geneid | 22803 |
---|---|
ensemblid | ENSG00000088930.8 |
hgncid | 12836 |
symbol | XRN2 |
name | 5'-3' exoribonuclease 2 |
refseq_nuc | NM_012255.5 |
refseq_prot | NP_036387.2 |
ensembl_nuc | ENST00000377191.5 |
ensembl_prot | ENSP00000366396.3 |
mane_status | MANE Select |
chr | chr20 |
start | 21303331 |
end | 21389825 |
strand | + |
ver | v1.2 |
region | chr20:21303331-21389825 |
region5000 | chr20:21298331-21394825 |
regionname0 | XRN2_chr20_21303331_21389825 |
regionname5000 | XRN2_chr20_21298331_21394825 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 950 | 275 | 84 | 46 | 105 | 14 | 24 | 79 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0002 | 0/0 | 950 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0003 | 0/0 | 950 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2853 | 257 | 68 | 44 | 105 | 14 | 24 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
c0002 | 0/0 | 2853 | 16 | 15 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
c0003 | 0/0 | 2853 | 2 | 2 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
c0004 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
c0005 | 0/0 | 2853 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
c0006 | 0/0 | 2853 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 558 | 195 | 66 | 34 | 71 | 10 | 13 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
t0002 | 0/0 | 558 | 63 | 17 | 5 | 32 | 4 | 5 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
t0003 | 1/0 | 556 | 19 | 3 | 7 | 3 | 0 | 5 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
t0004 | 0/0 | 558 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2853 | 257 | 68 | 44 | 105 | 14 | 24 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0001c0002 | 0/0 | 2853 | 16 | 15 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0001c0004 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0001c0006 | 0/0 | 2853 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0002c0003 | 0/0 | 2853 | 2 | 2 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0003c0005 | 0/0 | 2853 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3410 | 175 | 48 | 32 | 71 | 10 | 13 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0001c0001t0002 | 0/0 | 3410 | 62 | 17 | 5 | 31 | 4 | 5 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0001c0001t0003 | 1/0 | 3408 | 19 | 3 | 7 | 3 | 0 | 5 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0001c0001t0004 | 0/0 | 3410 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0001c0002t0001 | 0/0 | 3410 | 16 | 15 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0001c0004t0001 | 0/0 | 3410 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0001c0006t0001 | 0/0 | 3410 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0002c0003t0001 | 0/0 | 3410 | 2 | 2 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
a0003c0005t0002 | 0/0 | 3410 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | copy fasta | chr20 | 21298331 | 21394825 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0001c0006t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0002c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0002c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
a0003c0005t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | GBR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0156 | EUR | GBR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0148 | EUR | GBR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | FIN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00639 | hp1 | a0001 | c0006 | t0001 | g0228 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0146 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CDX | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0035 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0104 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0097 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0268 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0269 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18963 | hp2 | a0003 | c0005 | t0002 | g0139 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | YRI | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ASW | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | USA | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | USA | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA21309 | hp1 | a0002 | c0003 | t0001 | g0176 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0225 | REF | REF | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0153 | REF | REF | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:21356665
|
A | G | 1 | a0002 | 2 | HG03209.hp1 NA21309.hp1 |
missense_variant&splice_region_variant | MODERATE | c.2198A>G | p.Gln733Arg | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 23/30 | 2266/3408 | 2198/2853 | 733/950 | chr20 | 21356665 | ||
chr20:21386972
|
A | G | 1 | a0003 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.2753A>G | p.Tyr918Cys | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/30 | 2821/3408 | 2753/2853 | 918/950 | chr20 | 21386972 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:21331620
|
T | C | 1 | a0001c0004 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.636T>C | p.Ile212Ile | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 7/30 | 704/3408 | 636/2853 | 212/950 | chr20 | 21331620 | ||
chr20:21333579
|
A | G | 1 | a0001c0006 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.894A>G | p.Glu298Glu | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 10/30 | 962/3408 | 894/2853 | 298/950 | chr20 | 21333579 | ||
chr20:21365603
|
C | T | 1 | a0001c0002 | 16 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
synonymous_variant | LOW | c.2355C>T | p.Asp785Asp | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/30 | 2423/3408 | 2355/2853 | 785/950 | chr20 | 21365603 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:21303376
|
G | A | 1 | a0001c0001t0004 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/30 | 23 | chr20 | 21303376 | |||||
chr20:21389696
|
C | CTT | 8 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*358_*359insTT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 30/30 | 359 | chr20 | 21389696 | |||||
chr20:21389808
|
G | C | 2 | a0001c0001t0002a0003c0005t0002 | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*470G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 30/30 | 470 | chr20 | 21389808 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:21303598
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(76): Show | 81 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.75+125T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21303598 | ||||||
chr20:21303824
|
CTGT | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00423.hp1 NA18944.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+357_75+359delTT others(1): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21303824 | |||||
chr20:21304065
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.75+592C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304065 | ||||||
chr20:21304127
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.75+654G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304127 | ||||||
chr20:21304196
|
T | G | 1 | a0001c0001t0001g0015 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.75+723T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304196 | ||||||
chr20:21304348
|
C | CT | 6 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0273others(3): Show | 6 | HG02622.hp1 HG03669.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+891dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21304348 | |||||
chr20:21304348
|
CT | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 59 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.75+891delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21304348 | |||||
chr20:21304453
|
C | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+980C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304453 | ||||||
chr20:21304459
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.75+986T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304459 | ||||||
chr20:21304620
|
T | C | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG02809.hp2 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1147T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304620 | ||||||
chr20:21305028
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.75+1555T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305028 | ||||||
chr20:21305249
|
A | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+1776A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305249 | ||||||
chr20:21305335
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(146): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.75+1862A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305335 | ||||||
chr20:21305415
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.75+1942C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305415 | ||||||
chr20:21305452
|
GCCATGTT others(2675): Show |
G | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(145): Show | 152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.75+1989_75+4670del | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305452 | |||||
chr20:21305483
|
G | C | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+2010G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305483 | ||||||
chr20:21305553
|
C | CT | 29 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+2103dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305553 | |||||
chr20:21305553
|
C | CTT | 5 | a0001c0001t0001g0206a0001c0001t0002g0202a0001c0001t0002g0203others(2): Show | 5 | HG01361.hp2 HG02965.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+2102_75+2103dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305553 | |||||
chr20:21305553
|
C | CTTTTT | 9 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118others(6): Show | 9 | HG00741.hp1 HG01256.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+2099_75+2103dup others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305553 | |||||
chr20:21305553
|
C | CTTTTTT | 5 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0125others(2): Show | 5 | HG00738.hp2 HG01192.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+2098_75+2103dup others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305553 | |||||
chr20:21305614
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.75+2141A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305614 | ||||||
chr20:21305747
|
CT | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(48): Show | 52 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.75+2290delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305747 | |||||
chr20:21305795
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.75+2322G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305795 | ||||||
chr20:21305808
|
C | T | 2 | a0001c0001t0003g0122a0001c0001t0003g0127 | 2 | NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.75+2335C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305808 | ||||||
chr20:21306134
|
G | GT | 5 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(2): Show | 5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+2671dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21306134 | |||||
chr20:21306159
|
C | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+2686C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21306159 | ||||||
chr20:21306206
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.75+2733G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21306206 | ||||||
chr20:21306241
|
G | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+2768G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21306241 | ||||||
chr20:21306893
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.75+3420C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21306893 | ||||||
chr20:21307071
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.75+3598C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21307071 | ||||||
chr20:21307073
|
C | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+3600C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21307073 | ||||||
chr20:21307359
|
T | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG00140.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.75+3886T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21307359 | ||||||
chr20:21307462
|
A | G | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.75+3989A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21307462 | ||||||
chr20:21308156
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(145): Show | 152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.75+4683T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308156 | ||||||
chr20:21308173
|
G | A | 5 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118others(2): Show | 5 | HG01192.hp2 HG01943.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+4700G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308173 | ||||||
chr20:21308279
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.75+4806G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308279 | ||||||
chr20:21308345
|
T | C | 1 | a0001c0001t0002g0136 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.75+4872T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308345 | ||||||
chr20:21308497
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.75+5024G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308497 | ||||||
chr20:21308497
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75+5024G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308497 | ||||||
chr20:21308631
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.75+5158A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308631 | ||||||
chr20:21308641
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(33): Show | 37 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.75+5168A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308641 | ||||||
chr20:21308674
|
G | A | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+5201G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308674 | ||||||
chr20:21308873
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+5400A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308873 | ||||||
chr20:21308924
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.75+5451G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308924 | ||||||
chr20:21308947
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+5474C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308947 | ||||||
chr20:21308964
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.75+5491A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308964 | ||||||
chr20:21309152
|
T | G | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.75+5679T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309152 | ||||||
chr20:21309223
|
A | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.75+5750A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309223 | ||||||
chr20:21309243
|
A | G | 1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+5770A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309243 | ||||||
chr20:21309668
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 16 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+6195G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309668 | ||||||
chr20:21309850
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.75+6377A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309850 | ||||||
chr20:21309947
|
A | G | 1 | a0001c0002t0001g0095 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.75+6474A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309947 | ||||||
chr20:21309964
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(33): Show | 37 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.75+6491C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309964 | ||||||
chr20:21309996
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.75+6523T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309996 | ||||||
chr20:21310263
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+6790C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310263 | ||||||
chr20:21310528
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.75+7055A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310528 | ||||||
chr20:21310784
|
G | A | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+7311G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310784 | ||||||
chr20:21310831
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.75+7358G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310831 | ||||||
chr20:21310842
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.75+7369T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310842 | ||||||
chr20:21310893
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.75+7420C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310893 | ||||||
chr20:21310986
|
C | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+7513C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310986 | ||||||
chr20:21311003
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.75+7530T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311003 | ||||||
