geneid | 127544 |
---|---|
ensemblid | ENSG00000116514.17 |
hgncid | 26886 |
symbol | RNF19B |
name | ring finger protein 19B |
refseq_nuc | NM_001300826.2 |
refseq_prot | NP_001287755.1 |
ensembl_nuc | ENST00000235150.5 |
ensembl_prot | ENSP00000235150.4 |
mane_status | MANE Select |
chr | chr1 |
start | 32936449 |
end | 32964809 |
strand | - |
ver | v1.2 |
region | chr1:32936449-32964809 |
region5000 | chr1:32931449-32969809 |
regionname0 | RNF19B_chr1_32936449_32964809 |
regionname5000 | RNF19B_chr1_32931449_32969809 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 731 | 312 | 87 | 60 | 120 | 8 | 36 | 91 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0002 | 0/0 | 731 | 13 | 0 | 0 | 12 | 0 | 1 | 9 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0003 | 0/0 | 733 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0004 | 1/0 | 731 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0005 | 0/0 | 731 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2196 | 226 | 82 | 42 | 72 | 5 | 24 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
c0002 | 0/0 | 2196 | 70 | 2 | 10 | 48 | 3 | 7 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
c0003 | 0/0 | 2196 | 14 | 2 | 7 | 0 | 0 | 5 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
c0004 | 0/0 | 2196 | 13 | 0 | 0 | 12 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
c0005 | 0/0 | 2202 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
c0006 | 0/0 | 2196 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
c0007 | 1/0 | 2196 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
c0008 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
c0009 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 482 | 190 | 54 | 37 | 66 | 5 | 26 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
t0002 | 0/0 | 482 | 66 | 2 | 10 | 45 | 2 | 7 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
t0003 | 0/0 | 483 | 47 | 30 | 11 | 2 | 0 | 4 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
t0004 | 0/0 | 481 | 21 | 4 | 2 | 14 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
t0005 | 0/0 | 481 | 4 | 0 | 0 | 3 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
t0006 | 0/0 | 482 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
t0007 | 0/0 | 482 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 19 | 0 | 2 | 13 | 1 | 3 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0002 | 0/0 | 13 | 0 | 4 | 5 | 2 | 2 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0003 | 0/0 | 7 | 2 | 1 | 4 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0005 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2196 | 226 | 82 | 42 | 72 | 5 | 24 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0002 | 0/0 | 2196 | 70 | 2 | 10 | 48 | 3 | 7 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0003 | 0/0 | 2196 | 14 | 2 | 7 | 0 | 0 | 5 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0008 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0009 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0002c0004 | 0/0 | 2196 | 13 | 0 | 0 | 12 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0003c0005 | 0/0 | 2202 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0004c0007 | 1/0 | 2196 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0005c0006 | 0/0 | 2196 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2677 | 186 | 53 | 37 | 66 | 5 | 24 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0001t0003 | 0/0 | 2678 | 30 | 25 | 3 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0001t0004 | 0/0 | 2676 | 8 | 4 | 2 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0001t0006 | 0/0 | 2677 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0001t0007 | 0/0 | 2677 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0002t0002 | 0/0 | 2677 | 66 | 2 | 10 | 45 | 2 | 7 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0002t0005 | 0/0 | 2676 | 4 | 0 | 0 | 3 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0003t0001 | 0/0 | 2677 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0003t0003 | 0/0 | 2678 | 13 | 2 | 7 | 0 | 0 | 4 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0008t0001 | 0/0 | 2677 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0001c0009t0003 | 0/0 | 2678 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0002c0004t0004 | 0/0 | 2676 | 13 | 0 | 0 | 12 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0003c0005t0003 | 0/0 | 2684 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0004c0007t0001 | 1/0 | 2677 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
a0005c0006t0001 | 0/0 | 2677 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | copy fasta | chr1 | 32931449 | 32969809 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 13 | 0 | 4 | 5 | 2 | 2 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0003 | 0/0 | 7 | 2 | 1 | 4 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0005 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0001 | 0/0 | 19 | 0 | 2 | 13 | 1 | 3 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0002t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0003t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0008t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0001c0009t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0002c0004t0004g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0002c0004t0004g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0002c0004t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0002c0004t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0002c0004t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0002c0004t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0003c0005t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0003c0005t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0003c0005t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0004c0007t0001g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
a0005c0006t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | GBR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | GBR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00621 | hp2 | a0002 | c0004 | t0004 | g0255 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00673 | hp1 | a0002 | c0004 | t0004 | g0004 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00741 | hp1 | a0001 | c0003 | t0003 | g0045 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01109 | hp2 | a0001 | c0003 | t0003 | g0044 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01361 | hp1 | a0001 | c0003 | t0003 | g0006 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01433 | hp2 | a0001 | c0003 | t0003 | g0046 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01515 | hp2 | a0001 | c0002 | t0005 | g0056 | EUR | IBS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01891 | hp2 | a0001 | c0008 | t0001 | g0107 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01934 | hp2 | a0001 | c0009 | t0003 | g0257 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01943 | hp1 | a0001 | c0003 | t0003 | g0040 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02015 | hp2 | a0001 | c0002 | t0005 | g0053 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02040 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02080 | hp2 | a0001 | c0002 | t0005 | g0062 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | CDX | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | CDX | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02257 | hp2 | a0001 | c0003 | t0003 | g0038 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02293 | hp1 | a0001 | c0003 | t0003 | g0047 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02300 | hp2 | a0001 | c0003 | t0003 | g0006 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02698 | hp1 | a0001 | c0003 | t0003 | g0041 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02896 | hp2 | a0003 | c0005 | t0003 | g0029 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02897 | hp1 | a0003 | c0005 | t0003 | g0030 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02965 | hp1 | a0001 | c0003 | t0003 | g0039 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0048 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0076 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03654 | hp2 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03669 | hp1 | a0001 | c0003 | t0003 | g0043 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0055 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0067 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03927 | hp1 | a0001 | c0003 | t0003 | g0042 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04115 | hp2 | a0005 | c0006 | t0001 | g0026 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04184 | hp1 | a0002 | c0004 | t0004 | g0013 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | CHB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | CHB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18946 | hp1 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18954 | hp1 | a0002 | c0004 | t0004 | g0256 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18959 | hp2 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18961 | hp2 | a0001 | c0002 | t0005 | g0239 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18978 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18979 | hp1 | a0002 | c0004 | t0004 | g0254 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18980 | hp2 | a0002 | c0004 | t0004 | g0013 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18981 | hp1 | a0002 | c0004 | t0004 | g0253 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | LWK | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19064 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19067 | hp2 | a0002 | c0004 | t0004 | g0013 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19086 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19090 | hp1 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0057 | EUR | TSI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | GIH | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG06807 | hp1 | a0003 | c0005 | t0003 | g0028 | AFR | USA | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | USA | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | LWK | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0220 | REF | REF | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
homoSapiens_grch38 | hp1 | a0004 | c0007 | t0001 | g0027 | REF | REF | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:32964396
|
G | A | 1 | a0002 | 13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
missense_variant | MODERATE | c.290C>T | p.Ala97Val | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/9 | 414/2677 | 290/2196 | 97/731 | chr1 | 32964396 | ||
chr1:32964416
|
C | CGCCTCG | 1 | a0003 | 3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
disruptive_inframe_insertion | MODERATE | c.264_269dupCGAGGC | p.Ala90_Glu91insGluA others(2): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/9 | 393/2677 | 269/2196 | 90/731 | chr1 | 32964416 | ||
chr1:32964501
|
T | G | 4 | a0001a0002a0003others(1): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
missense_variant | MODERATE | c.185A>C | p.Gln62Pro | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/9 | 309/2677 | 185/2196 | 62/731 | chr1 | 32964501 | ||
chr1:32964520
|
G | T | 1 | a0005 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.166C>A | p.Pro56Thr | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/9 | 290/2677 | 166/2196 | 56/731 | chr1 | 32964520 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:32936914
|
C | T | 1 | a0001c0003 | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
synonymous_variant | LOW | c.2088G>A | p.Ser696Ser | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 2212/2677 | 2088/2196 | 696/731 | chr1 | 32936914 | ||
chr1:32936941
|
G | C | 1 | a0001c0003 | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
synonymous_variant | LOW | c.2061C>G | p.Pro687Pro | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 2185/2677 | 2061/2196 | 687/731 | chr1 | 32936941 | ||
chr1:32944092
|
G | A | 1 | a0001c0002 | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
synonymous_variant | LOW | c.1329C>T | p.Gly443Gly | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/9 | 1453/2677 | 1329/2196 | 443/731 | chr1 | 32944092 | ||
chr1:32948338
|
G | A | 1 | a0001c0008 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.867C>T | p.Cys289Cys | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/9 | 991/2677 | 867/2196 | 289/731 | chr1 | 32948338 | ||
chr1:32964569
|
G | A | 1 | a0001c0009 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.117C>T | p.Phe39Phe | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/9 | 241/2677 | 117/2196 | 39/731 | chr1 | 32964569 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:32936571
|
C | T | 2 | a0001c0002t0002a0001c0002t0005 | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*235G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 235 | chr1 | 32936571 | |||||
chr1:32936722
|
T | C | 1 | a0001c0001t0006 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 84 | chr1 | 32936722 | |||||
chr1:32936733
|
G | GA | 4 | a0001c0001t0003a0001c0003t0003a0001c0009t0003others(1): Show | 47 | HG00423.hp2 HG00639.hp1 HG00741.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*72dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 72 | chr1 | 32936733 | |||||
chr1:32936733
|
GA | G | 3 | a0001c0001t0004a0001c0002t0005a0002c0004t0004 | 25 | HG00621.hp2 HG00639.hp2 HG00673.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*72delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 72 | chr1 | 32936733 | |||||
chr1:32936805
|
T | G | 1 | a0001c0001t0007 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 1 | chr1 | 32936805 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:32937603
|
G | C | 5 | a0001c0001t0003g0009a0001c0001t0003g0086a0001c0001t0003g0087others(2): Show | 7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1743-344C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32937603 | ||||||
chr1:32937880
|
T | C | 50 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(47): Show | 83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1742+517A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32937880 | ||||||
chr1:32938140
|
C | CA | 42 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0105others(39): Show | 43 | HG00609.hp1 HG00639.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1742+256dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938140 | ||||||
chr1:32938140
|
C | CAA | 23 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0003g0016others(20): Show | 33 | HG00621.hp2 HG00673.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1742+255_1742+256d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938140 | ||||||
chr1:32938140
|
CA | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0083a0001c0001t0001g0119others(3): Show | 7 | NA18941.hp2 NA18960.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1742+256delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938140 | ||||||
chr1:32938141
|
A | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0196 | 2 | HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1742+256T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938141 | ||||||
chr1:32938295
|
G | A | 1 | a0001c0001t0004g0209 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1742+102C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938295 | ||||||
chr1:32938362
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0196 | 2 | HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1742+35A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938362 | ||||||
chr1:32938540
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1611-12C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938540 | ||||||
chr1:32938600
|
A | G | 1 | a0001c0001t0003g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1611-72T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938600 | ||||||
chr1:32938619
|
T | C | 1 | a0001c0002t0002g0066 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1611-91A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938619 | ||||||
chr1:32938766
|
C | T | 44 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1611-238G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938766 | ||||||
chr1:32938931
|
G | C | 1 | a0005c0006t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1611-403C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938931 | ||||||
chr1:32938970
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0177 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1611-442C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938970 | ||||||
chr1:32939290
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1611-762G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939290 | ||||||
chr1:32939442
|
A | C | 1 | a0001c0001t0001g0160 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1611-914T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939442 | ||||||
chr1:32939480
|
CTTA | C | 3 | a0001c0001t0001g0095a0001c0001t0003g0093a0001c0001t0003g0094 | 3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1611-955_1611-953d others(5): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939480 | ||||||
chr1:32939717
|
A | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(5): Show | 12 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1611-1189T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939717 | ||||||
chr1:32939864
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0162 | 2 | HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1611-1336G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939864 | ||||||
chr1:32939934
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1611-1406C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939934 | ||||||
