | g0024 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0153 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0233 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03130 | hp2 | a0001 | c0002 | t0004 | g0025 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0178 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03195 | hp1 | a0001 | c0005 | t0004 | g0182 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03209 | hp1 | a0001 | c0002 | t0004 | g0180 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03225 | hp1 | a0001 | c0002 | t0004 | g0203 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03225 | hp2 | a0001 | c0001 | t0018 | g0163 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0199 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03486 | hp2 | a0001 | c0002 | t0012 | g0220 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0229 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03579 | hp1 | a0001 | c0002 | t0004 | g0183 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0012 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03688 | hp1 | a0001 | c0001 | t0010 | g0094 | SAS | STU | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0216 | SAS | STU | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03942 | hp1 | a0001 | c0001 | t0021 | g0072 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0095 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | STU | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | STU | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18522 | hp1 | a0001 | c0002 | t0012 | g0026 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0154 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18943 | hp2 | a0001 | c0001 | t0017 | g0235 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18947 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18948 | hp1 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18961 | hp1 | a0001 | c0001 | t0014 | g0112 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18961 | hp2 | a0001 | c0001 | t0011 | g0027 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18968 | hp2 | a0001 | c0001 | t0014 | g0162 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18978 | hp1 | a0001 | c0001 | t0007 | g0145 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18994 | hp2 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18999 | hp2 | a0001 | c0001 | t0011 | g0234 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19030 | hp1 | a0001 | c0002 | t0004 | g0196 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19043 | hp2 | a0001 | c0002 | t0015 | g0256 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19064 | hp2 | a0001 | c0001 | t0011 | g0027 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19078 | hp2 | a0001 | c0001 | t0006 | g0092 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19090 | hp1 | a0001 | c0001 | t0017 | g0236 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19240 | hp1 | a0001 | c0001 | t0016 | g0164 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0147 | AFR | ASW | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ASW | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0064 | EUR | TSI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02109 | hp1 | a0001 | c0001 | t0008 | g0157 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02486 | hp1 | a0001 | c0002 | t0004 | g0025 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0188 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02559 | hp1 | a0001 | c0002 | t0013 | g0168 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03471 | hp1 | a0001 | c0002 | t0004 | g0012 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG06807 | hp1 | a0001 | c0002 | t0013 | g0169 | AFR | USA | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0167 | AFR | USA | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0093 | AFR | USA | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA20300 | hp2 | a0001 | c0001 | t0022 | g0170 | AFR | USA | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
NA21309 | hp2 | a0001 | c0004 | t0004 | g0171 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0127 | REF | REF | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0003 | REF | REF | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:37369050
|
C | T | 1 | a0001c0005 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.807C>T | p.Ala269Ala | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/8 | 989/5616 | 807/1458 | 269/485 | chr6 | 37369050 | ||
chr6:37371547
|
G | A | 1 | a0001c0004 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1011G>A | p.Lys337Lys | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/8 | 1193/5616 | 1011/1458 | 337/485 | chr6 | 37371547 | ||
chr6:37381257
|
G | A | 2 | a0001c0001a0001c0004 | 207 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
synonymous_variant | LOW | c.1344G>A | p.Thr448Thr | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/8 | 1526/5616 | 1344/1458 | 448/485 | chr6 | 37381257 | ||
chr6:37381290
|
G | A | 1 | a0001c0003 | 3 | HG01099.hp2 HG01106.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1377G>A | p.Lys459Lys | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/8 | 1559/5616 | 1377/1458 | 459/485 | chr6 | 37381290 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:37354015
|
G | T | 2 | a0001c0001t0006a0001c0001t0010 | 16 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-150G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/8 | 150 | chr6 | 37354015 | |||||
chr6:37354031
|
C | G | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(10): Show | 126 | HG00609.hp2 HG00741.hp1 HG00741.hp2 others(123): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-134C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/8 | chr6 | 37354031 | ||||||
chr6:37354076
|
G | T | 1 | a0001c0001t0016 | 2 | HG02055.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-89G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/8 | 89 | chr6 | 37354076 | |||||
chr6:37391130
|
C | T | 4 | a0001c0001t0009a0001c0001t0016a0001c0001t0022others(1): Show | 9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*372C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 372 | chr6 | 37391130 | |||||
chr6:37391348
|
A | T | 1 | a0001c0002t0012 | 3 | HG01884.hp2 HG03486.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*590A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 590 | chr6 | 37391348 | |||||
chr6:37391421
|
C | T | 1 | a0001c0001t0011 | 3 | NA18961.hp2 NA18999.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*663C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 663 | chr6 | 37391421 | |||||
chr6:37391433
|
G | A | 1 | a0001c0002t0013 | 2 | HG02559.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*675G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 675 | chr6 | 37391433 | |||||
chr6:37391539
|
C | T | 4 | a0001c0001t0009a0001c0001t0016a0001c0001t0022others(1): Show | 9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*781C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 781 | chr6 | 37391539 | |||||
chr6:37391771
|
A | G | 1 | a0001c0001t0021 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1013A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1013 | chr6 | 37391771 | |||||
chr6:37392170
|
A | G | 7 | a0001c0001t0004a0001c0001t0015a0001c0002t0004others(4): Show | 27 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1412A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1412 | chr6 | 37392170 | |||||
chr6:37392292
|
G | A | 1 | a0001c0001t0018 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1534G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1534 | chr6 | 37392292 | |||||
chr6:37392296
|
A | G | 1 | a0001c0001t0014 | 2 | NA18961.hp1 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1538A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1538 | chr6 | 37392296 | |||||
chr6:37392443
|
C | G | 1 | a0001c0001t0017 | 2 | NA18943.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1685C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1685 | chr6 | 37392443 | |||||
chr6:37392674
|
G | A | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0019others(1): Show | 28 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1916G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1916 | chr6 | 37392674 | |||||
chr6:37392778
|
A | G | 1 | a0001c0001t0018 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2020A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2020 | chr6 | 37392778 | |||||
chr6:37392781
|
T | C | 20 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(17): Show | 118 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2023T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2023 | chr6 | 37392781 | |||||
chr6:37393208
|
C | T | 1 | a0001c0001t0020 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2450C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2450 | chr6 | 37393208 | |||||
chr6:37393660
|
G | A | 1 | a0001c0002t0023 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2902G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2902 | chr6 | 37393660 | |||||
chr6:37393733
|
