geneid | 1525 |
---|---|
ensemblid | ENSG00000154639.19 |
hgncid | 2559 |
symbol | CXADR |
name | CXADR Ig-like cell adhesion molecule |
refseq_nuc | NM_001338.5 |
refseq_prot | NP_001329.1 |
ensembl_nuc | ENST00000284878.12 |
ensembl_prot | ENSP00000284878.7 |
mane_status | MANE Select |
chr | chr21 |
start | 17513043 |
end | 17570100 |
strand | + |
ver | v1.2 |
region | chr21:17513043-17570100 |
region5000 | chr21:17508043-17575100 |
regionname0 | CXADR_chr21_17513043_17570100 |
regionname5000 | CXADR_chr21_17508043_17575100 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 365 | 343 | 88 | 56 | 143 | 12 | 42 | 97 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0002 | 0/0 | 365 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0003 | 0/0 | 365 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0004 | 0/0 | 365 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0005 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1098 | 250 | 40 | 45 | 113 | 12 | 39 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0002 | 0/1 | 1098 | 67 | 25 | 8 | 30 | 0 | 3 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0003 | 0/0 | 1098 | 9 | 8 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0004 | 0/0 | 1098 | 7 | 7 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0005 | 0/0 | 1098 | 4 | 4 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0006 | 0/0 | 1098 | 3 | 2 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0007 | 0/0 | 1098 | 3 | 3 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0008 | 0/0 | 1098 | 2 | 0 | 0 | 0 | 0 | 2 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0009 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0010 | 0/0 | 1098 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0011 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0012 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
c0013 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4498 | 75 | 3 | 13 | 45 | 4 | 10 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0002 | 0/0 | 4497 | 51 | 16 | 3 | 19 | 1 | 12 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0003 | 0/0 | 4495 | 47 | 4 | 10 | 23 | 1 | 9 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0004 | 0/0 | 4496 | 12 | 0 | 0 | 12 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0005 | 0/0 | 4497 | 12 | 8 | 4 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0006 | 0/0 | 4495 | 10 | 8 | 2 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0007 | 0/0 | 4498 | 9 | 0 | 5 | 1 | 1 | 2 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0008 | 0/0 | 4494 | 8 | 0 | 0 | 7 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0009 | 0/0 | 4497 | 7 | 7 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0010 | 0/1 | 4496 | 7 | 2 | 3 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0011 | 0/0 | 4489 | 6 | 6 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0012 | 0/0 | 4498 | 5 | 0 | 0 | 5 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0013 | 0/0 | 4497 | 4 | 4 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0014 | 0/0 | 4496 | 4 | 3 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0015 | 0/0 | 4497 | 3 | 0 | 1 | 1 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0016 | 0/0 | 4492 | 3 | 0 | 1 | 1 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0017 | 0/0 | 4496 | 3 | 3 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0018 | 0/0 | 4497 | 3 | 3 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0019 | 0/0 | 4498 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0020 | 0/0 | 4494 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0021 | 0/0 | 4494 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0022 | 0/0 | 4498 | 2 | 0 | 1 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0023 | 0/0 | 4498 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0024 | 0/0 | 4499 | 2 | 0 | 2 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0025 | 0/0 | 4499 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0026 | 0/0 | 4498 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0027 | 0/0 | 4494 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0028 | 0/0 | 4496 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0029 | 0/0 | 4494 | 2 | 0 | 0 | 1 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0030 | 0/0 | 4496 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0031 | 0/0 | 4497 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0032 | 0/0 | 4497 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0033 | 0/0 | 4498 | 2 | 1 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0034 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0035 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0036 | 0/0 | 4495 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0037 | 0/0 | 4496 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0038 | 0/0 | 4495 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0039 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0040 | 0/0 | 4489 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0041 | 0/0 | 4498 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0042 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0043 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0044 | 0/0 | 4498 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0045 | 0/0 | 4498 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0046 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0047 | 0/0 | 4498 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0048 | 0/0 | 4498 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0049 | 0/0 | 4498 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0050 | 0/0 | 4499 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0051 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0052 | 0/0 | 4498 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0053 | 0/0 | 4496 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0054 | 0/0 | 4496 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0055 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0056 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0057 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0058 | 0/0 | 4496 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0059 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0060 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0061 | 0/0 | 4499 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0062 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0063 | 0/0 | 4496 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0064 | 0/0 | 4495 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0065 | 0/0 | 4496 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0066 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0067 | 0/0 | 4496 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0068 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0069 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0070 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0071 | 0/0 | 4496 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0072 | 0/0 | 4493 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0073 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0074 | 0/0 | 4498 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0075 | 0/0 | 4496 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0076 | 0/0 | 4496 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0077 | 0/0 | 4496 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0078 | 0/0 | 4496 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0079 | 0/0 | 4498 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0080 | 1/0 | 4496 | 1 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0081 | 0/0 | 4496 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0082 | 0/0 | 4495 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0083 | 0/0 | 4498 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0084 | 0/0 | 4496 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0085 | 0/0 | 4495 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
t0086 | 0/0 | 4496 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0311 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1098 | 250 | 40 | 45 | 113 | 12 | 39 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002 | 0/1 | 1098 | 67 | 25 | 8 | 30 | 0 | 3 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0003 | 0/0 | 1098 | 9 | 8 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0004 | 0/0 | 1098 | 7 | 7 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0006 | 0/0 | 1098 | 3 | 2 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0007 | 0/0 | 1098 | 3 | 3 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0009 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0011 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0013 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0002c0005 | 0/0 | 1098 | 4 | 4 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0003c0010 | 0/0 | 1098 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0004c0008 | 0/0 | 1098 | 2 | 0 | 0 | 0 | 0 | 2 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0005c0012 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5595 | 74 | 3 | 13 | 44 | 4 | 10 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0002 | 0/0 | 5594 | 49 | 14 | 3 | 19 | 1 | 12 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0003 | 0/0 | 5592 | 47 | 4 | 10 | 23 | 1 | 9 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0005 | 0/0 | 5594 | 12 | 8 | 4 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0007 | 0/0 | 5595 | 9 | 0 | 5 | 1 | 1 | 2 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0012 | 0/0 | 5595 | 5 | 0 | 0 | 5 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0015 | 0/0 | 5594 | 3 | 0 | 1 | 1 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0016 | 0/0 | 5589 | 2 | 0 | 0 | 1 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0017 | 0/0 | 5593 | 3 | 3 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0019 | 0/0 | 5595 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0022 | 0/0 | 5595 | 2 | 0 | 1 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0023 | 0/0 | 5595 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0024 | 0/0 | 5596 | 2 | 0 | 2 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0025 | 0/0 | 5596 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0026 | 0/0 | 5595 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0028 | 0/0 | 5593 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0029 | 0/0 | 5591 | 2 | 0 | 0 | 1 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0030 | 0/0 | 5593 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0031 | 0/0 | 5594 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0033 | 0/0 | 5595 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0041 | 0/0 | 5595 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0042 | 0/0 | 5594 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0043 | 0/0 | 5594 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0044 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0045 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0046 | 0/0 | 5594 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0047 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0048 | 0/0 | 5595 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0049 | 0/0 | 5595 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0050 | 0/0 | 5596 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0051 | 0/0 | 5597 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0052 | 0/0 | 5595 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0053 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0054 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0055 | 0/0 | 5594 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0056 | 0/0 | 5594 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0058 | 0/0 | 5593 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0065 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0066 | 0/0 | 5591 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0067 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0068 | 0/0 | 5589 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0076 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0079 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0080 | 1/0 | 5593 | 1 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0001t0081 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0004 | 0/0 | 5593 | 11 | 0 | 0 | 11 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0006 | 0/0 | 5592 | 10 | 8 | 2 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0008 | 0/0 | 5591 | 8 | 0 | 0 | 7 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0010 | 0/1 | 5593 | 6 | 2 | 2 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0011 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0013 | 0/0 | 5594 | 4 | 4 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0014 | 0/0 | 5593 | 4 | 3 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0020 | 0/0 | 5591 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0021 | 0/0 | 5591 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0027 | 0/0 | 5591 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0034 | 0/0 | 5591 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0035 | 0/0 | 5591 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0037 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0038 | 0/0 | 5592 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0039 | 0/0 | 5591 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0057 | 0/0 | 5590 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0059 | 0/0 | 5588 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0060 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0061 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0062 | 0/0 | 5591 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0070 | 0/0 | 5594 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0071 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0072 | 0/0 | 5590 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0073 | 0/0 | 5591 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0083 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0085 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0002t0086 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0003t0009 | 0/0 | 5594 | 7 | 7 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0003t0016 | 0/0 | 5589 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0003t0064 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0004t0011 | 0/0 | 5586 | 5 | 5 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0004t0040 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0004t0069 | 0/0 | 5591 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0006t0032 | 0/0 | 5594 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0006t0078 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0007t0002 | 0/0 | 5594 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0007t0033 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0009t0074 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0009t0075 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0011t0063 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0001c0013t0010 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0002c0005t0018 | 0/0 | 5594 | 3 | 3 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0002c0005t0077 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0003c0010t0004 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0003c0010t0036 | 0/0 | 5592 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0004c0008t0082 | 0/0 | 5592 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0004c0008t0084 | 0/0 | 5593 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
a0005c0012t0001 | 0/0 | 5595 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | copy fasta | chr21 | 17508043 | 17575100 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0015g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0015g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0015g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0016g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0016g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0017g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0017g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0019g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0019g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0022g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0022g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0023g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0023g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0024g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0024g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0025g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0025g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0026g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0026g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0028g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0028g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0029g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0029g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0030g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0030g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0031g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0031g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0033g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0041g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0042g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0043g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0044g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0045g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0046g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0047g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0048g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0049g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0050g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0051g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0052g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0053g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0054g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0055g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0056g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0058g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0065g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0066g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0067g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0068g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0076g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0079g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0080g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0081g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0311 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0013g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0014g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0014g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0014g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0020g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0020g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0021g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0021g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0027g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0027g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0034g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0035g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0037g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0038g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0039g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0057g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0059g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0060g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0061g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0062g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0070g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0071g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0072g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0073g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0083g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0085g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0086g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0016g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0064g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0040g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0069g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0006t0032g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0006t0032g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0006t0078g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0007t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0007t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0007t0033g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0009t0074g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0009t0075g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0011t0063g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0013t0010g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0002c0005t0018g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0002c0005t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0002c0005t0018g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0002c0005t0077g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0003c0010t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0003c0010t0036g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0004c0008t0082g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0004c0008t0084g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0005c0012t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0317 | EUR | GBR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | GBR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0318 | EUR | GBR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00140 | hp2 | a0001 | c0001 | t0052 | g0041 | EUR | GBR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00323 | hp1 | a0001 | c0001 | t0042 | g0273 | EUR | FIN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0286 | EUR | FIN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00423 | hp1 | a0001 | c0001 | t0025 | g0252 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00423 | hp2 | a0001 | c0002 | t0004 | g0325 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00609 | hp1 | a0001 | c0002 | t0004 | g0324 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00639 | hp1 | a0001 | c0002 | t0006 | g0101 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00639 | hp2 | a0001 | c0001 | t0045 | g0264 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00642 | hp1 | a0001 | c0002 | t0014 | g0075 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00642 | hp2 | a0001 | c0001 | t0007 | g0261 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00673 | hp2 | a0001 | c0002 | t0035 | g0340 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00733 | hp2 | a0001 | c0001 | t0007 | g0237 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00741 | hp1 | a0001 | c0001 | t0022 | g0262 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01069 | hp1 | a0001 | c0001 | t0054 | g0236 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01074 | hp1 | a0001 | c0001 | t0043 | g0119 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01074 | hp2 | a0001 | c0002 | t0083 | g0124 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01081 | hp2 | a0001 | c0001 | t0065 | g0063 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01099 | hp1 | a0001 | c0002 | t0086 | g0001 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01109 | hp2 | a0001 | c0006 | t0032 | g0012 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0180 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0179 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01175 | hp1 | a0001 | c0013 | t0010 | g0298 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01192 | hp2 | a0001 | c0002 | t0006 | g0001 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01243 | hp1 | a0001 | c0003 | t0016 | g0187 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0037 