geneid | 5971 |
---|---|
ensemblid | ENSG00000104856.15 |
hgncid | 9956 |
symbol | RELB |
name | RELB proto-oncogene, NF-kB subunit |
refseq_nuc | NM_006509.4 |
refseq_prot | NP_006500.2 |
ensembl_nuc | ENST00000221452.13 |
ensembl_prot | ENSP00000221452.7 |
mane_status | MANE Select |
chr | chr19 |
start | 45001464 |
end | 45038192 |
strand | + |
ver | v1.2 |
region | chr19:45001464-45038192 |
region5000 | chr19:44996464-45043192 |
regionname0 | RELB_chr19_45001464_45038192 |
regionname5000 | RELB_chr19_44996464_45043192 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1740 | 373 | 91 | 74 | 149 | 12 | 45 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
c0002 | 0/0 | 1740 | 4 | 4 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
c0003 | 0/0 | 1740 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
c0004 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
c0005 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
c0006 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
c0007 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 519 | 356 | 96 | 69 | 138 | 10 | 41 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
t0002 | 0/0 | 519 | 17 | 0 | 0 | 13 | 0 | 4 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
t0003 | 0/0 | 519 | 7 | 0 | 5 | 0 | 2 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
t0004 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
t0005 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1740 | 373 | 91 | 74 | 149 | 12 | 45 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0002 | 0/0 | 1740 | 4 | 4 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0003 | 0/0 | 1740 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0004 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0005 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0006 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0002c0007 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2258 | 348 | 91 | 69 | 136 | 10 | 40 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0001t0002 | 0/0 | 2258 | 16 | 0 | 0 | 12 | 0 | 4 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0001t0003 | 0/0 | 2258 | 7 | 0 | 5 | 0 | 2 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0001t0004 | 0/0 | 2258 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0001t0005 | 0/0 | 2258 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0002t0001 | 0/0 | 2258 | 4 | 4 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0003t0001 | 0/0 | 2258 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0004t0001 | 0/0 | 2258 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0005t0001 | 0/0 | 2258 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0001c0006t0002 | 0/0 | 2258 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
a0002c0007t0001 | 0/0 | 2258 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | copy fasta | chr19 | 44996464 | 45043192 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0005t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0001c0006t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
a0002c0007t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | GBR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | GBR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00423 | hp2 | a0002 | c0007 | t0001 | g0237 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0376 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0377 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0274 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0231 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0378 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CDX | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0379 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0176 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0380 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0374 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0256 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | YRI | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0375 | AFR | YRI | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0370 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19000 | hp1 | a0001 | c0005 | t0001 | g0354 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19004 | hp2 | a0001 | c0006 | t0002 | g0327 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | ASW | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ASW | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | GIH | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0381 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | USA | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | USA | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA20300 | hp1 | a0001 | c0004 | t0001 | g0242 | AFR | USA | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | USA | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0280 | REF | REF | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0048 | REF | REF | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:45011996
|
C | G | 1 | a0002 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.224C>G | p.Pro75Arg | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/12 | 340/2258 | 224/1740 | 75/579 | chr19 | 45011996 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:45001636
|
G | C | 1 | a0001c0003 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.57G>C | p.Pro19Pro | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/12 | 173/2258 | 57/1740 | 19/579 | chr19 | 45001636 | ||
chr19:45012177
|
G | A | 1 | a0001c0004 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.405G>A | p.Gln135Gln | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/12 | 521/2258 | 405/1740 | 135/579 | chr19 | 45012177 | ||
chr19:45032640
|
C | T | 1 | a0001c0006 | 1 | NA19004.hp2 | synonymous_variant | LOW | c.1098C>T | p.Tyr366Tyr | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/12 | 1214/2258 | 1098/1740 | 366/579 | chr19 | 45032640 | ||
chr19:45037508
|
C | T | 1 | a0001c0002 | 4 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.1458C>T | p.Asp486Asp | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 1574/2258 | 1458/1740 | 486/579 | chr19 | 45037508 | ||
chr19:45037667
|
C | T | 1 | a0001c0005 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.1617C>T | p.Tyr539Tyr | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 1733/2258 | 1617/1740 | 539/579 | chr19 | 45037667 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:45038070
|
G | A | 1 | a0001c0001t0004 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 280 | chr19 | 45038070 | |||||
chr19:45038120
|
C | T | 1 | a0001c0001t0005 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 330 | chr19 | 45038120 | |||||
chr19:45038140
|
G | T | 2 | a0001c0001t0002a0001c0006t0002 | 17 | HG02080.hp2 HG02523.hp2 HG02602.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 350 | chr19 | 45038140 | |||||
chr19:45038156
|
G | T | 1 | a0001c0001t0003 | 7 | HG01081.hp1 HG01192.hp2 HG01255.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*366G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 366 | chr19 | 45038156 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:45001765
|
G | T | 2 | a0001c0001t0001g0380a0001c0001t0001g0381 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.106+80G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45001765 | ||||||
chr19:45001884
|
G | C | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.106+199G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45001884 | ||||||
chr19:45001919
|
C | A | 3 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0001t0003g0005 | 3 | HG01192.hp2 HG01255.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.106+234C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45001919 | ||||||
chr19:45002058
|
C | T | 1 | a0001c0001t0001g0379 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.106+373C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002058 | ||||||
chr19:45002059
|
C | G | 1 | a0001c0001t0001g0378 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.106+374C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002059 | ||||||
chr19:45002077
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.106+392G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002077 | ||||||
chr19:45002090
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG00735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.106+405T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002090 | ||||||
chr19:45002126
|
G | T | 1 | a0001c0001t0001g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.106+441G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002126 | ||||||
chr19:45002163
|
A | C | 3 | a0001c0001t0001g0374a0001c0001t0001g0375a0001c0001t0001g0376 | 3 | HG01243.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.106+478A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002163 | ||||||
chr19:45002169
|
A | G | 4 | a0001c0001t0001g0371a0001c0001t0001g0372a0001c0001t0001g0373others(1): Show | 4 | HG00621.hp2 NA18962.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+484A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002169 | ||||||
chr19:45002184
|
C | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01943.hp1 HG01981.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+499C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002184 | ||||||
chr19:45002307
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.106+622T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002307 | ||||||
chr19:45002338
|
T | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | NA19009.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.107-611T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002338 | ||||||
chr19:45002407
|
C | G | 7 | a0001c0001t0001g0363a0001c0001t0001g0364a0001c0001t0001g0365others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-542C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002407 | ||||||
chr19:45002411
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.107-538G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002411 | ||||||
chr19:45002446
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.107-503G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002446 | ||||||
chr19:45002519
|
A | T | 4 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-430A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002519 | ||||||
chr19:45002545
|
G | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(8): Show | 11 | HG00597.hp2 HG02135.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-404G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002545 | ||||||
chr19:45002651
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.107-298C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002651 | ||||||
chr19:45003147
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.154+151C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003147 | ||||||
chr19:45003171
|
T | G | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+175T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003171 | ||||||
chr19:45003287
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.154+291C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003287 | ||||||
chr19:45003368
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154+372G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003368 | ||||||
chr19:45003424
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG00597.hp2 HG02135.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.154+428G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003424 | ||||||
chr19:45003441
|
C | G | 1 | a0001c0001t0001g0357 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.154+445C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003441 | ||||||
chr19:45003474
|
C | CA | 10 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG00140.hp2 HG01952.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.154+503dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | |||||
chr19:45003474
|
CA | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0070others(10): Show | 13 | HG00609.hp1 HG01109.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.154+503delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | |||||
chr19:45003474
|
CAA | C | 58 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.154+502_154+503del others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | |||||
chr19:45003474
|
CAAA | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.154+501_154+503del others(3): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | |||||
chr19:45003474
|
CAAAA | C | 30 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0329others(27): Show | 30 | HG00738.hp2 HG01109.hp1 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.154+500_154+503del others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | |||||
chr19:45003514
|
T | A | 340 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(337): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.154+518T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003514 | ||||||
chr19:45003549
|
A | G | 9 | a0001c0001t0001g0124a0001c0001t0001g0359a0001c0001t0001g0360others(6): Show | 9 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+553A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003549 | ||||||
chr19:45003567
|
T | C | 13 | a0001c0001t0001g0034a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00738.hp2 HG01123.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.154+571T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003567 | ||||||
chr19:45003890
|
T | G | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.154+894T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003890 | ||||||
chr19:45003893
|
G | GT | 5 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0068others(2): Show | 5 | HG01934.hp2 HG02300.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+905dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003893 | |||||
chr19:45003913
|
G | T | 5 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361others(2): Show | 5 | HG01123.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+917G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003913 | ||||||
chr19:45003915
|
G | GT | 83 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0040others(80): Show | 84 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.154+945dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | |||||
chr19:45003915
|
G | GTT | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(55): Show | 58 | HG00438.hp1 HG00597.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.154+944_154+945dup others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | |||||
chr19:45003915
|
G | GTTT | 81 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0077others(78): Show | 81 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.154+943_154+945dup others(3): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | |||||
chr19:45003915
|
G | GTTTT | 56 | a0001c0001t0001g0023a0001c0001t0001g0078a0001c0001t0001g0117others(53): Show | 56 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.154+942_154+945dup others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | |||||
chr19:45003915
|
G | T | 7 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361others(4): Show | 7 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+919G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003915 | ||||||
chr19:45003915
|
GTTTT | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0027others(7): Show | 10 | HG00609.hp1 HG01109.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.154+942_154+945del others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | |||||
chr19:45003915
|
GTTTTT | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(46): Show | 49 | HG00099.hp2 HG00597.hp2 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.154+941_154+945del others(5): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | |||||
chr19:45004244
|