C | T | 3 | a0001c0001t0005a0001c0001t0008a0001c0001t0020 | 27 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2975C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2975 | chr6 | 37393733 | |||||
chr6:37393762
|
A | C | 4 | a0001c0001t0009a0001c0001t0016a0001c0001t0022others(1): Show | 9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3004A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 3004 | chr6 | 37393762 | |||||
chr6:37394145
|
A | G | 1 | a0001c0002t0013 | 2 | HG02559.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3387A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 3387 | chr6 | 37394145 | |||||
chr6:37394454
|
G | A | 1 | a0001c0001t0022 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3696G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 3696 | chr6 | 37394454 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:37354383
|
C | G | 2 | a0001c0002t0001g0257a0001c0002t0015g0256 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.111+108C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354383 | ||||||
chr6:37354416
|
G | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(4): Show | 7 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+141G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354416 | ||||||
chr6:37354419
|
G | T | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.111+144G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354419 | ||||||
chr6:37354513
|
G | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02040.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.111+238G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354513 | ||||||
chr6:37354569
|
A | T | 99 | a0001c0001t0002g0172a0001c0001t0002g0200a0001c0001t0002g0209others(96): Show | 127 | HG00609.hp2 HG00741.hp1 HG00741.hp2 others(124): Show |
intron_variant | MODIFIER | c.111+294A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354569 | ||||||
chr6:37354595
|
G | A | 1 | a0001c0001t0022g0170 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.111+320G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354595 | ||||||
chr6:37354774
|
G | GC | 130 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(127): Show | 158 | HG00609.hp2 HG00741.hp1 HG00741.hp2 others(155): Show |
intron_variant | MODIFIER | c.111+501dupC | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 37354774 | |||||
chr6:37354896
|
G | A | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111+621G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354896 | ||||||
chr6:37355219
|
C | G | 1 | a0001c0002t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.111+944C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355219 | ||||||
chr6:37355263
|
A | G | 27 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(24): Show | 37 | HG02056.hp1 HG02109.hp2 HG02559.hp2 others(34): Show |
intron_variant | MODIFIER | c.111+988A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355263 | ||||||
chr6:37355269
|
T | C | 5 | a0001c0001t0002g0237a0001c0001t0011g0027a0001c0001t0011g0234others(2): Show | 6 | NA18943.hp2 NA18961.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+994T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355269 | ||||||
chr6:37355392
|
T | C | 3 | a0001c0001t0008g0146a0001c0001t0008g0147a0001c0001t0008g0148 | 3 | HG01361.hp1 HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.111+1117T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355392 | ||||||
chr6:37355482
|
G | A | 2 | a0001c0002t0001g0257a0001c0002t0015g0256 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.111+1207G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355482 | ||||||
chr6:37355733
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.111+1458G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355733 | ||||||
chr6:37356106
|
A | C | 2 | a0001c0002t0013g0168a0001c0002t0013g0169 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.111+1831A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356106 | ||||||
chr6:37356144
|
A | G | 2 | a0001c0001t0007g0166a0001c0001t0007g0167 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.111+1869A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356144 | ||||||
chr6:37356234
|
T | C | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.111+1959T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356234 | ||||||
chr6:37356336
|
ATGG | A | 21 | a0001c0001t0004g0184a0001c0001t0024g0176a0001c0002t0002g0175others(18): Show | 25 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.111+2063_111+2065d others(5): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 37356336 | |||||
chr6:37356740
|
G | A | 2 | a0001c0001t0007g0166a0001c0001t0007g0167 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.111+2465G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356740 | ||||||
chr6:37356892
|
C | T | 3 | a0001c0001t0016g0164a0001c0001t0016g0165a0001c0001t0018g0163 | 3 | HG02055.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.111+2617C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356892 | ||||||
chr6:37357081
|
G | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(107): Show | 140 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.111+2806G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357081 | ||||||
chr6:37357117
|
C | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(113): Show | 146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.111+2842C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357117 | ||||||
chr6:37357170
|
A | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.111+2895A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357170 | ||||||
chr6:37357200
|
G | A | 1 | a0001c0001t0006g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.111+2925G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357200 | ||||||
chr6:37357418
|
T | C | 2 | a0001c0001t0008g0030a0001c0001t0008g0031 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.112-3028T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357418 | ||||||
chr6:37357556
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.112-2890G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357556 | ||||||
chr6:37357639
|
T | G | 1 | a0001c0001t0006g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.112-2807T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357639 | ||||||
chr6:37357916
|
A | C | 30 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(27): Show | 40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-2530A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357916 | ||||||
chr6:37357936
|
C | T | 1 | a0001c0001t0007g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.112-2510C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357936 | ||||||
chr6:37358104
|
T | G | 1 | a0001c0001t0001g0066 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.112-2342T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358104 | ||||||
chr6:37358253
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18979.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.112-2193A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358253 | ||||||
chr6:37358441
|
T | A | 30 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(27): Show | 40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-2005T>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358441 | ||||||
chr6:37358468
|
A | G | 1 | a0001c0002t0001g0064 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.112-1978A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358468 | ||||||
chr6:37358819
|
G | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | NA18979.hp1 NA18982.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.112-1627G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358819 | ||||||
chr6:37358823
|
G | A | 30 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(27): Show | 40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-1623G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358823 | ||||||
chr6:37358913
|
A | G | 1 | a0001c0001t0003g0029 | 2 | NA18949.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.112-1533A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358913 | ||||||
chr6:37358996
|
T | C | 1 | a0001c0001t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.112-1450T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358996 | ||||||
chr6:37359022
|
G | A | 12 | a0001c0001t0022g0170a0001c0002t0001g0149a0001c0002t0002g0004others(9): Show | 16 | HG01943.hp1 HG02004.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.112-1424G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359022 | ||||||
chr6:37359089
|
C | CTG | 30 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(27): Show | 40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-1356_112-1355i others(4): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 37359089 | |||||
chr6:37359570
|
A | G | 1 | a0001c0002t0001g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.112-876A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359570 | ||||||
chr6:37359618
|
A | G | 30 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(27): Show | 40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-828A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359618 | ||||||
chr6:37359863
|