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0217 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01258 | hp1 | a0001 | c0001 | t0047 | g0265 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01258 | hp2 | a0001 | c0001 | t0007 | g0218 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01346 | hp1 | a0001 | c0002 | t0010 | g0228 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01346 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0299 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01361 | hp2 | a0001 | c0001 | t0024 | g0257 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01433 | hp1 | a0001 | c0002 | t0010 | g0316 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01496 | hp1 | a0001 | c0001 | t0015 | g0254 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01515 | hp1 | a0001 | c0001 | t0029 | g0202 | EUR | IBS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0203 | EUR | IBS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01884 | hp2 | a0001 | c0002 | t0011 | g0107 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01891 | hp1 | a0001 | c0002 | t0006 | g0103 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01975 | hp1 | a0001 | c0002 | t0027 | g0144 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02015 | hp2 | a0001 | c0002 | t0034 | g0332 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02027 | hp1 | a0005 | c0012 | t0001 | g0282 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02027 | hp2 | a0001 | c0002 | t0008 | g0039 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02055 | hp1 | a0001 | c0001 | t0028 | g0090 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02056 | hp2 | a0001 | c0002 | t0008 | g0161 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02071 | hp1 | a0001 | c0002 | t0004 | g0322 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02074 | hp1 | a0001 | c0002 | t0004 | g0342 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02074 | hp2 | a0001 | c0002 | t0021 | g0334 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02080 | hp2 | a0001 | c0001 | t0019 | g0323 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02129 | hp1 | a0001 | c0001 | t0046 | g0206 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02135 | hp2 | a0001 | c0001 | t0007 | g0233 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0102 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02145 | hp2 | a0001 | c0001 | t0079 | g0078 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02155 | hp1 | a0003 | c0010 | t0004 | g0343 | EAS | CDX | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CDX | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | CDX | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02257 | hp2 | a0001 | c0002 | t0013 | g0104 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02258 | hp1 | a0001 | c0001 | t0028 | g0091 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02258 | hp2 | a0002 | c0005 | t0018 | g0153 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02273 | hp1 | a0001 | c0001 | t0030 | g0166 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02280 | hp1 | a0001 | c0002 | t0013 | g0106 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02280 | hp2 | a0001 | c0004 | t0069 | g0305 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02300 | hp2 | a0001 | c0001 | t0024 | g0211 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02451 | hp2 | a0001 | c0006 | t0078 | g0010 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02523 | hp1 | a0001 | c0002 | t0021 | g0333 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02572 | hp2 | a0001 | c0004 | t0011 | g0038 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02615 | hp2 | a0001 | c0002 | t0006 | g0117 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02622 | hp1 | a0001 | c0004 | t0011 | g0188 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02622 | hp2 | a0002 | c0005 | t0018 | g0155 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02630 | hp1 | a0001 | c0003 | t0009 | g0182 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02630 | hp2 | a0001 | c0001 | t0067 | g0013 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02698 | hp1 | a0001 | c0002 | t0010 | g0310 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02698 | hp2 | a0001 | c0001 | t0007 | g0238 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02717 | hp1 | a0001 | c0007 | t0002 | g0092 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02717 | hp2 | a0001 | c0003 | t0009 | g0087 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02723 | hp1 | a0001 | c0002 | t0013 | g0105 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02723 | hp2 | a0001 | c0002 | t0006 | g0152 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0235 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02738 | hp1 | a0001 | c0001 | t0051 | g0207 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02738 | hp2 | a0001 | c0001 | t0016 | g0045 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0151 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02895 | hp1 | a0002 | c0005 | t0077 | g0149 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02895 | hp2 | a0001 | c0002 | t0085 | g0074 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02896 | hp1 | a0001 | c0003 | t0064 | g0147 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02896 | hp2 | a0001 | c0001 | t0017 | g0178 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02897 | hp1 | a0001 | c0002 | t0014 | g0077 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02897 | hp2 | a0001 | c0003 | t0009 | g0154 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02922 | hp1 | a0001 | c0002 | t0014 | g0079 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02922 | hp2 | a0001 | c0002 | t0006 | g0146 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02965 | hp2 | a0001 | c0001 | t0017 | g0098 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02970 | hp1 | a0001 | c0002 | t0061 | g0014 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0301 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02976 | hp2 | a0001 | c0009 | t0075 | g0191 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03041 | hp2 | a0001 | c0004 | t0011 | g0080 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03098 | hp1 | a0002 | c0005 | t0018 | g0145 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0302 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03139 | hp2 | a0001 | c0004 | t0040 | g0319 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03195 | hp2 | a0001 | c0006 | t0032 | g0011 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03209 | hp1 | a0001 | c0002 | t0006 | g0001 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03209 | hp2 | a0001 | c0001 | t0031 | g0185 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03225 | hp1 | a0001 | c0007 | t0002 | g0093 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03225 | hp2 | a0001 | c0002 | t0060 | g0003 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03486 | hp2 | a0001 | c0002 | t0027 | g0016 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03490 | hp1 | a0004 | c0008 | t0082 | g0312 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03490 | hp2 | a0001 | c0001 | t0066 | g0054 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03492 | hp1 | a0004 | c0008 | t0084 | g0313 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03516 | hp1 | a0001 | c0001 | t0031 | g0186 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03516 | hp2 | a0001 | c0003 | t0009 | g0022 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03540 | hp1 | a0001 | c0011 | t0063 | g0162 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03540 | hp2 | a0001 | c0009 | t0074 | g0190 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03654 | hp1 | a0001 | c0001 | t0048 | g0231 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03654 | hp2 | a0001 | c0002 | t0070 | g0026 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03704 | hp2 | a0001 | c0001 | t0015 | g0268 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0071 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0295 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04184 | hp1 | a0001 | c0001 | t0058 | g0246 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04184 | hp2 | a0001 | c0002 | t0008 | g0044 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18522 | hp2 | a0001 | c0003 | t0009 | g0021 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18747 | hp2 | a0001 | c0001 | t0025 | g0006 | EAS | CHB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18906 | hp1 | a0001 | c0002 | t0013 | g0108 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18906 | hp2 | a0001 | c0007 | t0033 | g0189 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18940 | hp2 | a0001 | c0001 | t0041 | g0260 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18941 | hp1 | a0001 | c0002 | t0008 | g0062 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18941 | hp2 | a0001 | c0001 | t0055 | g0307 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18944 | hp1 | a0001 | c0001 | t0076 | g0294 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18947 | hp1 | a0001 | c0001 | t0023 | g0242 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18948 | hp1 | a0001 | c0002 | t0008 | g0061 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18959 | hp1 | a0001 | c0002 | t0004 | g0330 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18966 | hp2 | a0001 | c0001 | t0026 | g0244 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18967 | hp1 | a0001 | c0002 | t0004 | g0337 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18967 | hp2 | a0001 | c0001 | t0068 | g0027 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18970 | hp2 | a0001 | c0001 | t0081 | g0165 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18971 | hp1 | a0001 | c0002 | t0037 | g0326 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18975 | hp2 | a0001 | c0001 | t0050 | g0219 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18977 | hp2 | a0001 | c0001 | t0016 | g0068 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18981 | hp2 | a0001 | c0002 | t0008 | g0160 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18983 | hp1 | a0001 | c0002 | t0071 | g0125 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18987 | hp1 | a0001 | c0002 | t0004 | g0329 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18988 | hp2 | a0001 | c0002 | t0072 | g0150 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18989 | hp2 | a0001 | c0001 | t0012 | g0089 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18993 | hp1 | a0001 | c0002 | t0020 | g0336 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18993 | hp2 | a0001 | c0001 | t0012 | g0132 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18994 | hp1 | a0001 | c0002 | t0020 | g0335 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18995 | hp1 | a0001 | c0002 | t0004 | g0338 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18995 | hp2 | a0001 | c0001 | t0056 | g0135 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18998 | hp1 | a0001 | c0002 | t0008 | g0060 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0341 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18999 | hp2 | a0001 | c0001 | t0012 | g0137 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19002 | hp1 | a0001 | c0001 | t0015 | g0250 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19005 | hp2 | a0001 | c0002 | t0039 | g0321 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19010 | hp1 | a0001 | c0002 | t0073 | g0285 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19010 | hp2 | a0001 | c0001 | t0049 | g0281 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19011 | hp1 | a0001 | c0002 | t0008 | g0177 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19030 | hp1 | a0001 | c0002 | t0010 | g0183 | AFR | LWK | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | LWK | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | LWK | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | LWK | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19062 | hp1 | a0001 | c0001 | t0012 | g0133 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19065 | hp1 | a0001 | c0002 | t0004 | g0339 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19068 | hp1 | a0001 | c0001 | t0023 | g0248 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19070 | hp1 | a0001 | c0002 | t0004 | g0327 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19072 | hp1 | a0003 | c0010 | t0036 | g0344 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19072 | hp2 | a0001 | c0001 | t0012 | g0134 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19075 | hp1 | a0001 | c0001 | t0053 | g0115 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19075 | hp2 | a0001 | c0001 | t0029 | g0309 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19079 | hp2 | a0001 | c0001 | t0026 | g0212 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19085 | hp1 | a0001 | c0002 | t0038 | g0328 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19086 | hp2 | a0001 | c0001 | t0019 | g0331 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19240 | hp1 | a0001 | c0002 | t0057 | g0019 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19240 | hp2 | a0001 | c0004 | t0011 | g0197 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ASW | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | ASW | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20752 | hp1 | a0001 | c0001 | t0033 | g0084 | EUR | TSI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20752 | hp2 | a0001 | c0001 | t0022 | g0118 | EUR | TSI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | GIH | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | GIH | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02109 | hp1 | a0001 | c0002 | t0059 | g0003 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02109 | hp2 | a0001 | c0003 | t0009 | g0024 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02486 | hp2 | a0001 | c0001 | t0017 | g0297 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02559 | hp1 | a0001 | c0001 | t0044 | g0210 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02559 | hp2 | a0001 | c0002 | t0014 | g0076 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03471 | hp1 | a0001 | c0004 | t0011 | g0195 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03471 | hp2 | a0001 | c0002 | t0062 | g0164 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG06807 | hp1 | a0001 | c0001 | t0030 | g0017 | AFR | USA | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG06807 | hp2 | a0001 | c0002 | t0010 | g0121 | AFR | USA | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20300 | hp1 | a0001 | c0003 | t0009 | g0023 | AFR | USA | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | USA | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0010 | g0311 | REF | REF | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0080 | g0088 | REF | REF | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:17513172
|
G | C | 1 | a0004 | 2 | HG03490.hp1 HG03492.hp1 |
missense_variant&splice_region_variant | MODERATE | c.43G>C | p.Asp15His | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/7 | 130/5593 | 43/1098 | 15/365 | chr21 | 17513172 | ||
chr21:17565507
|
A | G | 1 | a0005 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.913A>G | p.Met305Val | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1000/5593 | 913/1098 | 305/365 | chr21 | 17565507 | ||
chr21:17565577
|
G | A | 1 | a0003 | 2 | HG02155.hp1 NA19072.hp1 |
missense_variant | MODERATE | c.983G>A | p.Arg328His | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1070/5593 | 983/1098 | 328/365 | chr21 | 17565577 | ||
chr21:17565660
|
C | T | 1 | a0002 | 4 | HG02258.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.1066C>T | p.Pro356Ser | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1153/5593 | 1066/1098 | 356/365 | chr21 | 17565660 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:17513150
|
C | T | 1 | a0001c0013 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.21C>T | p.Phe7Phe | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/7 | 108/5593 | 21/1098 | 7/365 | chr21 | 17513150 | ||
chr21:17547103
|
A | G | 1 | a0001c0007 | 3 | HG02717.hp1 HG03225.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.120A>G | p.Pro40Pro | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/7 | 207/5593 | 120/1098 | 40/365 | chr21 | 17547103 | ||
chr21:17547148
|
C | A | 1 | a0001c0011 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.165C>A | p.Ile55Ile | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/7 | 252/5593 | 165/1098 | 55/365 | chr21 | 17547148 | ||
chr21:17551871
|
A | G | 2 | a0001c0003a0001c0004 | 16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
synonymous_variant | LOW | c.333A>G | p.Gln111Gln | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/7 | 420/5593 | 333/1098 | 111/365 | chr21 | 17551871 | ||
chr21:17560709
|
T | A | 1 | a0001c0009 | 2 | HG02976.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.579T>A | p.Thr193Thr | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/7 | 666/5593 | 579/1098 | 193/365 | chr21 | 17560709 | ||
chr21:17565440
|
A | G | 5 | a0001c0002a0001c0004a0001c0013others(2): Show | 79 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(76): Show |
synonymous_variant | LOW | c.846A>G | p.Pro282Pro | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 933/5593 | 846/1098 | 282/365 | chr21 | 17565440 | ||
chr21:17565644
|
G | A | 1 | a0001c0006 | 3 | HG01109.hp2 HG02451.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.1050G>A | p.Ala350Ala | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1137/5593 | 1050/1098 | 350/365 | chr21 | 17565644 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:17513072
|
T | C | 11 | a0001c0001t0019a0001c0002t0004a0001c0002t0020others(8): Show | 24 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-58T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/7 | 58 | chr21 | 17513072 | |||||
chr21:17513072
|
T | G | 1 | a0001c0004t0040 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/7 | 58 | chr21 | 17513072 | |||||
chr21:17565725
|
T | C | 3 | a0001c0002t0011a0001c0004t0011a0001c0004t0040 | 7 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*33T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 33 | chr21 | 17565725 | |||||
chr21:17565762
|
G | T | 9 | a0001c0002t0006a0001c0002t0010a0001c0002t0014others(6): Show | 26 | HG00639.hp1 HG00642.hp1 HG01074.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*70G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 70 | chr21 | 17565762 | |||||
chr21:17565800
|
ATAAGT | A | 3 | a0001c0002t0011a0001c0004t0011a0001c0004t0040 | 7 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*112_*116delGTTAA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 112 | INFO_REALIGN_3_PRIME | chr21 | 17565800 | ||||
chr21:17565858
|
G | A | 27 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(24): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*166G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 166 | chr21 | 17565858 | |||||
chr21:17565942
|
T | G | 48 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(45): Show | 147 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*250T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 250 | chr21 | 17565942 | |||||
chr21:17566091
|
G | T | 15 | a0001c0002t0004a0001c0002t0008a0001c0002t0020others(12): Show | 34 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*399G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 399 | chr21 | 17566091 | |||||
chr21:17566167
|
C | T | 2 | a0001c0002t0006a0001c0002t0086 | 11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*475C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 475 | chr21 | 17566167 | |||||
chr21:17566297
|
A | G | 1 | a0001c0001t0026 | 2 | NA18966.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*605A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 605 | chr21 | 17566297 | |||||
chr21:17566351
|
T | C | 1 | a0001c0002t0027 | 2 | HG01975.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*659T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 659 | chr21 | 17566351 | |||||
chr21:17566359
|
T | C | 31 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(28): Show | 107 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*667T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 667 | chr21 | 17566359 | |||||
chr21:17566421
|
T | C | 14 | a0001c0002t0004a0001c0002t0008a0001c0002t0020others(11): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*729T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 729 | chr21 | 17566421 | |||||
chr21:17566449
|
G | A | 4 | a0001c0002t0011a0001c0004t0011a0001c0004t0040others(1): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*757G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 757 | chr21 | 17566449 | |||||
chr21:17566662
|
ATGT | A | 14 | a0001c0002t0004a0001c0002t0008a0001c0002t0020others(11): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*981_*983delGTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 981 | INFO_REALIGN_3_PRIME | chr21 | 17566662 | ||||
chr21:17566684
|
G | A | 2 | a0001c0009t0074a0001c0009t0075 | 2 | HG02976.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*992G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 992 | chr21 | 17566684 | |||||
chr21:17566861
|
G | C | 1 | a0001c0001t0041 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1169G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1169 | chr21 | 17566861 | |||||
chr21:17566946
|
T | TA | 29 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(26): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1266dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1267 | INFO_REALIGN_3_PRIME | chr21 | 17566946 | ||||
chr21:17566946
|
TA | T | 34 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(31): Show | 114 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1266delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1266 | INFO_REALIGN_3_PRIME | chr21 | 17566946 | ||||
chr21:17566986
|
G | A | 91 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(88): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*1294G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1294 | chr21 | 17566986 | |||||
chr21:17567065
|
C | G | 1 | a0001c0001t0052 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1373C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1373 | chr21 | 17567065 | |||||
chr21:17567111
|
T | C | 31 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(28): Show | 107 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1419T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1419 | chr21 | 17567111 | |||||
chr21:17567128
|
C | T | 14 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(11): Show | 69 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1436C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1436 | chr21 | 17567128 | |||||
chr21:17567156
|
C | G | 2 | a0001c0002t0014a0001c0002t0085 | 5 | HG00642.hp1 HG02559.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1464C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1464 | chr21 | 17567156 | |||||
chr21:17567251
|
A | G | 1 | a0001c0001t0068 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1559A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1559 | chr21 | 17567251 | |||||
chr21:17567306
|
T | C | 1 | a0001c0002t0020 | 2 | NA18993.hp1 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1614T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1614 | chr21 | 17567306 | |||||
chr21:17567390
|
G | A | 2 | a0001c0001t0007a0001c0001t0042 | 10 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1698G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1698 | chr21 | 17567390 | |||||
chr21:17567511
|
C | T | 2 | a0001c0002t0039a0001c0002t0073 | 2 | NA19005.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1819C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1819 | chr21 | 17567511 | |||||
chr21:17567621
|
A | G | 27 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(24): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1929A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1929 | chr21 | 17567621 | |||||
chr21:17567638
|
T | C | 1 | a0001c0001t0052 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1946T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1946 | chr21 | 17567638 | |||||