chr1:32940264
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1611-1736C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940264 | ||||||
chr1:32940371
|
A | C | 44 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1611-1843T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940371 | ||||||
chr1:32940372
|
T | C | 1 | a0001c0001t0006g0223 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1611-1844A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940372 | ||||||
chr1:32940395
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1610+1857A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940395 | ||||||
chr1:32940498
|
A | C | 6 | a0002c0004t0004g0004a0002c0004t0004g0013a0002c0004t0004g0253others(3): Show | 13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1610+1754T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940498 | ||||||
chr1:32940542
|
A | G | 1 | a0001c0001t0003g0244 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1610+1710T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940542 | ||||||
chr1:32940642
|
T | G | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1610+1610A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940642 | ||||||
chr1:32940860
|
T | C | 2 | a0001c0001t0004g0159a0001c0001t0004g0161 | 2 | HG00639.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1610+1392A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940860 | ||||||
chr1:32941101
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0118 | 2 | NA18942.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1610+1151A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941101 | ||||||
chr1:32941154
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1610+1098A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941154 | ||||||
chr1:32941206
|
C | G | 100 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(97): Show | 139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.1610+1046G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941206 | ||||||
chr1:32941315
|
C | T | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1610+937G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941315 | ||||||
chr1:32941483
|
C | T | 12 | a0001c0003t0001g0048a0001c0003t0003g0006a0001c0003t0003g0038others(9): Show | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610+769G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941483 | ||||||
chr1:32941542
|
A | AAAAAT | 44 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1610+705_1610+709d others(7): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941542 | ||||||
chr1:32941553
|
AAAAT | A | 3 | a0003c0005t0003g0028a0003c0005t0003g0029a0003c0005t0003g0030 | 3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1610+695_1610+698d others(6): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941553 | ||||||
chr1:32941846
|
C | A | 12 | a0001c0003t0001g0048a0001c0003t0003g0006a0001c0003t0003g0038others(9): Show | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610+406G>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941846 | ||||||
chr1:32941994
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0177a0001c0001t0001g0212others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1610+258C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941994 | ||||||
chr1:32942011
|
C | T | 12 | a0001c0003t0001g0048a0001c0003t0003g0006a0001c0003t0003g0038others(9): Show | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610+241G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32942011 | ||||||
chr1:32942053
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1610+199G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32942053 | ||||||
chr1:32942092
|
G | A | 50 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(47): Show | 83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1610+160C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32942092 | ||||||
chr1:32942159
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1610+93C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32942159 | ||||||
chr1:32942537
|
T | G | 37 | a0001c0001t0001g0017a0001c0001t0001g0095a0001c0001t0001g0104others(34): Show | 41 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1403-78A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942537 | ||||||
chr1:32942554
|
T | C | 1 | a0001c0001t0003g0244 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1403-95A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942554 | ||||||
chr1:32942721
|
C | T | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1403-262G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942721 | ||||||
chr1:32942799
|
A | C | 4 | a0001c0001t0001g0179a0001c0001t0001g0189a0001c0001t0001g0199others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1403-340T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942799 | ||||||
chr1:32942859
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1403-400C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942859 | ||||||
chr1:32942868
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1403-409G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942868 | ||||||
chr1:32943034
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1403-575C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943034 | ||||||
chr1:32943140
|
CA | C | 94 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(91): Show | 130 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.1403-682delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943140 | ||||||
chr1:32943192
|
T | TCTACGTT others(9): Show |
2 | a0003c0005t0003g0029a0003c0005t0003g0030 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1403-749_1403-734d others(18): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943192 | ||||||
chr1:32943212
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1403-753G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943212 | ||||||
chr1:32943325
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1402+694T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943325 | ||||||
chr1:32943408
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0003g0093a0001c0001t0003g0094 | 3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1402+611C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943408 | ||||||
chr1:32943578
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1402+441G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943578 | ||||||
chr1:32943628
|
A | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(5): Show | 12 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1402+391T>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943628 | ||||||
chr1:32943654
|
T | C | 1 | a0001c0002t0002g0079 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1402+365A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943654 | ||||||
chr1:32943831
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0182 | 2 | NA18956.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1402+188G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943831 | ||||||
chr1:32943950
|
C | T | 100 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(97): Show | 139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.1402+69G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943950 | ||||||
chr1:32943999
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1402+20T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943999 | ||||||
chr1:32944199
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1262-40A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944199 | ||||||
chr1:32944217
|
C | T | 3 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0003g0243 | 3 | HG00639.hp1 HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1262-58G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944217 | ||||||
chr1:32944439
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1262-280T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944439 | ||||||
chr1:32944632
|
G | A | 1 | a0001c0002t0002g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1262-473C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944632 | ||||||
chr1:32944835
|
C | A | 1 | a0001c0001t0003g0243 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1262-676G>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944835 | ||||||
chr1:32944836
|
C | T | 1 | a0002c0004t0004g0254 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1262-677G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944836 | ||||||
chr1:32944849
|
C | T | 12 | a0001c0003t0001g0048a0001c0003t0003g0006a0001c0003t0003g0038others(9): Show | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1261+665G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944849 | ||||||
chr1:32944890
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1261+624C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944890 | ||||||