C | G | 5 | a0001c0001t0007g0166a0001c0001t0007g0167a0001c0002t0013g0168others(2): Show | 5 | HG02559.hp1 HG03098.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-583C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359863 | ||||||
chr6:37359885
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.112-561G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359885 | ||||||
chr6:37360036
|
A | G | 1 | a0001c0002t0002g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.112-410A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37360036 | ||||||
chr6:37360223
|
C | T | 51 | a0001c0001t0002g0172a0001c0001t0003g0230a0001c0001t0004g0184others(48): Show | 58 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.112-223C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37360223 | ||||||
chr6:37360388
|
G | A | 30 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(27): Show | 40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-58G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37360388 | ||||||
chr6:37360402
|
G | A | 3 | a0001c0001t0005g0013a0001c0001t0005g0218a0001c0001t0005g0219 | 5 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-44G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37360402 | ||||||
chr6:37360439
|
C | CT | 86 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(83): Show | 103 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(100): Show |
splice_region_variant&intron_variant | LOW | c.112-6dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 37360439 | |||||
chr6:37360623
|
C | CT | 27 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(24): Show | 37 | HG02056.hp1 HG02109.hp2 HG02559.hp2 others(34): Show |
intron_variant | MODIFIER | c.240+63dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37360623 | |||||
chr6:37360623
|
CT | C | 54 | a0001c0001t0001g0014a0001c0001t0001g0067a0001c0001t0001g0068others(51): Show | 62 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.240+63delT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37360623 | |||||
chr6:37360777
|
A | G | 35 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(32): Show | 45 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(42): Show |
intron_variant | MODIFIER | c.240+203A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37360777 | ||||||
chr6:37360788
|
A | C | 1 | a0001c0001t0001g0140 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.240+214A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37360788 | ||||||
chr6:37361225
|
A | G | 84 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(81): Show | 101 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(98): Show |
intron_variant | MODIFIER | c.240+651A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361225 | ||||||
chr6:37361505
|
C | T | 1 | a0001c0002t0001g0139 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.240+931C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361505 | ||||||
chr6:37361552
|
C | T | 1 | a0001c0001t0006g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.240+978C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361552 | ||||||
chr6:37361772
|
G | A | 49 | a0001c0001t0002g0172a0001c0001t0003g0230a0001c0001t0004g0184others(46): Show | 56 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.240+1198G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361772 | ||||||
chr6:37361796
|
C | T | 1 | a0001c0002t0001g0137 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.240+1222C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361796 | ||||||
chr6:37361984
|
C | G | 4 | a0001c0001t0003g0029a0001c0001t0003g0217a0001c0001t0003g0253others(1): Show | 5 | NA18949.hp2 NA18962.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+1410C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361984 | ||||||
chr6:37362024
|
A | G | 11 | a0001c0002t0001g0054a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 11 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.240+1450A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362024 | ||||||
chr6:37362102
|
C | T | 6 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+1528C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362102 | ||||||
chr6:37362117
|
C | T | 1 | a0001c0002t0002g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.240+1543C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362117 | ||||||
chr6:37362263
|
T | C | 1 | a0001c0001t0001g0015 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.240+1689T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362263 | ||||||
chr6:37362458
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.240+1884T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362458 | ||||||
chr6:37362515
|
A | G | 5 | a0001c0002t0002g0211a0001c0002t0002g0212a0001c0002t0002g0213others(2): Show | 5 | NA18955.hp1 NA18956.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+1941A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362515 | ||||||
chr6:37362516
|
TTTAA | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(154): Show | 193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.240+1945_240+1948d others(6): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37362516 | |||||
chr6:37362543
|
G | A | 1 | a0001c0002t0012g0220 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.240+1969G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362543 | ||||||
chr6:37362679
|
A | G | 6 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+2105A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362679 | ||||||
chr6:37362838
|
T | C | 2 | a0001c0001t0008g0030a0001c0001t0008g0031 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.240+2264T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362838 | ||||||
chr6:37362975
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(81): Show | 109 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.240+2401C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362975 | ||||||
chr6:37363240
|
C | G | 1 | a0001c0002t0001g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.240+2666C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363240 | ||||||
chr6:37363273
|
C | G | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0066others(13): Show | 18 | HG00323.hp2 HG02015.hp1 HG03669.hp2 others(15): Show |
intron_variant | MODIFIER | c.240+2699C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363273 | ||||||
chr6:37363499
|
A | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG00609.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.240+2925A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363499 | ||||||
chr6:37363564
|
T | C | 1 | a0001c0001t0005g0218 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.240+2990T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363564 | ||||||
chr6:37363578
|
C | T | 1 | a0001c0002t0004g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.240+3004C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363578 | ||||||
chr6:37363680
|
A | ATTAC | 31 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(28): Show | 41 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.240+3108_240+3109i others(6): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37363680 | |||||
chr6:37363698
|
C | T | 1 | a0001c0002t0001g0063 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.240+3124C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363698 | ||||||
chr6:37363720
|
T | C | 3 | a0001c0001t0007g0166a0001c0001t0007g0167a0001c0004t0004g0171 | 3 | HG03098.hp2 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.240+3146T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363720 | ||||||
chr6:37363876
|
C | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.240+3302C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363876 | ||||||
chr6:37363986
|
T | C | 1 | a0001c0001t0021g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.240+3412T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363986 | ||||||
chr6:37364023
|
T | C | 29 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(26): Show | 39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.240+3449T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364023 | ||||||
chr6:37364039
|
C | T | 1 | a0001c0001t0008g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.240+3465C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364039 | ||||||
chr6:37364178
|
C | CA | 129 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(126): Show | 163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.240+3625dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364178 | |||||
chr6:37364178
|
C | CAA | 25 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0052others(22): Show | 27 | HG00741.hp1 HG01109.hp1 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.240+3624_240+3625d others(4): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364178 | |||||
chr6:37364178
|
C | CAAAAAA | 23 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(20): Show | 32 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.240+3620_240+3625d others(8): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364178 | |||||
chr6:37364178
|