C | T | 2 | a0001c0001t0001g0375a0001c0001t0001g0376 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.154+1248C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004244 | ||||||
chr19:45004284
|
G | A | 16 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(13): Show | 16 | HG00597.hp2 HG02109.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.154+1288G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004284 | ||||||
chr19:45004322
|
G | A | 1 | a0001c0001t0001g0374 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154+1326G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004322 | ||||||
chr19:45004413
|
A | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00597.hp2 HG00738.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.154+1417A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004413 | ||||||
chr19:45004423
|
C | T | 1 | a0001c0006t0002g0327 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.154+1427C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004423 | ||||||
chr19:45004438
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.154+1442G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004438 | ||||||
chr19:45004503
|
C | T | 1 | a0001c0001t0001g0379 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.154+1507C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004503 | ||||||
chr19:45004557
|
C | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG00408.hp2 HG02080.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+1561C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004557 | ||||||
chr19:45004617
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.154+1621C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004617 | ||||||
chr19:45004697
|
A | G | 14 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0124others(11): Show | 14 | HG00738.hp2 HG01123.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.154+1701A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004697 | ||||||
chr19:45004823
|
T | C | 5 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0002t0001g0128others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+1827T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004823 | ||||||
chr19:45004892
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154+1896G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004892 | ||||||
chr19:45004935
|
C | G | 1 | a0001c0001t0001g0116 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.154+1939C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004935 | ||||||
chr19:45005014
|
A | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(49): Show | 52 | HG00099.hp2 HG00609.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.154+2018A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005014 | ||||||
chr19:45005026
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0042 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.154+2030C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005026 | ||||||
chr19:45005031
|
C | T | 1 | a0001c0001t0001g0379 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.154+2035C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005031 | ||||||
chr19:45005087
|
C | T | 44 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 44 | HG00099.hp2 HG00609.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.154+2091C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005087 | ||||||
chr19:45005093
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0328 | 2 | HG01934.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.154+2097C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005093 | ||||||
chr19:45005123
|
A | T | 1 | a0001c0001t0001g0290 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.154+2127A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005123 | ||||||
chr19:45005154
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.154+2158G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005154 | ||||||
chr19:45005156
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+2160G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005156 | ||||||
chr19:45005264
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.154+2268G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005264 | ||||||
chr19:45005296
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | HG02717.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.154+2300T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005296 | ||||||
chr19:45005439
|
G | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0002t0001g0128others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+2443G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005439 | ||||||
chr19:45005589
|
C | G | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0023others(157): Show | 160 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.154+2593C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005589 | ||||||
chr19:45005613
|
C | CT | 9 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0123others(6): Show | 9 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+2625dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45005613 | |||||
chr19:45005766
|
C | A | 339 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(336): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.154+2770C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005766 | ||||||
chr19:45005773
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.154+2777T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005773 | ||||||
chr19:45005792
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0197 | 2 | HG00558.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.154+2796C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005792 | ||||||
chr19:45006244
|
G | A | 4 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+3248G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006244 | ||||||
chr19:45006446
|
C | G | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.155-3368C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006446 | ||||||
chr19:45006502
|
C | T | 8 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0131others(5): Show | 8 | HG01099.hp2 HG01109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-3312C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006502 | ||||||
chr19:45006683
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.155-3131G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006683 | ||||||
chr19:45006696
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.155-3118C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006696 | ||||||
chr19:45006714
|
A | G | 5 | a0001c0001t0001g0194a0001c0001t0001g0226a0001c0001t0002g0105others(2): Show | 5 | NA18950.hp2 NA18973.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-3100A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006714 | ||||||
chr19:45006800
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.155-3014A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006800 | ||||||
chr19:45006822
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2992G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006822 | ||||||
chr19:45006832
|
G | T | 1 | a0001c0001t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2982G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006832 | ||||||
chr19:45006834
|
A | T | 1 | a0001c0001t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2980A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006834 | ||||||
chr19:45006836
|
T | G | 1 | a0001c0001t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2978T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006836 | ||||||
chr19:45006837
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2977C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006837 | ||||||
chr19:45006838
|
C | A | 1 | a0001c0001t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2976C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006838 | ||||||
chr19:45006839
|
C | G | 1 | a0001c0001t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2975C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006839 | ||||||
chr19:45006847
|
C | A | 1 | a0001c0001t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2967C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006847 | ||||||
chr19:45006955
|
GA | G | 8 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0144others(5): Show | 8 | HG00099.hp1 HG02897.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-2842delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45006955 | |||||
chr19:45007154
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.155-2660C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007154 | ||||||
chr19:45007268
|
TA | T | 14 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(11): Show | 14 | HG00408.hp1 HG01175.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.155-2543delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45007268 | |||||
chr19:45007368
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-2446C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007368 | ||||||
chr19:45007631
|
G | A | 1 | a0002c0007t0001g0237 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.155-2183G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007631 | ||||||
chr19:45007687
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.155-2127G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007687 | ||||||
chr19:45007762
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.155-2052G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007762 | ||||||
chr19:45007773
|
G | A | 4 | a0001c0001t0001g0127a0001c0002t0001g0128a0001c0002t0001g0130others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-2041G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007773 | ||||||
chr19:45007783
|
G | A | 1 | a0001c0001t0002g0335 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.155-2031G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007783 | ||||||
chr19:45007783
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.155-2031G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007783 | ||||||
chr19:45007816
|
CCA | C | 94 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(91): Show | 94 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.155-1994_155-1993d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45007816 | |||||
chr19:45007882
|
C | A | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(87): Show | 90 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.155-1932C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007882 | ||||||
chr19:45008000
|
C | CA | 31 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0024others(28): Show | 31 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.155-1791dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45008000 | |||||
chr19:45008000
|
CA | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.155-1791delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45008000 | |||||
chr19:45008000
|
CAA | C | 22 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(19): Show | 22 | HG01256.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.155-1792_155-1791d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45008000 | |||||
chr19:45008018
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0119a0001c0001t0001g0159others(5): Show | 8 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-1796A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008018 | ||||||
chr19:45008036
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.155-1778G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008036 | ||||||
chr19:45008165
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.155-1649G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008165 | ||||||
chr19:45008186
|
A | G | 3 | a0001c0001t0001g0271a0001c0001t0001g0290a0001c0001t0001g0314 | 3 | HG01928.hp2 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.155-1628A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008186 | ||||||
chr19:45008269
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.155-1545G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008269 | ||||||
chr19:45008323
|
C | A | 1 | a0001c0001t0002g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.155-1491C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008323 | ||||||
chr19:45008347
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0001g0330 | 3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.155-1467C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008347 | ||||||
chr19:45008381
|
G | A | 1 | a0001c0001t0001g0357 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.155-1433G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008381 | ||||||
chr19:45008403
|
A | G | 2 | a0001c0001t0001g0192a0001c0001t0002g0113 | 2 | NA18971.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.155-1411A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008403 | ||||||
chr19:45008404
|
C | A | 3 | a0001c0001t0001g0294a0001c0001t0001g0350a0001c0001t0001g0378 | 3 | HG02015.hp2 NA19080.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.155-1410C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008404 | ||||||
chr19:45008874
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.155-940G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008874 | ||||||
chr19:45008970
|
T | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0035others(18): Show | 21 | HG00733.hp2 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.155-844T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008970 | ||||||
chr19:45009106
|
A | C | 7 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0381others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-708A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009106 | ||||||
chr19:45009157
|
T | G | 19 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0070others(16): Show | 19 | HG01069.hp2 HG01123.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.155-657T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009157 | ||||||
chr19:45009167
|
G | A | 5 | a0001c0001t0001g0308a0001c0001t0001g0362a0001c0001t0002g0283others(2): Show | 5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-647G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009167 | ||||||
chr19:45009190
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02717.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-624C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009190 | ||||||
chr19:45009205
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.155-609C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009205 | ||||||
chr19:45009206
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 99 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.155-608G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009206 | ||||||
chr19:45009301
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.155-513G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009301 | ||||||
chr19:45009418
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0119others(16): Show | 19 | HG00733.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.155-396A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009418 | ||||||
chr19:45009888
|
GGCCTTC | G | 74 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.163+67_163+72delGC others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45009888 | ||||||
chr19:45009956
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.163+134T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45009956 | ||||||
chr19:45009978
|
G | A | 71 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(68): Show | 71 | HG00673.hp1 HG00673.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.163+156G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45009978 | ||||||
chr19:45010159
|
C | T | 59 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(56): Show | 59 | HG00673.hp1 HG00673.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.163+337C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010159 | ||||||
chr19:45010200
|
G | C | 19 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(16): Show | 19 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.163+378G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010200 | ||||||