chr21:17567657
|
G | A | 4 | a0001c0002t0011a0001c0004t0011a0001c0004t0040others(1): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1965G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1965 | chr21 | 17567657 | |||||
chr21:17567770
|
C | T | 1 | a0001c0002t0070 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2078C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2078 | chr21 | 17567770 | |||||
chr21:17567862
|
C | CT | 25 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(22): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2181dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2182 | INFO_REALIGN_3_PRIME | chr21 | 17567862 | ||||
chr21:17567862
|
CT | C | 16 | a0001c0001t0028a0001c0002t0004a0001c0002t0008others(13): Show | 36 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2181delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2181 | INFO_REALIGN_3_PRIME | chr21 | 17567862 | ||||
chr21:17568012
|
T | C | 5 | a0001c0002t0013a0001c0002t0057a0001c0002t0059others(2): Show | 8 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2320T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2320 | chr21 | 17568012 | |||||
chr21:17568125
|
C | CT | 41 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(38): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*2454dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2455 | INFO_REALIGN_3_PRIME | chr21 | 17568125 | ||||
chr21:17568125
|
C | CTT | 22 | a0001c0001t0025a0001c0001t0029a0001c0001t0033others(19): Show | 51 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2453_*2454dupTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2455 | INFO_REALIGN_3_PRIME | chr21 | 17568125 | ||||
chr21:17568125
|
C | CTTT | 11 | a0001c0001t0003a0001c0001t0028a0001c0001t0051others(8): Show | 67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2452_*2454dupTTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2455 | INFO_REALIGN_3_PRIME | chr21 | 17568125 | ||||
chr21:17568161
|
G | C | 49 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(46): Show | 148 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*2469G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2469 | chr21 | 17568161 | |||||
chr21:17568168
|
A | G | 35 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(32): Show | 115 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2476A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2476 | chr21 | 17568168 | |||||
chr21:17568189
|
C | T | 1 | a0001c0001t0046 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2497C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2497 | chr21 | 17568189 | |||||
chr21:17568191
|
G | C | 2 | a0001c0001t0046a0001c0001t0047 | 2 | HG01258.hp1 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2499G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2499 | chr21 | 17568191 | |||||
chr21:17568206
|
G | T | 31 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(28): Show | 107 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2514G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2514 | chr21 | 17568206 | |||||
chr21:17568207
|
C | T | 1 | a0001c0002t0070 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2515C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2515 | chr21 | 17568207 | |||||
chr21:17568215
|
G | A | 2 | a0001c0001t0022a0001c0001t0044 | 3 | HG00741.hp1 HG02559.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2523G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2523 | chr21 | 17568215 | |||||
chr21:17568330
|
G | A | 34 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(31): Show | 114 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2638G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2638 | chr21 | 17568330 | |||||
chr21:17568379
|
C | T | 7 | a0001c0002t0004a0001c0002t0035a0001c0002t0037others(4): Show | 17 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2687C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2687 | chr21 | 17568379 | |||||
chr21:17568406
|
G | A | 4 | a0001c0002t0011a0001c0004t0011a0001c0004t0040others(1): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2714G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2714 | chr21 | 17568406 | |||||
chr21:17568407
|
C | T | 1 | a0001c0001t0049 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2715C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2715 | chr21 | 17568407 | |||||
chr21:17568498
|
CTT | C | 34 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(31): Show | 114 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2808_*2809delTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2808 | INFO_REALIGN_3_PRIME | chr21 | 17568498 | ||||
chr21:17568529
|
A | G | 2 | a0001c0006t0032a0001c0006t0078 | 3 | HG01109.hp2 HG02451.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2837A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2837 | chr21 | 17568529 | |||||
chr21:17568540
|
G | T | 2 | a0001c0001t0031a0001c0001t0079 | 3 | HG02145.hp2 HG03209.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2848G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2848 | chr21 | 17568540 | |||||
chr21:17568557
|
C | CT | 25 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(22): Show | 92 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2882dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2883 | INFO_REALIGN_3_PRIME | chr21 | 17568557 | ||||
chr21:17568557
|
C | CTT | 5 | a0001c0001t0067a0001c0002t0011a0001c0004t0011others(2): Show | 9 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2881_*2882dupTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2883 | INFO_REALIGN_3_PRIME | chr21 | 17568557 | ||||
chr21:17568557
|
CT | C | 42 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(39): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*2882delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2882 | INFO_REALIGN_3_PRIME | chr21 | 17568557 | ||||
chr21:17568566
|
T | C | 4 | a0001c0001t0031a0001c0001t0079a0002c0005t0018others(1): Show | 7 | HG02145.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2874T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2874 | chr21 | 17568566 | |||||
chr21:17568582
|
A | G | 34 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(31): Show | 114 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2890A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2890 | chr21 | 17568582 | |||||
chr21:17568605
|
G | C | 30 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(27): Show | 106 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2913G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2913 | chr21 | 17568605 | |||||
chr21:17568671
|
G | T | 2 | a0001c0001t0012a0001c0001t0056 | 6 | NA18989.hp2 NA18993.hp2 NA18995.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2979G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2979 | chr21 | 17568671 | |||||
chr21:17568743
|
G | C | 4 | a0001c0002t0011a0001c0004t0011a0001c0004t0040others(1): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3051G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3051 | chr21 | 17568743 | |||||
chr21:17568769
|
G | A | 34 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(31): Show | 114 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*3077G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3077 | chr21 | 17568769 | |||||
chr21:17568781
|
C | G | 2 | a0001c0002t0027a0001c0002t0062 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3089C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3089 | chr21 | 17568781 | |||||
chr21:17568797
|
C | G | 9 | a0001c0001t0003a0001c0001t0016a0001c0001t0029others(6): Show | 57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3105C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3105 | chr21 | 17568797 | |||||
chr21:17568828
|
A | G | 1 | a0001c0002t0037 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3136A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3136 | chr21 | 17568828 | |||||
chr21:17568945
|
A | G | 18 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(15): Show | 77 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3253A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3253 | chr21 | 17568945 | |||||
chr21:17569132
|
A | G | 1 | a0001c0001t0055 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3440A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3440 | chr21 | 17569132 | |||||
chr21:17569133
|
T | C | 1 | a0001c0002t0070 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3441T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3441 | chr21 | 17569133 | |||||
chr21:17569366
|
T | TTA | 17 | a0001c0002t0004a0001c0002t0008a0001c0002t0020others(14): Show | 36 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3686_*3687dupAT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3688 | INFO_REALIGN_3_PRIME | chr21 | 17569366 | ||||
chr21:17569366
|
TTA | T | 16 | a0001c0001t0003a0001c0001t0016a0001c0001t0029others(13): Show | 68 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3686_*3687delAT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3686 | INFO_REALIGN_3_PRIME | chr21 | 17569366 | ||||
chr21:17569383
|
C | T | 26 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(23): Show | 102 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*3691C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3691 | chr21 | 17569383 | |||||
chr21:17569397
|
A | G | 1 | a0001c0001t0048 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3705A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3705 | chr21 | 17569397 | |||||
chr21:17569515
|
A | G | 1 | a0001c0001t0028 | 2 | HG02055.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3823A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3823 | chr21 | 17569515 | |||||
chr21:17569657
|
G | C | 34 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(31): Show | 114 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*3965G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3965 | chr21 | 17569657 | |||||
chr21:17569753
|
G | A | 2 | a0001c0001t0028a0001c0011t0063 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4061G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4061 | chr21 | 17569753 | |||||
chr21:17569758
|
C | T | 2 | a0004c0008t0082a0004c0008t0084 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4066C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4066 | chr21 | 17569758 | |||||
chr21:17569787
|
T | C | 2 | a0001c0003t0009a0001c0003t0064 | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4095T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4095 | chr21 | 17569787 | |||||
chr21:17569870
|
G | A | 3 | a0001c0001t0023a0001c0001t0050a0001c0001t0055 | 4 | NA18941.hp2 NA18947.hp1 NA18975.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4178G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4178 | chr21 | 17569870 | |||||
chr21:17569905
|
G | A | 28 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(25): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*4213G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4213 | chr21 | 17569905 | |||||
chr21:17569931
|
G | A | 7 | a0001c0002t0011a0001c0002t0057a0001c0002t0059others(4): Show | 11 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4239G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4239 | chr21 | 17569931 | |||||
chr21:17570025
|
C | G | 2 | a0001c0002t0027a0001c0002t0062 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4333C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4333 | chr21 | 17570025 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:17513186
|
A | C | 24 | a0001c0001t0019g0323a0001c0001t0019g0331a0001c0002t0004g0322others(21): Show | 24 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.43+14A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513186 | ||||||
chr21:17513228
|
C | G | 30 | a0001c0001t0001g0306a0001c0001t0001g0314a0001c0001t0001g0315others(27): Show | 31 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.43+56C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513228 | ||||||
chr21:17513267
|
C | G | 1 | a0003c0010t0036g0344 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.43+95C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513267 | ||||||
chr21:17513356
|
C | A | 17 | a0001c0001t0019g0323a0001c0001t0019g0331a0001c0002t0004g0322others(14): Show | 17 | HG00423.hp2 HG00609.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.43+184C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513356 | ||||||
chr21:17513408
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+236C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513408 | ||||||
chr21:17513410
|
G | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.43+238G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513410 | ||||||
chr21:17513423
|
G | A | 1 | a0001c0001t0007g0008 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.43+251G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513423 | ||||||
chr21:17513454
|
C | T | 23 | a0001c0001t0019g0323a0001c0001t0019g0331a0001c0002t0004g0322others(20): Show | 23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+282C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513454 | ||||||
chr21:17513575
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.43+403T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513575 | ||||||
chr21:17513580
|
C | T | 97 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0199others(94): Show | 99 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.43+408C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513580 | ||||||
chr21:17513624
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0001t0067g0013others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+452T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513624 | ||||||
chr21:17513642
|
A | C | 1 | a0001c0001t0001g0291 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+470A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513642 | ||||||
chr21:17513649
|
A | G | 3 | a0001c0001t0002g0196a0001c0004t0011g0195a0001c0004t0011g0197 | 3 | HG02886.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.43+477A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513649 | ||||||
chr21:17513651
|
G | A | 23 | a0001c0001t0019g0323a0001c0001t0019g0331a0001c0002t0004g0322others(20): Show | 23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+479G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513651 | ||||||
chr21:17513657
|
G | T | 2 | a0001c0002t0059g0003a0001c0002t0060g0003 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.43+485G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513657 | ||||||
chr21:17513942
|
A | C | 1 | a0001c0001t0003g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.43+770A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513942 | ||||||
chr21:17513950
|
G | C | 1 | a0001c0001t0002g0018 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.43+778G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513950 | ||||||
chr21:17514192
|
C | A | 6 | a0001c0001t0002g0007a0001c0001t0002g0292a0001c0001t0002g0293others(3): Show | 7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+1020C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514192 | ||||||
chr21:17514201
|
G | A | 1 | a0001c0002t0057g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+1029G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514201 | ||||||
chr21:17514208
|
T | G | 1 | a0001c0001t0003g0004 | 2 | NA18953.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.43+1036T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514208 | ||||||
chr21:17514447
|
G | A | 5 | a0001c0001t0003g0020a0001c0003t0009g0021a0001c0003t0009g0022others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+1275G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514447 | ||||||
chr21:17514524
|
C | T | 3 | a0001c0001t0002g0286a0001c0001t0002g0287a0001c0001t0002g0288 | 3 | HG00323.hp2 NA18954.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.43+1352C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514524 | ||||||
chr21:17514565
|
GA | G | 240 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.43+1407delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17514565 | |||||
chr21:17514565
|
GAAA | G | 15 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+1405_43+1407del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17514565 | |||||
chr21:17514567
|
A | G | 3 | a0001c0001t0002g0196a0001c0004t0011g0195a0001c0004t0011g0197 | 3 | HG02886.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.43+1395A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514567 | ||||||
chr21:17514637
|
CT | C | 7 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(4): Show | 7 | HG01243.hp1 HG01257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+1479delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17514637 | |||||
chr21:17514685
|
G | A | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+1513G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514685 | ||||||
chr21:17514733
|
A | G | 5 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0007t0033g0189others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+1561A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514733 | ||||||
chr21:17514739
|
T | G | 24 | a0001c0001t0019g0323a0001c0001t0019g0331a0001c0002t0004g0322others(21): Show | 24 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.43+1567T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514739 | ||||||
chr21:17514794
|
C | T | 2 | a0001c0001t0031g0185a0001c0001t0031g0186 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.43+1622C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514794 | ||||||
chr21:17514813
|
T | C | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+1641T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514813 | ||||||
chr21:17514883
|
C | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0110a0001c0001t0001g0112others(83): Show | 88 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.43+1711C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514883 | ||||||
chr21:17514886
|
A | T | 8 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0001t0067g0013others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+1714A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514886 | ||||||
chr21:17514973
|
A | AT | 14 | a0001c0001t0001g0184a0001c0001t0002g0015a0001c0001t0002g0192others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.43+1813dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17514973 | |||||
chr21:17515130
|
C | A | 2 | a0001c0001t0003g0203a0001c0001t0029g0202 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.43+1958C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515130 | ||||||
chr21:17515146
|
G | GA | 346 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(343): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.43+1976dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17515146 | |||||
chr21:17515165
|
C | T | 86 | a0001c0001t0001g0009a0001c0001t0001g0110a0001c0001t0001g0112others(83): Show | 88 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.43+1993C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515165 | ||||||
chr21:17515283
|
A | G | 85 | a0001c0001t0001g0009a0001c0001t0001g0110a0001c0001t0001g0112others(82): Show | 87 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.43+2111A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515283 | ||||||
chr21:17515360
|
T | A | 258 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.43+2188T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515360 | ||||||
chr21:17515408
|
G | A | 16 | a0001c0001t0002g0015a0001c0001t0002g0109a0001c0001t0002g0192others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.43+2236G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515408 | ||||||
chr21:17515432
|
A | T | 11 | a0001c0001t0003g0020a0001c0002t0006g0103a0001c0002t0011g0107others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+2260A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515432 | ||||||
chr21:17515447
|
C | CA | 16 | a0001c0001t0001g0204a0001c0001t0002g0015a0001c0001t0002g0192others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.43+2286dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17515447 | |||||
chr21:17515476
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.43+2304T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515476 | ||||||
chr21:17515509
|
A | G | 1 | a0001c0002t0057g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+2337A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515509 | ||||||
chr21:17515559
|
C | T | 1 | a0001c0002t0010g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.43+2387C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515559 | ||||||
chr21:17515602
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0001t0067g0013others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+2430G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515602 | ||||||
chr21:17515636
|
C | A | 6 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0302others(3): Show | 6 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+2464C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515636 | ||||||
chr21:17515662
|
A | T | 1 | a0001c0004t0040g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.43+2490A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515662 | ||||||
chr21:17515717
|
A | C | 1 | a0001c0001t0001g0291 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+2545A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515717 | ||||||
chr21:17515808
|
A | C | 24 | a0001c0001t0002g0007a0001c0001t0002g0094a0001c0001t0002g0095others(21): Show | 25 | HG00639.hp1 HG01361.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.43+2636A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515808 | ||||||
chr21:17516072
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.43+2900G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516072 | ||||||
chr21:17516162
|
C | G | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+2990C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516162 | ||||||
chr21:17516223
|
G | A | 6 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0302others(3): Show | 6 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+3051G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516223 | ||||||
chr21:17516400
|
G | A | 6 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0302others(3): Show | 6 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+3228G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516400 | ||||||
chr21:17516464
|
G | T | 15 | a0001c0001t0001g0306a0001c0001t0001g0314a0001c0001t0001g0315others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+3292G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516464 | ||||||
chr21:17516546
|
T | C | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+3374T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516546 | ||||||
chr21:17516653
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.43+3481C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516653 | ||||||
chr21:17516815
|
AGT | A | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0199others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.43+3646_43+3647del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17516815 | |||||
chr21:17516952
|
GA | G | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+3788delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17516952 | |||||
chr21:17517156
|
A | G | 2 | a0001c0003t0016g0187a0001c0004t0011g0188 | 2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+3984A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517156 | ||||||
chr21:17517447
|
G | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02523.hp2 NA18943.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+4275G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517447 | ||||||
chr21:17517553
|
G | C | 8 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0001t0067g0013others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+4381G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517553 | ||||||
chr21:17517570
|
A | G | 3 | a0001c0001t0001g0284a0001c0002t0039g0321a0001c0002t0073g0285 | 3 | NA19005.hp1 NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.43+4398A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517570 | ||||||
chr21:17517666
|