C | CAAAAAAA | 5 | a0001c0001t0003g0028a0001c0001t0003g0238a0001c0001t0003g0253others(2): Show | 6 | HG03209.hp2 HG03471.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+3619_240+3625d others(9): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364178 | |||||
chr6:37364261
|
T | TAAAACCA others(274): Show |
1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.240+3697_240+3698i others(283): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | |||||
chr6:37364261
|
T | TAAAACCA others(274): Show |
4 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(1): Show | 4 | HG02647.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+3697_240+3698i others(283): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | |||||
chr6:37364261
|
T | TAAAACCA others(275): Show |
1 | a0001c0001t0009g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.240+3697_240+3698i others(284): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | |||||
chr6:37364261
|
T | TAAAACCA others(276): Show |
1 | a0001c0001t0015g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.240+3697_240+3698i others(285): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | |||||
chr6:37364261
|
T | TAAAACCA others(274): Show |
1 | a0001c0001t0007g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.240+3697_240+3698i others(283): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | |||||
chr6:37364261
|
T | TAAAACCA others(275): Show |
1 | a0001c0001t0007g0166 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.240+3697_240+3698i others(284): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | |||||
chr6:37364437
|
A | G | 1 | a0001c0001t0003g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.240+3863A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364437 | ||||||
chr6:37364440
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.240+3866G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364440 | ||||||
chr6:37364489
|
T | A | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240+3915T>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364489 | ||||||
chr6:37364781
|
A | G | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.241-3703A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364781 | ||||||
chr6:37364801
|
G | A | 29 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(26): Show | 39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.241-3683G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364801 | ||||||
chr6:37365255
|
T | C | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.241-3229T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365255 | ||||||
chr6:37365329
|
C | T | 3 | a0001c0001t0016g0164a0001c0001t0016g0165a0001c0001t0018g0163 | 3 | HG02055.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-3155C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365329 | ||||||
chr6:37365394
|
G | T | 29 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(26): Show | 39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.241-3090G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365394 | ||||||
chr6:37365508
|
A | G | 6 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-2976A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365508 | ||||||
chr6:37365542
|
G | A | 64 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(61): Show | 78 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(75): Show |
intron_variant | MODIFIER | c.241-2942G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365542 | ||||||
chr6:37365674
|
A | G | 29 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(26): Show | 39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.241-2810A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365674 | ||||||
chr6:37365801
|
A | AG | 33 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(30): Show | 37 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.241-2682dupG | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37365801 | |||||
chr6:37365811
|
T | C | 1 | a0001c0002t0001g0039 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.241-2673T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365811 | ||||||
chr6:37365831
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.241-2653A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365831 | ||||||
chr6:37365908
|
C | A | 1 | a0001c0001t0007g0106 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.241-2576C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365908 | ||||||
chr6:37366020
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(181): Show | 230 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.241-2464C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366020 | ||||||
chr6:37366091
|
C | G | 29 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(26): Show | 39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.241-2393C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366091 | ||||||
chr6:37366394
|
T | C | 64 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(61): Show | 78 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(75): Show |
intron_variant | MODIFIER | c.241-2090T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366394 | ||||||
chr6:37366658
|
C | T | 6 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-1826C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366658 | ||||||
chr6:37366683
|
T | TCCCTCAT others(10): Show |
2 | a0001c0002t0001g0105a0001c0002t0001g0130 | 2 | HG00639.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.241-1800_241-1784d others(19): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37366683 | |||||
chr6:37366953
|
C | T | 1 | a0001c0002t0004g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.241-1531C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366953 | ||||||
chr6:37366983
|
C | T | 64 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(61): Show | 78 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(75): Show |
intron_variant | MODIFIER | c.241-1501C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366983 | ||||||
chr6:37367064
|
G | A | 31 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0237others(28): Show | 41 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.241-1420G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367064 | ||||||
chr6:37367071
|
T | C | 1 | a0001c0001t0003g0239 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.241-1413T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367071 | ||||||
chr6:37367142
|
G | A | 2 | a0001c0001t0016g0164a0001c0001t0016g0165 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-1342G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367142 | ||||||
chr6:37367175
|
G | A | 1 | a0001c0001t0005g0224 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.241-1309G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367175 | ||||||
chr6:37367360
|
C | G | 1 | a0001c0002t0001g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.241-1124C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367360 | ||||||
chr6:37367369
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.241-1115A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367369 | ||||||
chr6:37367387
|
T | C | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.241-1097T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367387 | ||||||
chr6:37367553
|
A | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-931A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367553 | ||||||
chr6:37367565
|
G | A | 3 | a0001c0001t0016g0164a0001c0001t0016g0165a0001c0001t0018g0163 | 3 | HG02055.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-919G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367565 | ||||||
chr6:37367588
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.241-896G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367588 | ||||||
chr6:37367683
|
T | C | 5 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0016g0164others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-801T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367683 | ||||||
chr6:37367684
|
G | C | 1 | a0001c0001t0005g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.241-800G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367684 | ||||||
chr6:37367722
|
A | G | 26 | a0001c0001t0002g0237a0001c0001t0002g0245a0001c0001t0003g0006others(23): Show | 36 | HG02056.hp1 HG02109.hp2 HG02559.hp2 others(33): Show |
intron_variant | MODIFIER | c.241-762A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367722 | ||||||
chr6:37367845
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.241-639G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367845 | ||||||
chr6:37368057
|
C | T | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.241-427C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37368057 | ||||||
chr6:37368440
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0128 | 3 | NA18948.hp2 NA18979.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.241-44C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37368440 | ||||||
chr6:37369375
|
A | C | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.975+157A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37369375 | ||||||
chr6:37369583
|
T | C | 6 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+365T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37369583 | ||||||