chr20:21311200
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.75+7727C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311200 | ||||||
chr20:21311454
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+7981G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311454 | ||||||
chr20:21311590
|
G | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.75+8117G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311590 | ||||||
chr20:21311606
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | NA18995.hp1 NA19056.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+8133T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311606 | ||||||
chr20:21311625
|
T | C | 1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+8152T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311625 | ||||||
chr20:21311632
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+8159A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311632 | ||||||
chr20:21311721
|
C | T | 4 | a0001c0001t0002g0181a0001c0001t0002g0198a0001c0001t0002g0199others(1): Show | 4 | HG02965.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+8248C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311721 | ||||||
chr20:21312153
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.75+8680C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312153 | ||||||
chr20:21312173
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.75+8700C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312173 | ||||||
chr20:21312188
|
C | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8715C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312188 | ||||||
chr20:21312191
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8718C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312191 | ||||||
chr20:21312192
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8719A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312192 | ||||||
chr20:21312195
|
C | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8722C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312195 | ||||||
chr20:21312196
|
T | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8723T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312196 | ||||||
chr20:21312197
|
C | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8724C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312197 | ||||||
chr20:21312198
|
T | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8725T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312198 | ||||||
chr20:21312205
|
C | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8732C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312205 | ||||||
chr20:21312206
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8733A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312206 | ||||||
chr20:21312235
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8762C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312235 | ||||||
chr20:21312237
|
C | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8764C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312237 | ||||||
chr20:21312275
|
GCTAAGTT others(9): Show |
G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8803_75+8818del others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312275 | ||||||
chr20:21312293
|
T | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8820T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312293 | ||||||
chr20:21312297
|
T | G | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8824T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312297 | ||||||
chr20:21312299
|
T | A | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8826T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312299 | ||||||
chr20:21312302
|
T | A | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8829T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312302 | ||||||
chr20:21312324
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8851C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312324 | ||||||
chr20:21312325
|
C | CCGGTTAG others(16): Show |
1 | a0001c0001t0002g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8852_75+8853ins others(23): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312325 | ||||||
chr20:21312363
|
G | C | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.75+8890G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312363 | ||||||
chr20:21312391
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.75+8918G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312391 | ||||||
chr20:21312441
|
T | A | 2 | a0001c0001t0002g0138a0003c0005t0002g0139 | 2 | NA18963.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.75+8968T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312441 | ||||||
chr20:21312597
|
C | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.75+9124C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312597 | ||||||
chr20:21312602
|
A | AT | 8 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(5): Show | 8 | HG00423.hp2 HG00738.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+9153dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21312602 | |||||
chr20:21312602
|
AT | A | 28 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(25): Show | 28 | HG00558.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.75+9153delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21312602 | |||||
chr20:21312602
|
ATT | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(30): Show | 34 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+9152_75+9153del others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21312602 | |||||
chr20:21312602
|
ATTTTTTT others(2): Show |
A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(146): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.75+9145_75+9153del others(9): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21312602 | |||||
chr20:21312901
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+9428C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312901 | ||||||
chr20:21313178
|
C | T | 2 | a0001c0001t0002g0182a0001c0001t0002g0196 | 2 | NA19058.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.75+9705C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21313178 | ||||||
chr20:21313246
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.75+9773C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21313246 | ||||||
chr20:21313952
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.75+10479C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21313952 | ||||||
chr20:21314179
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.75+10706C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314179 | ||||||
chr20:21314277
|
T | C | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+10804T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314277 | ||||||
chr20:21314429
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.75+10956G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314429 | ||||||
chr20:21314588
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.75+11115G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314588 | ||||||
chr20:21314589
|
C | T | 2 | a0001c0001t0002g0083a0001c0001t0002g0195 | 2 | NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.75+11116C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314589 | ||||||
chr20:21314804
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.75+11331G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314804 | ||||||
chr20:21314871
|
G | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.75+11398G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314871 | ||||||
chr20:21314958
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.76-11321C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314958 | ||||||
chr20:21315012
|
C | G | 1 | a0001c0001t0002g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.76-11267C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315012 | ||||||
chr20:21315350
|
C | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-10929C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315350 | ||||||
chr20:21315487
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.76-10792G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315487 | ||||||
chr20:21315845
|
T | C | 1 | a0001c0001t0003g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76-10434T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315845 | ||||||
chr20:21315869
|
TC | T | 3 | a0001c0001t0003g0115a0001c0001t0003g0122a0001c0001t0003g0127 | 3 | HG03654.hp2 NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.76-10407delC | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21315869 | |||||
chr20:21315921
|
C | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.76-10358C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315921 | ||||||
chr20:21315991
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.76-10288G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315991 | ||||||
chr20:21315993
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.76-10286T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315993 | ||||||
chr20:21316001
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.76-10278G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316001 | ||||||
chr20:21316022
|
G | C | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.76-10257G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316022 | ||||||
chr20:21316042
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.76-10237C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316042 | ||||||
chr20:21316186
|
G | A | 1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.76-10093G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316186 | ||||||
chr20:21316670
|
C | A | 1 | a0001c0001t0003g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76-9609C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316670 | ||||||
chr20:21316741
|
T | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(16): Show | 20 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.76-9538T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316741 | ||||||
chr20:21316748
|
T | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(2): Show | 5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-9531T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316748 | ||||||
chr20:21316863
|
A | T | 3 | a0001c0001t0002g0165a0001c0001t0002g0173a0001c0001t0002g0174 | 3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.76-9416A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316863 | ||||||
chr20:21317031
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.76-9248A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317031 | ||||||
chr20:21317047
|
C | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.76-9232C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317047 | ||||||
chr20:21317301
|
AT | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(152): Show | 159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.76-8967delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21317301 | |||||
chr20:21317340
|
C | T | 1 | a0002c0003t0001g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.76-8939C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317340 | ||||||
chr20:21317496
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.76-8783T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317496 | ||||||
chr20:21317564
|
G | T | 1 | a0001c0002t0001g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.76-8715G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317564 | ||||||
chr20:21317808
|
C | T | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-8471C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317808 | ||||||
chr20:21318076
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0002g0165a0001c0001t0002g0173others(1): Show | 4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-8203C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318076 | ||||||
chr20:21318093
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(149): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.76-8186T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318093 | ||||||
chr20:21318094
|
G | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(149): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.76-8185G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318094 | ||||||
chr20:21318385
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.76-7894A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318385 | ||||||
chr20:21318399
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0172 | 2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.76-7880A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318399 | ||||||
chr20:21318412
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.76-7867C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318412 | ||||||
chr20:21318536
|
T | TTA | 8 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(5): Show | 8 | HG01934.hp2 HG01943.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-7742_76-7741ins others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21318536 | |||||
chr20:21318544
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.76-7735G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318544 | ||||||
chr20:21318603
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.76-7676G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318603 | ||||||
chr20:21318716
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.76-7563A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318716 | ||||||
chr20:21318762
|
A | T | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.76-7517A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318762 | ||||||
chr20:21318861
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.76-7418C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318861 | ||||||
chr20:21319024
|
T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-7255T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319024 | ||||||
chr20:21319241
|
C | T | 1 | a0001c0001t0003g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76-7038C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319241 | ||||||
chr20:21319302
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-6977C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319302 | ||||||
chr20:21319392
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.76-6887G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319392 | ||||||
chr20:21319493
|
T | C | 1 | a0001c0001t0003g0113 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.76-6786T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319493 | ||||||
chr20:21319586
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.76-6693A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319586 | ||||||
chr20:21319617
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.76-6662C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319617 | ||||||
chr20:21319751
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.76-6528G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319751 | ||||||
chr20:21320029
|
T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-6250T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320029 | ||||||
chr20:21320066
|
C | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-6213C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320066 | ||||||
chr20:21320137
|
T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-6142T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320137 | ||||||
chr20:21320264
|
CATTTATT others(9): Show |
C | 5 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(2): Show | 5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-5984_76-5969del others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320264 | |||||
chr20:21320267
|
T | TTATTTAT others(5): Show |
139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(136): Show | 143 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.76-6000_76-5989dup others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320267 | |||||
chr20:21320279
|
G | GTATT | 15 | a0001c0001t0003g0112a0001c0001t0003g0114a0001c0001t0003g0115others(12): Show | 15 | HG00738.hp2 HG01192.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-5988_76-5985dup others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320279 | |||||
chr20:21320279
|
G | GTATTTAT others(9): Show |
12 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0040others(9): Show | 12 | HG02148.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-5989_76-5988ins others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320279 | |||||
chr20:21320279
|
G | GTATTTAT others(17): Show |
1 | a0001c0001t0001g0219 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.76-5989_76-5988ins others(24): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320279 | |||||
chr20:21320295
|
G | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.76-5984G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320295 | ||||||
chr20:21320540
|
C | G | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-5739C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320540 | ||||||
chr20:21320722
|