chr1:32944967
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0003g0093a0001c0001t0003g0094 | 3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1261+547G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944967 | ||||||
chr1:32944968
|
G | T | 1 | a0001c0001t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1261+546C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944968 | ||||||
chr1:32945078
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1261+436G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945078 | ||||||
chr1:32945146
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1261+368G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945146 | ||||||
chr1:32945297
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1261+217C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945297 | ||||||
chr1:32945377
|
T | G | 1 | a0001c0003t0003g0043 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1261+137A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945377 | ||||||
chr1:32945414
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0232 | 3 | HG01081.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1261+100G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945414 | ||||||
chr1:32945724
|
C | T | 2 | a0001c0002t0002g0061a0001c0002t0002g0069 | 2 | HG01256.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1147-96G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945724 | ||||||
chr1:32945726
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1147-98T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945726 | ||||||
chr1:32945841
|
C | G | 12 | a0001c0003t0001g0048a0001c0003t0003g0006a0001c0003t0003g0038others(9): Show | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1147-213G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945841 | ||||||
chr1:32945880
|
A | ATT | 42 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(39): Show | 68 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1147-254_1147-253d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945880 | ||||||
chr1:32945925
|
C | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1147-297G>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945925 | ||||||
chr1:32946032
|
T | A | 1 | a0001c0001t0003g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1146+370A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946032 | ||||||
chr1:32946089
|
C | T | 1 | a0001c0001t0003g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1146+313G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946089 | ||||||
chr1:32946125
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0003g0241a0001c0001t0003g0242others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+277G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946125 | ||||||
chr1:32946174
|
G | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0101a0001c0001t0003g0111 | 4 | HG01891.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+228C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946174 | ||||||
chr1:32946201
|
A | T | 1 | a0001c0001t0003g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1146+201T>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946201 | ||||||
chr1:32946242
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1146+160C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946242 | ||||||
chr1:32946271
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1146+131T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946271 | ||||||
chr1:32946784
|
G | C | 1 | a0001c0001t0003g0243 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.984-220C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32946784 | ||||||
chr1:32946843
|
A | G | 1 | a0001c0002t0002g0069 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.984-279T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32946843 | ||||||
chr1:32946995
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.984-431G>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32946995 | ||||||
chr1:32947297
|
TTTTG | T | 3 | a0003c0005t0003g0028a0003c0005t0003g0029a0003c0005t0003g0030 | 3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.984-737_984-734del others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947297 | ||||||
chr1:32947435
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA18939.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.983+787C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947435 | ||||||
chr1:32947495
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.983+727G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947495 | ||||||
chr1:32947589
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.983+633C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947589 | ||||||
chr1:32947658
|
T | TA | 10 | a0001c0001t0001g0095a0001c0001t0001g0187a0001c0001t0001g0193others(7): Show | 10 | HG01106.hp2 HG01934.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.983+563dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947658 | ||||||
chr1:32947711
|
A | C | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.983+511T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947711 | ||||||
chr1:32947801
|
A | C | 1 | a0001c0002t0002g0052 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.983+421T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947801 | ||||||
chr1:32948093
|
T | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0152 | 2 | HG00609.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.983+129A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32948093 | ||||||
chr1:32948439
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0232 | 3 | HG01081.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.842-76C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948439 | ||||||
chr1:32948515
|
G | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 11 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.842-152C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948515 | ||||||
chr1:32948516
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.842-153C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948516 | ||||||
chr1:32948647
|
A | C | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.842-284T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948647 | ||||||
chr1:32948973
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.841+596C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948973 | ||||||
chr1:32949031
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.841+538T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949031 | ||||||
chr1:32949062
|
T | C | 48 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(45): Show | 54 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.841+507A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949062 | ||||||
chr1:32949266
|
T | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.841+303A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949266 | ||||||
chr1:32949329
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.841+240T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949329 | ||||||
chr1:32949412
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.841+157A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949412 | ||||||
chr1:32949799
|
A | G | 3 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0003g0243 | 3 | HG00639.hp1 HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.636-25T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949799 | ||||||
chr1:32949808
|
G | GT | 48 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(45): Show | 54 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.636-35dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949808 | ||||||
chr1:32949850
|
AAC | A | 5 | a0001c0001t0003g0009a0001c0001t0003g0086a0001c0001t0003g0087others(2): Show | 7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.636-78_636-77delGT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949850 | ||||||
chr1:32949865
|
T | C | 48 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(45): Show | 54 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.636-91A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949865 | ||||||
chr1:32949958
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.636-184C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949958 | ||||||
chr1:32949971
|
CT | C | 12 | a0001c0003t0001g0048a0001c0003t0003g0006a0001c0003t0003g0038others(9): Show | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.636-198delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949971 | ||||||
chr1:32950022
|
T | C | 100 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(97): Show | 139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.636-248A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950022 | ||||||
chr1:32950220
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.636-446C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950220 | ||||||