chr6:37370258
|
G | A | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.975+1040G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370258 | ||||||
chr6:37370529
|
T | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-983T>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370529 | ||||||
chr6:37370566
|
G | A | 2 | a0001c0002t0001g0051a0001c0002t0002g0201 | 2 | HG01346.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.976-946G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370566 | ||||||
chr6:37370573
|
A | T | 63 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(60): Show | 77 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(74): Show |
intron_variant | MODIFIER | c.976-939A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370573 | ||||||
chr6:37370638
|
C | G | 3 | a0001c0002t0002g0175a0001c0002t0002g0189a0001c0002t0004g0174 | 3 | HG01884.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.976-874C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370638 | ||||||
chr6:37370701
|
C | CT | 212 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(209): Show | 270 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.976-796dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 37370701 | |||||
chr6:37370701
|
C | CTT | 7 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(4): Show | 7 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.976-797_976-796dup others(2): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 37370701 | |||||
chr6:37370925
|
A | C | 1 | a0001c0002t0001g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.976-587A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370925 | ||||||
chr6:37371193
|
G | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(94): Show | 127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.976-319G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371193 | ||||||
chr6:37371241
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(94): Show | 127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.976-271A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371241 | ||||||
chr6:37371298
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.976-214C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371298 | ||||||
chr6:37371343
|
T | C | 28 | a0001c0001t0002g0245a0001c0001t0003g0006a0001c0001t0003g0007others(25): Show | 38 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.976-169T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371343 | ||||||
chr6:37371454
|
G | A | 3 | a0001c0002t0002g0175a0001c0002t0002g0189a0001c0002t0004g0174 | 3 | HG01884.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.976-58G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371454 | ||||||
chr6:37371591
|
A | G | 1 | a0001c0001t0007g0020 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1038+17A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371591 | ||||||
chr6:37371743
|
C | A | 1 | a0001c0002t0004g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1038+169C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371743 | ||||||
chr6:37371794
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1038+220A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371794 | ||||||
chr6:37371805
|
T | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0001g0134 | 3 | HG00323.hp2 NA18975.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1038+231T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371805 | ||||||
chr6:37371846
|
T | C | 4 | a0001c0001t0005g0221a0001c0001t0005g0226a0001c0001t0005g0250others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+272T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371846 | ||||||
chr6:37371975
|
T | C | 34 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(31): Show | 38 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.1038+401T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371975 | ||||||
chr6:37372545
|
G | A | 2 | a0001c0001t0007g0166a0001c0001t0007g0167 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1038+971G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372545 | ||||||
chr6:37372604
|
C | T | 1 | a0001c0001t0003g0252 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1038+1030C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372604 | ||||||
chr6:37372691
|
C | T | 1 | a0001c0001t0003g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1038+1117C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372691 | ||||||
chr6:37372697
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1038+1123C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372697 | ||||||
chr6:37372698
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1038+1124G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372698 | ||||||
chr6:37372786
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1038+1212A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372786 | ||||||
chr6:37372796
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0091 | 3 | NA18940.hp1 NA18960.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1038+1222C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372796 | ||||||
chr6:37372838
|
G | A | 23 | a0001c0001t0005g0013a0001c0001t0005g0173a0001c0001t0005g0218others(20): Show | 25 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1038+1264G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372838 | ||||||
chr6:37372841
|
T | C | 19 | a0001c0001t0002g0172a0001c0001t0003g0230a0001c0001t0004g0184others(16): Show | 23 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1038+1267T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372841 | ||||||
chr6:37372996
|
A | G | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1038+1422A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372996 | ||||||
chr6:37373025
|
C | G | 19 | a0001c0001t0002g0172a0001c0001t0003g0230a0001c0001t0004g0184others(16): Show | 23 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1038+1451C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373025 | ||||||
chr6:37373249
|
C | CCTT | 63 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(60): Show | 77 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(74): Show |
intron_variant | MODIFIER | c.1039-1369_1039-136 others(7): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 37373249 | |||||
chr6:37373458
|
G | A | 9 | a0001c0001t0008g0146a0001c0001t0008g0147a0001c0001t0008g0148others(6): Show | 9 | HG01361.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1039-1162G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373458 | ||||||
chr6:37373516
|
C | A | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1039-1104C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373516 | ||||||
chr6:37373553
|
C | T | 19 | a0001c0001t0002g0172a0001c0001t0003g0230a0001c0001t0004g0184others(16): Show | 23 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-1067C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373553 | ||||||
chr6:37373615
|
C | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1039-1005C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373615 | ||||||
chr6:37373646
|
C | G | 63 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(60): Show | 77 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(74): Show |
intron_variant | MODIFIER | c.1039-974C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373646 | ||||||
chr6:37373850
|
A | G | 24 | a0001c0001t0005g0013a0001c0001t0005g0173a0001c0001t0005g0218others(21): Show | 26 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1039-770A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373850 | ||||||
chr6:37373920
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1039-700A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373920 | ||||||
chr6:37374006
|
A | G | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1039-614A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374006 | ||||||
chr6:37374082
|
T | C | 9 | a0001c0001t0008g0146a0001c0001t0008g0147a0001c0001t0008g0148others(6): Show | 9 | HG01361.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1039-538T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374082 | ||||||
chr6:37374144
|
A | G | 63 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(60): Show | 77 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(74): Show |
intron_variant | MODIFIER | c.1039-476A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374144 | ||||||
chr6:37374359
|
T | G | 1 | a0001c0001t0009g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1039-261T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374359 | ||||||
chr6:37374373
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1039-247A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374373 | ||||||
chr6:37374414
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1039-206G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374414 | ||||||
chr6:37375083
|
T | C | 1 | a0001c0002t0001g0139 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1128+374T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375083 | ||||||
chr6:37375301
|
G | T | 1 | a0001c0002t0002g0215 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1128+592G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375301 | ||||||