G | C | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-5557G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320722 | ||||||
chr20:21320815
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.76-5464C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320815 | ||||||
chr20:21320839
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.76-5440C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320839 | ||||||
chr20:21321058
|
C | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-5221C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321058 | ||||||
chr20:21321078
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.76-5201C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321078 | ||||||
chr20:21321207
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.76-5072A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321207 | ||||||
chr20:21321240
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.76-5039C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321240 | ||||||
chr20:21321256
|
G | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-5023G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321256 | ||||||
chr20:21321263
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.76-5016G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321263 | ||||||
chr20:21321301
|
C | CTG | 19 | a0001c0001t0001g0046a0001c0001t0002g0156a0001c0001t0002g0157others(16): Show | 19 | HG00099.hp2 HG00738.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-4930_76-4929dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
C | CTGTG | 6 | a0001c0001t0002g0138a0001c0001t0002g0140a0001c0001t0002g0163others(3): Show | 6 | HG01981.hp1 NA18941.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-4932_76-4929dup others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
C | CTGTGTGT others(3): Show |
1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.76-4938_76-4929dup others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
CTG | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 39 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.76-4930_76-4929del others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
CTGTG | C | 47 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0016others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.76-4932_76-4929del others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
CTGTGTG | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 115 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.76-4934_76-4929del others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
CTGTGTGT others(1): Show |
C | 11 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0096others(8): Show | 11 | HG00280.hp2 HG00639.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-4936_76-4929del others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
CTGTGTGT others(3): Show |
C | 12 | a0001c0001t0001g0135a0001c0001t0001g0207a0001c0001t0001g0211others(9): Show | 12 | HG00639.hp2 HG01074.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-4938_76-4929del others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0220 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76-4940_76-4929del others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
CTGTGTGT others(9): Show |
C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-4944_76-4929del others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
CTGTGTGT others(11): Show |
C | 3 | a0001c0001t0001g0206a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG01167.hp1 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.76-4946_76-4929del others(18): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321301
|
CTGTGTGT others(25): Show |
C | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.76-4960_76-4929del others(32): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | |||||
chr20:21321353
|
G | A | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-4926G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321353 | ||||||
chr20:21321358
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0105others(36): Show | 40 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.76-4921C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321358 | ||||||
chr20:21321689
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.76-4590G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321689 | ||||||
chr20:21321713
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.76-4566G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321713 | ||||||
chr20:21321772
|
T | G | 2 | a0001c0001t0002g0191a0001c0001t0002g0202 | 2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.76-4507T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321772 | ||||||
chr20:21321814
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | NA18946.hp2 NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.76-4465G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321814 | ||||||
chr20:21321847
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.76-4432T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321847 | ||||||
chr20:21321851
|
A | G | 3 | a0001c0001t0001g0227a0001c0001t0001g0230a0001c0001t0001g0256 | 3 | HG00280.hp2 HG00639.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.76-4428A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321851 | ||||||
chr20:21321927
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.76-4352C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321927 | ||||||
chr20:21321943
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.76-4336T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321943 | ||||||
chr20:21322009
|
T | G | 1 | a0001c0001t0002g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-4270T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322009 | ||||||
chr20:21322096
|
C | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-4183C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322096 | ||||||
chr20:21322247
|
G | A | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-4032G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322247 | ||||||
chr20:21322299
|
C | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-3980C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322299 | ||||||
chr20:21322732
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.76-3547C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322732 | ||||||
chr20:21322802
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.76-3477A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322802 | ||||||
chr20:21322867
|
A | G | 1 | a0001c0001t0003g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.76-3412A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322867 | ||||||
chr20:21324192
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0029 | 3 | NA18991.hp2 NA19064.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.76-2087A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324192 | ||||||
chr20:21324202
|
A | G | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG00140.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.76-2077A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324202 | ||||||
chr20:21324497
|
C | CT | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 114 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.76-1769dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21324497 | |||||
chr20:21324497
|
C | CTT | 38 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 39 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.76-1770_76-1769dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21324497 | |||||
chr20:21324514
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.76-1765C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324514 | ||||||
chr20:21324670
|
G | C | 1 | a0001c0001t0002g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.76-1609G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324670 | ||||||
chr20:21324762
|
T | C | 15 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0086others(12): Show | 15 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-1517T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324762 | ||||||
chr20:21324776
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.76-1503C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324776 | ||||||
chr20:21325393
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.76-886G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325393 | ||||||
chr20:21325499
|
T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-780T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325499 | ||||||
chr20:21325609
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.76-670G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325609 | ||||||
chr20:21325653
|
G | T | 1 | a0001c0001t0002g0195 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.76-626G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325653 | ||||||
chr20:21325675
|
A | G | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.76-604A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325675 | ||||||
chr20:21325819
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.76-460A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325819 | ||||||
chr20:21325857
|
T | G | 1 | a0001c0001t0001g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.76-422T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325857 | ||||||
chr20:21326469
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.204-21A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 2/29 | chr20 | 21326469 | ||||||
chr20:21326813
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.315+212G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21326813 | ||||||
chr20:21327058
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.315+457G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327058 | ||||||
chr20:21327066
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0105others(54): Show | 58 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.315+465G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327066 | ||||||
chr20:21327090
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.315+489C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327090 | ||||||
chr20:21327116
|
C | T | 4 | a0001c0001t0002g0136a0001c0001t0002g0147a0001c0001t0002g0166others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+515C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327116 | ||||||
chr20:21327173
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.315+572G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327173 | ||||||
chr20:21327243
|
G | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(2): Show | 5 | HG00423.hp1 NA18944.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+642G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327243 | ||||||
chr20:21327480
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.315+879G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327480 | ||||||
chr20:21327884
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.316-675A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327884 | ||||||
chr20:21327934
|
A | C | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.316-625A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327934 | ||||||
chr20:21328174
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(145): Show | 152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.316-385G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21328174 | ||||||
chr20:21328832
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.427+162A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21328832 | ||||||
chr20:21329123
|
C | T | 6 | a0001c0001t0002g0083a0001c0001t0002g0141a0001c0001t0002g0142others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.427+453C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329123 | ||||||
chr20:21329188
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(2): Show | 5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.427+518G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329188 | ||||||
chr20:21329516
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.427+846C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329516 | ||||||
chr20:21329677
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.428-804C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329677 | ||||||
chr20:21329698
|
AATAGTG | A | 5 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0170others(2): Show | 5 | HG01891.hp1 HG02976.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-778_428-773del others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329698 | |||||
chr20:21329770
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0024others(1): Show | 4 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-711G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329770 | ||||||
chr20:21329835
|
CA | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(149): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.428-640delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329835 | |||||
chr20:21329856
|
G | GGT | 24 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0128others(21): Show | 24 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.428-584_428-583dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329856
|
G | GGTGT | 8 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0110others(5): Show | 8 | HG01934.hp1 HG01975.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-586_428-583dup others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329856
|
G | GGTGTGT | 6 | a0001c0001t0001g0178a0001c0001t0001g0271a0001c0001t0002g0143others(3): Show | 6 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-588_428-583dup others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329856
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0270 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.428-596_428-583dup others(14): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329856
|
GGT | G | 35 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0037others(32): Show | 35 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.428-584_428-583del others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329856
|
GGTGT | G | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 78 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.428-586_428-583del others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329856
|
GGTGTGT | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0040others(52): Show | 56 | HG00280.hp2 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.428-588_428-583del others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329856
|
GGTGTGTG others(1): Show |
G | 7 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0023others(4): Show | 8 | HG01884.hp2 HG02015.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.428-590_428-583del others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329856
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0002g0136 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.428-592_428-583del others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329856
|
GGTGTGTG others(5): Show |
G | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG00423.hp1 HG03239.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-594_428-583del others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | |||||
chr20:21329908
|
C | T | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.428-573C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329908 | ||||||
chr20:21330204
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.428-277A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21330204 | ||||||
chr20:21330367
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.428-114C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21330367 | ||||||
chr20:21330468
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.428-13C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21330468 | ||||||
chr20:21331003
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.576+298A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | chr20 | 21331003 | ||||||
chr20:21331268
|
G | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.577-293G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | chr20 | 21331268 | ||||||
chr20:21331350
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.577-211C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | chr20 | 21331350 | ||||||
chr20:21331399
|
T | TCA | 19 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0108others(16): Show | 19 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.577-124_577-123dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | |||||
chr20:21331399
|
T | TCACA | 17 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0128others(14): Show | 18 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.577-126_577-123dup others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | |||||
chr20:21331399
|
T | TCACACA | 5 | a0001c0001t0001g0134a0001c0001t0001g0270a0001c0001t0001g0271others(2): Show | 5 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.577-128_577-123dup others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | |||||
chr20:21331399
|