C | T | 3 | a0001c0001t0002g0196a0001c0004t0011g0195a0001c0004t0011g0197 | 3 | HG02886.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.43+4494C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517666 | ||||||
chr21:17517680
|
A | C | 11 | a0001c0001t0003g0020a0001c0002t0006g0103a0001c0002t0011g0107others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+4508A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517680 | ||||||
chr21:17517683
|
T | TTGAAGA | 39 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(36): Show | 39 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.43+4516_43+4517ins others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17517683 | |||||
chr21:17517734
|
A | G | 15 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+4562A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517734 | ||||||
chr21:17517741
|
A | T | 2 | a0001c0003t0016g0187a0001c0004t0011g0188 | 2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+4569A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517741 | ||||||
chr21:17517899
|
G | A | 15 | a0001c0001t0001g0306a0001c0001t0001g0314a0001c0001t0001g0315others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+4727G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517899 | ||||||
chr21:17517958
|
C | T | 2 | a0001c0003t0016g0187a0001c0004t0011g0188 | 2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+4786C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517958 | ||||||
chr21:17518043
|
C | T | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+4871C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518043 | ||||||
chr21:17518122
|
G | A | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+4950G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518122 | ||||||
chr21:17518141
|
G | A | 2 | a0001c0001t0002g0303a0001c0001t0002g0304 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.43+4969G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518141 | ||||||
chr21:17518141
|
GA | G | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+4970delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518141 | ||||||
chr21:17518170
|
G | T | 1 | a0001c0003t0009g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.43+4998G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518170 | ||||||
chr21:17518181
|
G | A | 6 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+5009G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518181 | ||||||
chr21:17518230
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.43+5058A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518230 | ||||||
chr21:17518264
|
AC | A | 3 | a0001c0001t0005g0179a0001c0001t0005g0180a0001c0001t0017g0178 | 3 | HG01168.hp2 HG01169.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.43+5094delC | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17518264 | |||||
chr21:17518266
|
C | A | 280 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(277): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.43+5094C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518266 | ||||||
chr21:17518308
|
A | G | 25 | a0001c0001t0019g0323a0001c0001t0019g0331a0001c0001t0068g0027others(22): Show | 25 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.43+5136A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518308 | ||||||
chr21:17518335
|
C | G | 3 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0002t0027g0016 | 3 | HG02055.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.43+5163C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518335 | ||||||
chr21:17518560
|
A | T | 1 | a0001c0001t0001g0291 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+5388A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518560 | ||||||
chr21:17518806
|
C | T | 6 | a0001c0001t0002g0007a0001c0001t0002g0292a0001c0001t0002g0293others(3): Show | 7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+5634C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518806 | ||||||
chr21:17518892
|
A | G | 15 | a0001c0001t0001g0306a0001c0001t0001g0314a0001c0001t0001g0315others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+5720A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518892 | ||||||
chr21:17518908
|
T | C | 1 | a0001c0003t0009g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.43+5736T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518908 | ||||||
chr21:17518953
|
C | T | 1 | a0001c0001t0017g0297 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43+5781C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518953 | ||||||
chr21:17519003
|
A | G | 2 | a0001c0002t0020g0335a0001c0002t0020g0336 | 2 | NA18993.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.43+5831A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519003 | ||||||
chr21:17519024
|
C | T | 5 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0283others(2): Show | 5 | HG02027.hp1 NA18960.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+5852C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519024 | ||||||
chr21:17519040
|
C | T | 2 | a0001c0001t0002g0303a0001c0001t0002g0304 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.43+5868C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519040 | ||||||
chr21:17519063
|
G | A | 1 | a0001c0002t0057g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+5891G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519063 | ||||||
chr21:17519082
|
T | G | 2 | a0001c0003t0016g0187a0001c0004t0011g0188 | 2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+5910T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519082 | ||||||
chr21:17519445
|
A | G | 1 | a0001c0001t0003g0025 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.43+6273A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519445 | ||||||
chr21:17519610
|
G | C | 1 | a0001c0001t0002g0116 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.43+6438G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519610 | ||||||
chr21:17519634
|
C | T | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+6462C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519634 | ||||||
chr21:17519691
|
T | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA19011.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.43+6519T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519691 | ||||||
chr21:17519696
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.43+6524G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519696 | ||||||
chr21:17519707
|
T | C | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+6535T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519707 | ||||||
chr21:17519734
|
G | C | 13 | a0001c0001t0002g0015a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+6562G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519734 | ||||||
chr21:17519758
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.43+6586C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519758 | ||||||
chr21:17519806
|
A | G | 2 | a0001c0001t0001g0277a0001c0001t0002g0276 | 2 | HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.43+6634A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519806 | ||||||
chr21:17519976
|
T | TAC | 15 | a0001c0001t0002g0007a0001c0001t0002g0196a0001c0001t0002g0292others(12): Show | 16 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.43+6819_43+6820dup others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17519976 | |||||
chr21:17519993
|
G | A | 1 | a0001c0002t0006g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.43+6821G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519993 | ||||||
chr21:17519996
|
C | T | 1 | a0001c0002t0008g0177 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.43+6824C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519996 | ||||||
chr21:17520041
|
C | A | 1 | a0001c0002t0057g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+6869C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520041 | ||||||
chr21:17520346
|
G | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0199others(105): Show | 110 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.43+7174G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520346 | ||||||
chr21:17520407
|
T | C | 85 | a0001c0001t0001g0009a0001c0001t0001g0110a0001c0001t0001g0112others(82): Show | 87 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.43+7235T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520407 | ||||||
chr21:17520586
|
A | T | 1 | a0001c0001t0001g0275 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.43+7414A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520586 | ||||||
chr21:17520648
|
G | A | 226 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(223): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.43+7476G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520648 | ||||||
chr21:17520779
|
T | C | 21 | a0001c0001t0001g0306a0001c0001t0001g0314a0001c0001t0001g0315others(18): Show | 21 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.43+7607T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520779 | ||||||
chr21:17520802
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.43+7630C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520802 | ||||||
chr21:17520843
|
A | G | 23 | a0001c0001t0019g0323a0001c0001t0019g0331a0001c0002t0004g0322others(20): Show | 23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+7671A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520843 | ||||||
chr21:17520844
|
T | C | 1 | a0001c0001t0046g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43+7672T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520844 | ||||||
chr21:17520898
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0043g0119 | 2 | HG01074.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.43+7726G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520898 | ||||||
chr21:17521022
|
T | G | 8 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0302others(5): Show | 8 | HG01243.hp1 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+7850T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521022 | ||||||
chr21:17521053
|
A | G | 336 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(333): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.43+7881A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521053 | ||||||
chr21:17521083
|
T | C | 5 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0007t0033g0189others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+7911T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521083 | ||||||
chr21:17521117
|
A | T | 1 | a0001c0001t0002g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.43+7945A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521117 | ||||||
chr21:17521131
|
A | G | 15 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0002t0006g0103others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+7959A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521131 | ||||||
chr21:17521179
|
G | A | 6 | a0001c0001t0002g0007a0001c0001t0002g0292a0001c0001t0002g0293others(3): Show | 7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+8007G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521179 | ||||||
chr21:17521280
|
G | A | 2 | a0001c0002t0010g0121a0001c0002t0010g0183 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.43+8108G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521280 | ||||||
chr21:17521300
|
G | A | 1 | a0001c0002t0004g0322 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.43+8128G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521300 | ||||||
chr21:17521318
|
TTTA | T | 17 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0109others(14): Show | 18 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.43+8164_43+8166del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17521318 | |||||
chr21:17521345
|
C | T | 6 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+8173C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521345 | ||||||
chr21:17521375
|
T | A | 185 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0040others(182): Show | 187 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.43+8203T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521375 | ||||||
chr21:17521464
|
A | G | 12 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0302others(9): Show | 12 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+8292A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521464 | ||||||
chr21:17521537
|
G | A | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+8365G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521537 | ||||||
chr21:17521548
|
C | CCTGA | 3 | a0001c0002t0057g0019a0001c0003t0016g0187a0001c0004t0011g0188 | 3 | HG01243.hp1 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.43+8378_43+8381dup others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17521548 | |||||
chr21:17521559
|
GTGA | G | 10 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0002t0057g0019others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+8389_43+8391del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17521559 | |||||
chr21:17521694
|
G | A | 1 | a0001c0002t0027g0144 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.43+8522G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521694 | ||||||
chr21:17522133
|
G | C | 129 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0007others(126): Show | 132 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.43+8961G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522133 | ||||||
chr21:17522154
|
C | CT | 11 | a0001c0001t0002g0007a0001c0001t0002g0292a0001c0001t0002g0293others(8): Show | 12 | HG02683.hp2 HG02717.hp1 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.43+8992dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17522154 | |||||
chr21:17522164
|
T | G | 1 | a0001c0002t0004g0324 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.43+8992T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522164 | ||||||
chr21:17522195
|
C | T | 1 | a0001c0002t0057g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+9023C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522195 | ||||||
chr21:17522197
|
A | G | 5 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(2): Show | 5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+9025A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522197 | ||||||
chr21:17522198
|
G | C | 1 | a0001c0001t0002g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.43+9026G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522198 | ||||||
chr21:17522200
|
G | T | 5 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(2): Show | 5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+9028G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522200 | ||||||
chr21:17522209
|
C | T | 9 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(6): Show | 9 | HG00741.hp2 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+9037C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522209 | ||||||
chr21:17522315
|
AT | A | 58 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0018others(55): Show | 60 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.43+9147delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17522315 | |||||
chr21:17522335
|
C | T | 2 | a0001c0001t0003g0302a0001c0002t0006g0301 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.43+9163C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522335 | ||||||
chr21:17522347
|
C | T | 1 | a0001c0001t0005g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.43+9175C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522347 | ||||||
chr21:17522348
|
A | G | 90 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0007others(87): Show | 93 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.43+9176A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522348 | ||||||
chr21:17522360
|
C | G | 42 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0059others(39): Show | 42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.43+9188C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522360 | ||||||
chr21:17522375
|
C | T | 1 | a0001c0002t0057g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+9203C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522375 | ||||||
chr21:17522391
|
G | A | 22 | a0001c0001t0019g0331a0001c0002t0004g0322a0001c0002t0004g0324others(19): Show | 22 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+9219G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522391 | ||||||
chr21:17522480
|
A | G | 10 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0002t0057g0019others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+9308A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522480 | ||||||
chr21:17522693
|
T | C | 1 | a0001c0001t0028g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.43+9521T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522693 | ||||||
chr21:17522909
|
T | C | 6 | a0001c0001t0002g0007a0001c0001t0002g0292a0001c0001t0002g0293others(3): Show | 7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+9737T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522909 | ||||||
chr21:17522958
|
A | G | 10 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0002t0057g0019others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+9786A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522958 | ||||||
chr21:17522974
|
T | C | 1 | a0001c0001t0051g0207 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.43+9802T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522974 | ||||||
chr21:17523049
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0042g0273 | 2 | HG00099.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.43+9877A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523049 | ||||||
chr21:17523406
|
C | G | 3 | a0001c0002t0021g0333a0001c0002t0021g0334a0001c0002t0034g0332 | 3 | HG02015.hp2 HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.43+10234C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523406 | ||||||
chr21:17523491
|
C | G | 2 | a0001c0003t0016g0187a0001c0004t0011g0188 | 2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+10319C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523491 | ||||||
chr21:17523542
|
CAT | C | 6 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(3): Show | 6 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+10372_43+10373d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17523542 | |||||
chr21:17523579
|
G | A | 9 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+10407G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523579 | ||||||
chr21:17523652
|
T | A | 9 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0001t0067g0013others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+10480T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523652 | ||||||
chr21:17523670
|
A | T | 1 | a0001c0004t0011g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.43+10498A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523670 | ||||||
chr21:17523753
|
G | A | 182 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0040others(179): Show | 184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.43+10581G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523753 | ||||||
chr21:17523894
|
T | C | 39 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(36): Show | 39 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.43+10722T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523894 | ||||||
chr21:17523928
|
G | A | 93 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0007others(90): Show | 96 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.43+10756G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523928 | ||||||
chr21:17524003
|
C | T | 5 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0007t0033g0189others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+10831C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524003 | ||||||
chr21:17524028
|
T | TTG | 11 | a0001c0001t0001g0272a0001c0002t0004g0337a0001c0002t0004g0338others(8): Show | 11 | HG00673.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+10869_43+10870d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524028 | |||||
chr21:17524041
|
T | TGTGC | 4 | a0001c0001t0002g0196a0001c0001t0017g0297a0001c0004t0011g0195others(1): Show | 4 | HG02486.hp2 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+10870_43+10871i others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524041 | |||||
chr21:17524043
|
C | CGT | 90 | a0001c0001t0001g0009a0001c0001t0001g0271a0001c0001t0002g0002others(87): Show | 93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.43+10894_43+10895d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524043 | |||||
chr21:17524043
|
C | T | 4 | a0001c0001t0002g0196a0001c0001t0017g0297a0001c0004t0011g0195others(1): Show | 4 | HG02486.hp2 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+10871C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524043 | ||||||
chr21:17524043
|
CGT | C | 5 | a0001c0001t0079g0078a0001c0002t0014g0075a0001c0002t0014g0076others(2): Show | 5 | HG00642.hp1 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+10894_43+10895d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524043 | |||||
chr21:17524090
|
C | T | 1 | a0001c0001t0002g0176 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.43+10918C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524090 | ||||||
chr21:17524172
|
G | T | 4 | a0001c0001t0001g0270a0001c0001t0001g0275a0001c0001t0003g0004others(1): Show | 5 | NA18948.hp2 NA18953.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+11000G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524172 | ||||||
chr21:17524195
|
A | T | 61 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0018others(58): Show | 63 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.43+11023A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524195 | ||||||
chr21:17524219
|
C | T | 3 | a0001c0002t0057g0019a0001c0003t0016g0187a0001c0004t0011g0188 | 3 | HG01243.hp1 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.43+11047C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524219 | ||||||
chr21:17524240
|
C | T | 2 | a0001c0003t0009g0023a0001c0003t0009g0024 | 2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.43+11068C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524240 | ||||||
chr21:17524347
|
A | G | 1 | a0001c0001t0002g0296 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.43+11175A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524347 | ||||||
chr21:17524427
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.43+11255T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524427 | ||||||
chr21:17524490
|
C | T | 60 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0018others(57): Show | 62 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.43+11318C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524490 | ||||||
chr21:17524575
|
C | CA | 18 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0318others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.43+11430dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | |||||
chr21:17524575
|
CA | C | 33 | a0001c0001t0001g0040a0001c0001t0003g0020a0001c0001t0003g0042others(30): Show | 33 | HG00140.hp2 HG00423.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.43+11430delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | |||||
chr21:17524575
|
CAA | C | 68 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0067others(65): Show | 68 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.43+11429_43+11430d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | |||||
chr21:17524575
|
CAAA | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0110others(115): Show | 120 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.43+11428_43+11430d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | |||||
chr21:17524575
|
CAAAAAA | C | 73 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0015others(70): Show | 76 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.43+11425_43+11430d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | |||||
chr21:17524575
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0201a0001c0001t0015g0268 | 2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.43+11421_43+11430d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | |||||
chr21:17524575
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(2): Show | 5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+11418_43+11430d others(15): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | |||||
chr21:17524765