chr6:37375392
|
A | G | 3 | a0001c0001t0007g0166a0001c0001t0007g0167a0001c0004t0004g0171 | 3 | HG03098.hp2 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1128+683A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375392 | ||||||
chr6:37375535
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1128+826C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375535 | ||||||
chr6:37375648
|
T | G | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1128+939T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375648 | ||||||
chr6:37375688
|
G | A | 1 | a0001c0001t0008g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1128+979G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375688 | ||||||
chr6:37375694
|
A | G | 1 | a0001c0001t0020g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1128+985A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375694 | ||||||
chr6:37375924
|
C | T | 3 | a0001c0001t0007g0166a0001c0001t0007g0167a0001c0004t0004g0171 | 3 | HG03098.hp2 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1129-1002C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375924 | ||||||
chr6:37375928
|
G | C | 6 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129-998G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375928 | ||||||
chr6:37375982
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1129-944G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375982 | ||||||
chr6:37375983
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1129-943G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375983 | ||||||
chr6:37376070
|
T | C | 19 | a0001c0001t0002g0172a0001c0001t0003g0230a0001c0001t0004g0184others(16): Show | 23 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1129-856T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376070 | ||||||
chr6:37376399
|
A | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-527A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376399 | ||||||
chr6:37376546
|
G | C | 12 | a0001c0001t0001g0098a0001c0001t0006g0002a0001c0001t0006g0065others(9): Show | 17 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1129-380G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376546 | ||||||
chr6:37376560
|
C | T | 1 | a0001c0001t0008g0148 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1129-366C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376560 | ||||||
chr6:37376613
|
C | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-313C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376613 | ||||||
chr6:37377061
|
C | CT | 60 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0049others(57): Show | 65 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.1236+56dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | |||||
chr6:37377061
|
C | CTT | 9 | a0001c0001t0001g0052a0001c0001t0001g0127a0001c0001t0006g0065others(6): Show | 11 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.1236+55_1236+56dup others(2): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | |||||
chr6:37377061
|
CT | C | 10 | a0001c0001t0001g0053a0001c0001t0001g0142a0001c0001t0005g0222others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1236+56delT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | |||||
chr6:37377061
|
CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+49_1236+56del others(8): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | |||||
chr6:37377061
|
CTTTTTTT others(3): Show |
C | 26 | a0001c0001t0002g0245a0001c0001t0003g0006a0001c0001t0003g0007others(23): Show | 36 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1236+47_1236+56del others(10): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | |||||
chr6:37377367
|
A | G | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1236+334A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377367 | ||||||
chr6:37377674
|
G | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1236+641G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377674 | ||||||
chr6:37377775
|
A | G | 1 | a0001c0002t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1236+742A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377775 | ||||||
chr6:37377787
|
A | C | 1 | a0001c0001t0003g0247 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1236+754A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377787 | ||||||
chr6:37377928
|
T | C | 64 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(61): Show | 78 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(75): Show |
intron_variant | MODIFIER | c.1236+895T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377928 | ||||||
chr6:37378225
|
C | T | 30 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(27): Show | 34 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1236+1192C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378225 | ||||||
chr6:37378336
|
C | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+1303C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378336 | ||||||
chr6:37378375
|
C | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1236+1342C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378375 | ||||||
chr6:37378588
|
G | A | 4 | a0001c0002t0002g0187a0001c0002t0002g0188a0001c0002t0002g0232others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+1555G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378588 | ||||||
chr6:37378600
|
C | CA | 58 | a0001c0001t0001g0033a0001c0001t0001g0078a0001c0001t0001g0088others(55): Show | 72 | HG00609.hp1 HG00741.hp1 HG01243.hp2 others(69): Show |
intron_variant | MODIFIER | c.1236+1590dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37378600 | |||||
chr6:37378600
|
C | CAA | 6 | a0001c0001t0001g0107a0001c0001t0002g0237a0001c0001t0003g0241others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+1589_1236+159 others(6): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37378600 | |||||
chr6:37378600
|
CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+1578_1236+159 others(17): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37378600 | |||||
chr6:37378831
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1236+1798T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378831 | ||||||
chr6:37379079
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1236+2046C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379079 | ||||||
chr6:37379102
|
C | T | 8 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0009g0151others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1237-2048C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379102 | ||||||
chr6:37379457
|
G | A | 2 | a0001c0002t0001g0055a0001c0002t0001g0056 | 2 | HG00642.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1237-1693G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379457 | ||||||
chr6:37379527
|
A | G | 3 | a0001c0001t0005g0013a0001c0001t0005g0218a0001c0001t0005g0219 | 5 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-1623A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379527 | ||||||
chr6:37379659
|
G | A | 1 | a0001c0002t0001g0041 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1237-1491G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379659 | ||||||
chr6:37379668
|
G | T | 1 | a0001c0002t0002g0213 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1237-1482G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379668 | ||||||
chr6:37379763
|
G | A | 63 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(60): Show | 77 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(74): Show |
intron_variant | MODIFIER | c.1237-1387G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379763 | ||||||
chr6:37379912
|
G | GTTTGTTT others(6): Show |
1 | a0001c0001t0003g0247 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1237-1234_1237-122 others(17): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37379912 | |||||
chr6:37380466
|
C | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1237-684C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380466 | ||||||
chr6:37380540
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(188): Show | 237 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.1237-610A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380540 | ||||||
chr6:37380543
|
C | T | 20 | a0001c0001t0002g0172a0001c0001t0003g0230a0001c0001t0024g0176others(17): Show | 24 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1237-607C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380543 | ||||||
chr6:37380563
|
C | T | 1 | a0001c0001t0019g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1237-587C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380563 | ||||||
chr6:37380583
|
A | C | 2 | a0001c0001t0007g0166a0001c0001t0007g0167 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1237-567A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380583 | ||||||
chr6:37380665
|
C | T | 1 | a0001c0002t0002g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1237-485C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380665 | ||||||
chr6:37380670
|
C | CA | 32 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0121others(29): Show | 44 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1237-463dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37380670 | |||||