chr1:32950335
|
T | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0101a0001c0001t0003g0111 | 4 | HG01891.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.636-561A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950335 | ||||||
chr1:32950424
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.636-650G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950424 | ||||||
chr1:32950457
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.636-683G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950457 | ||||||
chr1:32950488
|
C | T | 3 | a0003c0005t0003g0028a0003c0005t0003g0029a0003c0005t0003g0030 | 3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.636-714G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950488 | ||||||
chr1:32950570
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.636-796C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950570 | ||||||
chr1:32950684
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.636-910C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950684 | ||||||
chr1:32950755
|
G | C | 1 | a0001c0001t0003g0109 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.636-981C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950755 | ||||||
chr1:32950764
|
C | T | 5 | a0001c0001t0001g0082a0001c0001t0003g0109a0003c0005t0003g0028others(2): Show | 5 | HG02630.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.636-990G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950764 | ||||||
chr1:32950774
|
C | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.636-1000G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950774 | ||||||
chr1:32950843
|
C | CT | 10 | a0001c0001t0001g0115a0001c0001t0001g0164a0001c0001t0001g0240others(7): Show | 17 | HG00621.hp2 HG00673.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.636-1070dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950843 | ||||||
chr1:32950843
|
CT | C | 55 | a0001c0001t0001g0247a0001c0001t0003g0016a0001c0001t0003g0096others(52): Show | 82 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.636-1070delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950843 | ||||||
chr1:32950932
|
C | T | 48 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(45): Show | 54 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.636-1158G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950932 | ||||||
chr1:32951027
|
T | C | 100 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(97): Show | 139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.636-1253A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951027 | ||||||
chr1:32951080
|
G | A | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636-1306C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951080 | ||||||
chr1:32951234
|
A | T | 1 | a0001c0002t0002g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.636-1460T>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951234 | ||||||
chr1:32951306
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.636-1532C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951306 | ||||||
chr1:32951484
|
A | T | 6 | a0002c0004t0004g0004a0002c0004t0004g0013a0002c0004t0004g0253others(3): Show | 13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.636-1710T>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951484 | ||||||
chr1:32951510
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.636-1736G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951510 | ||||||
chr1:32951547
|
T | C | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-1773A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951547 | ||||||
chr1:32951649
|
G | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0177 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.636-1875C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951649 | ||||||
chr1:32951857
|
G | A | 4 | a0001c0001t0001g0124a0001c0001t0003g0241a0001c0001t0003g0242others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.636-2083C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951857 | ||||||
chr1:32951957
|
GC | G | 3 | a0003c0005t0003g0028a0003c0005t0003g0029a0003c0005t0003g0030 | 3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.636-2184delG | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951957 | ||||||
chr1:32951958
|
C | CT | 27 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0104others(24): Show | 29 | HG00673.hp2 HG01106.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.636-2185dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951958 | ||||||
chr1:32951958
|
CT | C | 68 | a0001c0001t0001g0124a0001c0001t0001g0192a0001c0001t0003g0009others(65): Show | 102 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.636-2185delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951958 | ||||||
chr1:32952184
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.636-2410T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952184 | ||||||
chr1:32952212
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.636-2438A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952212 | ||||||
chr1:32952429
|
T | TA | 49 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0025others(46): Show | 55 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.636-2656dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952429
|
T | TAA | 22 | a0001c0001t0001g0024a0001c0001t0001g0126a0001c0001t0001g0143others(19): Show | 23 | HG00639.hp2 HG01070.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.636-2657_636-2656d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952429
|
T | TAAA | 7 | a0001c0001t0001g0011a0001c0001t0001g0091a0001c0001t0001g0145others(4): Show | 9 | HG01243.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.636-2658_636-2656d others(5): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952429
|
TA | T | 8 | a0001c0001t0001g0085a0001c0001t0001g0116a0001c0001t0001g0118others(5): Show | 8 | HG01074.hp2 HG02083.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.636-2656delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952429
|
TAA | T | 7 | a0001c0001t0001g0163a0001c0001t0003g0094a0001c0001t0003g0102others(4): Show | 7 | HG00741.hp1 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.636-2657_636-2656d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952429
|
TAAA | T | 18 | a0001c0001t0001g0095a0001c0001t0003g0016a0001c0001t0003g0093others(15): Show | 21 | HG01361.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.636-2658_636-2656d others(5): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952429
|
TAAAA | T | 22 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0104others(19): Show | 23 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.636-2659_636-2656d others(6): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952429
|
TAAAAA | T | 44 | a0001c0001t0003g0009a0001c0001t0003g0088a0001c0001t0003g0109others(41): Show | 72 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.636-2660_636-2656d others(7): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952429
|
TAAAAAA | T | 8 | a0001c0001t0003g0087a0001c0002t0005g0239a0002c0004t0004g0004others(5): Show | 15 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.636-2661_636-2656d others(8): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952429
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.636-2668_636-2656d others(15): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | ||||||
chr1:32952449
|
A | C | 47 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(44): Show | 79 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.636-2675T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952449 | ||||||
chr1:32952452
|
A | C | 1 | a0001c0001t0003g0097 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.636-2678T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952452 | ||||||
chr1:32952478
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.636-2704G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952478 | ||||||
chr1:32952552
|
C | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(9): Show | 16 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.636-2778G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952552 | ||||||
chr1:32952599
|
G | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0021others(54): Show | 72 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.636-2825C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952599 | ||||||
chr1:32952611
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636-2837C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952611 | ||||||
chr1:32952650
|
G | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0095a0001c0001t0001g0104others(34): Show | 41 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.636-2876C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952650 | ||||||
chr1:32952748
|