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.43+11593C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524765 | ||||||
chr21:17524779
|
C | T | 6 | a0001c0001t0002g0007a0001c0001t0002g0292a0001c0001t0002g0293others(3): Show | 7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+11607C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524779 | ||||||
chr21:17525079
|
T | C | 1 | a0001c0001t0055g0307 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.43+11907T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525079 | ||||||
chr21:17525205
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0002g0215 | 2 | HG02132.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.43+12033T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525205 | ||||||
chr21:17525244
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+12072G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525244 | ||||||
chr21:17525358
|
A | T | 1 | a0001c0001t0001g0267 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.43+12186A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525358 | ||||||
chr21:17525369
|
A | C | 1 | a0001c0001t0028g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.43+12197A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525369 | ||||||
chr21:17525474
|
C | T | 10 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0002t0057g0019others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+12302C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525474 | ||||||
chr21:17525608
|
T | A | 93 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0007others(90): Show | 96 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.43+12436T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525608 | ||||||
chr21:17525725
|
A | G | 7 | a0001c0002t0004g0337a0001c0002t0004g0338a0001c0002t0004g0339others(4): Show | 7 | HG00673.hp2 HG02074.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+12553A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525725 | ||||||
chr21:17525759
|
T | C | 1 | a0001c0001t0017g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.43+12587T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525759 | ||||||
chr21:17525909
|
A | T | 1 | a0001c0001t0001g0266 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.43+12737A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525909 | ||||||
chr21:17526014
|
T | C | 9 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+12842T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526014 | ||||||
chr21:17526045
|
A | C | 1 | a0001c0004t0011g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.43+12873A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526045 | ||||||
chr21:17526054
|
C | T | 22 | a0001c0001t0019g0331a0001c0002t0004g0322a0001c0002t0004g0324others(19): Show | 22 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+12882C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526054 | ||||||
chr21:17526279
|
T | C | 62 | a0001c0001t0001g0009a0001c0001t0001g0122a0001c0001t0002g0002others(59): Show | 64 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.43+13107T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526279 | ||||||
chr21:17526364
|
A | T | 9 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+13192A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526364 | ||||||
chr21:17526508
|
G | A | 1 | a0001c0001t0003g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.43+13336G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526508 | ||||||
chr21:17526577
|
G | T | 9 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+13405G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526577 | ||||||
chr21:17526583
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+13411G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526583 | ||||||
chr21:17526831
|
G | GTTTTGT | 6 | a0001c0001t0067g0013a0001c0002t0061g0014a0001c0002t0062g0164others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+13675_43+13680d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17526831 | |||||
chr21:17526911
|
A | C | 9 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0001t0067g0013others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+13739A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526911 | ||||||
chr21:17527093
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+13921T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527093 | ||||||
chr21:17527174
|
G | A | 8 | a0001c0001t0079g0078a0001c0002t0010g0121a0001c0002t0010g0183others(5): Show | 8 | HG00642.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+14002G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527174 | ||||||
chr21:17527194
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.43+14022G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527194 | ||||||
chr21:17527285
|
A | C | 2 | a0001c0003t0016g0187a0001c0004t0011g0188 | 2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+14113A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527285 | ||||||
chr21:17527372
|
G | A | 22 | a0001c0001t0019g0331a0001c0002t0004g0322a0001c0002t0004g0324others(19): Show | 22 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+14200G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527372 | ||||||
chr21:17527385
|
C | T | 6 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(3): Show | 6 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+14213C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527385 | ||||||
chr21:17527509
|
G | T | 5 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(2): Show | 5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+14337G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527509 | ||||||
chr21:17527653
|
T | C | 2 | a0001c0001t0007g0217a0001c0001t0007g0218 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.43+14481T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527653 | ||||||
chr21:17527681
|
G | A | 1 | a0001c0002t0037g0326 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43+14509G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527681 | ||||||
chr21:17527688
|
C | G | 1 | a0001c0004t0011g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.43+14516C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527688 | ||||||
chr21:17527726
|
C | A | 42 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0059others(39): Show | 42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.43+14554C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527726 | ||||||
chr21:17527800
|
T | TTTTA | 11 | a0001c0001t0002g0196a0001c0001t0005g0163a0001c0001t0017g0297others(8): Show | 12 | HG01099.hp1 HG01192.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.43+14648_43+14651d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17527800 | |||||
chr21:17527820
|
A | T | 1 | a0001c0001t0047g0265 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.43+14648A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527820 | ||||||
chr21:17527842
|
C | T | 42 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0059others(39): Show | 42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.43+14670C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527842 | ||||||
chr21:17527932
|
C | T | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+14760C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527932 | ||||||
chr21:17527957
|
A | G | 9 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+14785A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527957 | ||||||
chr21:17528060
|
A | C | 1 | a0001c0002t0027g0144 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.43+14888A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528060 | ||||||
chr21:17528068
|
C | CT | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0112others(111): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.43+14919dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | |||||
chr21:17528068
|
C | CTT | 22 | a0001c0001t0001g0110a0001c0001t0001g0139a0001c0001t0001g0140others(19): Show | 22 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+14918_43+14919d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | |||||
chr21:17528068
|
CT | C | 47 | a0001c0001t0002g0015a0001c0001t0002g0082a0001c0001t0002g0094others(44): Show | 47 | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.43+14919delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | |||||
chr21:17528068
|
CTT | C | 92 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0007others(89): Show | 95 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.43+14918_43+14919d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | |||||
chr21:17528068
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0303 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.43+14910_43+14919d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | |||||
chr21:17528071
|
T | G | 8 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0001t0067g0013others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+14899T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528071 | ||||||
chr21:17528072
|
T | G | 1 | a0001c0006t0078g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.43+14900T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528072 | ||||||
chr21:17528073
|
T | C | 11 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(8): Show | 11 | HG00741.hp2 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+14901T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528073 | ||||||
chr21:17528074
|
T | C | 20 | a0001c0001t0019g0331a0001c0002t0004g0322a0001c0002t0004g0324others(17): Show | 20 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.43+14902T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528074 | ||||||
chr21:17528075
|
T | C | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+14903T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528075 | ||||||
chr21:17528100
|
G | T | 1 | a0001c0001t0002g0320 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.43+14928G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528100 | ||||||
chr21:17528265
|
G | A | 24 | a0001c0001t0003g0020a0001c0001t0019g0331a0001c0002t0004g0322others(21): Show | 24 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.43+15093G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528265 | ||||||
chr21:17528363
|
C | T | 10 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0002t0057g0019others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+15191C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528363 | ||||||
chr21:17528709
|
A | G | 1 | a0001c0001t0046g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43+15537A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528709 | ||||||
chr21:17528832
|
T | C | 337 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.43+15660T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528832 | ||||||
chr21:17528852
|
C | T | 23 | a0001c0001t0019g0331a0001c0002t0004g0322a0001c0002t0004g0324others(20): Show | 23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+15680C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528852 | ||||||
chr21:17528938
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.43+15766C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528938 | ||||||
chr21:17528965
|
G | A | 2 | a0001c0001t0002g0303a0001c0001t0002g0304 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.43+15793G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528965 | ||||||
chr21:17529034
|
C | CT | 31 | a0001c0001t0001g0113a0001c0001t0001g0263a0001c0001t0001g0283others(28): Show | 31 | HG00639.hp2 HG00741.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.43+15884dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529034 | |||||
chr21:17529034
|
CT | C | 25 | a0001c0001t0001g0050a0001c0001t0001g0209a0001c0001t0001g0221others(22): Show | 25 | HG00544.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.43+15884delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529034 | |||||
chr21:17529034
|
CTTTTTTT others(5): Show |
C | 95 | a0001c0001t0001g0009a0001c0001t0001g0122a0001c0001t0002g0002others(92): Show | 98 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.43+15873_43+15884d others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529034 | |||||
chr21:17529034
|
CTTTTTTT others(7): Show |
C | 22 | a0001c0001t0019g0331a0001c0002t0004g0322a0001c0002t0004g0324others(19): Show | 22 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+15871_43+15884d others(16): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529034 | |||||
chr21:17529100
|
G | A | 9 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+15928G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529100 | ||||||
chr21:17529252
|
C | T | 4 | a0001c0001t0031g0185a0001c0001t0031g0186a0001c0007t0002g0092others(1): Show | 4 | HG02717.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+16080C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529252 | ||||||
chr21:17529266
|
C | T | 1 | a0001c0003t0009g0022 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.43+16094C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529266 | ||||||
chr21:17529315
|
G | C | 42 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0059others(39): Show | 42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.43+16143G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529315 | ||||||
chr21:17529502
|
A | G | 181 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0040others(178): Show | 183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.43+16330A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529502 | ||||||
chr21:17529651
|
G | A | 127 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0007others(124): Show | 130 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.43+16479G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529651 | ||||||
chr21:17529774
|
C | A | 337 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.43+16602C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529774 | ||||||
chr21:17529795
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.43+16623T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529795 | ||||||
chr21:17529922
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.43+16750T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529922 | ||||||
chr21:17529931
|
ATTTTTC | A | 23 | a0001c0001t0019g0331a0001c0002t0004g0322a0001c0002t0004g0324others(20): Show | 23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+16777_43+16782d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529931 | |||||
chr21:17529955
|
T | C | 10 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0002t0057g0019others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+16783T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529955 | ||||||
chr21:17529970
|
A | G | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+16798A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529970 | ||||||
chr21:17530028
|
A | G | 1 | a0001c0004t0011g0080 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.43+16856A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530028 | ||||||
chr21:17530051
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.43+16879C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530051 | ||||||
chr21:17530059
|
T | C | 337 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.43+16887T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530059 | ||||||
chr21:17530114
|
A | AT | 104 | a0001c0001t0001g0009a0001c0001t0001g0314a0001c0001t0001g0318others(101): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.44-16895dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | |||||
chr21:17530114
|
A | ATT | 13 | a0001c0001t0001g0315a0001c0001t0002g0303a0001c0001t0002g0304others(10): Show | 13 | HG01175.hp1 HG01175.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-16896_44-16895d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | |||||
chr21:17530114
|
A | ATTT | 59 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0059others(56): Show | 59 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.44-16897_44-16895d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | |||||
chr21:17530114
|
A | ATTTT | 21 | a0001c0001t0001g0067a0001c0001t0001g0112a0001c0001t0001g0224others(18): Show | 21 | HG01109.hp1 HG01261.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.44-16898_44-16895d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | |||||
chr21:17530114
|
A | ATTTTT | 104 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0113others(101): Show | 106 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.44-16899_44-16895d others(7): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | |||||
chr21:17530114
|
A | ATTTTTT | 21 | a0001c0001t0001g0006a0001c0001t0001g0199a0001c0001t0001g0213others(18): Show | 21 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.44-16900_44-16895d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | |||||
chr21:17530205
|
A | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0139a0001c0001t0001g0140others(4): Show | 7 | HG02132.hp2 HG02135.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-16822A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530205 | ||||||
chr21:17530220
|
C | T | 13 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0302others(10): Show | 13 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-16807C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530220 | ||||||
chr21:17530224
|
C | G | 9 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-16803C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530224 | ||||||
chr21:17530294
|
AT | A | 9 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-16730delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530294 | |||||
chr21:17530453
|
G | C | 13 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0302others(10): Show | 13 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-16574G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530453 | ||||||
chr21:17530551
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.44-16476C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530551 | ||||||
chr21:17530641
|
C | T | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-16386C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530641 | ||||||
chr21:17530755
|
G | A | 62 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0018others(59): Show | 64 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.44-16272G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530755 | ||||||
chr21:17530762
|
C | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0003t0009g0021others(4): Show | 7 | HG01109.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-16265C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530762 | ||||||
chr21:17530766
|
A | G | 1 | a0001c0001t0079g0078 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.44-16261A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530766 | ||||||
chr21:17530792
|
C | T | 4 | a0001c0002t0008g0160a0001c0002t0008g0161a0001c0002t0008g0177others(1): Show | 4 | HG02056.hp2 NA18981.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-16235C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530792 | ||||||
chr21:17530820
|
A | C | 10 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0002t0057g0019others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-16207A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530820 | ||||||
chr21:17530892
|
T | A | 2 | a0001c0001t0002g0303a0001c0001t0002g0304 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.44-16135T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530892 | ||||||
chr21:17531038
|
G | A | 6 | a0001c0001t0079g0078a0001c0002t0014g0075a0001c0002t0014g0076others(3): Show | 6 | HG00642.hp1 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-15989G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531038 | ||||||
chr21:17531109
|
C | G | 1 | a0001c0001t0002g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.44-15918C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531109 | ||||||
chr21:17531118
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.44-15909C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531118 | ||||||
chr21:17531146
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.44-15881A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531146 | ||||||
chr21:17531162
|
G | A | 3 | a0001c0001t0022g0118a0001c0001t0022g0262a0001c0001t0044g0210 | 3 | HG00741.hp1 HG02559.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.44-15865G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531162 | ||||||
chr21:17531164
|
G | A | 3 | a0001c0003t0009g0154a0001c0003t0009g0182a0001c0003t0064g0147 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.44-15863G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531164 | ||||||
chr21:17531170
|
G | A | 1 | a0001c0001t0046g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.44-15857G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531170 | ||||||
chr21:17531214
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.44-15813G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531214 | ||||||
chr21:17531229
|
G | A | 1 | a0001c0001t0003g0072 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.44-15798G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531229 | ||||||
chr21:17531277
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.44-15750C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531277 | ||||||
chr21:17531298
|
C | CA | 6 | a0001c0001t0002g0007a0001c0001t0002g0292a0001c0001t0002g0293others(3): Show | 7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-15716dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531298 | |||||
chr21:17531298
|
CA | C | 111 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0015others(108): Show | 113 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.44-15716delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531298 | |||||
chr21:17531298
|
CAA | C | 13 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0302others(10): Show | 13 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-15717_44-15716d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531298 | |||||
chr21:17531319
|
A | G | 3 | a0001c0002t0057g0019a0001c0003t0016g0187a0001c0004t0011g0188 | 3 | HG01243.hp1 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.44-15708A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531319 | ||||||
chr21:17531339
|
T | G | 42 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0059others(39): Show | 42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.44-15688T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531339 | ||||||
chr21:17531347
|
C | T | 1 | a0001c0001t0003g0066 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-15680C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531347 | ||||||
chr21:17531415
|
A | G | 11 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0002t0010g0183others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-15612A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531415 | ||||||
chr21:17531438
|
T | C | 43 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0291others(40): Show | 43 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.44-15589T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531438 | ||||||
chr21:17531536
|
A | G | 335 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(332): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.44-15491A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531536 | ||||||
chr21:17531555
|
G | C | 1 | a0001c0001t0003g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.44-15472G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531555 | ||||||
chr21:17531573
|
C | T | 3 | a0001c0001t0002g0100a0001c0002t0006g0101a0001c0002t0006g0102 | 3 | HG00639.hp1 HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.44-15454C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531573 | ||||||
chr21:17531721
|
A | G | 4 | a0001c0002t0006g0001a0001c0002t0006g0117a0001c0002t0006g0152others(1): Show | 5 | HG01099.hp1 HG01192.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-15306A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531721 | ||||||
chr21:17531779
|
CTT | C | 26 | a0001c0001t0002g0100a0001c0001t0002g0196a0001c0001t0005g0163others(23): Show | 27 | HG00639.hp1 HG00642.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.44-15244_44-15243d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531779 | |||||
chr21:17531786
|