chr19:45010240
|
T | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(100): Show | 103 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.163+418T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010240 | ||||||
chr19:45010293
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 98 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.163+471C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010293 | ||||||
chr19:45010309
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163+487T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010309 | ||||||
chr19:45010313
|
T | TCAAAAAG others(315): Show |
1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163+507_163+508ins others(322): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010313
|
T | TCAAAAAG others(314): Show |
6 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0236others(3): Show | 6 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010313
|
T | TCAAAAAG others(314): Show |
1 | a0001c0001t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010313
|
T | TCAAAAAG others(314): Show |
5 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0280others(2): Show | 5 | HG01069.hp2 HG01123.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010313
|
T | TCAAAAAG others(313): Show |
1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163+507_163+508ins others(320): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010313
|
T | TCAAAAAG others(312): Show |
6 | a0001c0001t0001g0127a0001c0001t0001g0358a0001c0002t0001g0100others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(319): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010313
|
T | TCAAAAAG others(313): Show |
63 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 63 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(320): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010313
|
T | TCAAAAAG others(314): Show |
12 | a0001c0001t0001g0007a0001c0001t0001g0109a0001c0001t0001g0119others(9): Show | 12 | HG00438.hp1 HG01175.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010313
|
T | TCAAAAAG others(315): Show |
1 | a0001c0001t0001g0103 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.163+507_163+508ins others(322): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010313
|
T | TCAAAAAG others(313): Show |
1 | a0001c0001t0001g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.163+507_163+508ins others(320): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | |||||
chr19:45010314
|
C | CAAAAAGA others(313): Show |
2 | a0001c0001t0001g0166a0001c0001t0001g0213 | 2 | HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.163+507_163+508ins others(320): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010314 | |||||
chr19:45010314
|
C | CAAAAAGA others(314): Show |
1 | a0001c0001t0001g0212 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010314 | |||||
chr19:45010350
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.163+528A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010350 | ||||||
chr19:45010357
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 100 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.163+535T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010357 | ||||||
chr19:45010451
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.163+629G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010451 | ||||||
chr19:45010481
|
A | G | 1 | a0001c0001t0001g0380 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.163+659A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010481 | ||||||
chr19:45010516
|
T | G | 7 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0381others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+694T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010516 | ||||||
chr19:45010596
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0062 | 2 | HG01071.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.163+774C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010596 | ||||||
chr19:45010720
|
C | T | 1 | a0001c0001t0003g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.163+898C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010720 | ||||||
chr19:45010828
|
C | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02155.hp2 NA18998.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.163+1006C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010828 | ||||||
chr19:45010829
|
C | A | 4 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0279others(1): Show | 4 | HG01069.hp2 HG01123.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+1007C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010829 | ||||||
chr19:45010980
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.164-956C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010980 | ||||||
chr19:45011174
|
A | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0381 | 2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.164-762A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011174 | ||||||
chr19:45011191
|
C | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(245): Show | 248 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.164-745C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011191 | ||||||
chr19:45011204
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.164-732G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011204 | ||||||
chr19:45011214
|
G | A | 71 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(68): Show | 71 | HG00673.hp1 HG00673.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.164-722G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011214 | ||||||
chr19:45011232
|
G | A | 12 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0124others(9): Show | 12 | HG01069.hp2 HG01123.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-704G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011232 | ||||||
chr19:45011247
|
C | T | 8 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0135others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-689C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011247 | ||||||
chr19:45011255
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.164-681C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011255 | ||||||
chr19:45011272
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0002g0113 | 2 | NA18971.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.164-664C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011272 | ||||||
chr19:45011292
|
T | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(264): Show | 267 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.164-644T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011292 | ||||||
chr19:45011408
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.164-528C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011408 | ||||||
chr19:45011418
|
T | C | 1 | a0001c0001t0001g0304 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.164-518T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011418 | ||||||
chr19:45011419
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.164-517C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011419 | ||||||
chr19:45011443
|
T | G | 79 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(76): Show | 79 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.164-493T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011443 | ||||||
chr19:45011455
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0374 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-481C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011455 | ||||||
chr19:45011488
|
A | G | 5 | a0001c0001t0001g0127a0001c0002t0001g0100a0001c0002t0001g0128others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-448A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011488 | ||||||
chr19:45011519
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.164-417C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011519 | ||||||
chr19:45011756
|
C | CTG | 10 | a0001c0001t0001g0069a0001c0001t0001g0108a0001c0001t0001g0120others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-139_164-138dup others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | |||||
chr19:45011756
|
C | CTGTG | 6 | a0001c0001t0001g0043a0001c0001t0001g0099a0001c0001t0001g0124others(3): Show | 6 | HG01943.hp2 HG02647.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-141_164-138dup others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | |||||
chr19:45011756
|
C | CTGTGTG | 6 | a0001c0001t0001g0037a0001c0001t0001g0125a0001c0001t0001g0207others(3): Show | 6 | HG00140.hp2 HG01192.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-143_164-138dup others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | |||||
chr19:45011756
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.164-147_164-138dup others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | |||||
chr19:45011756
|
C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0052a0001c0001t0002g0083 | 2 | HG02004.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.164-149_164-138dup others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | |||||
chr19:45011756
|
C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0053 | 2 | HG00323.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.164-151_164-138dup others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | |||||
chr19:45011756
|
C | CTGTGTGT others(9): Show |
3 | a0001c0001t0001g0041a0001c0001t0001g0055a0001c0001t0001g0065 | 3 | HG01934.hp1 HG01952.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.164-153_164-138dup others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | |||||
chr19:45011756
|
C | CTGTGTGT others(13): Show |
2 | a0001c0001t0001g0056a0001c0001t0001g0079 | 2 | HG01496.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.164-157_164-138dup others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | |||||
chr19:45011756
|
C | G | 5 | a0001c0001t0001g0127a0001c0002t0001g0100a0001c0002t0001g0128others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-180C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011756 | ||||||
chr19:45011789
|
T | A | 1 | a0001c0004t0001g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.164-147T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011789 | ||||||
chr19:45011791
|
T | A | 2 | a0001c0001t0001g0381a0001c0004t0001g0242 | 2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.164-145T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011791 | ||||||
chr19:45011793
|
T | A | 2 | a0001c0001t0001g0381a0001c0004t0001g0242 | 2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.164-143T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011793 | ||||||
chr19:45011793
|
TGTGTGAG others(11): Show |
T | 1 | a0001c0001t0001g0362 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.164-141_164-124del others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011793 | |||||
chr19:45011795
|
T | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0381a0001c0004t0001g0242 | 3 | HG02109.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.164-141T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011795 | ||||||
chr19:45011795
|
TGTGAGAG others(5): Show |
T | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.164-139_164-128del others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011795 | |||||
chr19:45011795
|
TGTGAGAG others(9): Show |
T | 3 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361 | 3 | HG01123.hp1 HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.164-139_164-124del others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011795 | |||||
chr19:45011795
|
TGTGAGAG others(11): Show |
T | 4 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(1): Show | 4 | HG01109.hp2 HG02683.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-139_164-122del others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011795 | |||||
chr19:45011795
|
TGTGAGAG others(13): Show |
T | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164-139_164-120del others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011795 | |||||
chr19:45011797
|
T | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0381a0001c0002t0001g0128others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-139T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011797 | ||||||
chr19:45011797
|
T | TGAGAGAG others(13): Show |
1 | a0001c0001t0001g0291 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.164-120_164-101dup others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGAGAG others(3): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0066 | 2 | HG01069.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGAGAG others(5): Show |
1 | a0001c0001t0003g0003 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGAGAG others(7): Show |
1 | a0001c0001t0001g0243 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGAGAG others(9): Show |
1 | a0001c0001t0001g0010 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGAGAG others(11): Show |
1 | a0001c0001t0001g0009 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGAGAG others(13): Show |
1 | a0001c0001t0001g0234 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGAG others(7): Show |
5 | a0001c0001t0001g0076a0001c0001t0001g0122a0001c0001t0001g0123others(2): Show | 5 | HG00438.hp2 HG01106.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGAG others(9): Show |
5 | a0001c0001t0001g0006a0001c0001t0001g0126a0001c0001t0001g0235others(2): Show | 5 | HG02015.hp2 HG02738.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGAG others(11): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0245 | 2 | HG02071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGAG others(13): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0244 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGAG others(17): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0117 | 2 | NA19082.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0038 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(5): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0150 | 2 | HG02922.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0102a0001c0001t0001g0149 | 2 | HG00544.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(11): Show |
6 | a0001c0001t0001g0078a0001c0001t0001g0101a0001c0001t0001g0286others(3): Show | 6 | HG01255.hp2 HG02040.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(13): Show |
4 | a0001c0001t0001g0024a0001c0001t0001g0073a0001c0001t0001g0247others(1): Show | 4 | HG00597.hp2 HG00609.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(15): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG01981.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(21): Show |
1 | a0001c0001t0001g0246 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(5): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0288 | 4 | HG01168.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(7): Show |
3 | a0001c0001t0001g0051a0001c0001t0001g0152a0001c0001t0001g0372 | 3 | HG00621.hp2 HG02965.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0151 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0098 | 2 | NA18953.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(13): Show |
3 | a0001c0001t0001g0049a0001c0001t0001g0293a0001c0001t0001g0301 | 3 | HG02056.hp1 NA18997.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(15): Show |
5 | a0001c0001t0001g0015a0001c0001t0001g0044a0001c0001t0001g0238others(2): Show | 5 | HG00423.hp1 HG01943.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(17): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0202 | 3 | HG02293.hp2 HG03209.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(19): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0249 | 2 | HG01074.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(21): Show |
1 | a0001c0001t0001g0018 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(23): Show |
1 | a0001c0001t0001g0248 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(30): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(25): Show |