TCA | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(103): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.577-124_577-123del others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | |||||
chr20:21331399
|
TCACA | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(38): Show | 41 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.577-126_577-123del others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | |||||
chr20:21331399
|
TCACACA | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(11): Show | 14 | HG00621.hp2 HG00673.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.577-128_577-123del others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | |||||
chr20:21331470
|
T | C | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.577-91T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | chr20 | 21331470 | ||||||
chr20:21331644
|
C | T | 3 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0205 | 3 | HG02965.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.649+11C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 7/29 | chr20 | 21331644 | ||||||
chr20:21331650
|
A | G | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.649+17A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 7/29 | chr20 | 21331650 | ||||||
chr20:21331687
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(33): Show | 37 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.649+54G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 7/29 | chr20 | 21331687 | ||||||
chr20:21332015
|
C | G | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.700+197C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 8/29 | chr20 | 21332015 | ||||||
chr20:21332206
|
G | T | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.701-77G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 8/29 | chr20 | 21332206 | ||||||
chr20:21332255
|
C | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(15): Show | 19 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.701-28C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 8/29 | chr20 | 21332255 | ||||||
chr20:21332471
|
T | TA | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(147): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.858+42dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 21332471 | |||||
chr20:21332743
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.858+303C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21332743 | ||||||
chr20:21332806
|
T | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.858+366T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21332806 | ||||||
chr20:21332880
|
A | G | 4 | a0001c0001t0002g0181a0001c0001t0002g0198a0001c0001t0002g0199others(1): Show | 4 | HG02965.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+440A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21332880 | ||||||
chr20:21332994
|
G | T | 1 | a0001c0001t0002g0146 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.859-550G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21332994 | ||||||
chr20:21333019
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.859-525G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333019 | ||||||
chr20:21333021
|
G | C | 1 | a0001c0001t0001g0015 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.859-523G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333021 | ||||||
chr20:21333137
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.859-407C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333137 | ||||||
chr20:21333199
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.859-345A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333199 | ||||||
chr20:21333201
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.859-343C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333201 | ||||||
chr20:21333217
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.859-327G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333217 | ||||||
chr20:21333441
|
T | C | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.859-103T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333441 | ||||||
chr20:21333457
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.859-87G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333457 | ||||||
chr20:21333503
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.859-41C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333503 | ||||||
chr20:21333521
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.859-23C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333521 | ||||||
chr20:21333538
|
T | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 16 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.859-6T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333538 | ||||||
chr20:21333902
|
G | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG02896.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068-35G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 11/29 | chr20 | 21333902 | ||||||
chr20:21334218
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1233+33C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334218 | ||||||
chr20:21334444
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1233+259C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334444 | ||||||
chr20:21334493
|
A | G | 2 | a0001c0001t0001g0253a0001c0004t0001g0104 | 2 | HG02976.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1233+308A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334493 | ||||||
chr20:21334595
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1233+410G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334595 | ||||||
chr20:21334933
|
AGAG | A | 15 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0086others(12): Show | 15 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1233+749_1233+751d others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334933 | ||||||
chr20:21335022
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1233+837T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335022 | ||||||
chr20:21335151
|
A | T | 1 | a0001c0001t0003g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1233+966A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335151 | ||||||
chr20:21335281
|
G | A | 4 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+1096G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335281 | ||||||
chr20:21335516
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1233+1331G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335516 | ||||||
chr20:21335562
|
G | C | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1233+1377G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335562 | ||||||
chr20:21335736
|
T | C | 1 | a0001c0001t0003g0115 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1233+1551T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335736 | ||||||
chr20:21335898
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1233+1713G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335898 | ||||||
chr20:21335961
|
C | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1233+1776C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335961 | ||||||
chr20:21336335
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1233+2150G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21336335 | ||||||
chr20:21336851
|
G | A | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1234-2193G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21336851 | ||||||
chr20:21336860
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1234-2184T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21336860 | ||||||
chr20:21337210
|
A | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1234-1834A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21337210 | ||||||
chr20:21337212
|
G | T | 1 | a0001c0001t0001g0208 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1234-1832G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21337212 | ||||||
chr20:21337263
|
A | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(32): Show | 36 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1234-1781A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21337263 | ||||||
chr20:21337285
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1234-1759G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21337285 | ||||||
chr20:21338060
|
T | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1234-984T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338060 | ||||||
chr20:21338188
|
A | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1234-856A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338188 | ||||||
chr20:21338339
|
A | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0047others(29): Show | 32 | HG00621.hp2 HG00673.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1234-705A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338339 | ||||||
chr20:21338340
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1234-704G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338340 | ||||||
chr20:21338623
|
T | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 222 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1234-421T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338623 | ||||||
chr20:21338731
|
T | C | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1234-313T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338731 | ||||||
chr20:21338896
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1234-148T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338896 | ||||||
chr20:21338910
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1234-134G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338910 | ||||||
chr20:21339180
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1278+92A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339180 | ||||||
chr20:21339190
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 250 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1278+102A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339190 | ||||||
chr20:21339611
|
G | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1278+523G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339611 | ||||||
chr20:21339697
|
C | A | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0237others(2): Show | 5 | HG00735.hp1 HG02723.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+609C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339697 | ||||||
chr20:21339916
|
A | C | 4 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0268others(1): Show | 4 | HG01256.hp1 HG02683.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279-805A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339916 | ||||||
chr20:21339966
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1279-755A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339966 | ||||||
chr20:21340015
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1279-706T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21340015 | ||||||
chr20:21340255
|
A | C | 1 | a0001c0001t0004g0035 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1279-466A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21340255 | ||||||
chr20:21340656
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 221 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1279-65C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21340656 | ||||||
chr20:21340696
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1279-25T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21340696 | ||||||
chr20:21341054
|
C | CGTA | 19 | a0001c0001t0001g0075a0001c0001t0003g0112a0001c0001t0003g0113others(16): Show | 19 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1410+204_1410+206d others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr20 | 21341054 | |||||
chr20:21341264
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1410+412G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341264 | ||||||
chr20:21341572
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1410+720C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341572 | ||||||
chr20:21341584
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1410+732G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341584 | ||||||
chr20:21341652
|
A | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1410+800A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341652 | ||||||
chr20:21341653
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1410+801C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341653 | ||||||
chr20:21341654
|
A | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1410+802A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341654 | ||||||
chr20:21341655
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1410+803C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341655 | ||||||
chr20:21342320
|
C | T | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG01069.hp2 HG02683.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1410+1468C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342320 | ||||||
chr20:21342342
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1410+1490A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342342 | ||||||
chr20:21342438
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1410+1586C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342438 | ||||||
chr20:21342755
|
C | T | 2 | a0001c0002t0001g0085a0001c0002t0001g0086 | 2 | HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1411-1335C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342755 | ||||||
chr20:21342907
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1411-1183G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342907 | ||||||
chr20:21342976
|
A | T | 1 | a0001c0001t0001g0039 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1411-1114A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342976 | ||||||
chr20:21343356
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0109 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1411-734G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343356 | ||||||
chr20:21343410
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1411-680C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343410 | ||||||
chr20:21343820
|
T | G | 1 | a0001c0001t0001g0264 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1411-270T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343820 | ||||||
chr20:21343872
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1411-218G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343872 | ||||||
chr20:21343884
|
A | G | 1 | a0001c0002t0001g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1411-206A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343884 | ||||||
chr20:21344251
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0023others(6): Show | 10 | HG01978.hp1 HG02004.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.1529+43A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344251 | ||||||
chr20:21344382
|
A | T | 1 | a0001c0001t0002g0162 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1529+174A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344382 | ||||||
chr20:21344384
|
G | A | 1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1529+176G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344384 | ||||||
chr20:21344560
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1529+352T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344560 | ||||||
chr20:21344584
|
T | G | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1529+376T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344584 | ||||||
chr20:21344667
|
A | C | 1 | a0001c0001t0003g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1529+459A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344667 | ||||||
chr20:21344796
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0241a0001c0001t0001g0255 | 3 | HG00099.hp1 HG01496.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1529+588C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344796 | ||||||
chr20:21344965
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1529+757C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344965 | ||||||
chr20:21344983
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1529+775C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344983 | ||||||
chr20:21345073
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1529+865T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345073 | ||||||
chr20:21345222
|
G | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1529+1014G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345222 | ||||||
chr20:21345355
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1530-1060A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345355 | ||||||
chr20:21345429
|
G | C | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1530-986G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345429 | ||||||
chr20:21345460
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1530-955T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345460 | ||||||
chr20:21345940
|
AT | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1530-468delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr20 | 21345940 | |||||
chr20:21346044
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1530-371T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21346044 | ||||||
chr20:21346127