C | CA | 16 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0176others(13): Show | 16 | HG01109.hp1 HG01346.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.636-2975dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952748 | ||||||
chr1:32952748
|
CA | C | 9 | a0001c0001t0001g0197a0001c0001t0001g0219a0001c0001t0003g0009others(6): Show | 11 | HG01069.hp1 HG01258.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.636-2975delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952748 | ||||||
chr1:32952748
|
CAA | C | 93 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(90): Show | 130 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.636-2976_636-2975d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952748 | ||||||
chr1:32952791
|
C | T | 1 | a0001c0002t0002g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.636-3017G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952791 | ||||||
chr1:32952819
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.636-3045C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952819 | ||||||
chr1:32952962
|
A | AT | 77 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0025others(74): Show | 109 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.636-3189dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952962 | ||||||
chr1:32952962
|
A | ATT | 6 | a0001c0001t0001g0134a0001c0001t0003g0086a0001c0001t0003g0096others(3): Show | 6 | HG01943.hp2 HG02257.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.636-3190_636-3189d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952962 | ||||||
chr1:32952962
|
AT | A | 20 | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0092others(17): Show | 21 | HG01070.hp2 HG01081.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.636-3189delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952962 | ||||||
chr1:32952986
|
A | G | 9 | a0001c0001t0003g0016a0001c0001t0003g0096a0001c0001t0003g0097others(6): Show | 10 | HG01891.hp1 HG02647.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.636-3212T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952986 | ||||||
chr1:32953001
|
T | G | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636-3227A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953001 | ||||||
chr1:32953002
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636-3228G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953002 | ||||||
chr1:32953048
|
C | T | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-3274G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953048 | ||||||
chr1:32953074
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636-3300G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953074 | ||||||
chr1:32953199
|
T | C | 50 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(47): Show | 83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.636-3425A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953199 | ||||||
chr1:32953304
|
T | C | 3 | a0001c0002t0002g0008a0001c0002t0002g0071a0001c0002t0002g0073 | 5 | NA18747.hp1 NA18942.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.636-3530A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953304 | ||||||
chr1:32953374
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.636-3600A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953374 | ||||||
chr1:32953383
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.636-3609C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953383 | ||||||
chr1:32953605
|
C | T | 94 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(91): Show | 131 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.636-3831G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953605 | ||||||
chr1:32953641
|
T | C | 12 | a0001c0003t0001g0048a0001c0003t0003g0006a0001c0003t0003g0038others(9): Show | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.636-3867A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953641 | ||||||
chr1:32953901
|
C | CT | 20 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0131others(17): Show | 27 | HG00673.hp1 HG01106.hp2 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.636-4128dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953901 | ||||||
chr1:32953901
|
CT | C | 58 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0024others(55): Show | 65 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.636-4128delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953901 | ||||||
chr1:32953981
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.636-4207A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953981 | ||||||
chr1:32953983
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.636-4209T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953983 | ||||||
chr1:32954155
|
T | G | 50 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(47): Show | 83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.636-4381A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954155 | ||||||
chr1:32954249
|
T | C | 1 | a0001c0002t0002g0071 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.636-4475A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954249 | ||||||
chr1:32954319
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.636-4545A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954319 | ||||||
chr1:32954504
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0003g0093a0001c0001t0003g0094 | 3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.636-4730G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954504 | ||||||
chr1:32954520
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.636-4746G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954520 | ||||||
chr1:32954529
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0211 | 2 | HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.636-4755T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954529 | ||||||
chr1:32954570
|
C | T | 1 | a0001c0002t0002g0051 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.636-4796G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954570 | ||||||
chr1:32954591
|
T | C | 1 | a0001c0003t0003g0047 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.636-4817A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954591 | ||||||
chr1:32954738
|
C | CA | 45 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(42): Show | 67 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.636-4965dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954738 | ||||||
chr1:32954746
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.636-4972T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954746 | ||||||
chr1:32954751
|
A | C | 1 | a0001c0001t0003g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.636-4977T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954751 | ||||||
chr1:32954751
|
AAAC | A | 4 | a0001c0002t0002g0012a0001c0002t0002g0072a0001c0002t0002g0238others(1): Show | 6 | NA18947.hp2 NA18950.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.636-4980_636-4978d others(5): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954751 | ||||||
chr1:32954818
|
T | C | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-5044A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954818 | ||||||
chr1:32954836
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.636-5062T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954836 | ||||||
chr1:32954884
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.636-5110C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954884 | ||||||
chr1:32955331
|
T | C | 3 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0232 | 3 | HG01081.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.636-5557A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955331 | ||||||
chr1:32955533
|
C | G | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.636-5759G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955533 | ||||||
chr1:32955566
|
C | CA | 7 | a0001c0001t0001g0196a0002c0004t0004g0004a0002c0004t0004g0013others(4): Show | 14 | HG00621.hp2 HG00673.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.636-5793dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955566 | ||||||
chr1:32955579
|
T | A | 1 | a0001c0002t0002g0073 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.636-5805A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955579 | ||||||
chr1:32955653
|
G | A | 2 | a0001c0002t0002g0051a0001c0002t0002g0052 | 2 | NA18612.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.636-5879C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955653 | ||||||
chr1:32955730
|
C | T | 94 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(91): Show | 131 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.636-5956G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955730 | ||||||
chr1:32955748
|
C | CA | 8 | a0001c0001t0001g0025a0001c0001t0001g0197a0001c0001t0001g0198others(5): Show | 9 | HG02280.hp1 HG02809.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.636-5975dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955748 | ||||||