1 | a0001c0001t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(32): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(14): Show |
1 | a0001c0001t0001g0060 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(21): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(9): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0153 | 2 | HG03486.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(11): Show |
4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | HG00099.hp2 HG01256.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(13): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0326 | 2 | HG00609.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(15): Show |
4 | a0001c0001t0001g0143a0001c0001t0001g0302a0001c0001t0002g0061others(1): Show | 4 | HG00423.hp2 HG01071.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(17): Show |
2 | a0001c0001t0001g0294a0001c0001t0001g0325 | 2 | HG01358.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(21): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0289 | 2 | NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(23): Show |
1 | a0001c0001t0001g0250 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(30): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0379 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0373a0001c0001t0003g0253 | 2 | HG01361.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(13): Show |
5 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0090others(2): Show | 5 | HG01257.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(15): Show |
1 | a0001c0001t0001g0350 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(19): Show |
1 | a0001c0001t0001g0251 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(13): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0064 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(21): Show |
1 | a0001c0001t0002g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0054 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0068 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(17): Show |
1 | a0001c0001t0001g0154 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(19): Show |
1 | a0001c0001t0001g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
T | TGTGTGTG others(17): Show |
1 | a0001c0001t0001g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
TGA | T | 21 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0146others(18): Show | 21 | HG01175.hp1 HG01517.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.164-102_164-101del others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
TGAGA | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(31): Show | 34 | HG00673.hp2 HG00733.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.164-104_164-101del others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
TGAGAGA | T | 42 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0029others(39): Show | 42 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.164-106_164-101del others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
TGAGAGAG others(1): Show |
T | 34 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0104others(31): Show | 34 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.164-108_164-101del others(8): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
TGAGAGAG others(3): Show |
T | 37 | a0001c0001t0001g0025a0001c0001t0001g0086a0001c0001t0001g0109others(34): Show | 37 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.164-110_164-101del others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
TGAGAGAG others(5): Show |
T | 18 | a0001c0001t0001g0027a0001c0001t0001g0070a0001c0001t0001g0084others(15): Show | 18 | HG00558.hp1 HG00597.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-112_164-101del others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
TGAGAGAG others(7): Show |
T | 11 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0162others(8): Show | 11 | HG00544.hp1 HG01243.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-114_164-101del others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
TGAGAGAG others(9): Show |
T | 4 | a0001c0001t0001g0033a0001c0001t0001g0097a0001c0001t0001g0119others(1): Show | 4 | HG01891.hp1 HG03209.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-116_164-101del others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011797
|
TGAGAGAG others(13): Show |
T | 1 | a0001c0001t0001g0032 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.164-120_164-101del others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | |||||
chr19:45011799
|
A | T | 45 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0037others(42): Show | 45 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.164-137A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011799 | ||||||
chr19:45011801
|
A | T | 65 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0037others(62): Show | 65 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.164-135A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011801 | ||||||
chr19:45011803
|
A | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(94): Show | 97 | HG00673.hp1 HG00673.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-133A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011803 | ||||||
chr19:45011805
|
A | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(131): Show | 134 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.164-131A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011805 | ||||||
chr19:45011807
|
A | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(163): Show | 166 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.164-129A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011807 | ||||||
chr19:45011809
|
A | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 198 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.164-127A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011809 | ||||||
chr19:45011811
|
A | T | 184 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(181): Show | 184 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.164-125A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011811 | ||||||
chr19:45011813
|
A | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 96 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.164-123A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011813 | ||||||
chr19:45011815
|
A | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(72): Show | 75 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.164-121A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011815 | ||||||
chr19:45011817
|
A | T | 14 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0085others(11): Show | 14 | HG00544.hp1 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.164-119A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011817 | ||||||
chr19:45011819
|
A | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0368a0001c0001t0001g0374 | 3 | HG02258.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-117A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011819 | ||||||
chr19:45011821
|
A | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0374 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-115A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011821 | ||||||
chr19:45011872
|
C | CT | 6 | a0001c0001t0001g0060a0001c0001t0001g0308a0001c0001t0002g0061others(3): Show | 6 | HG02602.hp1 HG02602.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-49dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011872 | |||||
chr19:45011872
|
CT | C | 39 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0055others(36): Show | 39 | HG00099.hp1 HG00597.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.164-49delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011872 | |||||
chr19:45011890
|
T | G | 1 | a0001c0001t0001g0380 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.164-46T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011890 | ||||||
chr19:45012297
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.504+21C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012297 | ||||||
chr19:45012315
|
G | A | 7 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0381others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+39G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012315 | ||||||
chr19:45012518
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0075 | 2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.504+242C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012518 | ||||||
chr19:45012595
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0280 | 3 | HG01069.hp2 HG01123.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.504+319T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012595 | ||||||
chr19:45012667
|
G | T | 1 | a0001c0001t0001g0380 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.504+391G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012667 | ||||||
chr19:45012744
|
A | G | 3 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG00639.hp2 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.504+468A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012744 | ||||||
chr19:45012745
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.504+469A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012745 | ||||||
chr19:45012746
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.504+470G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012746 | ||||||
chr19:45012746
|
G | GA | 165 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.504+482dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45012746 | |||||
chr19:45012792
|
T | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.504+516T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012792 | ||||||
chr19:45012814
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.504+538C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012814 | ||||||
chr19:45012879
|
T | G | 7 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0381others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+603T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012879 | ||||||
chr19:45013128
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0309 | 2 | HG00558.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.504+852A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013128 | ||||||
chr19:45013197
|
A | G | 3 | a0001c0001t0001g0211a0001c0001t0001g0347a0001c0001t0001g0358 | 3 | HG01109.hp1 HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.504+921A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013197 | ||||||
chr19:45013211
|
G | A | 78 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(75): Show | 78 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.504+935G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013211 | ||||||
chr19:45013234
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0092 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.504+958C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013234 | ||||||
chr19:45013303
|
CTAATTTT others(12): Show |
C | 1 | a0001c0001t0001g0304 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.504+1030_504+1048d others(21): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45013303 | |||||
chr19:45013341
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0374 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+1065A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013341 | ||||||
chr19:45013373
|
T | A | 77 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(74): Show | 77 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.504+1097T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013373 | ||||||
chr19:45013437
|
G | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0001g0330 | 3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.504+1161G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013437 | ||||||
chr19:45013445
|
T | C | 7 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0381others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+1169T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013445 | ||||||
chr19:45013455
|
T | TAC | 99 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0028others(96): Show | 99 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.504+1180_504+1181i others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45013455 | |||||
chr19:45013491
|
C | T | 8 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0380others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+1215C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013491 | ||||||
chr19:45013520
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.504+1244C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013520 | ||||||
chr19:45013623
|
G | A | 70 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(67): Show | 70 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.504+1347G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013623 | ||||||
chr19:45013959
|
T | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG02647.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+1683T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013959 | ||||||
chr19:45014010
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.504+1734T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014010 | ||||||
chr19:45014027
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.504+1751C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014027 | ||||||
chr19:45014115
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.504+1839T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014115 | ||||||
chr19:45014128
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.504+1852C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014128 | ||||||
chr19:45014168
|
C | CT | 88 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+1910dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014168 | |||||
chr19:45014168
|
C | CTT | 9 | a0001c0001t0001g0006a0001c0001t0001g0070a0001c0001t0001g0117others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.504+1909_504+1910d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014168 | |||||
chr19:45014168
|
CTTTT | C | 42 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.504+1907_504+1910d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014168 | |||||
chr19:45014238
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.504+1962C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014238 | ||||||
chr19:45014239
|
G | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(66): Show | 69 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.504+1963G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014239 | ||||||
chr19:45014255
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.504+1979C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014255 | ||||||
chr19:45014263
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.504+1987A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014263 | ||||||
chr19:45014527
|
G | GT | 264 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(261): Show | 264 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.504+2261dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014527 | |||||
chr19:45014528
|
T | G | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.504+2252T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014528 | ||||||
chr19:45014666
|
C | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0279others(1): Show | 4 | HG01069.hp2 HG01123.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+2390C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014666 | ||||||
chr19:45014815
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0090 | 3 | HG01256.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.504+2539G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014815 | ||||||
chr19:45014852
|
T | C | 1 | a0001c0001t0001g0380 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.504+2576T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014852 | ||||||
chr19:45014903
|