G | C | 1 | a0001c0001t0022g0262 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.44-15241G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531786 | ||||||
chr21:17531937
|
G | GT | 187 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0040others(184): Show | 189 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.44-15076dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531937 | |||||
chr21:17531937
|
G | GTT | 42 | a0001c0001t0001g0243a0001c0001t0001g0253a0001c0001t0001g0291others(39): Show | 43 | HG00597.hp1 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.44-15077_44-15076d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531937 | |||||
chr21:17531998
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.44-15029G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531998 | ||||||
chr21:17532008
|
C | T | 2 | a0001c0001t0003g0064a0001c0001t0003g0071 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.44-15019C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532008 | ||||||
chr21:17532009
|
A | C | 2 | a0001c0001t0003g0064a0001c0001t0003g0071 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.44-15018A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532009 | ||||||
chr21:17532042
|
C | T | 5 | a0001c0001t0001g0112a0001c0001t0001g0209a0001c0001t0001g0221others(2): Show | 5 | HG02040.hp2 HG02155.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-14985C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532042 | ||||||
chr21:17532183
|
C | T | 258 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(255): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.44-14844C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532183 | ||||||
chr21:17532196
|
G | C | 3 | a0001c0006t0032g0011a0001c0006t0032g0012a0001c0006t0078g0010 | 3 | HG01109.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.44-14831G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532196 | ||||||
chr21:17532261
|
G | C | 10 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(7): Show | 10 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.44-14766G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532261 | ||||||
chr21:17532309
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0006t0032g0011others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-14718G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532309 | ||||||
chr21:17532339
|
A | G | 2 | a0001c0001t0002g0196a0001c0001t0017g0297 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.44-14688A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532339 | ||||||
chr21:17532402
|
ACTGT | A | 16 | a0001c0001t0002g0015a0001c0001t0005g0029a0001c0001t0005g0030others(13): Show | 16 | HG00741.hp2 HG01109.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.44-14622_44-14619d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17532402 | |||||
chr21:17532432
|
A | G | 3 | a0001c0002t0057g0019a0001c0002t0059g0003a0001c0002t0060g0003 | 3 | HG02109.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-14595A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532432 | ||||||
chr21:17532445
|
A | C | 2 | a0001c0002t0020g0335a0001c0002t0020g0336 | 2 | NA18993.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.44-14582A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532445 | ||||||
chr21:17532474
|
C | T | 181 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.44-14553C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532474 | ||||||
chr21:17532507
|
AG | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0040others(109): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.44-14519delG | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532507 | ||||||
chr21:17532508
|
G | A | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-14519G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532508 | ||||||
chr21:17532636
|
GGCACTGC others(5): Show |
G | 35 | a0001c0001t0003g0141a0001c0001t0003g0172a0001c0002t0004g0322others(32): Show | 35 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.44-14388_44-14377d others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17532636 | |||||
chr21:17532770
|
G | A | 1 | a0001c0001t0046g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.44-14257G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532770 | ||||||
chr21:17532785
|
T | C | 1 | a0001c0002t0010g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.44-14242T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532785 | ||||||
chr21:17533041
|
G | A | 11 | a0001c0002t0006g0001a0001c0002t0006g0101a0001c0002t0006g0102others(8): Show | 12 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-13986G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533041 | ||||||
chr21:17533080
|
T | A | 66 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(63): Show | 67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-13947T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533080 | ||||||
chr21:17533153
|
A | T | 1 | a0001c0001t0017g0098 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.44-13874A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533153 | ||||||
chr21:17533581
|
G | A | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-13446G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533581 | ||||||
chr21:17533587
|
A | G | 17 | a0001c0002t0006g0001a0001c0002t0006g0101a0001c0002t0006g0102others(14): Show | 18 | HG00639.hp1 HG00642.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.44-13440A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533587 | ||||||
chr21:17533631
|
G | T | 1 | a0001c0001t0003g0269 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.44-13396G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533631 | ||||||
chr21:17533712
|
A | G | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-13315A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533712 | ||||||
chr21:17533824
|
C | G | 4 | a0001c0001t0001g0291a0001c0001t0025g0252a0001c0001t0026g0212others(1): Show | 4 | HG00423.hp1 NA18966.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-13203C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533824 | ||||||
chr21:17533873
|
G | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(117): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.44-13154G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533873 | ||||||
chr21:17533900
|
T | C | 1 | a0001c0001t0017g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.44-13127T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533900 | ||||||
chr21:17534007
|
A | AAT | 7 | a0001c0001t0002g0100a0001c0001t0002g0215a0001c0001t0005g0036others(4): Show | 7 | HG02258.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-13000_44-12999d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534007 | |||||
chr21:17534007
|
A | AATATAT | 15 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(12): Show | 15 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-13004_44-12999d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534007 | |||||
chr21:17534007
|
AAT | A | 102 | a0001c0001t0001g0009a0001c0001t0001g0059a0001c0001t0001g0120others(99): Show | 105 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.44-13000_44-12999d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534007 | |||||
chr21:17534007
|
AATAT | A | 7 | a0001c0004t0011g0038a0001c0004t0011g0080a0001c0004t0011g0188others(4): Show | 7 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-13002_44-12999d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534007 | |||||
chr21:17534012
|
ATATATAT others(11): Show |
A | 4 | a0001c0002t0014g0076a0001c0002t0014g0077a0001c0002t0014g0079others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-12998_44-12981d others(20): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534012 | |||||
chr21:17534019
|
T | TATATAGC others(17): Show |
1 | a0001c0003t0016g0187 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.44-13003_44-13002i others(26): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | |||||
chr21:17534019
|
T | TATATAGC others(19): Show |
1 | a0001c0001t0001g0113 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.44-13003_44-13002i others(28): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | |||||
chr21:17534019
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0201 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.44-13001_44-13000i others(28): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | |||||
chr21:17534019
|
T | TATATATA others(21): Show |
107 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0040others(104): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.44-13001_44-13000i others(30): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | |||||
chr21:17534019
|
T | TATATATA others(53): Show |
1 | a0001c0001t0015g0254 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.44-13001_44-13000i others(62): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | |||||
chr21:17534027
|
T | G | 31 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0002t0008g0039others(28): Show | 31 | HG01109.hp2 HG02015.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.44-13000T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534027 | ||||||
chr21:17534028
|
A | C | 31 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0002t0008g0039others(28): Show | 31 | HG01109.hp2 HG02015.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.44-12999A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534028 | ||||||
chr21:17534029
|
G | T | 31 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0002t0008g0039others(28): Show | 31 | HG01109.hp2 HG02015.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.44-12998G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534029 | ||||||
chr21:17534030
|
C | A | 31 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0002t0008g0039others(28): Show | 31 | HG01109.hp2 HG02015.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.44-12997C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534030 | ||||||
chr21:17534030
|
C | CTA | 21 | a0001c0001t0002g0175a0001c0001t0002g0320a0001c0002t0004g0322others(18): Show | 21 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.44-12982_44-12981d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534030 | |||||
chr21:17534030
|
CTA | C | 75 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(72): Show | 76 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.44-12982_44-12981d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534030 | |||||
chr21:17534032
|
A | ATATATAT others(15): Show |
1 | a0001c0002t0061g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-12981_44-12980i others(24): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534032 | |||||
chr21:17534045
|
T | C | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-12982T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534045 | ||||||
chr21:17534060
|
C | CTA | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0040others(118): Show | 122 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.44-12958_44-12957d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | |||||
chr21:17534060
|
C | CTATATAT others(23): Show |
2 | a0001c0001t0001g0291a0001c0001t0007g0317 | 2 | HG00099.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.44-12957_44-12956i others(32): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | |||||
chr21:17534060
|
C | CTATATAT others(25): Show |
2 | a0001c0001t0001g0009a0001c0001t0019g0331 | 2 | HG01928.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.44-12957_44-12956i others(34): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | |||||
chr21:17534060
|
C | CTATATAT others(51): Show |
1 | a0001c0001t0001g0222 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.44-12957_44-12956i others(60): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | |||||
chr21:17534060
|
C | CTATATAT others(27): Show |
3 | a0001c0001t0001g0120a0001c0001t0043g0119a0001c0009t0075g0191 | 3 | HG01074.hp1 HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.44-12957_44-12956i others(36): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | |||||
chr21:17534069
|
T | TATAC | 18 | a0001c0001t0001g0112a0001c0001t0001g0234a0001c0001t0001g0245others(15): Show | 19 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.44-12957_44-12956i others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534069 | |||||
chr21:17534069
|
T | TATATACA others(27): Show |
1 | a0001c0001t0001g0059 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.44-12957_44-12956i others(36): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534069 | |||||
chr21:17534071
|
C | T | 144 | a0001c0001t0001g0067a0001c0001t0001g0122a0001c0001t0001g0200others(141): Show | 146 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.44-12956C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534071 | ||||||
chr21:17534073
|
C | T | 1 | a0001c0001t0003g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.44-12954C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534073 | ||||||
chr21:17534079
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.44-12948C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534079 | ||||||
chr21:17534081
|
C | CATATAT | 3 | a0001c0001t0002g0225a0001c0002t0008g0160a0001c0003t0009g0021 | 3 | HG03041.hp1 NA18522.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.44-12931_44-12926d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534081 | |||||
chr21:17534081
|
C | T | 14 | a0001c0001t0001g0059a0001c0001t0001g0112a0001c0001t0001g0138others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-12946C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534081 | ||||||
chr21:17534081
|
CAT | C | 27 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0111others(24): Show | 28 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.44-12927_44-12926d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534081 | |||||
chr21:17534081
|
CATAT | C | 3 | a0002c0005t0018g0145a0002c0005t0018g0153a0002c0005t0018g0155 | 3 | HG02258.hp2 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.44-12929_44-12926d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534081 | |||||
chr21:17534083
|
T | C | 13 | a0001c0001t0001g0067a0001c0001t0001g0122a0001c0001t0001g0200others(10): Show | 13 | HG01069.hp1 HG01517.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-12944T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534083 | ||||||
chr21:17534085
|
T | C | 3 | a0001c0001t0031g0185a0001c0001t0031g0186a0001c0001t0079g0078 | 3 | HG02145.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.44-12942T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534085 | ||||||
chr21:17534098
|
A | AT | 9 | a0001c0001t0003g0086a0001c0001t0003g0142a0001c0001t0003g0173others(6): Show | 9 | HG00597.hp2 HG02165.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.44-12928dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534098 | |||||
chr21:17534098
|
A | T | 9 | a0001c0001t0003g0020a0001c0001t0003g0043a0001c0001t0003g0058others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-12929A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534098 | ||||||
chr21:17534098
|
ATAT | A | 6 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(3): Show | 6 | HG00323.hp2 HG01069.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-12927_44-12925d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534098 | |||||
chr21:17534099
|
TA | T | 4 | a0001c0001t0002g0171a0001c0001t0003g0025a0001c0001t0003g0047others(1): Show | 4 | HG00609.hp2 HG01433.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-12927delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534099 | ||||||
chr21:17534100
|
A | AT | 6 | a0001c0002t0010g0121a0001c0002t0010g0183a0001c0002t0014g0075others(3): Show | 6 | HG00642.hp1 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-12902dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | |||||
chr21:17534100
|
A | ATATATAT | 6 | a0001c0002t0008g0039a0001c0002t0008g0161a0001c0002t0008g0177others(3): Show | 6 | HG02027.hp2 HG02056.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-12926_44-12925i others(9): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | |||||
chr21:17534100
|
A | ATATATAT others(2): Show |
9 | a0001c0002t0004g0337a0001c0002t0004g0338a0001c0002t0004g0339others(6): Show | 9 | HG00673.hp2 HG02074.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-12926_44-12925i others(11): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | |||||
chr21:17534100
|
A | ATATATTT others(2): Show |
8 | a0001c0002t0004g0325a0001c0002t0004g0327a0001c0002t0004g0329others(5): Show | 8 | HG00423.hp2 HG02155.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-12926_44-12925i others(11): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | |||||
chr21:17534100
|
A | ATATATTT others(4): Show |
1 | a0001c0002t0004g0324 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.44-12926_44-12925i others(13): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | |||||
chr21:17534100
|
A | ATATATTT others(5): Show |
1 | a0001c0002t0004g0322 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.44-12926_44-12925i others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | |||||
chr21:17534100
|
A | ATTT | 11 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0002t0006g0001others(8): Show | 12 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-12904_44-12902d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | |||||
chr21:17534100
|
A | T | 52 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0042others(49): Show | 53 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.44-12927A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534100 | ||||||
chr21:17534100
|
AT | A | 9 | a0001c0001t0005g0179a0001c0002t0010g0228a0001c0002t0010g0310others(6): Show | 9 | HG01074.hp2 HG01169.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-12902delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | |||||
chr21:17534101
|
T | TA | 29 | a0001c0001t0001g0067a0001c0001t0001g0122a0001c0001t0001g0140others(26): Show | 29 | HG00673.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.44-12926_44-12925i others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534101 | ||||||
chr21:17534101
|
T | TATA | 3 | a0001c0001t0001g0184a0001c0001t0007g0235a0001c0002t0061g0014 | 3 | HG02735.hp1 HG02735.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.44-12926_44-12925i others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534101 | ||||||
chr21:17534102
|
T | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(105): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.44-12925T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534102 | ||||||
chr21:17534103
|
T | A | 23 | a0001c0001t0001g0067a0001c0001t0001g0122a0001c0001t0001g0140others(20): Show | 23 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.44-12924T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534103 | ||||||
chr21:17534104
|
T | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(89): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.44-12923T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534104 | ||||||
chr21:17534105
|
T | A | 14 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(11): Show | 14 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.44-12922T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534105 | ||||||
chr21:17534106
|
T | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0120others(6): Show | 10 | HG00735.hp1 HG01074.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-12921T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534106 | ||||||
chr21:17534107
|
T | A | 1 | a0001c0002t0061g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-12920T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534107 | ||||||
chr21:17534110
|
T | A | 2 | a0001c0001t0028g0091a0001c0011t0063g0162 | 2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-12917T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534110 | ||||||
chr21:17534211
|
G | A | 96 | a0001c0001t0002g0015a0001c0001t0003g0004a0001c0001t0003g0020others(93): Show | 98 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.44-12816G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534211 | ||||||
chr21:17534215
|
C | T | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-12812C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534215 | ||||||
chr21:17534257
|
C | T | 1 | a0001c0002t0061g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-12770C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534257 | ||||||
chr21:17534258
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-12769G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534258 | ||||||
chr21:17534278
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0199a0001c0001t0001g0222others(5): Show | 8 | HG00558.hp1 HG02083.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-12749G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534278 | ||||||
chr21:17534571
|
G | T | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-12456G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534571 | ||||||
chr21:17534583
|
G | C | 13 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0003t0009g0021others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-12444G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534583 | ||||||
chr21:17534767
|
A | ATTTGTCT others(3): Show |
2 | a0001c0001t0001g0234a0001c0001t0001g0271 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.44-12257_44-12248d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534767 | |||||
chr21:17534787
|
T | G | 1 | a0001c0013t0010g0298 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.44-12240T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534787 | ||||||
chr21:17534789
|
C | CT | 119 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0040others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.44-12224dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | |||||
chr21:17534789
|
C | CTTTTTTT others(2): Show |
12 | a0001c0001t0003g0043a0001c0002t0006g0001a0001c0002t0006g0101others(9): Show | 13 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-12232_44-12224d others(11): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | |||||
chr21:17534789
|
C | CTTTTTTT others(3): Show |
71 | a0001c0001t0002g0015a0001c0001t0003g0004a0001c0001t0003g0020others(68): Show | 72 | HG00438.hp1 HG00597.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.44-12233_44-12224d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | |||||
chr21:17534789
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0003g0046a0001c0001t0028g0091a0001c0002t0010g0183others(4): Show | 7 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-12234_44-12224d others(13): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | |||||
chr21:17534789
|
C | CTTTTTTT others(5): Show |
31 | a0001c0001t0003g0028a0001c0001t0028g0090a0001c0002t0004g0322others(28): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.44-12235_44-12224d others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | |||||
chr21:17534789
|
C | CTTTTTTT others(6): Show |
2 | a0001c0002t0008g0044a0003c0010t0036g0344 | 2 | HG04184.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.44-12236_44-12224d others(15): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | |||||
chr21:17534859
|
A | C | 1 | a0001c0001t0012g0132 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.44-12168A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534859 | ||||||
chr21:17534941
|
C | T | 3 | a0001c0001t0002g0286a0001c0001t0002g0287a0001c0001t0002g0288 | 3 | HG00323.hp2 NA18954.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.44-12086C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534941 | ||||||
chr21:17535304
|
T | G | 19 | a0001c0001t0003g0028a0001c0002t0004g0322a0001c0002t0004g0324others(16): Show | 19 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.44-11723T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535304 | ||||||
chr21:17535506
|
A | G | 5 | a0001c0001t0003g0141a0001c0001t0003g0172a0001c0001t0003g0173others(2): Show | 5 | HG00597.hp2 HG02083.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-11521A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535506 | ||||||
chr21:17535658
|
T | C | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-11369T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535658 | ||||||
chr21:17535659
|