chr1:32955748
|
CA | C | 75 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0082others(72): Show | 112 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.636-5975delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955748 | ||||||
chr1:32955766
|
A | G | 1 | a0002c0004t0004g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.636-5992T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955766 | ||||||
chr1:32955860
|
T | C | 50 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(47): Show | 83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.636-6086A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955860 | ||||||
chr1:32955972
|
A | G | 9 | a0001c0001t0003g0016a0001c0001t0003g0096a0001c0001t0003g0097others(6): Show | 10 | HG01891.hp1 HG02647.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.636-6198T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955972 | ||||||
chr1:32956087
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.636-6313G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956087 | ||||||
chr1:32956124
|
G | C | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-6350C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956124 | ||||||
chr1:32956136
|
T | C | 4 | a0001c0001t0001g0082a0003c0005t0003g0028a0003c0005t0003g0029others(1): Show | 4 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.636-6362A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956136 | ||||||
chr1:32956177
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.636-6403G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956177 | ||||||
chr1:32956269
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.636-6495G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956269 | ||||||
chr1:32956344
|
T | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.636-6570A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956344 | ||||||
chr1:32956420
|
C | T | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-6646G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956420 | ||||||
chr1:32956743
|
G | GAA | 100 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(97): Show | 139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.636-6970_636-6969i others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956743 | ||||||
chr1:32956856
|
GC | G | 5 | a0001c0001t0003g0009a0001c0001t0003g0086a0001c0001t0003g0087others(2): Show | 7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.636-7083delG | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956856 | ||||||
chr1:32956978
|
G | C | 6 | a0002c0004t0004g0004a0002c0004t0004g0013a0002c0004t0004g0253others(3): Show | 13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+7073C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956978 | ||||||
chr1:32957074
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.635+6977T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957074 | ||||||
chr1:32957170
|
T | A | 1 | a0001c0001t0001g0203 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.635+6881A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957170 | ||||||
chr1:32957253
|
C | T | 6 | a0002c0004t0004g0004a0002c0004t0004g0013a0002c0004t0004g0253others(3): Show | 13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+6798G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957253 | ||||||
chr1:32957381
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.635+6670A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957381 | ||||||
chr1:32957605
|
G | A | 44 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.635+6446C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957605 | ||||||
chr1:32957758
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA18940.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.635+6293G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957758 | ||||||
chr1:32957759
|
G | A | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635+6292C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957759 | ||||||
chr1:32957774
|
C | T | 3 | a0003c0005t0003g0028a0003c0005t0003g0029a0003c0005t0003g0030 | 3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.635+6277G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957774 | ||||||
chr1:32957874
|
T | C | 5 | a0001c0001t0003g0009a0001c0001t0003g0086a0001c0001t0003g0087others(2): Show | 7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.635+6177A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957874 | ||||||
chr1:32958005
|
C | G | 1 | a0001c0001t0003g0109 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.635+6046G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958005 | ||||||
chr1:32958045
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.635+6006T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958045 | ||||||
chr1:32958066
|
A | G | 1 | a0001c0003t0001g0048 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.635+5985T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958066 | ||||||
chr1:32958135
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 7 | NA18942.hp1 NA18960.hp2 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.635+5916T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958135 | ||||||
chr1:32958224
|
C | T | 6 | a0002c0004t0004g0004a0002c0004t0004g0013a0002c0004t0004g0253others(3): Show | 13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+5827G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958224 | ||||||
chr1:32958231
|
T | C | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635+5820A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958231 | ||||||
chr1:32958245
|
T | C | 10 | a0001c0003t0001g0048a0001c0003t0003g0006a0001c0003t0003g0040others(7): Show | 12 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.635+5806A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958245 | ||||||
chr1:32958626
|
G | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | NA18983.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.635+5425C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958626 | ||||||
chr1:32958798
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0036 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.635+5253T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958798 | ||||||
chr1:32958808
|
A | C | 1 | a0001c0001t0003g0244 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.635+5243T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958808 | ||||||
chr1:32958928
|
G | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA18939.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.635+5123C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958928 | ||||||
chr1:32958971
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.635+5080T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958971 | ||||||
chr1:32959177
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.635+4874T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959177 | ||||||
chr1:32959360
|
G | A | 1 | a0001c0001t0004g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635+4691C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959360 | ||||||
chr1:32959744
|
A | G | 1 | a0001c0002t0002g0077 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.635+4307T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959744 | ||||||
chr1:32959807
|
G | A | 1 | a0001c0001t0004g0209 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.635+4244C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959807 | ||||||
chr1:32959845
|
A | G | 99 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(96): Show | 138 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.635+4206T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959845 | ||||||
chr1:32959881
|
C | CA | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0210others(6): Show | 9 | HG01175.hp2 HG02055.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.635+4169dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959881 | ||||||
chr1:32959881
|
CA | C | 90 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0083others(87): Show | 129 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.635+4169delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959881 | ||||||
chr1:32959952
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.635+4099C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959952 | ||||||
chr1:32960023
|
C | G | 3 | a0001c0001t0001g0095a0001c0001t0003g0093a0001c0001t0003g0094 | 3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635+4028G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960023 | ||||||
chr1:32960037
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.635+4014G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960037 | ||||||
chr1:32960060
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | HG00099.hp2 HG01192.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.635+3991T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960060 | ||||||