AT | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(259): Show | 262 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.504+2644delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014903 | |||||
chr19:45014965
|
T | C | 285 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(282): Show | 285 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.504+2689T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014965 | ||||||
chr19:45014988
|
C | T | 6 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0236others(3): Show | 6 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+2712C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014988 | ||||||
chr19:45014989
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.504+2713G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014989 | ||||||
chr19:45015087
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+2811G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015087 | ||||||
chr19:45015164
|
A | G | 1 | a0001c0001t0002g0370 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.504+2888A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015164 | ||||||
chr19:45015281
|
C | T | 1 | a0001c0001t0001g0380 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.504+3005C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015281 | ||||||
chr19:45015411
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.504+3135C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015411 | ||||||
chr19:45015459
|
G | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0224 | 3 | HG02647.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.504+3183G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015459 | ||||||
chr19:45015579
|
A | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0272a0001c0001t0001g0315 | 3 | HG02683.hp2 HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.504+3303A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015579 | ||||||
chr19:45015595
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.504+3319C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015595 | ||||||
chr19:45015730
|
A | G | 332 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(329): Show | 332 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(329): Show |
intron_variant | MODIFIER | c.504+3454A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015730 | ||||||
chr19:45015734
|
C | CA | 9 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0066others(6): Show | 9 | HG01069.hp2 HG01123.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.504+3470dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45015734 | |||||
chr19:45015734
|
C | CAA | 7 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0381others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+3469_504+3470d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45015734 | |||||
chr19:45015744
|
AAAG | A | 6 | a0001c0001t0001g0092a0001c0001t0001g0265a0001c0001t0001g0269others(3): Show | 6 | HG02897.hp2 NA18747.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+3471_504+3473d others(5): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45015744 | |||||
chr19:45015745
|
AAG | A | 81 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(78): Show | 81 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.504+3471_504+3472d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45015745 | |||||
chr19:45015746
|
AG | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 163 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.504+3471delG | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015746 | ||||||
chr19:45015747
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0034others(27): Show | 30 | HG01069.hp2 HG01109.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.504+3471G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015747 | ||||||
chr19:45015842
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.504+3566G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015842 | ||||||
chr19:45015954
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.504+3678A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015954 | ||||||
chr19:45016006
|
A | AT | 9 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0033others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.504+3740dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45016006 | |||||
chr19:45016006
|
A | T | 77 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(74): Show | 77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.504+3730A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016006 | ||||||
chr19:45016009
|
T | A | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.504+3733T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016009 | ||||||
chr19:45016048
|
G | C | 2 | a0001c0001t0001g0336a0001c0001t0001g0349 | 2 | NA18961.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.504+3772G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016048 | ||||||
chr19:45016099
|
C | G | 1 | a0001c0001t0001g0285 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+3823C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016099 | ||||||
chr19:45016233
|
C | T | 1 | a0001c0002t0001g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.504+3957C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016233 | ||||||
chr19:45016240
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.504+3964C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016240 | ||||||
chr19:45016321
|
GAGAA | G | 7 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0066others(4): Show | 7 | HG01069.hp2 HG01123.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+4051_504+4054d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45016321 | |||||
chr19:45016541
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.504+4265C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016541 | ||||||
chr19:45016776
|
G | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0159a0001c0001t0001g0160others(4): Show | 7 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+4500G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016776 | ||||||
chr19:45016850
|
A | AAAAC | 16 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0162others(13): Show | 16 | HG00544.hp1 HG02129.hp1 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+4598_504+4601d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45016850 | |||||
chr19:45016850
|
AAAACAAA others(1): Show |
A | 3 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0001g0330 | 3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.504+4594_504+4601d others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45016850 | |||||
chr19:45017027
|
A | C | 14 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0085others(11): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.504+4751A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017027 | ||||||
chr19:45017246
|
T | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA19056.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.505-4807T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017246 | ||||||
chr19:45017254
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.505-4799G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017254 | ||||||
chr19:45017281
|
G | T | 1 | a0001c0001t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.505-4772G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017281 | ||||||
chr19:45017316
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.505-4737A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017316 | ||||||
chr19:45017355
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0280 | 3 | HG01069.hp2 HG01123.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.505-4698G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017355 | ||||||
chr19:45017449
|
T | TAAAAAAA others(1): Show |
151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.505-4597_505-4590d others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(2): Show |
12 | a0001c0001t0001g0020a0001c0001t0001g0196a0001c0001t0001g0207others(9): Show | 12 | HG01243.hp1 HG02145.hp2 HG04228.hp2 others(9): Show |
intron_variant | MODIFIER | c.505-4598_505-4590d others(11): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(3): Show |
60 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0072others(57): Show | 60 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.505-4599_505-4590d others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(4): Show |
28 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0027others(25): Show | 28 | HG00609.hp2 HG01109.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-4600_505-4590d others(13): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(5): Show |
6 | a0001c0001t0001g0028a0001c0001t0001g0097a0001c0001t0001g0279others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-4601_505-4590d others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(15): Show |
1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.505-4590_505-4589i others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.505-4590_505-4589i others(25): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(18): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0066 | 2 | HG01069.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.505-4590_505-4589i others(27): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(20): Show |
4 | a0001c0001t0001g0273a0001c0001t0001g0317a0001c0001t0001g0318others(1): Show | 4 | HG00733.hp2 HG02486.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-4590_505-4589i others(29): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(21): Show |
5 | a0001c0001t0001g0034a0001c0001t0001g0160a0001c0001t0001g0236others(2): Show | 5 | HG02622.hp1 HG02970.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-4590_505-4589i others(30): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(22): Show |
1 | a0001c0001t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.505-4590_505-4589i others(31): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(24): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0330 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505-4590_505-4589i others(33): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(25): Show |
1 | a0001c0001t0001g0280 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.505-4590_505-4589i others(34): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017449
|
T | TAAAAAAA others(19): Show |
1 | a0001c0001t0001g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.505-4590_505-4589i others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | |||||
chr19:45017450
|
A | AAAAAAAA others(18): Show |
6 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0002t0001g0100others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-4590_505-4589i others(27): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017450 | |||||
chr19:45017464
|
C | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0001g0330 | 3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-4589C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017464 | ||||||
chr19:45017603
|
T | A | 1 | a0001c0001t0001g0294 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.505-4450T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017603 | ||||||
chr19:45017663
|
C | CT | 6 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0001g0163others(3): Show | 6 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-4375dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017663 | |||||
chr19:45017695
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.505-4358C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017695 | ||||||
chr19:45017701
|
G | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0072others(5): Show | 8 | HG01109.hp2 HG02055.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.505-4352G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017701 | ||||||
chr19:45017707
|
G | C | 1 | a0001c0001t0001g0304 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.505-4346G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017707 | ||||||
chr19:45017786
|
C | T | 14 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0066others(11): Show | 14 | HG01069.hp2 HG01123.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.505-4267C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017786 | ||||||
chr19:45017908
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.505-4145G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017908 | ||||||
chr19:45017935
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.505-4118G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017935 | ||||||
chr19:45018055
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.505-3998T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018055 | ||||||
chr19:45018064
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.505-3989C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018064 | ||||||
chr19:45018168
|
A | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(280): Show | 283 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.505-3885A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018168 | ||||||
chr19:45018229
|
C | T | 7 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0066others(4): Show | 7 | HG01069.hp2 HG01123.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-3824C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018229 | ||||||
chr19:45018246
|
T | C | 7 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0381others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-3807T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018246 | ||||||
chr19:45018342
|
T | C | 1 | a0001c0001t0001g0365 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.505-3711T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018342 | ||||||
chr19:45018352
|
T | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(265): Show | 268 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.505-3701T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018352 | ||||||
chr19:45018359
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.505-3694G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018359 | ||||||
chr19:45018372
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.505-3681C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018372 | ||||||
chr19:45018489
|
C | CAG | 283 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(280): Show | 283 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.505-3564_505-3563i others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018489 | ||||||
chr19:45018507
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.505-3546G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018507 | ||||||
chr19:45018576
|
C | T | 7 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0381others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-3477C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018576 | ||||||
chr19:45018670
|
A | AT | 3 | a0001c0001t0001g0019a0001c0001t0001g0375a0001c0001t0001g0376 | 3 | HG01243.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505-3380dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45018670 | |||||
chr19:45018673
|
TA | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0066others(15): Show | 18 | HG00733.hp2 HG01069.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.505-3379delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018673 | ||||||
chr19:45018674
|
A | T | 347 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.505-3379A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018674 | ||||||
chr19:45018790
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.505-3263C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018790 | ||||||
chr19:45018833
|
C | T | 84 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(81): Show | 84 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.505-3220C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018833 | ||||||
chr19:45018923
|
G | A | 76 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.505-3130G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018923 | ||||||