|
G | A | 1 | a0002c0003t0001g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1530-288G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21346127 | ||||||
chr20:21346152
|
A | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0066 | 3 | HG02572.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1530-263A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21346152 | ||||||
chr20:21346240
|
C | T | 7 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0068others(4): Show | 7 | HG00621.hp2 HG02132.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530-175C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21346240 | ||||||
chr20:21346568
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1665+18T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346568 | ||||||
chr20:21346611
|
C | T | 1 | a0002c0003t0001g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1665+61C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346611 | ||||||
chr20:21346632
|
G | C | 1 | a0001c0001t0002g0181 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1665+82G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346632 | ||||||
chr20:21346807
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1665+257C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346807 | ||||||
chr20:21346867
|
T | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1665+317T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346867 | ||||||
chr20:21347004
|
G | A | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1665+454G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347004 | ||||||
chr20:21347071
|
T | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1665+521T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347071 | ||||||
chr20:21347079
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1665+529A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347079 | ||||||
chr20:21347263
|
C | T | 1 | a0001c0001t0001g0225 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1665+713C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347263 | ||||||
chr20:21347269
|
T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1665+719T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347269 | ||||||
chr20:21347549
|
C | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1666-597C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347549 | ||||||
chr20:21347648
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1666-498A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347648 | ||||||
chr20:21347740
|
G | A | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1666-406G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347740 | ||||||
chr20:21347749
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0105others(54): Show | 58 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1666-397C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347749 | ||||||
chr20:21347789
|
G | A | 1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1666-357G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347789 | ||||||
chr20:21348077
|
GT | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1666-61delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr20 | 21348077 | |||||
chr20:21348314
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(31): Show | 35 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1774-27G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 18/29 | chr20 | 21348314 | ||||||
chr20:21348329
|
T | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1774-12T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 18/29 | chr20 | 21348329 | ||||||
chr20:21348811
|
T | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(15): Show | 19 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1863+381T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21348811 | ||||||
chr20:21348871
|
G | A | 32 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0047others(29): Show | 32 | HG00621.hp2 HG00673.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1863+441G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21348871 | ||||||
chr20:21348904
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1863+474A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21348904 | ||||||
chr20:21348949
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1864-440A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21348949 | ||||||
chr20:21349142
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1864-247T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21349142 | ||||||
chr20:21349312
|
A | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(32): Show | 36 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1864-77A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21349312 | ||||||
chr20:21349476
|
T | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 38 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1936+15T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21349476 | ||||||
chr20:21349537
|
T | G | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1936+76T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21349537 | ||||||
chr20:21349664
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1936+203G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21349664 | ||||||
chr20:21349677
|
T | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1936+216T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21349677 | ||||||
chr20:21350225
|
A | G | 1 | a0001c0001t0001g0225 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1936+764A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350225 | ||||||
chr20:21350298
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | NA18995.hp1 NA19056.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936+837G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350298 | ||||||
chr20:21350353
|
C | T | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1936+892C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350353 | ||||||
chr20:21350394
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1936+933C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350394 | ||||||
chr20:21350395
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1936+934G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350395 | ||||||
chr20:21350399
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1936+938G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350399 | ||||||
chr20:21350404
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1936+943T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350404 | ||||||
chr20:21350441
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1936+980G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350441 | ||||||
chr20:21350504
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1936+1043C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350504 | ||||||
chr20:21350525
|
C | CA | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(75): Show | 80 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1936+1092dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | |||||
chr20:21350525
|
C | CAA | 26 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0047others(23): Show | 27 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1936+1091_1936+109 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | |||||
chr20:21350525
|
CA | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(30): Show | 34 | HG00323.hp1 HG00558.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1936+1092delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | |||||
chr20:21350525
|
CAA | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG00423.hp1 HG01891.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1936+1091_1936+109 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | |||||
chr20:21350525
|
CAAA | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0128others(29): Show | 33 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1936+1090_1936+109 others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | |||||
chr20:21350525
|
CAAAA | C | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(6): Show | 9 | HG01975.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1936+1089_1936+109 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | |||||
chr20:21350525
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1936+1081_1936+109 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | |||||
chr20:21350525
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1936+1077_1936+109 others(20): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | |||||
chr20:21350695
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1936+1234T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350695 | ||||||
chr20:21350734
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1936+1273G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350734 | ||||||
chr20:21350768
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1936+1307C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350768 | ||||||
chr20:21350796
|
T | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA18962.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1936+1335T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350796 | ||||||
chr20:21350903
|
T | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(149): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1936+1442T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350903 | ||||||
chr20:21351041
|
A | G | 1 | a0001c0002t0001g0095 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1936+1580A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351041 | ||||||
chr20:21351224
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1936+1763T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351224 | ||||||
chr20:21351264
|
T | C | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1936+1803T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351264 | ||||||
chr20:21351627
|
G | A | 2 | a0001c0001t0002g0156a0001c0001t0002g0157 | 2 | HG00099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1936+2166G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351627 | ||||||
chr20:21351709
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1936+2248C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351709 | ||||||
chr20:21351811
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1936+2350A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351811 | ||||||
chr20:21352016
|
C | T | 1 | a0001c0006t0001g0228 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1936+2555C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352016 | ||||||
chr20:21352024
|
G | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(149): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1936+2563G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352024 | ||||||
chr20:21352071
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1936+2610A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352071 | ||||||
chr20:21352228
|
A | G | 18 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0003g0114others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1937-2561A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352228 | ||||||
chr20:21352279
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1937-2510A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352279 | ||||||
chr20:21352432
|
A | G | 1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1937-2357A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352432 | ||||||
chr20:21352448
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1937-2341T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352448 | ||||||
chr20:21352573
|
C | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1937-2216C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352573 | ||||||
chr20:21352804
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1937-1985A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352804 | ||||||
chr20:21353013
|
G | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1937-1776G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353013 | ||||||
chr20:21353030
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(149): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1937-1759G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353030 | ||||||
chr20:21353223
|
G | GAT | 8 | a0001c0001t0001g0105a0001c0001t0002g0170a0001c0001t0002g0199others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1937-1525_1937-152 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353223
|
G | GATAT | 5 | a0001c0001t0001g0175a0001c0002t0001g0085a0001c0002t0001g0094others(2): Show | 5 | HG02965.hp2 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1937-1527_1937-152 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353223
|
GAT | G | 11 | a0001c0001t0001g0132a0001c0001t0002g0146a0001c0001t0002g0158others(8): Show | 11 | HG00738.hp2 HG01192.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1937-1525_1937-152 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353223
|
GATAT | G | 17 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0131others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1937-1527_1937-152 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353223
|
GATATAT | G | 27 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0107others(24): Show | 28 | HG00438.hp1 HG00735.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1937-1529_1937-152 others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353223
|
GATATATA others(1): Show |
G | 19 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0162others(16): Show | 19 | HG00423.hp2 HG00558.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1937-1531_1937-152 others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353223
|
GATATATA others(3): Show |
G | 17 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0002g0083others(14): Show | 17 | HG00099.hp2 HG00741.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1937-1533_1937-152 others(14): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353223
|
GATATATA others(5): Show |
G | 3 | a0001c0001t0002g0136a0001c0001t0002g0145a0001c0001t0002g0181 | 3 | HG02257.hp2 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1937-1535_1937-152 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353223
|
GATATATA others(9): Show |
G | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1937-1539_1937-152 others(20): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353223
|
GATATATA others(23): Show |
G | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1937-1553_1937-152 others(34): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | |||||
chr20:21353240
|
ATATATAT others(19): Show |
A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(147): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1937-1547_1937-152 others(30): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353240 | |||||
chr20:21353242
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1937-1545_1937-152 others(28): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353242 | |||||
chr20:21353252
|
ATATATAT others(7): Show |
A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1937-1535_1937-152 others(18): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353252 | |||||
chr20:21353266
|
C | A | 1 | a0001c0002t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1937-1523C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353266 | ||||||
chr20:21353301
|
A | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1937-1488A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353301 | ||||||
chr20:21353794
|
T | TA | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(142): Show | 149 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1937-979dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353794 | |||||
chr20:21353817
|
T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1937-972T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353817 | ||||||
chr20:21353824
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1937-965G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353824 | ||||||
chr20:21353889
|
C | T | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1937-900C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353889 | ||||||
chr20:21354014
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1937-775T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354014 | ||||||
chr20:21354034
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0109 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1937-755C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354034 | ||||||
chr20:21354159
|
T | A | 4 | a0001c0001t0001g0096a0001c0001t0001g0135a0002c0003t0001g0097others(1): Show | 4 | HG03209.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1937-630T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354159 | ||||||
chr20:21354264
|
TTAG | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1937-521_1937-519d others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21354264 | |||||
chr20:21354326
|
A | T | 56 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.1937-463A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354326 | ||||||
chr20:21354414
|
A | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1937-375A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354414 | ||||||
chr20:21354475
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1937-314T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354475 | ||||||
chr20:21354591
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1937-198G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354591 | ||||||
chr20:21355126
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2020+254C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355126 | ||||||
chr20:21355162
|
C | T | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2020+290C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355162 | ||||||
chr20:21355367
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2020+495C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355367 | ||||||
chr20:21355674
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2021-406C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355674 | ||||||
chr20:21355705
|
T | A | 4 | a0001c0001t0001g0217a0001c0001t0001g0244a0001c0001t0002g0166others(1): Show | 4 | HG02273.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2021-375T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355705 | ||||||
chr20:21355771
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2021-309T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355771 | ||||||
chr20:21356186
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2118+9C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 22/29 | chr20 | 21356186 | ||||||
chr20:21356187
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.2118+10G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 22/29 | chr20 | 21356187 | ||||||
chr20:21356430
|
T | G | 3 | a0001c0001t0002g0165a0001c0001t0002g0173a0001c0001t0002g0174 | 3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2119-156T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 22/29 | chr20 | 21356430 | ||||||
chr20:21356755
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2198+90A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 23/29 | chr20 | 21356755 | ||||||
chr20:21356867
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2198+202G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 23/29 | chr20 | 21356867 | ||||||
chr20:21357138
|
G | GT | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2198+474dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 21357138 | |||||
chr20:21358063
|
G | T | 2 | a0001c0002t0001g0088a0001c0002t0001g0094 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2255+271G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21358063 | ||||||
chr20:21358703
|
G | C | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2255+911G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21358703 | ||||||
chr20:21358748
|
CGTTTATC others(17): Show |
C | 3 | a0001c0001t0002g0165a0001c0001t0002g0173a0001c0001t0002g0174 | 3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2255+969_2255+992d others(26): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21358748 | |||||
chr20:21358760
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2255+968C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21358760 | ||||||
chr20:21358950
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2255+1158C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21358950 | ||||||
chr20:21359078
|
A | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0219 | 2 | NA19000.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2255+1286A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359078 | ||||||
chr20:21359124
|
G | A | 62 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2255+1332G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359124 | ||||||
chr20:21359219
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2255+1427A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359219 | ||||||
chr20:21359253
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0135 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2255+1461C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359253 | ||||||
chr20:21359254
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2255+1462G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359254 | ||||||
chr20:21359365
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2255+1573T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359365 | ||||||
chr20:21359409
|
G | T | 1 | a0001c0001t0003g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2255+1617G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359409 | ||||||
chr20:21359468
|
C | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2255+1676C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359468 | ||||||
chr20:21359524
|
C | CA | 63 | a0001c0001t0001g0244a0001c0001t0001g0262a0001c0001t0002g0083others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2255+1746dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21359524 | |||||
chr20:21359834
|
A | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2255+2042A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359834 | ||||||
chr20:21359913
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2255+2121A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359913 | ||||||
chr20:21360061
|
A | G | 62 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2255+2269A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21360061 | ||||||
chr20:21360353
|
C | T | 63 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2255+2561C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21360353 | ||||||
chr20:21360457
|
G | GT | 18 | a0001c0001t0001g0022a0001c0001t0001g0175a0001c0001t0001g0179others(15): Show | 18 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2255+2679dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21360457 | |||||
chr20:21360695
|
A | AT | 17 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(14): Show | 18 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2255+2909dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21360695 | |||||
chr20:21361348
|
T | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2255+3556T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361348 | ||||||
chr20:21361695
|
A | G | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2256-3726A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361695 | ||||||
chr20:21361740
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2256-3681T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361740 | ||||||
chr20:21361840
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2256-3581A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361840 | ||||||
chr20:21361912
|
T | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2256-3509T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361912 | ||||||
chr20:21362088
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2256-3333G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362088 | ||||||
chr20:21362153
|
A | G | 1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2256-3268A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362153 | ||||||
chr20:21362332
|
G | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2256-3089G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362332 | ||||||
chr20:21362691
|
C | A | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2256-2730C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362691 | ||||||
chr20:21362834
|
G | A | 1 | a0002c0003t0001g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2256-2587G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362834 | ||||||
chr20:21362997
|
T | C | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2256-2424T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362997 | ||||||
chr20:21363228
|
T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2256-2193T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363228 | ||||||
chr20:21363306
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2256-2115G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363306 | ||||||
chr20:21363780
|
T | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2256-1641T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363780 | ||||||
chr20:21363808
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2256-1613A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363808 | ||||||
chr20:21363815
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2256-1606T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363815 | ||||||
chr20:21363816
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2256-1605G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363816 | ||||||
chr20:21364010
|
C | T | 61 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.2256-1411C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21364010 | ||||||
chr20:21364153
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2256-1268G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21364153 | ||||||
chr20:21364804
|
C | CA | 36 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0073others(33): Show | 37 | HG00140.hp2 HG00621.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.2256-601dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21364804 | |||||
chr20:21364804
|
CA | C | 12 | a0001c0001t0001g0210a0001c0001t0002g0182a0001c0001t0003g0112others(9): Show | 12 | HG00738.hp2 HG00741.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.2256-601delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21364804 | |||||
chr20:21364935
|
A | C | 20 | a0001c0001t0002g0151a0001c0001t0002g0156a0001c0001t0002g0157others(17): Show | 20 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.2256-486A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21364935 | ||||||
chr20:21364942
|
C | T | 27 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0045others(24): Show | 27 | HG00621.hp2 HG00673.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.2256-479C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21364942 | ||||||
chr20:21365079
|
C | A | 1 | a0001c0001t0001g0244 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2256-342C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21365079 | ||||||
chr20:21365184
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2256-237C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21365184 | ||||||
chr20:21365770
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0046 | 2 | HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2456+66G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21365770 | ||||||
chr20:21365800
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0002g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2456+111_2456+143d others(35): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21365800 | |||||
chr20:21365803
|
TATATA | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2456+105_2456+109d others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21365803 | |||||
chr20:21365877
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2456+173A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21365877 | ||||||
chr20:21365881
|
T | TTATATAA others(19): Show |
1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2456+184_2456+209d others(28): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21365881 | |||||
chr20:21365896
|
TTA | T | 3 | a0001c0001t0002g0165a0001c0001t0002g0173a0001c0001t0002g0174 | 3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2456+201_2456+202d others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21365896 | |||||
chr20:21365966
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2456+262T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21365966 | ||||||
chr20:21366012
|
A | ATATATAA others(30): Show |
1 | a0001c0001t0001g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2456+352_2456+388d others(39): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366012 | |||||
chr20:21366020
|
T | TATATATA others(71): Show |
1 | a0001c0001t0002g0164 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2456+352_2456+429d others(80): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366020 | |||||
chr20:21366057
|
T | C | 1 | a0001c0001t0002g0158 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2456+353T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366057 | ||||||
chr20:21366057
|
T | TATATATA others(34): Show |
3 | a0001c0001t0001g0200a0001c0001t0001g0206a0002c0003t0001g0176 | 3 | HG01361.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2456+412_2456+452d others(43): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366057 | |||||
chr20:21366057
|
T | TATATATA others(75): Show |
2 | a0001c0001t0001g0175a0001c0001t0001g0201 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2456+371_2456+452d others(84): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366057 | |||||
chr20:21366094
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2456+390A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366094 | ||||||
chr20:21366109
|
ATATAT | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(28): Show | 32 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2456+412_2456+416d others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366109 | |||||
chr20:21366120
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2456+416T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366120 | ||||||
chr20:21366125
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0018 | 2 | HG01071.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2456+421G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366125 | ||||||
chr20:21366126
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0018 | 2 | HG01071.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2456+422T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366126 | ||||||
chr20:21366128
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0018 | 2 | HG01071.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2456+424T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366128 | ||||||
chr20:21366139
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(28): Show | 32 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2456+435C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366139 | ||||||
chr20:21366147
|
A | T | 1 | a0001c0001t0001g0032 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2456+443A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366147 | ||||||
chr20:21366150
|
A | ATATAT | 30 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(27): Show | 31 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.2456+448_2456+452d others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366150 | |||||
chr20:21366150
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0018 | 2 | HG01071.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2456+446A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366150 | ||||||
chr20:21366163
|
T | TTATA | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2456+462_2456+465d others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366163 | |||||
chr20:21366192
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2456+488T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366192 | ||||||
chr20:21366218
|
T | TTA | 4 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0170others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2456+526_2456+527d others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366218 | |||||
chr20:21366469
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2456+765A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366469 | ||||||
chr20:21366737
|
A | C | 60 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.2456+1033A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366737 | ||||||
chr20:21366762
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2456+1058T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366762 | ||||||
chr20:21367076
|
G | T | 1 | a0001c0001t0001g0010 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2456+1372G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367076 | ||||||
chr20:21367340
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2457-1123A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367340 | ||||||
chr20:21367561
|
G | A | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2457-902G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367561 | ||||||
chr20:21367643
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2457-820G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367643 | ||||||
chr20:21367792
|
C | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2457-671C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367792 | ||||||
chr20:21367990
|
A | G | 2 | a0001c0002t0001g0091a0001c0004t0001g0104 | 2 | HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2457-473A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367990 | ||||||
chr20:21368344
|
T | C | 16 | a0001c0001t0001g0180a0001c0002t0001g0084a0001c0002t0001g0085others(13): Show | 16 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2457-119T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21368344 | ||||||
chr20:21368974
|
C | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2584+384C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21368974 | ||||||
chr20:21369091