A | C | 13 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0003t0009g0021others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-11368A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535659 | ||||||
chr21:17535756
|
C | T | 2 | a0001c0001t0003g0198a0001c0001t0003g0229 | 2 | NA18961.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.44-11271C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535756 | ||||||
chr21:17535968
|
A | G | 6 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-11059A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535968 | ||||||
chr21:17536013
|
T | A | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-11014T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536013 | ||||||
chr21:17536076
|
C | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0138 | 3 | HG00735.hp1 HG01192.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.44-10951C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536076 | ||||||
chr21:17536110
|
T | C | 1 | a0001c0001t0003g0072 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.44-10917T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536110 | ||||||
chr21:17536149
|
A | T | 7 | a0001c0001t0002g0007a0001c0001t0002g0156a0001c0001t0002g0157others(4): Show | 8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-10878A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536149 | ||||||
chr21:17536186
|
A | C | 144 | a0001c0001t0001g0059a0001c0001t0002g0015a0001c0001t0003g0004others(141): Show | 146 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.44-10841A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536186 | ||||||
chr21:17536187
|
C | T | 1 | a0001c0002t0027g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-10840C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536187 | ||||||
chr21:17536232
|
A | G | 10 | a0001c0002t0006g0001a0001c0002t0006g0101a0001c0002t0006g0102others(7): Show | 11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-10795A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536232 | ||||||
chr21:17536260
|
T | C | 8 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(5): Show | 8 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-10767T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536260 | ||||||
chr21:17536312
|
A | G | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-10715A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536312 | ||||||
chr21:17536392
|
C | T | 2 | a0004c0008t0082g0312a0004c0008t0084g0313 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.44-10635C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536392 | ||||||
chr21:17536403
|
G | A | 1 | a0001c0001t0068g0027 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.44-10624G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536403 | ||||||
chr21:17536503
|
C | A | 143 | a0001c0001t0002g0015a0001c0001t0003g0004a0001c0001t0003g0020others(140): Show | 145 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.44-10524C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536503 | ||||||
chr21:17536742
|
A | G | 1 | a0001c0001t0003g0300 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.44-10285A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536742 | ||||||
chr21:17536949
|
G | A | 10 | a0001c0002t0006g0001a0001c0002t0006g0101a0001c0002t0006g0102others(7): Show | 11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-10078G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536949 | ||||||
chr21:17536995
|
T | A | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-10032T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536995 | ||||||
chr21:17537018
|
A | G | 1 | a0001c0001t0081g0165 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.44-10009A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537018 | ||||||
chr21:17537055
|
A | G | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-9972A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537055 | ||||||
chr21:17537105
|
T | C | 2 | a0001c0002t0014g0077a0001c0002t0085g0074 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.44-9922T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537105 | ||||||
chr21:17537118
|
A | G | 11 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-9909A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537118 | ||||||
chr21:17537437
|
T | C | 1 | a0001c0002t0027g0144 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.44-9590T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537437 | ||||||
chr21:17537554
|
G | A | 2 | a0001c0002t0027g0016a0001c0002t0027g0144 | 2 | HG01975.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.44-9473G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537554 | ||||||
chr21:17537623
|
A | G | 5 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0006t0032g0011others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-9404A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537623 | ||||||
chr21:17537722
|
A | C | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-9305A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537722 | ||||||
chr21:17537725
|
A | G | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-9302A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537725 | ||||||
chr21:17537728
|
A | G | 144 | a0001c0001t0001g0059a0001c0001t0002g0015a0001c0001t0003g0004others(141): Show | 146 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.44-9299A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537728 | ||||||
chr21:17537761
|
CT | C | 4 | a0001c0002t0004g0337a0001c0002t0004g0338a0001c0002t0004g0339others(1): Show | 4 | HG00673.hp2 NA18967.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-9265delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537761 | ||||||
chr21:17537880
|
C | T | 1 | a0001c0001t0003g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.44-9147C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537880 | ||||||
chr21:17537903
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0030g0017 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44-9124T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537903 | ||||||
chr21:17538184
|
A | G | 2 | a0001c0001t0005g0034a0001c0001t0005g0035 | 2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.44-8843A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538184 | ||||||
chr21:17538189
|
T | C | 144 | a0001c0001t0001g0059a0001c0001t0002g0015a0001c0001t0003g0004others(141): Show | 146 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.44-8838T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538189 | ||||||
chr21:17538199
|
C | G | 8 | a0001c0003t0016g0187a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-8828C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538199 | ||||||
chr21:17538200
|
C | T | 1 | a0001c0001t0015g0268 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.44-8827C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538200 | ||||||
chr21:17538201
|
G | A | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-8826G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538201 | ||||||
chr21:17538220
|
CA | C | 346 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(343): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.44-8806delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538220 | ||||||
chr21:17538262
|
A | G | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-8765A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538262 | ||||||
chr21:17538285
|
C | G | 4 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0001t0003g0299others(1): Show | 4 | HG01109.hp1 HG01361.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-8742C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538285 | ||||||
chr21:17538341
|
G | T | 6 | a0001c0001t0001g0201a0001c0001t0001g0291a0001c0001t0015g0268others(3): Show | 6 | HG00423.hp1 HG01257.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-8686G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538341 | ||||||
chr21:17538396
|
G | A | 1 | a0001c0001t0066g0054 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.44-8631G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538396 | ||||||
chr21:17538470
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.44-8557C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538470 | ||||||
chr21:17538594
|
C | T | 2 | a0002c0005t0018g0153a0002c0005t0018g0155 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.44-8433C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538594 | ||||||
chr21:17538644
|
G | A | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-8383G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538644 | ||||||
chr21:17538680
|
G | C | 1 | a0001c0001t0016g0045 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.44-8347G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538680 | ||||||
chr21:17538702
|
G | A | 3 | a0001c0001t0012g0132a0001c0001t0012g0133a0001c0001t0012g0134 | 3 | NA18993.hp2 NA19062.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.44-8325G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538702 | ||||||
chr21:17539026
|
C | T | 11 | a0001c0001t0001g0209a0001c0001t0001g0221a0001c0001t0001g0224others(8): Show | 11 | HG02040.hp2 HG02080.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-8001C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539026 | ||||||
chr21:17539027
|
G | A | 15 | a0001c0002t0008g0039a0001c0002t0008g0060a0001c0002t0008g0061others(12): Show | 15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-8000G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539027 | ||||||
chr21:17539175
|
A | G | 1 | a0001c0001t0022g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.44-7852A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539175 | ||||||
chr21:17539325
|
CCAGCTTT others(16): Show |
C | 1 | a0001c0001t0022g0262 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.44-7701_44-7679del others(23): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539325 | ||||||
chr21:17539342
|
G | A | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-7685G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539342 | ||||||
chr21:17539395
|
C | T | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-7632C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539395 | ||||||
chr21:17539409
|
G | A | 3 | a0001c0002t0027g0016a0001c0002t0027g0144a0001c0002t0062g0164 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.44-7618G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539409 | ||||||
chr21:17539503
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-7524A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539503 | ||||||
chr21:17539518
|
G | C | 1 | a0001c0001t0003g0308 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.44-7509G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539518 | ||||||
chr21:17539637
|
T | C | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-7390T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539637 | ||||||
chr21:17539800
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.44-7227C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539800 | ||||||
chr21:17539807
|
C | T | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-7220C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539807 | ||||||
chr21:17539808
|
C | T | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-7219C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539808 | ||||||
chr21:17539882
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.44-7145C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539882 | ||||||
chr21:17539884
|
A | G | 3 | a0001c0001t0031g0185a0001c0001t0031g0186a0001c0001t0079g0078 | 3 | HG02145.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.44-7143A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539884 | ||||||
chr21:17539918
|
G | GT | 6 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-7108dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17539918 | |||||
chr21:17539930
|
T | G | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-7097T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539930 | ||||||
chr21:17539939
|
C | T | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-7088C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539939 | ||||||
chr21:17540062
|
G | A | 2 | a0001c0002t0021g0333a0001c0002t0034g0332 | 2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.44-6965G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540062 | ||||||
chr21:17540110
|
C | T | 1 | a0001c0004t0011g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.44-6917C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540110 | ||||||
chr21:17540140
|
C | T | 1 | a0001c0001t0068g0027 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.44-6887C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540140 | ||||||
chr21:17540178
|
G | C | 3 | a0001c0001t0002g0196a0001c0001t0002g0304a0001c0001t0017g0297 | 3 | HG02451.hp1 HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.44-6849G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540178 | ||||||
chr21:17540309
|
C | T | 1 | a0001c0001t0007g0317 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.44-6718C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540309 | ||||||
chr21:17540310
|
G | A | 1 | a0001c0001t0017g0297 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.44-6717G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540310 | ||||||
chr21:17540312
|
C | A | 1 | a0002c0005t0018g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44-6715C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540312 | ||||||
chr21:17540338
|
A | C | 1 | a0002c0005t0018g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44-6689A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540338 | ||||||
chr21:17540356
|
A | T | 3 | a0001c0002t0057g0019a0001c0002t0059g0003a0001c0002t0060g0003 | 3 | HG02109.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-6671A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540356 | ||||||
chr21:17540358
|
T | G | 1 | a0001c0001t0001g0270 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.44-6669T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540358 | ||||||
chr21:17540393
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.44-6634A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540393 | ||||||
chr21:17540400
|
T | C | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-6627T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540400 | ||||||
chr21:17540407
|
AT | A | 3 | a0001c0001t0024g0211a0001c0001t0024g0257a0001c0001t0045g0264 | 3 | HG00639.hp2 HG01361.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.44-6618delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17540407 | |||||
chr21:17540490
|
G | A | 1 | a0001c0002t0061g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-6537G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540490 | ||||||
chr21:17540764
|
G | C | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-6263G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540764 | ||||||
chr21:17540894
|
C | T | 55 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(52): Show | 56 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.44-6133C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540894 | ||||||
chr21:17540985
|
G | A | 1 | a0001c0002t0008g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.44-6042G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540985 | ||||||
chr21:17541026
|
C | G | 1 | a0001c0004t0069g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.44-6001C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541026 | ||||||
chr21:17541077
|
G | A | 1 | a0001c0002t0061g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-5950G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541077 | ||||||
chr21:17541234
|
A | C | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-5793A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541234 | ||||||
chr21:17541248
|
C | G | 1 | a0001c0001t0003g0143 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.44-5779C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541248 | ||||||
chr21:17541278
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.44-5749C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541278 | ||||||
chr21:17541358
|
C | T | 11 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(8): Show | 11 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-5669C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541358 | ||||||
chr21:17541372
|
G | A | 18 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(15): Show | 18 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-5655G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541372 | ||||||
chr21:17541379
|
C | T | 1 | a0001c0002t0027g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-5648C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541379 | ||||||
chr21:17541380
|
G | A | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-5647G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541380 | ||||||
chr21:17541396
|
C | CA | 11 | a0001c0001t0001g0283a0001c0002t0006g0001a0001c0002t0006g0101others(8): Show | 12 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-5620dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17541396 | |||||
chr21:17541474
|
C | T | 2 | a0001c0001t0028g0090a0001c0001t0028g0091 | 2 | HG02055.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.44-5553C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541474 | ||||||
chr21:17541499
|
A | G | 68 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(65): Show | 69 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.44-5528A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541499 | ||||||
chr21:17541521
|
A | G | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-5506A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541521 | ||||||
chr21:17541596
|
C | A | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-5431C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541596 | ||||||
chr21:17541617
|
A | AT | 24 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0327others(21): Show | 24 | HG00609.hp1 HG00642.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.44-5393dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17541617 | |||||
chr21:17541617
|
A | ATT | 15 | a0001c0002t0004g0325a0001c0002t0004g0337a0001c0002t0008g0039others(12): Show | 15 | HG00423.hp2 HG02015.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-5394_44-5393dup others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17541617 | |||||
chr21:17541617
|
AT | A | 268 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.44-5393delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17541617 | |||||
chr21:17541774
|
G | C | 66 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(63): Show | 67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-5253G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541774 | ||||||
chr21:17541863
|
A | G | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-5164A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541863 | ||||||
chr21:17541903
|
C | A | 4 | a0001c0002t0014g0076a0001c0002t0014g0077a0001c0002t0014g0079others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-5124C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541903 | ||||||
chr21:17541916
|
T | C | 3 | a0001c0001t0024g0211a0001c0001t0024g0257a0001c0001t0045g0264 | 3 | HG00639.hp2 HG01361.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.44-5111T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541916 | ||||||
chr21:17542001
|
A | G | 1 | a0001c0001t0002g0192 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.44-5026A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542001 | ||||||
chr21:17542024
|
ACT | A | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-5000_44-4999del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17542024 | |||||
chr21:17542052
|
T | A | 66 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(63): Show | 67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-4975T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542052 | ||||||
chr21:17542068
|
A | G | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-4959A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542068 | ||||||
chr21:17542147
|
A | G | 4 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0225others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-4880A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542147 | ||||||
chr21:17542168
|
TA | T | 8 | a0001c0002t0008g0039a0001c0002t0008g0060a0001c0002t0008g0061others(5): Show | 8 | HG02027.hp2 HG02056.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-4858delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542168 | ||||||
chr21:17542249
|
A | G | 3 | a0001c0003t0009g0154a0001c0003t0009g0182a0001c0003t0064g0147 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.44-4778A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542249 | ||||||
chr21:17542315
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.44-4712C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542315 | ||||||
chr21:17542614
|
G | A | 4 | a0001c0001t0023g0242a0001c0001t0023g0248a0001c0001t0050g0219others(1): Show | 4 | NA18941.hp2 NA18947.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-4413G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542614 | ||||||
chr21:17542655
|
T | C | 2 | a0001c0001t0001g0267a0001c0001t0051g0207 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.44-4372T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542655 | ||||||
chr21:17542693
|
C | T | 1 | a0001c0002t0008g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.44-4334C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542693 | ||||||
chr21:17542741
|
A | G | 12 | a0001c0001t0002g0196a0001c0001t0002g0304a0001c0001t0005g0163others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-4286A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542741 | ||||||
chr21:17542870
|
C | G | 74 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(71): Show | 75 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.44-4157C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542870 | ||||||
chr21:17542900
|
G | A | 119 | a0001c0001t0002g0196a0001c0001t0002g0304a0001c0001t0003g0004others(116): Show | 120 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.44-4127G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542900 | ||||||
chr21:17542918
|
G | A | 6 | a0001c0001t0002g0015a0001c0001t0017g0297a0001c0001t0030g0017others(3): Show | 6 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-4109G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542918 | ||||||
chr21:17543000
|
A | T | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-4027A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543000 | ||||||
chr21:17543019
|
T | C | 7 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0225others(4): Show | 7 | HG02717.hp1 HG03041.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-4008T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543019 | ||||||
chr21:17543035
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.44-3992G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543035 | ||||||
chr21:17543097
|
A | G | 1 | a0001c0001t0002g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.44-3930A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543097 | ||||||
chr21:17543114
|
G | A | 1 | a0001c0001t0012g0133 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.44-3913G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543114 | ||||||
chr21:17543157
|
A | G | 15 | a0001c0002t0008g0039a0001c0002t0008g0060a0001c0002t0008g0061others(12): Show | 15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-3870A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543157 | ||||||
chr21:17543312
|
C | T | 66 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(63): Show | 67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-3715C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543312 | ||||||
chr21:17543411
|
A | G | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-3616A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543411 | ||||||
chr21:17543494
|
C | T | 76 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0018others(73): Show | 78 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.44-3533C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543494 | ||||||
chr21:17543620
|
C | T | 1 | a0001c0003t0016g0187 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.44-3407C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543620 | ||||||