chr19:45018923
|
G | T | 7 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0381others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-3130G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018923 | ||||||
chr19:45018952
|
C | T | 84 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(81): Show | 84 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.505-3101C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018952 | ||||||
chr19:45018972
|
T | A | 1 | a0001c0001t0001g0270 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.505-3081T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018972 | ||||||
chr19:45018978
|
A | G | 5 | a0001c0001t0001g0308a0001c0001t0001g0362a0001c0001t0002g0283others(2): Show | 5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-3075A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018978 | ||||||
chr19:45019031
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0002g0283 | 3 | HG02738.hp2 HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.505-3022G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019031 | ||||||
chr19:45019054
|
C | G | 1 | a0001c0001t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.505-2999C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019054 | ||||||
chr19:45019062
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.505-2991T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019062 | ||||||
chr19:45019147
|
G | A | 5 | a0001c0001t0001g0308a0001c0001t0001g0362a0001c0001t0002g0283others(2): Show | 5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2906G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019147 | ||||||
chr19:45019194
|
C | G | 6 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0236others(3): Show | 6 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2859C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019194 | ||||||
chr19:45019385
|
C | T | 14 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0066others(11): Show | 14 | HG01069.hp2 HG01123.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.505-2668C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019385 | ||||||
chr19:45019415
|
C | G | 5 | a0001c0001t0001g0308a0001c0001t0001g0362a0001c0001t0002g0283others(2): Show | 5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2638C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019415 | ||||||
chr19:45019459
|
G | A | 2 | a0001c0001t0001g0375a0001c0001t0001g0376 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505-2594G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019459 | ||||||
chr19:45019474
|
C | T | 76 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.505-2579C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019474 | ||||||
chr19:45019740
|
C | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.505-2313C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019740 | ||||||
chr19:45019801
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 4 | HG00673.hp1 HG02071.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-2252C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019801 | ||||||
chr19:45019803
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.505-2250G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019803 | ||||||
chr19:45019869
|
G | T | 70 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(67): Show | 70 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.505-2184G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019869 | ||||||
chr19:45019893
|
TCTCAAAC others(34): Show |
T | 5 | a0001c0001t0001g0308a0001c0001t0001g0362a0001c0001t0002g0283others(2): Show | 5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2148_505-2108d others(43): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45019893 | |||||
chr19:45020111
|
T | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.505-1942T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020111 | ||||||
chr19:45020144
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0001g0330 | 3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-1909A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020144 | ||||||
chr19:45020201
|
G | A | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(278): Show | 281 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.505-1852G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020201 | ||||||
chr19:45020325
|
G | A | 155 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(152): Show | 155 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.505-1728G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020325 | ||||||
chr19:45020380
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.505-1673C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020380 | ||||||
chr19:45020402
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0001g0330 | 3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-1651T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020402 | ||||||
chr19:45020553
|
C | CT | 178 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(175): Show | 178 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.505-1478dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020553 | |||||
chr19:45020553
|
C | CTT | 85 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0023others(82): Show | 85 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.505-1479_505-1478d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020553 | |||||
chr19:45020553
|
C | CTTT | 9 | a0001c0001t0001g0229a0001c0001t0001g0257a0001c0001t0001g0258others(6): Show | 9 | HG00621.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.505-1480_505-1478d others(5): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020553 | |||||
chr19:45020553
|
CT | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0060others(3): Show | 6 | HG01261.hp2 HG01517.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-1478delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020553 | |||||
chr19:45020588
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.505-1465C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020588 | ||||||
chr19:45020593
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.505-1460T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020593 | ||||||
chr19:45020621
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.505-1432G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020621 | ||||||
chr19:45020626
|
T | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(280): Show | 283 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.505-1427T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020626 | ||||||
chr19:45020643
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0001g0123a0001c0001t0001g0143others(6): Show | 9 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.505-1410C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020643 | ||||||
chr19:45020747
|
T | TG | 269 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(266): Show | 269 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.505-1302dupG | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020747 | |||||
chr19:45020757
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.505-1296C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020757 | ||||||
chr19:45020778
|
C | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.505-1275C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020778 | ||||||
chr19:45020837
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.505-1216G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020837 | ||||||
chr19:45020861
|
C | T | 22 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0070others(19): Show | 22 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.505-1192C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020861 | ||||||
chr19:45020952
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.505-1101A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020952 | ||||||
chr19:45020990
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.505-1063T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020990 | ||||||
chr19:45021034
|
G | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0001g0330 | 3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-1019G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021034 | ||||||
chr19:45021047
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.505-1006C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021047 | ||||||
chr19:45021099
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.505-954C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021099 | ||||||
chr19:45021105
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.505-948C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021105 | ||||||
chr19:45021106
|
G | A | 7 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0127others(4): Show | 7 | HG01069.hp2 HG01123.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-947G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021106 | ||||||
chr19:45021186
|
A | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0070others(24): Show | 27 | HG00673.hp1 HG01123.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-867A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021186 | ||||||
chr19:45021244
|
C | T | 1 | a0001c0006t0002g0327 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.505-809C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021244 | ||||||
chr19:45021295
|
A | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0028others(27): Show | 30 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.505-758A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021295 | ||||||
chr19:45021335
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.505-718A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021335 | ||||||
chr19:45021391
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.505-662G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021391 | ||||||
chr19:45021399
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.505-654G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021399 | ||||||
chr19:45021421
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(69): Show | 72 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.505-632G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021421 | ||||||
chr19:45021456
|
C | CA | 29 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(26): Show | 29 | HG00733.hp2 HG01081.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.505-578dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45021456 | |||||
chr19:45021456
|
CA | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0020others(64): Show | 67 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.505-578delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45021456 | |||||
chr19:45021573
|
C | CT | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 248 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.505-459dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45021573 | |||||
chr19:45021573
|
C | CTT | 12 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(9): Show | 12 | HG00438.hp1 HG01981.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.505-460_505-459dup others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45021573 | |||||
chr19:45021604
|
A | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(264): Show | 268 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.505-449A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021604 | ||||||
chr19:45021723
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.505-330C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021723 | ||||||
chr19:45021735
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.505-318G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021735 | ||||||
chr19:45021780
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0377a0001c0001t0002g0083 | 3 | HG01358.hp1 HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.505-273A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021780 | ||||||
chr19:45021867
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0001g0330 | 3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-186G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021867 | ||||||
chr19:45021911
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.505-142G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021911 | ||||||
chr19:45021937
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0362 | 3 | HG02896.hp1 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.505-116C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021937 | ||||||
chr19:45021949
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.505-104C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021949 | ||||||
chr19:45022231
|
G | A | 24 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0094others(21): Show | 24 | HG00621.hp2 HG02040.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.662+21G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45022231 | ||||||
chr19:45022547
|
CT | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(269): Show | 273 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.662+354delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45022547 | |||||
chr19:45022547
|
CTT | C | 15 | a0001c0001t0001g0108a0001c0001t0001g0119a0001c0001t0001g0125others(12): Show | 15 | HG01123.hp1 HG01261.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.662+353_662+354del others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45022547 | |||||
chr19:45022663
|
C | T | 4 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0188others(1): Show | 4 | HG01081.hp1 HG01192.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+453C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45022663 | ||||||
chr19:45022774
|
G | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0330 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.662+564G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45022774 | ||||||
chr19:45023393
|
T | TTTCC | 52 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(49): Show | 53 | HG00544.hp2 HG00609.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.662+1220_662+1223d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | |||||
chr19:45023393
|
T | TTTCCTTC others(1): Show |
44 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0051others(41): Show | 44 | HG00099.hp1 HG00621.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.662+1216_662+1223d others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | |||||
chr19:45023393
|
T | TTTCCTTC others(5): Show |
43 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(40): Show | 43 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.662+1212_662+1223d others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | |||||
chr19:45023393
|
T | TTTCCTTC others(9): Show |
11 | a0001c0001t0001g0034a0001c0001t0001g0099a0001c0001t0001g0126others(8): Show | 11 | HG00639.hp2 HG01257.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.662+1208_662+1223d others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | |||||
chr19:45023393
|
T | TTTCCTTC others(13): Show |
1 | a0001c0001t0001g0027 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.662+1204_662+1223d others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | |||||
chr19:45023393
|
T | TTTCCTTC others(17): Show |
1 | a0001c0001t0001g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.662+1200_662+1223d others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | |||||
chr19:45023393
|
TTTCC | T | 19 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0055others(16): Show | 19 | HG00140.hp1 HG01109.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.662+1220_662+1223d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | |||||
chr19:45023434
|
G | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0275a0001c0001t0001g0317others(1): Show | 4 | HG02257.hp2 HG02486.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+1224G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023434 | ||||||
chr19:45023466