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2584+501G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369091 | ||||||
chr20:21369211
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2584+621C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369211 | ||||||
chr20:21369491
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2584+901T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369491 | ||||||
chr20:21369518
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2584+928C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369518 | ||||||
chr20:21369523
|
C | G | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2584+933C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369523 | ||||||
chr20:21370254
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2584+1664A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21370254 | ||||||
chr20:21370577
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(211): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2584+1987A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21370577 | ||||||
chr20:21370698
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2584+2108G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21370698 | ||||||
chr20:21371025
|
TC | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0074others(1): Show | 4 | HG01884.hp1 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2584+2436delC | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371025 | ||||||
chr20:21371092
|
ACC | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(2): Show | 5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2584+2505_2584+250 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21371092 | |||||
chr20:21371120
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2584+2530C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371120 | ||||||
chr20:21371180
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2584+2590A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371180 | ||||||
chr20:21371274
|
C | G | 1 | a0001c0001t0001g0238 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2584+2684C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371274 | ||||||
chr20:21371598
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2584+3008A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371598 | ||||||
chr20:21371667
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2584+3077C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371667 | ||||||
chr20:21371735
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2584+3145T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371735 | ||||||
chr20:21371862
|
G | A | 4 | a0001c0001t0002g0136a0001c0001t0002g0147a0001c0001t0002g0166others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2584+3272G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371862 | ||||||
chr20:21372326
|
C | G | 2 | a0001c0001t0002g0191a0001c0001t0002g0202 | 2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2584+3736C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372326 | ||||||
chr20:21372373
|
G | T | 3 | a0001c0001t0002g0165a0001c0001t0002g0173a0001c0001t0002g0174 | 3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2584+3783G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372373 | ||||||
chr20:21372382
|
T | TA | 7 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0069others(4): Show | 7 | HG00621.hp1 HG00621.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2584+3794dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21372382 | |||||
chr20:21372450
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2584+3860G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372450 | ||||||
chr20:21372538
|
G | T | 1 | a0001c0001t0002g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2584+3948G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372538 | ||||||
chr20:21372706
|
A | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2584+4116A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372706 | ||||||
chr20:21372764
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2584+4174G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372764 | ||||||
chr20:21372771
|
A | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2584+4181A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372771 | ||||||
chr20:21372841
|
G | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2584+4251G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372841 | ||||||
chr20:21372882
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2584+4292T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372882 | ||||||
chr20:21372929
|
C | G | 1 | a0001c0001t0001g0270 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2584+4339C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372929 | ||||||
chr20:21373012
|
CT | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2584+4431delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21373012 | |||||
chr20:21373277
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2584+4687C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21373277 | ||||||
chr20:21373540
|
G | A | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2584+4950G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21373540 | ||||||
chr20:21374086
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2584+5496T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21374086 | ||||||
chr20:21374243
|
C | T | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2584+5653C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21374243 | ||||||
chr20:21374422
|
T | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(145): Show | 152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.2584+5832T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21374422 | ||||||
chr20:21374981
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2584+6391G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21374981 | ||||||
chr20:21375010
|
C | CT | 90 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0034others(87): Show | 91 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.2584+6445dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | |||||
chr20:21375010
|
C | CTT | 40 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(37): Show | 42 | HG00140.hp2 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.2584+6444_2584+644 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | |||||
chr20:21375010
|
CTTT | C | 31 | a0001c0001t0001g0206a0001c0001t0002g0136a0001c0001t0002g0140others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.2584+6443_2584+644 others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | |||||
chr20:21375010
|
CTTTT | C | 33 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0002g0083others(30): Show | 33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.2584+6442_2584+644 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | |||||
chr20:21375010
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2584+6436_2584+644 others(14): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | |||||
chr20:21375010
|
CTTTTTTT others(4): Show |
C | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0018others(13): Show | 16 | HG01071.hp2 HG02132.hp1 HG02965.hp2 others(13): Show |
intron_variant | MODIFIER | c.2584+6435_2584+644 others(15): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | |||||
chr20:21375010
|
CTTTTTTT others(5): Show |
C | 26 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(23): Show | 27 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.2584+6434_2584+644 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | |||||
chr20:21375056
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2584+6466A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375056 | ||||||
chr20:21375187
|
AT | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0078a0001c0001t0002g0193others(2): Show | 5 | HG00558.hp2 HG01884.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.2584+6609delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375187 | |||||
chr20:21375189
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2584+6599T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375189 | ||||||
chr20:21375208
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(145): Show | 152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.2584+6618A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375208 | ||||||
chr20:21375618
|
T | C | 5 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(2): Show | 5 | HG01975.hp1 NA18948.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-6376T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375618 | ||||||
chr20:21375818
|
ATTTATTT others(4): Show |
A | 1 | a0001c0001t0001g0020 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2585-6164_2585-615 others(15): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375818 | |||||
chr20:21375826
|
ATTT | A | 13 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0039others(10): Show | 13 | HG00621.hp1 HG00621.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.2585-6164_2585-616 others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375826 | |||||
chr20:21375829
|
T | TA | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 118 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2585-6165_2585-616 others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375829 | ||||||
chr20:21375829
|
T | TATTTA | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(16): Show | 19 | HG01361.hp1 HG01884.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.2585-6165_2585-616 others(9): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375829 | ||||||
chr20:21375829
|
T | TTTTA | 5 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0170others(2): Show | 5 | HG01891.hp1 HG02976.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2585-6141_2585-613 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375829 | |||||
chr20:21375829
|
T | TTTTATTT others(5): Show |
3 | a0001c0001t0001g0135a0001c0001t0002g0141a0001c0001t0002g0143 | 3 | HG02559.hp2 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2585-6149_2585-613 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375829 | |||||
chr20:21375829
|
T | TTTTATTT others(9): Show |
1 | a0001c0001t0002g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2585-6153_2585-613 others(20): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375829 | |||||
chr20:21375907
|
C | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(31): Show | 35 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.2585-6087C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375907 | ||||||
chr20:21376039
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2585-5955C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376039 | ||||||
chr20:21376040
|
G | A | 8 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0086others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2585-5954G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376040 | ||||||
chr20:21376418
|
A | G | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.2585-5576A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376418 | ||||||
chr20:21376499
|
A | G | 63 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0206others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2585-5495A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376499 | ||||||
chr20:21376649
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2585-5345C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376649 | ||||||
chr20:21376849
|
G | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(11): Show | 15 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2585-5145G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376849 | ||||||
chr20:21377006
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2585-4988C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377006 | ||||||
chr20:21377022
|
TA | T | 15 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0086others(12): Show | 15 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2585-4964delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377022 | |||||
chr20:21377080
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2585-4914T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377080 | ||||||
chr20:21377110
|
G | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0215 | 2 | NA18946.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2585-4884G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377110 | ||||||
chr20:21377243
|
C | CATATGAT | 5 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(2): Show | 5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-4750_2585-474 others(11): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377243 | |||||
chr20:21377255
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(2): Show | 5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-4739C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377255 | ||||||
chr20:21377264
|
C | CTTT | 15 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 16 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.2585-4718_2585-471 others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTCT others(6): Show |
1 | a0001c0001t0001g0262 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2585-4725_2585-472 others(17): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTCT others(14): Show |
1 | a0001c0001t0002g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2585-4725_2585-472 others(25): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2585-4725_2585-471 others(14): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2585-4726_2585-471 others(15): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(5): Show |
72 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(69): Show | 73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2585-4727_2585-471 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(6): Show |
80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 83 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.2585-4728_2585-471 others(17): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(7): Show |
17 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0001g0080others(14): Show | 17 | HG00438.hp2 HG02027.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2585-4729_2585-471 others(18): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(23): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0135a0001c0006t0001g0228 | 2 | HG00639.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(19): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(9): Show |
1 | a0002c0003t0001g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(20): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(21): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0002g0188a0001c0001t0002g0196 | 2 | NA18948.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(23): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(13): Show |
4 | a0001c0001t0002g0083a0001c0001t0002g0182a0001c0001t0002g0191others(1): Show | 4 | NA18968.hp2 NA18985.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(24): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(14): Show |
5 | a0001c0001t0002g0165a0001c0001t0002g0174a0001c0001t0002g0192others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(25): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(15): Show |
8 | a0001c0001t0002g0138a0001c0001t0002g0173a0001c0001t0002g0181others(5): Show | 8 | HG00423.hp2 HG00558.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(26): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(16): Show |
10 | a0001c0001t0002g0136a0001c0001t0002g0140a0001c0001t0002g0147others(7): Show | 10 | HG00438.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(27): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(17): Show |
5 | a0001c0001t0002g0145a0001c0001t0002g0156a0001c0001t0002g0158others(2): Show | 5 | HG00099.hp2 HG02165.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(28): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(18): Show |
12 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0148others(9): Show | 12 | HG00140.hp1 HG00280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(29): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0002g0155 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(30): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(20): Show |
4 | a0001c0001t0002g0142a0001c0001t0002g0154a0001c0001t0002g0170others(1): Show | 4 | HG01891.hp1 HG03540.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(31): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0002g0146 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(32): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0002g0272 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(33): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377264
|
C | CTTTTTTT others(23): Show |
3 | a0001c0001t0002g0141a0001c0001t0002g0167a0001c0001t0002g0177 | 3 | HG02559.hp2 HG02976.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(34): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | |||||
chr20:21377295
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2585-4699C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377295 | ||||||
chr20:21377339