chr6:37380670
|
CA | C | 25 | a0001c0001t0001g0098a0001c0001t0001g0120a0001c0001t0005g0173others(22): Show | 25 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1237-463delA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37380670 | |||||
chr6:37380685
|
A | T | 1 | a0001c0001t0001g0080 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1237-465A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380685 | ||||||
chr6:37380957
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1237-193A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380957 | ||||||
chr6:37381144
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(161): Show | 208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
splice_region_variant&intron_variant | LOW | c.1237-6C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37381144 | ||||||
chr6:37381517
|
G | A | 1 | a0001c0001t0021g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1441+163G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37381517 | ||||||
chr6:37381542
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1441+188C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37381542 | ||||||
chr6:37382031
|
A | G | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(1): Show | 4 | HG02083.hp1 HG02523.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441+677A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382031 | ||||||
chr6:37382108
|
T | C | 1 | a0001c0002t0001g0042 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1441+754T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382108 | ||||||
chr6:37382274
|
G | T | 15 | a0001c0001t0015g0150a0001c0002t0004g0012a0001c0002t0004g0177others(12): Show | 17 | HG00741.hp1 HG01243.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1441+920G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382274 | ||||||
chr6:37382280
|
G | A | 38 | a0001c0001t0002g0237a0001c0001t0003g0006a0001c0001t0003g0007others(35): Show | 55 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1441+926G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382280 | ||||||
chr6:37382959
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0079 | 2 | NA18995.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1441+1605C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382959 | ||||||
chr6:37382972
|
C | CA | 6 | a0001c0002t0001g0047a0001c0002t0001g0141a0001c0002t0002g0205others(3): Show | 6 | HG00639.hp1 HG02135.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441+1634dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37382972 | |||||
chr6:37383037
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0084a0001c0001t0001g0087others(3): Show | 7 | HG00323.hp2 HG02015.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441+1683A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383037 | ||||||
chr6:37383197
|
A | G | 9 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(6): Show | 9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1441+1843A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383197 | ||||||
chr6:37383300
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1441+1946T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383300 | ||||||
chr6:37383438
|
C | G | 2 | a0001c0002t0013g0168a0001c0002t0013g0169 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1441+2084C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383438 | ||||||
chr6:37383506
|
T | C | 1 | a0001c0001t0008g0157 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1441+2152T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383506 | ||||||
chr6:37383629
|
A | G | 1 | a0001c0001t0003g0239 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1441+2275A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383629 | ||||||
chr6:37383705
|
G | A | 4 | a0001c0002t0002g0187a0001c0002t0002g0188a0001c0002t0002g0232others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441+2351G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383705 | ||||||
chr6:37383726
|
G | A | 1 | a0001c0002t0002g0194 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1441+2372G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383726 | ||||||
chr6:37383830
|
A | AT | 26 | a0001c0001t0005g0013a0001c0001t0005g0173a0001c0001t0005g0218others(23): Show | 28 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1441+2482dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37383830 | |||||
chr6:37383921
|
C | G | 22 | a0001c0001t0015g0150a0001c0002t0004g0012a0001c0002t0004g0024others(19): Show | 26 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1441+2567C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383921 | ||||||
chr6:37383951
|
G | A | 3 | a0001c0001t0008g0146a0001c0001t0008g0148a0001c0001t0020g0159 | 3 | HG01361.hp1 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1441+2597G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383951 | ||||||
chr6:37384131
|
A | AT | 31 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0108others(28): Show | 39 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1441+2796dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37384131 | |||||
chr6:37384131
|
A | ATT | 41 | a0001c0001t0003g0007a0001c0001t0003g0028a0001c0001t0003g0029others(38): Show | 53 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.1441+2795_1441+279 others(6): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37384131 | |||||
chr6:37384131
|
AT | A | 15 | a0001c0001t0001g0022a0001c0001t0001g0069a0001c0001t0001g0075others(12): Show | 15 | HG01099.hp2 HG01167.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1441+2796delT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37384131 | |||||
chr6:37384390
|
G | C | 96 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0028others(93): Show | 118 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.1441+3036G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37384390 | ||||||
chr6:37384400
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1441+3046C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37384400 | ||||||
chr6:37384964
|
G | A | 1 | a0001c0001t0018g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1441+3610G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37384964 | ||||||
chr6:37385018
|
A | AT | 14 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0066others(11): Show | 16 | HG00323.hp2 HG02015.hp1 NA18612.hp1 others(13): Show |
intron_variant | MODIFIER | c.1441+3676dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37385018 | |||||
chr6:37385035
|
T | C | 96 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0028others(93): Show | 118 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.1441+3681T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385035 | ||||||
chr6:37385080
|
C | G | 1 | a0001c0005t0004g0182 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1441+3726C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385080 | ||||||
chr6:37385099
|
C | T | 4 | a0001c0001t0005g0221a0001c0001t0005g0226a0001c0001t0005g0250others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441+3745C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385099 | ||||||
chr6:37385164
|
C | T | 22 | a0001c0001t0015g0150a0001c0002t0004g0012a0001c0002t0004g0024others(19): Show | 26 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1441+3810C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385164 | ||||||
chr6:37385174
|
C | T | 22 | a0001c0001t0015g0150a0001c0002t0004g0012a0001c0002t0004g0024others(19): Show | 26 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1441+3820C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385174 | ||||||
chr6:37385343
|
G | T | 35 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0028others(32): Show | 51 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1441+3989G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385343 | ||||||
chr6:37385452
|
C | T | 1 | a0001c0002t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1441+4098C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385452 | ||||||
chr6:37385488
|
G | A | 2 | a0001c0001t0006g0092a0001c0001t0006g0138 | 2 | HG02523.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1441+4134G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385488 | ||||||
chr6:37385499
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1441+4145C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385499 | ||||||
chr6:37385623
|
C | T | 2 | a0001c0002t0004g0203a0001c0002t0004g0206 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1441+4269C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385623 | ||||||
chr6:37385719
|
C | A | 2 | a0001c0001t0010g0122a0001c0001t0010g0125 | 2 | HG00438.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1441+4365C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385719 | ||||||
chr6:37385740
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1441+4386T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385740 | ||||||
chr6:37385855
|
A | AT | 45 | a0001c0001t0001g0014a0001c0001t0001g0068a0001c0001t0001g0069others(42): Show | 51 | HG00642.hp1 HG01361.hp1 HG01891.hp2 others(48): Show |
intron_variant | MODIFIER | c.1441+4518dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37385855 | |||||