|
C | T | 1 | a0001c0001t0002g0113 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.662+1256C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023466 | ||||||
chr19:45023626
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.662+1416G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023626 | ||||||
chr19:45023639
|
C | T | 19 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0115others(16): Show | 19 | HG00621.hp1 HG02135.hp1 NA18612.hp2 others(16): Show |
intron_variant | MODIFIER | c.662+1429C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023639 | ||||||
chr19:45023640
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.662+1430G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023640 | ||||||
chr19:45023676
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0149a0001c0001t0001g0311 | 3 | HG01261.hp2 HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.662+1466G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023676 | ||||||
chr19:45023740
|
C | CT | 73 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0033others(70): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.662+1558dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023740 | |||||
chr19:45023740
|
C | CTT | 21 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0041others(18): Show | 21 | HG00735.hp1 HG01192.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.662+1557_662+1558d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023740 | |||||
chr19:45023740
|
CT | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(158): Show | 162 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.662+1558delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023740 | |||||
chr19:45023740
|
CTT | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0052others(9): Show | 12 | HG02004.hp2 HG02055.hp2 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.662+1557_662+1558d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023740 | |||||
chr19:45023791
|
C | A | 1 | a0001c0001t0003g0261 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.663-1538C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023791 | ||||||
chr19:45023880
|
AGCTGGGA others(218): Show |
A | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663-1432_663-1208d others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023880 | |||||
chr19:45023915
|
TAATTTTT others(85): Show |
T | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(274): Show | 278 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.663-1321_663-1230d others(94): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023915 | |||||
chr19:45023940
|
GGGGTTTC others(84): Show |
G | 1 | a0001c0001t0002g0370 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.663-1385_663-1295d others(93): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023940 | |||||
chr19:45024026
|
A | G | 1 | a0001c0001t0001g0367 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.663-1303A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024026 | ||||||
chr19:45024184
|
C | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0149a0001c0001t0001g0311 | 3 | HG01261.hp2 HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.663-1145C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024184 | ||||||
chr19:45024223
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663-1106G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024223 | ||||||
chr19:45024310
|
C | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(263): Show | 267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.663-1019C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024310 | ||||||
chr19:45024335
|
T | G | 1 | a0001c0001t0002g0370 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.663-994T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024335 | ||||||
chr19:45024371
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663-958C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024371 | ||||||
chr19:45024383
|
C | G | 6 | a0001c0001t0001g0133a0001c0001t0001g0236a0001c0001t0001g0273others(3): Show | 6 | HG00733.hp2 HG01243.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.663-946C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024383 | ||||||
chr19:45024531
|
C | G | 2 | a0001c0001t0001g0338a0001c0001t0001g0340 | 2 | HG02523.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.663-798C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024531 | ||||||
chr19:45024549
|
C | A | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663-780C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024549 | ||||||
chr19:45024589
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0182 | 2 | NA19043.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.663-740C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024589 | ||||||
chr19:45024598
|
G | A | 6 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0001g0100others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.663-731G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024598 | ||||||
chr19:45024699
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0185a0001c0003t0001g0256 | 3 | HG03239.hp2 HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.663-630G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024699 | ||||||
chr19:45024900
|
C | T | 4 | a0001c0001t0001g0108a0001c0001t0001g0359a0001c0001t0001g0360others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-429C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024900 | ||||||
chr19:45024929
|
G | A | 4 | a0001c0001t0001g0108a0001c0001t0001g0359a0001c0001t0001g0360others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-400G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024929 | ||||||
chr19:45025040
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.663-289G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025040 | ||||||
chr19:45025107
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.663-222C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025107 | ||||||
chr19:45025111
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.663-218G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025111 | ||||||
chr19:45025156
|
C | T | 2 | a0001c0001t0001g0374a0001c0001t0001g0381 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.663-173C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025156 | ||||||
chr19:45025181
|
C | A | 1 | a0001c0001t0001g0298 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.663-148C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025181 | ||||||
chr19:45025253
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.663-76C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025253 | ||||||
chr19:45025292
|
C | T | 4 | a0001c0001t0001g0108a0001c0001t0001g0359a0001c0001t0001g0360others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-37C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025292 | ||||||
chr19:45025451
|
C | A | 1 | a0001c0001t0001g0115 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.754+31C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 6/11 | chr19 | 45025451 | ||||||
chr19:45025532
|
C | A | 1 | a0001c0001t0001g0216 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.755-74C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 6/11 | chr19 | 45025532 | ||||||
chr19:45025541
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 192 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.755-65T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 6/11 | chr19 | 45025541 | ||||||
chr19:45025575
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.755-31A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 6/11 | chr19 | 45025575 | ||||||
chr19:45026449
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(186): Show | 190 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.886+712G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026449 | ||||||
chr19:45026449
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.886+712G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026449 | ||||||
chr19:45026553
|
G | GA | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(262): Show | 266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.886+825dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45026553 | |||||
chr19:45026567
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.886+830A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026567 | ||||||
chr19:45026589
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0059 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.886+852G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026589 | ||||||
chr19:45026677
|
G | C | 1 | a0001c0001t0001g0015 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.886+940G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026677 | ||||||
chr19:45026748
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 192 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.886+1011A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026748 | ||||||
chr19:45026956
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.886+1219G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026956 | ||||||
chr19:45027034
|
C | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0149a0001c0001t0001g0311 | 3 | HG01261.hp2 HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.886+1297C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027034 | ||||||
chr19:45027084
|
T | A | 1 | a0001c0001t0001g0049 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.886+1347T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027084 | ||||||
chr19:45027093
|
C | T | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0027others(66): Show | 69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.886+1356C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027093 | ||||||
chr19:45027181
|
C | G | 1 | a0001c0001t0002g0335 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.886+1444C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027181 | ||||||
chr19:45027219
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.886+1482C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027219 | ||||||
chr19:45027232
|
C | CA | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 194 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.886+1510dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45027232 | |||||
chr19:45027232
|
C | CAA | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(64): Show | 67 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.886+1509_886+1510d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45027232 | |||||
chr19:45027235
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.886+1498A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027235 | ||||||
chr19:45027257
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.886+1520C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027257 | ||||||
chr19:45027294
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(275): Show | 279 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.886+1557A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027294 | ||||||
chr19:45027313
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.887-1575C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027313 | ||||||
chr19:45027350
|
TGGCTGCA others(4): Show |
T | 1 | a0001c0001t0001g0049 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.887-1535_887-1525d others(13): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45027350 | |||||
chr19:45027466
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0330 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.887-1422C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027466 | ||||||
chr19:45027678
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.887-1210C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027678 | ||||||
chr19:45027794
|
T | C | 4 | a0001c0001t0001g0108a0001c0001t0001g0359a0001c0001t0001g0360others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.887-1094T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027794 | ||||||
chr19:45027905
|
G | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0129others(5): Show | 8 | HG00738.hp2 HG01074.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.887-983G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027905 | ||||||
chr19:45028258
|
G | A | 5 | a0001c0001t0001g0126a0001c0002t0001g0100a0001c0002t0001g0128others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.887-630G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028258 | ||||||
chr19:45028262
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.887-626T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028262 | ||||||
chr19:45028336
|
GT | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.887-548delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45028336 | |||||
chr19:45028348
|
T | G | 1 | a0001c0001t0001g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.887-540T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028348 | ||||||
chr19:45028360
|
GT | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0042others(2): Show | 6 | HG01358.hp2 HG03490.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.887-522delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45028360 | |||||
chr19:45028603
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.887-285G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028603 | ||||||
chr19:45028624
|
A | G | 5 | a0001c0001t0001g0126a0001c0002t0001g0100a0001c0002t0001g0128others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.887-264A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028624 | ||||||
chr19:45028637
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.887-251G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028637 | ||||||
chr19:45028680
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0294a0001c0001t0001g0296others(1): Show | 4 | HG00673.hp1 NA18952.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.887-208G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028680 | ||||||
chr19:45028751
|
G | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 192 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.887-137G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028751 | ||||||
chr19:45029187
|
C | T | 13 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(10): Show | 13 | HG00733.hp2 HG01123.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.991+195C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029187 | ||||||
chr19:45029188
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.991+196G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029188 | ||||||
chr19:45029201
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+209G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029201 | ||||||
chr19:45029317
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.991+325C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029317 | ||||||
chr19:45029367
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0330 | 3 | HG02572.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.991+375A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029367 | ||||||
chr19:45029389
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.991+397T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029389 | ||||||
chr19:45029576
|
G | T | 8 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0149others(5): Show | 8 | HG01261.hp2 HG01433.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+584G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029576 | ||||||
chr19:45029939
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0311 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.991+947G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029939 | ||||||
chr19:45029965
|
C | T | 8 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0149others(5): Show | 8 | HG01261.hp2 HG01433.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+973C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029965 | ||||||
chr19:45029996