chr1:32960072
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.635+3979A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960072 | ||||||
chr1:32960091
|
A | G | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.635+3960T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960091 | ||||||
chr1:32960210
|
ATGG | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG01258.hp1 NA19030.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.635+3838_635+3840d others(5): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960210 | ||||||
chr1:32960501
|
T | A | 6 | a0001c0002t0002g0077a0001c0002t0002g0078a0001c0002t0002g0079others(3): Show | 6 | HG02071.hp1 HG02074.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.635+3550A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960501 | ||||||
chr1:32960794
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635+3257G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960794 | ||||||
chr1:32960899
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0006g0223 | 3 | NA18959.hp2 NA18961.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.635+3152C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960899 | ||||||
chr1:32961005
|
G | A | 94 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(91): Show | 131 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.635+3046C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961005 | ||||||
chr1:32961008
|
G | C | 1 | a0001c0001t0003g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.635+3043C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961008 | ||||||
chr1:32961015
|
CA | C | 99 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(96): Show | 138 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.635+3035delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961015 | ||||||
chr1:32961069
|
T | C | 42 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0095others(39): Show | 46 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.635+2982A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961069 | ||||||
chr1:32961106
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.635+2945A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961106 | ||||||
chr1:32961212
|
T | C | 5 | a0001c0001t0003g0009a0001c0001t0003g0086a0001c0001t0003g0087others(2): Show | 7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.635+2839A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961212 | ||||||
chr1:32961281
|
T | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | NA18974.hp1 NA18982.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.635+2770A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961281 | ||||||
chr1:32961355
|
G | T | 2 | a0001c0002t0002g0054a0001c0002t0002g0245 | 2 | NA19060.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.635+2696C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961355 | ||||||
chr1:32961375
|
A | C | 1 | a0001c0009t0003g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.635+2676T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961375 | ||||||
chr1:32961451
|
A | G | 5 | a0001c0001t0003g0009a0001c0001t0003g0086a0001c0001t0003g0087others(2): Show | 7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.635+2600T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961451 | ||||||
chr1:32961557
|
A | G | 101 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0091others(98): Show | 140 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.635+2494T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961557 | ||||||
chr1:32961630
|
T | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG03490.hp1 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.635+2421A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961630 | ||||||
chr1:32961719
|
A | G | 50 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(47): Show | 83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.635+2332T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961719 | ||||||
chr1:32961877
|
C | T | 1 | a0001c0002t0005g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.635+2174G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961877 | ||||||
chr1:32961975
|
G | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01074.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.635+2076C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961975 | ||||||
chr1:32961980
|
T | G | 2 | a0001c0001t0001g0232a0001c0009t0003g0257 | 2 | HG01081.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.635+2071A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961980 | ||||||
chr1:32962000
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.635+2051A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962000 | ||||||
chr1:32962197
|
G | C | 6 | a0002c0004t0004g0004a0002c0004t0004g0013a0002c0004t0004g0253others(3): Show | 13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+1854C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962197 | ||||||
chr1:32962248
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.635+1803G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962248 | ||||||
chr1:32962249
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.635+1802C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962249 | ||||||
chr1:32962428
|
G | T | 4 | a0001c0001t0001g0082a0003c0005t0003g0028a0003c0005t0003g0029others(1): Show | 4 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.635+1623C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962428 | ||||||
chr1:32962640
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.635+1411A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962640 | ||||||
chr1:32962768
|
GA | G | 51 | a0001c0001t0001g0247a0001c0002t0002g0001a0001c0002t0002g0007others(48): Show | 84 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.635+1282delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962768 | ||||||
chr1:32962807
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.635+1244C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962807 | ||||||
chr1:32963039
|
GA | G | 3 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0052 | 3 | NA18612.hp1 NA18969.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.635+1011delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963039 | ||||||
chr1:32963108
|
G | C | 3 | a0001c0002t0002g0012a0001c0002t0002g0238a0001c0002t0005g0239 | 5 | NA18947.hp2 NA18950.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+943C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963108 | ||||||
chr1:32963294
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.635+757G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963294 | ||||||
chr1:32963299
|
C | T | 12 | a0001c0003t0001g0048a0001c0003t0003g0006a0001c0003t0003g0038others(9): Show | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.635+752G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963299 | ||||||
chr1:32963335
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.635+716C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963335 | ||||||
chr1:32963424
|
T | A | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.635+627A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963424 | ||||||
chr1:32963444
|
G | A | 3 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0003g0243 | 3 | HG00639.hp1 HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.635+607C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963444 | ||||||
chr1:32963489
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.635+562C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963489 | ||||||
chr1:32963712
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.635+339G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963712 | ||||||
chr1:32963718
|
CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.635+319_635+332del others(14): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963718 | ||||||
chr1:32963783
|
C | CA | 6 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG01981.hp2 HG02071.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.635+267dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963783 | ||||||
chr1:32963807
|
C | G | 1 | a0001c0002t0002g0032 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.635+244G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963807 | ||||||
chr1:32963938
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.635+113C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963938 | ||||||
chr1:32964007
|
T | TCGGCTGC others(28): Show |
1 | a0001c0001t0003g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.635+9_635+43dupGGG others(32): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32964007 | ||||||
chr1:32964019
|
C | G | 1 | a0001c0002t0002g0031 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.635+32G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32964019 |