|
C | G | 1 | a0001c0001t0002g0145 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2585-4655C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377339 | ||||||
chr20:21377528
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2585-4466G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377528 | ||||||
chr20:21377537
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2585-4457C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377537 | ||||||
chr20:21377538
|
G | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0206 | 3 | HG01361.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2585-4456G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377538 | ||||||
chr20:21377561
|
G | GT | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.2585-4422dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377561 | |||||
chr20:21377561
|
G | GTT | 63 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2585-4423_2585-442 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377561 | |||||
chr20:21378353
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2585-3641C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378353 | ||||||
chr20:21378389
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2585-3605C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378389 | ||||||
chr20:21378723
|
T | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-3271T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378723 | ||||||
chr20:21378906
|
A | G | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.2585-3088A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378906 | ||||||
chr20:21378907
|
C | T | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2585-3087C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378907 | ||||||
chr20:21379002
|
T | C | 16 | a0001c0001t0001g0180a0001c0002t0001g0084a0001c0002t0001g0085others(13): Show | 16 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2585-2992T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379002 | ||||||
chr20:21379027
|
A | G | 62 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2585-2967A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379027 | ||||||
chr20:21379035
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2585-2959C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379035 | ||||||
chr20:21379149
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2585-2845A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379149 | ||||||
chr20:21379535
|
C | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0188a0001c0001t0002g0195 | 3 | NA18948.hp1 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2585-2459C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379535 | ||||||
chr20:21379570
|
A | G | 16 | a0001c0001t0001g0180a0001c0002t0001g0084a0001c0002t0001g0085others(13): Show | 16 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2585-2424A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379570 | ||||||
chr20:21379617
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2585-2377T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379617 | ||||||
chr20:21379623
|
G | A | 62 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2585-2371G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379623 | ||||||
chr20:21379624
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2585-2370G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379624 | ||||||
chr20:21379828
|
A | C | 2 | a0001c0001t0002g0167a0001c0001t0002g0169 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2585-2166A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379828 | ||||||
chr20:21379890
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2585-2104A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379890 | ||||||
chr20:21380023
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2585-1971C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380023 | ||||||
chr20:21380092
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2585-1902A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380092 | ||||||
chr20:21380163
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0048 | 4 | HG02027.hp2 NA18963.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2585-1831G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380163 | ||||||
chr20:21380228
|
A | G | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-1766A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380228 | ||||||
chr20:21380523
|
T | C | 5 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0170others(2): Show | 5 | HG01891.hp1 HG02976.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2585-1471T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380523 | ||||||
chr20:21380849
|
G | C | 3 | a0001c0001t0002g0151a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG00099.hp2 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2585-1145G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380849 | ||||||
chr20:21380990
|
T | C | 3 | a0001c0001t0001g0227a0001c0001t0001g0230a0001c0001t0001g0256 | 3 | HG00280.hp2 HG00639.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2585-1004T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380990 | ||||||
chr20:21380999
|
G | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-995G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380999 | ||||||
chr20:21381046
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0002g0156a0001c0001t0002g0157 | 3 | HG00099.hp2 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2585-948G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381046 | ||||||
chr20:21381100
|
TTTTC | T | 10 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(7): Show | 10 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.2585-890_2585-887d others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21381100 | |||||
chr20:21381180
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2585-814G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381180 | ||||||
chr20:21381262
|
T | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-732T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381262 | ||||||
chr20:21381284
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2585-710C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381284 | ||||||
chr20:21381324
|
T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-670T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381324 | ||||||
chr20:21381424
|
C | G | 1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2585-570C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381424 | ||||||
chr20:21381466
|
T | C | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2585-528T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381466 | ||||||
chr20:21381713
|
TACACAC | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2585-257_2585-252d others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21381713 | |||||
chr20:21381713
|
TACACACA others(1): Show |
T | 24 | a0001c0001t0001g0017a0001c0001t0001g0067a0001c0001t0001g0096others(21): Show | 24 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.2585-259_2585-252d others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21381713 | |||||
chr20:21381713
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0163 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2585-261_2585-252d others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21381713 | |||||
chr20:21381815
|
G | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-179G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381815 | ||||||
chr20:21381861
|
A | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0175others(2): Show | 5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-133A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381861 | ||||||
chr20:21381961
|
A | C | 1 | a0001c0001t0002g0181 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2585-33A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381961 | ||||||
chr20:21382065
|
TA | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2648+12delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr20 | 21382065 | |||||
chr20:21382120
|
T | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2648+63T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382120 | ||||||
chr20:21382125
|
A | C | 2 | a0002c0003t0001g0097a0002c0003t0001g0176 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2648+68A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382125 | ||||||
chr20:21382183
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2648+126C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382183 | ||||||
chr20:21382284
|
A | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0105others(38): Show | 42 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.2648+227A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382284 | ||||||
chr20:21382323
|
T | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0105others(37): Show | 41 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.2648+266T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382323 | ||||||
chr20:21382338
|
G | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2648+281G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382338 | ||||||
chr20:21382344
|
G | C | 1 | a0001c0001t0001g0245 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2648+287G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382344 | ||||||
chr20:21382440
|
G | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0105others(37): Show | 41 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.2648+383G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382440 | ||||||
chr20:21382797
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2648+740A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382797 | ||||||
chr20:21382799
|
T | G | 3 | a0001c0001t0002g0187a0001c0001t0002g0192a0001c0001t0002g0197 | 3 | HG00423.hp2 HG00438.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2648+742T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382799 | ||||||
chr20:21382940
|
C | A | 1 | a0001c0001t0003g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2648+883C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382940 | ||||||
chr20:21383017
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2648+960A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383017 | ||||||
chr20:21383166
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2648+1109A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383166 | ||||||
chr20:21383176
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2648+1119C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383176 | ||||||
chr20:21383228
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(211): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2648+1171A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383228 | ||||||
chr20:21383602
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2648+1545G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383602 | ||||||
chr20:21383651
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2648+1594C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383651 | ||||||
chr20:21384281
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2648+2224A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384281 | ||||||
chr20:21384325
|
C | G | 64 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0002g0083others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.2648+2268C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384325 | ||||||
chr20:21384341
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0105others(36): Show | 40 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.2648+2284C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384341 | ||||||
chr20:21384423
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2648+2366A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384423 | ||||||
chr20:21384742
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2649-2126C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384742 | ||||||
chr20:21384774
|
G | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2649-2094G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384774 | ||||||
chr20:21384825
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0105others(100): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2649-2043G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384825 | ||||||
chr20:21384882
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2649-1986T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384882 | ||||||
chr20:21384920
|
G | A | 63 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2649-1948G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384920 | ||||||
chr20:21385396
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2649-1472T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385396 | ||||||
chr20:21385622
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2649-1246T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385622 | ||||||
chr20:21385639
|
C | CAA | 63 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2649-1225_2649-122 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr20 | 21385639 | |||||
chr20:21385775
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2649-1093C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385775 | ||||||
chr20:21385791
|
A | G | 26 | a0001c0001t0002g0138a0001c0001t0002g0140a0001c0001t0002g0144others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.2649-1077A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385791 | ||||||
chr20:21385857
|
A | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(11): Show | 15 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2649-1011A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385857 | ||||||
chr20:21385869
|
G | C | 1 | a0002c0003t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2649-999G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385869 | ||||||
chr20:21386162
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2649-706C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21386162 | ||||||
chr20:21386195
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2649-673A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21386195 | ||||||
chr20:21386803
|
C | T | 1 | a0002c0003t0001g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2649-65C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21386803 | ||||||
chr20:21386822
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2649-46G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21386822 | ||||||
chr20:21387103
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 37 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.2787+97A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21387103 | ||||||
chr20:21387369
|
AAAGT | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0105others(37): Show | 41 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.2787+368_2787+371d others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr20 | 21387369 | |||||
chr20:21387502
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2787+496A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21387502 | ||||||
chr20:21387524
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2787+518G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21387524 | ||||||
chr20:21387725
|
G | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.2787+719G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21387725 | ||||||
chr20:21387948
|
C | T | 26 | a0001c0001t0002g0138a0001c0001t0002g0140a0001c0001t0002g0144others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.2787+942C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21387948 | ||||||
chr20:21387955
|
G | GAGT | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2787+950_2787+951i others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr20 | 21387955 | |||||
chr20:21388294
|
G | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(147): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2788-979G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388294 | ||||||
chr20:21388375
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0109 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2788-898G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388375 | ||||||
chr20:21388670
|
T | C | 63 | a0001c0001t0002g0083a0001c0001t0002g0136a0001c0001t0002g0138others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2788-603T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388670 | ||||||
chr20:21388701
|
A | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG00673.hp1 NA18946.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2788-572A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388701 | ||||||
chr20:21388874
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2788-399T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388874 | ||||||
chr20:21389023
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0106others(14): Show | 18 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2788-250G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21389023 | ||||||
chr20:21389072
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2788-201C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21389072 |