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+1004T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029996 | ||||||
chr19:45030142
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.991+1150G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030142 | ||||||
chr19:45030185
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+1193A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030185 | ||||||
chr19:45030191
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.991+1199C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030191 | ||||||
chr19:45030303
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.991+1311T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030303 | ||||||
chr19:45030370
|
A | C | 1 | a0001c0001t0001g0258 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.991+1378A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030370 | ||||||
chr19:45030477
|
T | A | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.991+1485T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030477 | ||||||
chr19:45030759
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.991+1767C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030759 | ||||||
chr19:45030783
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(186): Show | 190 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.992-1751C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030783 | ||||||
chr19:45030865
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.992-1669G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030865 | ||||||
chr19:45031038
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0219 | 2 | NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.992-1496A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031038 | ||||||
chr19:45031102
|
A | G | 5 | a0001c0001t0001g0111a0001c0001t0001g0133a0001c0001t0001g0236others(2): Show | 5 | HG00733.hp2 HG00741.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1432A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031102 | ||||||
chr19:45031189
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.992-1345C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031189 | ||||||
chr19:45031201
|
T | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.992-1333T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031201 | ||||||
chr19:45031231
|
G | A | 5 | a0001c0001t0001g0126a0001c0002t0001g0100a0001c0002t0001g0128others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1303G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031231 | ||||||
chr19:45031265
|
A | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.992-1269A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031265 | ||||||
chr19:45031587
|
T | G | 1 | a0001c0004t0001g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.992-947T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031587 | ||||||
chr19:45031609
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.992-925T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031609 | ||||||
chr19:45031679
|
C | A | 1 | a0001c0001t0001g0350 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.992-855C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031679 | ||||||
chr19:45031700
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.992-834T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031700 | ||||||
chr19:45031724
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0064a0001c0001t0001g0279 | 3 | HG03130.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.992-810T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031724 | ||||||
chr19:45031736
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0030others(66): Show | 70 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.992-798C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031736 | ||||||
chr19:45031786
|
C | T | 10 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0127others(7): Show | 10 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-748C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031786 | ||||||
chr19:45031787
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.992-747G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031787 | ||||||
chr19:45031827
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0069a0001c0001t0001g0201others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.992-707C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031827 | ||||||
chr19:45031973
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.992-561T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031973 | ||||||
chr19:45032048
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0263a0001c0001t0001g0352 | 3 | NA18612.hp2 NA19057.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.992-486C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032048 | ||||||
chr19:45032052
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.992-482G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032052 | ||||||
chr19:45032072
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0323 | 2 | HG01099.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.992-462T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032072 | ||||||
chr19:45032129
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.992-405G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032129 | ||||||
chr19:45032258
|
C | A | 14 | a0001c0001t0001g0034a0001c0001t0001g0124a0001c0001t0001g0138others(11): Show | 14 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.992-276C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032258 | ||||||
chr19:45032313
|
G | A | 6 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG02109.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.992-221G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032313 | ||||||
chr19:45032373
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.992-161C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032373 | ||||||
chr19:45032402
|
G | C | 10 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0127others(7): Show | 10 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-132G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032402 | ||||||
chr19:45032414
|
CA | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 192 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.992-108delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr19 | 45032414 | |||||
chr19:45032430
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.992-104T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032430 | ||||||
chr19:45032778
|
C | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1207+29C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032778 | ||||||
chr19:45032803
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0001t0003g0253 | 3 | HG01192.hp2 HG01361.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1207+54T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032803 | ||||||
chr19:45032912
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0251 | 2 | NA18973.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1207+163T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032912 | ||||||
chr19:45032935
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1207+186C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032935 | ||||||
chr19:45032938
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1207+189T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032938 | ||||||
chr19:45032957
|
T | A | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00733.hp2 HG01109.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207+208T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032957 | ||||||
chr19:45033020
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1207+271C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033020 | ||||||
chr19:45033267
|
C | G | 1 | a0001c0001t0001g0366 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1207+518C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033267 | ||||||
chr19:45033275
|
G | A | 1 | a0001c0001t0001g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1207+526G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033275 | ||||||
chr19:45033315
|
C | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG01943.hp1 HG01952.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+566C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033315 | ||||||
chr19:45033382
|
C | A | 1 | a0001c0001t0001g0353 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1207+633C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033382 | ||||||
chr19:45033477
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1207+728G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033477 | ||||||
chr19:45033488
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1207+739C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033488 | ||||||
chr19:45033610
|
G | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0365others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-634G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033610 | ||||||
chr19:45033750
|
T | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0138others(2): Show | 5 | HG02622.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-494T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033750 | ||||||
chr19:45033762
|
C | T | 26 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1208-482C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033762 | ||||||
chr19:45033763
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1208-481G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033763 | ||||||
chr19:45033853
|
C | CT | 7 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0125others(4): Show | 7 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-388dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 45033853 | |||||
chr19:45033857
|
A | T | 26 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1208-387A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033857 | ||||||
chr19:45033858
|
A | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0034others(17): Show | 20 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1208-386A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033858 | ||||||
chr19:45033859
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0002t0001g0128others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-385A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033859 | ||||||
chr19:45033912
|
C | T | 4 | a0001c0002t0001g0100a0001c0002t0001g0128a0001c0002t0001g0130others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-332C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033912 | ||||||
chr19:45034019
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1208-225C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45034019 | ||||||
chr19:45034159
|
A | AAAAT | 24 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0034others(21): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1208-61_1208-58dup others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 45034159 | |||||
chr19:45034159
|
AAAAT | A | 162 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0022others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1208-61_1208-58del others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 45034159 | |||||
chr19:45034565
|
G | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG02886.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1354+37G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034565 | ||||||
chr19:45034575
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1354+47G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034575 | ||||||
chr19:45034703
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1354+175C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034703 | ||||||
chr19:45034797
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1354+269A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034797 | ||||||
chr19:45034841
|
TC | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 15 | HG00423.hp2 HG01943.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.1354+314delC | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034841 | ||||||
chr19:45034842
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1354+314C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034842 | ||||||
chr19:45034943
|
C | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0149a0001c0001t0001g0311 | 3 | HG01261.hp2 HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1354+415C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034943 | ||||||
chr19:45035447
|
G | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0330 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1354+919G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035447 | ||||||
chr19:45035539
|
C | CAACAACA others(15): Show |
4 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0365others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354+1013_1354+101 others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 45035539 | |||||
chr19:45035539
|
C | CAACAACA others(18): Show |
1 | a0001c0001t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1354+1013_1354+101 others(29): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 45035539 | |||||
chr19:45035576
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1354+1048C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035576 | ||||||
chr19:45035745
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1354+1217G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035745 | ||||||
chr19:45035878
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1354+1350T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035878 | ||||||
chr19:45035901
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1354+1373C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035901 | ||||||
chr19:45035975
|
G | A | 1 | a0001c0001t0001g0373 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1355-1430G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035975 | ||||||
chr19:45036384
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1355-1021C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036384 | ||||||
chr19:45036578
|
T | C | 4 | a0001c0002t0001g0100a0001c0002t0001g0128a0001c0002t0001g0130others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1355-827T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036578 | ||||||
chr19:45036607
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1355-798A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036607 | ||||||
chr19:45036726
|
G | A | 1 | a0001c0001t0004g0199 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1355-679G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036726 | ||||||
chr19:45036778
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1355-627A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036778 | ||||||
chr19:45036879
|
C | T | 1 | a0001c0001t0001g0375 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1355-526C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036879 | ||||||
chr19:45036917
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1355-488G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036917 | ||||||
chr19:45036955
|
T | C | 1 | a0001c0001t0003g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1355-450T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036955 | ||||||
chr19:45037108
|
G | A | 4 | a0001c0002t0001g0100a0001c0002t0001g0128a0001c0002t0001g0130others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1355-297G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45037108 | ||||||
chr19:45037149
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1355-256G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45037149 | ||||||
chr19:45037182
|
G | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0326 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1355-223G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45037182 | ||||||
chr19:45037243
|
T | C | 1 | a0001c0001t0001g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1355-162T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45037243 |