chr6:37385855
|
AT | A | 7 | a0001c0001t0001g0066a0001c0001t0001g0142a0001c0001t0003g0241others(4): Show | 7 | HG02896.hp2 HG03654.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441+4518delT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37385855 | |||||
chr6:37386075
|
A | G | 3 | a0001c0001t0004g0184a0001c0001t0007g0166a0001c0001t0007g0167 | 3 | HG03098.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1442-4667A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386075 | ||||||
chr6:37386096
|
A | G | 1 | a0001c0001t0003g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1442-4646A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386096 | ||||||
chr6:37386178
|
A | ACCTTATT others(39): Show |
1 | a0001c0002t0001g0023 | 2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1442-4563_1442-456 others(50): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37386178 | |||||
chr6:37386180
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0120 | 2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1442-4562A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386180 | ||||||
chr6:37386181
|
G | C | 1 | a0001c0002t0001g0023 | 2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1442-4561G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386181 | ||||||
chr6:37386182
|
T | C | 1 | a0001c0002t0001g0023 | 2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1442-4560T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386182 | ||||||
chr6:37386283
|
A | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(187): Show | 238 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.1442-4459A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386283 | ||||||
chr6:37386422
|
C | T | 22 | a0001c0001t0015g0150a0001c0002t0004g0012a0001c0002t0004g0024others(19): Show | 26 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1442-4320C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386422 | ||||||
chr6:37386659
|
C | T | 95 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0028others(92): Show | 117 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.1442-4083C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386659 | ||||||
chr6:37386756
|
T | A | 15 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0066others(12): Show | 17 | HG00323.hp2 HG02015.hp1 NA18612.hp1 others(14): Show |
intron_variant | MODIFIER | c.1442-3986T>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386756 | ||||||
chr6:37386827
|
C | T | 1 | a0001c0001t0018g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1442-3915C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386827 | ||||||
chr6:37387012
|
T | C | 1 | a0001c0001t0006g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1442-3730T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387012 | ||||||
chr6:37387437
|
G | A | 1 | a0001c0001t0018g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1442-3305G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387437 | ||||||
chr6:37387482
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1442-3260A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387482 | ||||||
chr6:37387489
|
C | T | 35 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0028others(32): Show | 51 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1442-3253C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387489 | ||||||
chr6:37387577
|
T | C | 9 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(6): Show | 9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1442-3165T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387577 | ||||||
chr6:37387623
|
T | C | 1 | a0001c0001t0009g0153 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1442-3119T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387623 | ||||||
chr6:37388106
|
A | G | 62 | a0001c0001t0002g0237a0001c0001t0003g0006a0001c0001t0003g0007others(59): Show | 80 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1442-2636A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388106 | ||||||
chr6:37388139
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1442-2603G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388139 | ||||||
chr6:37388200
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0142 | 2 | NA18982.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1442-2542A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388200 | ||||||
chr6:37388270
|
T | C | 2 | a0001c0002t0004g0196a0001c0002t0015g0256 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1442-2472T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388270 | ||||||
chr6:37388522
|
G | C | 26 | a0001c0001t0005g0013a0001c0001t0005g0173a0001c0001t0005g0218others(23): Show | 28 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1442-2220G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388522 | ||||||
chr6:37388642
|
G | A | 2 | a0001c0002t0002g0179a0001c0002t0002g0231 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1442-2100G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388642 | ||||||
chr6:37388683
|
C | T | 1 | a0001c0001t0008g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1442-2059C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388683 | ||||||
chr6:37388773
|
C | CA | 67 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0034others(64): Show | 85 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1442-1955dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37388773 | |||||
chr6:37388913
|
A | G | 2 | a0001c0002t0004g0196a0001c0002t0015g0256 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1442-1829A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388913 | ||||||
chr6:37388935
|
T | TAAAAAAA others(1): Show |
6 | a0001c0001t0003g0244a0001c0001t0004g0184a0001c0001t0005g0250others(3): Show | 6 | HG01257.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1442-1801_1442-179 others(12): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37388935 | |||||
chr6:37388935
|
T | TAAAAAAA others(2): Show |
87 | a0001c0001t0002g0237a0001c0001t0003g0006a0001c0001t0003g0007others(84): Show | 109 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.1442-1802_1442-179 others(13): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37388935 | |||||
chr6:37388935
|
T | TAAAAAAA others(3): Show |
4 | a0001c0001t0003g0241a0001c0001t0006g0093a0001c0001t0007g0166others(1): Show | 4 | HG03098.hp2 HG06807.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1442-1803_1442-179 others(14): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37388935 | |||||
chr6:37389024
|
A | G | 1 | a0001c0002t0002g0192 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1442-1718A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389024 | ||||||
chr6:37389140
|
G | C | 19 | a0001c0001t0015g0150a0001c0002t0004g0012a0001c0002t0004g0024others(16): Show | 23 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1442-1602G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389140 | ||||||
chr6:37389286
|
G | A | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1442-1456G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389286 | ||||||
chr6:37389328
|
G | A | 17 | a0001c0001t0015g0150a0001c0002t0004g0012a0001c0002t0004g0024others(14): Show | 21 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1442-1414G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389328 | ||||||
chr6:37389525
|
G | A | 2 | a0001c0001t0007g0166a0001c0001t0007g0167 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1442-1217G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389525 | ||||||
chr6:37389622
|
G | T | 1 | a0001c0001t0004g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1442-1120G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389622 | ||||||
chr6:37390246
|
A | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(232): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.1442-496A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390246 | ||||||
chr6:37390253
|
T | C | 1 | a0001c0001t0005g0228 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1442-489T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390253 | ||||||
chr6:37390283
|
GGGTGAT | G | 11 | a0001c0001t0007g0166a0001c0001t0007g0167a0001c0001t0009g0151others(8): Show | 11 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1442-453_1442-448d others(8): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37390283 | |||||
chr6:37390334
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1442-408C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390334 | ||||||
chr6:37390442
|
C | CA | 6 | a0001c0001t0001g0115a0001c0001t0011g0027a0001c0001t0011g0234others(3): Show | 7 | NA18957.hp1 NA18961.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1442-298dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37390442 | |||||
chr6:37390533
|
G | A | 5 | a0001c0001t0009g0151a0001c0001t0009g0152a0001c0001t0009g0153others(2): Show | 5 | HG02630.hp1 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442-209G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390533 | ||||||
chr6:37390665
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1442-77C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390665 |