chr21:17543820
|
G | A | 12 | a0001c0001t0002g0015a0001c0001t0005g0163a0001c0001t0030g0017others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.44-3207G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543820 | ||||||
chr21:17543983
|
G | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0204a0001c0001t0001g0205others(7): Show | 11 | HG00597.hp1 HG01258.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-3044G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543983 | ||||||
chr21:17544223
|
C | G | 2 | a0001c0009t0074g0190a0001c0009t0075g0191 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.44-2804C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544223 | ||||||
chr21:17544295
|
A | G | 36 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0263others(33): Show | 36 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.44-2732A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544295 | ||||||
chr21:17544301
|
A | G | 1 | a0001c0001t0003g0048 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.44-2726A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544301 | ||||||
chr21:17544436
|
C | T | 1 | a0001c0001t0017g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.44-2591C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544436 | ||||||
chr21:17544438
|
T | A | 2 | a0001c0002t0027g0016a0001c0002t0027g0144 | 2 | HG01975.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.44-2589T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544438 | ||||||
chr21:17544467
|
G | C | 15 | a0001c0002t0008g0039a0001c0002t0008g0060a0001c0002t0008g0061others(12): Show | 15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-2560G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544467 | ||||||
chr21:17544521
|
GCTGCAGA others(13): Show |
G | 57 | a0001c0001t0002g0015a0001c0001t0003g0004a0001c0001t0003g0020others(54): Show | 58 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.44-2503_44-2484del others(20): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17544521 | |||||
chr21:17544541
|
A | C | 9 | a0001c0002t0027g0016a0001c0002t0027g0144a0001c0002t0062g0164others(6): Show | 9 | HG01975.hp1 HG02109.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-2486A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544541 | ||||||
chr21:17544714
|
A | G | 74 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(71): Show | 75 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.44-2313A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544714 | ||||||
chr21:17544744
|
T | C | 2 | a0001c0009t0074g0190a0001c0009t0075g0191 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.44-2283T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544744 | ||||||
chr21:17544764
|
A | T | 1 | a0001c0001t0017g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.44-2263A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544764 | ||||||
chr21:17544780
|
C | T | 10 | a0001c0001t0005g0163a0001c0001t0033g0084a0001c0002t0011g0107others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-2247C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544780 | ||||||
chr21:17544804
|
C | T | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-2223C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544804 | ||||||
chr21:17544865
|
A | G | 66 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(63): Show | 67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-2162A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544865 | ||||||
chr21:17544962
|
CCT | C | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-2062_44-2061del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17544962 | |||||
chr21:17545007
|
C | T | 66 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(63): Show | 67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-2020C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545007 | ||||||
chr21:17545072
|
G | GT | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0059others(88): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.44-1930dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | |||||
chr21:17545072
|
G | GTT | 33 | a0001c0001t0001g0009a0001c0001t0001g0040a0001c0001t0001g0050others(30): Show | 33 | HG00140.hp1 HG00408.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.44-1931_44-1930dup others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | |||||
chr21:17545072
|
GT | G | 27 | a0001c0001t0002g0018a0001c0001t0002g0081a0001c0001t0002g0085others(24): Show | 27 | HG00423.hp2 HG00621.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.44-1930delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | |||||
chr21:17545072
|
GTT | G | 87 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0082others(84): Show | 89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.44-1931_44-1930del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | |||||
chr21:17545072
|
GTTT | G | 6 | a0001c0001t0003g0086a0001c0001t0003g0300a0001c0001t0005g0032others(3): Show | 6 | HG01169.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-1932_44-1930del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | |||||
chr21:17545072
|
GTTTT | G | 14 | a0001c0001t0003g0020a0001c0001t0003g0053a0001c0001t0003g0057others(11): Show | 14 | HG01109.hp1 HG01361.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-1933_44-1930del others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | |||||
chr21:17545072
|
GTTTTT | G | 53 | a0001c0001t0003g0004a0001c0001t0003g0025a0001c0001t0003g0028others(50): Show | 54 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.44-1934_44-1930del others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | |||||
chr21:17545391
|
T | A | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-1636T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545391 | ||||||
chr21:17545400
|
T | C | 4 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0001t0003g0299others(1): Show | 4 | HG01109.hp1 HG01361.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-1627T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545400 | ||||||
chr21:17545613
|
G | T | 2 | a0001c0001t0012g0133a0001c0001t0012g0134 | 2 | NA19062.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.44-1414G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545613 | ||||||
chr21:17545666
|
G | A | 7 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0225others(4): Show | 7 | HG02717.hp1 HG03041.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-1361G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545666 | ||||||
chr21:17545771
|
G | GTT | 64 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(61): Show | 65 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.44-1256_44-1255ins others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545771 | ||||||
chr21:17545772
|
G | T | 75 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(72): Show | 76 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.44-1255G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545772 | ||||||
chr21:17545781
|
G | GT | 9 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0157others(6): Show | 10 | HG02683.hp2 HG03098.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-1231dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545781 | |||||
chr21:17545781
|
G | T | 3 | a0001c0001t0003g0047a0001c0001t0003g0141a0001c0001t0016g0045 | 3 | HG02738.hp2 HG03688.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.44-1246G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545781 | ||||||
chr21:17545781
|
GT | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.44-1231delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545781 | |||||
chr21:17545784
|
T | G | 1 | a0001c0001t0002g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.44-1243T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545784 | ||||||
chr21:17545820
|
C | T | 6 | a0001c0001t0001g0240a0001c0001t0007g0008a0001c0001t0007g0233others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-1207C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545820 | ||||||
chr21:17545937
|
A | G | 6 | a0001c0004t0011g0038a0001c0004t0011g0080a0001c0004t0011g0188others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-1090A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545937 | ||||||
chr21:17545951
|
G | C | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-1076G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545951 | ||||||
chr21:17546034
|
C | T | 1 | a0001c0001t0016g0045 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.44-993C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546034 | ||||||
chr21:17546068
|
C | T | 4 | a0001c0004t0011g0038a0001c0004t0011g0188a0001c0004t0011g0197others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-959C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546068 | ||||||
chr21:17546111
|
G | A | 3 | a0001c0002t0027g0016a0001c0002t0027g0144a0001c0002t0062g0164 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.44-916G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546111 | ||||||
chr21:17546126
|
G | T | 1 | a0001c0001t0003g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.44-901G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546126 | ||||||
chr21:17546258
|
A | G | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-769A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546258 | ||||||
chr21:17546260
|
C | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0081others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.44-767C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546260 | ||||||
chr21:17546260
|
C | T | 193 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.44-767C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546260 | ||||||
chr21:17546306
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.44-721T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546306 | ||||||
chr21:17546322
|
T | A | 1 | a0001c0001t0001g0306 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.44-705T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546322 | ||||||
chr21:17546358
|
C | T | 7 | a0001c0001t0002g0007a0001c0001t0002g0156a0001c0001t0002g0157others(4): Show | 8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-669C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546358 | ||||||
chr21:17546408
|
G | A | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.44-619G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546408 | ||||||
chr21:17546665
|
T | C | 2 | a0001c0007t0002g0092a0001c0007t0002g0093 | 2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.44-362T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546665 | ||||||
chr21:17546672
|
G | A | 1 | a0001c0007t0033g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.44-355G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546672 | ||||||
chr21:17546736
|
C | G | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-291C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546736 | ||||||
chr21:17546737
|
T | G | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-290T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546737 | ||||||
chr21:17546936
|
A | G | 2 | a0001c0003t0009g0021a0001c0003t0009g0087 | 2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.44-91A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546936 | ||||||
chr21:17546940
|
A | G | 1 | a0001c0002t0061g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-87A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546940 | ||||||
chr21:17546962
|
C | T | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-65C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546962 | ||||||
chr21:17547236
|
A | T | 1 | a0003c0010t0004g0343 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.210+43A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547236 | ||||||
chr21:17547257
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.210+64C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547257 | ||||||
chr21:17547364
|
G | A | 2 | a0001c0007t0002g0092a0001c0007t0002g0093 | 2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.210+171G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547364 | ||||||
chr21:17547434
|
G | A | 8 | a0001c0003t0016g0187a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+241G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547434 | ||||||
chr21:17547534
|
C | T | 1 | a0001c0001t0003g0173 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.210+341C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547534 | ||||||
chr21:17547617
|
G | A | 2 | a0001c0002t0004g0322a0001c0002t0004g0324 | 2 | HG00609.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.210+424G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547617 | ||||||
chr21:17547762
|
A | AT | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.210+577dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17547762 | |||||
chr21:17547895
|
T | G | 2 | a0001c0002t0059g0003a0001c0002t0060g0003 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.210+702T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547895 | ||||||
chr21:17547937
|
C | G | 59 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(56): Show | 60 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.210+744C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547937 | ||||||
chr21:17548085
|
A | C | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+892A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548085 | ||||||
chr21:17548112
|
A | G | 13 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(10): Show | 13 | HG01884.hp2 HG01975.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.210+919A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548112 | ||||||
chr21:17548319
|
T | C | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+1126T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548319 | ||||||
chr21:17548350
|
C | A | 1 | a0001c0002t0008g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.210+1157C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548350 | ||||||
chr21:17548368
|
C | G | 16 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(13): Show | 16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.210+1175C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548368 | ||||||
chr21:17548373
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.210+1180C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548373 | ||||||
chr21:17548514
|
T | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.210+1321T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548514 | ||||||
chr21:17548613
|
G | A | 17 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(14): Show | 17 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.210+1420G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548613 | ||||||
chr21:17548616
|
C | T | 2 | a0001c0002t0059g0003a0001c0002t0060g0003 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.210+1423C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548616 | ||||||
chr21:17548664
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.210+1471G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548664 | ||||||
chr21:17548746
|
A | G | 1 | a0001c0001t0019g0323 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.210+1553A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548746 | ||||||
chr21:17549030
|
G | C | 1 | a0001c0001t0002g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.210+1837G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549030 | ||||||
chr21:17549075
|
T | A | 1 | a0001c0001t0017g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.210+1882T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549075 | ||||||
chr21:17549262
|
C | T | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.210+2069C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549262 | ||||||
chr21:17549420
|
C | A | 16 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(13): Show | 16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.210+2227C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549420 | ||||||
chr21:17549503
|
G | T | 46 | a0001c0001t0005g0163a0001c0002t0004g0322a0001c0002t0004g0324others(43): Show | 46 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.211-2246G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549503 | ||||||
chr21:17549736
|
C | G | 1 | a0001c0002t0006g0102 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.211-2013C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549736 | ||||||
chr21:17549737
|
C | T | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.211-2012C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549737 | ||||||
chr21:17549861
|
A | G | 2 | a0004c0008t0082g0312a0004c0008t0084g0313 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.211-1888A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549861 | ||||||
chr21:17549944
|
C | T | 8 | a0001c0003t0016g0187a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-1805C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549944 | ||||||
chr21:17550016
|
A | G | 3 | a0001c0002t0027g0016a0001c0002t0027g0144a0001c0002t0062g0164 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211-1733A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550016 | ||||||
chr21:17550036
|
A | T | 1 | a0001c0001t0002g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.211-1713A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550036 | ||||||
chr21:17550043
|
A | G | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.211-1706A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550043 | ||||||
chr21:17550085
|
G | A | 1 | a0001c0002t0061g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.211-1664G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550085 | ||||||
chr21:17550109
|
C | G | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-1640C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550109 | ||||||
chr21:17550135
|
T | C | 3 | a0001c0002t0027g0016a0001c0002t0027g0144a0001c0002t0062g0164 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211-1614T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550135 | ||||||
chr21:17550216
|
T | C | 16 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(13): Show | 16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.211-1533T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550216 | ||||||
chr21:17550280
|
G | T | 3 | a0001c0002t0027g0016a0001c0002t0027g0144a0001c0002t0062g0164 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211-1469G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550280 | ||||||
chr21:17550351
|
C | CA | 118 | a0001c0001t0001g0059a0001c0001t0002g0015a0001c0001t0003g0004others(115): Show | 120 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.211-1382dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17550351 | |||||
chr21:17550351
|
C | CAA | 192 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(189): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.211-1383_211-1382d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17550351 | |||||
chr21:17550351
|
C | CAAA | 10 | a0001c0001t0002g0007a0001c0001t0002g0081a0001c0001t0002g0083others(7): Show | 11 | HG00639.hp2 HG01099.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-1384_211-1382d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17550351 | |||||
chr21:17550370
|
T | G | 2 | a0001c0009t0074g0190a0001c0009t0075g0191 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.211-1379T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550370 | ||||||
chr21:17550377
|
T | C | 1 | a0001c0001t0002g0320 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.211-1372T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550377 | ||||||
chr21:17550381
|
T | G | 1 | a0001c0004t0069g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.211-1368T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550381 | ||||||
chr21:17550454
|
C | T | 8 | a0001c0003t0016g0187a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-1295C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550454 | ||||||
chr21:17550613
|
A | G | 59 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(56): Show | 60 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.211-1136A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550613 | ||||||
chr21:17550664
|
T | C | 1 | a0001c0003t0016g0187 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.211-1085T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550664 | ||||||
chr21:17550795
|
G | T | 1 | a0003c0010t0004g0343 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.211-954G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550795 | ||||||
chr21:17551097
|
T | TA | 10 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0196others(7): Show | 10 | HG02451.hp1 HG02486.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-651dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17551097 | |||||
chr21:17551142
|
A | G | 1 | a0001c0003t0009g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-607A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551142 | ||||||
chr21:17551186
|
G | A | 1 | a0001c0001t0002g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.211-563G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551186 | ||||||
chr21:17551308
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.211-441G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551308 | ||||||
chr21:17551331
|
T | C | 16 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(13): Show | 16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.211-418T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551331 | ||||||
chr21:17551392
|
CAAAAA | C | 8 | a0001c0003t0016g0187a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-356_211-352del others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551392 | ||||||
chr21:17551424
|
C | T | 1 | a0001c0004t0040g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.211-325C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551424 | ||||||
chr21:17551547
|
A | G | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-202A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551547 | ||||||
chr21:17551702
|
T | G | 9 | a0001c0001t0003g0049a0001c0003t0009g0021a0001c0003t0009g0022others(6): Show | 9 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.211-47T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551702 | ||||||
chr21:17551710
|
G | T | 1 | a0001c0002t0008g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.211-39G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551710 | ||||||
chr21:17552019
|
T | C | 10 | a0001c0001t0005g0163a0001c0002t0011g0107a0001c0002t0013g0104others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.415+66T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552019 | ||||||
chr21:17552245
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0171 | 2 | HG00438.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.415+292G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552245 | ||||||
chr21:17552383
|
A | C | 21 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(18): Show | 21 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.415+430A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552383 | ||||||
chr21:17552385
|
A | C | 2 | a0001c0001t0001g0184a0001c0001t0052g0041 | 2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.415+432A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552385 | ||||||
chr21:17552436
|
A | G | 2 | a0001c0001t0002g0304a0001c0001t0017g0297 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.415+483A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552436 | ||||||
chr21:17552481
|
T | G | 211 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.415+528T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552481 | ||||||
chr21:17552573
|
T | TTA | 9 | a0001c0002t0011g0107a0001c0003t0016g0187a0001c0004t0011g0038others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.415+621_415+622dup others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17552573 | |||||
chr21:17552741
|
G | A | 130 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0040others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.415+788G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552741 | ||||||
chr21:17552955
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.415+1002C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552955 | ||||||
chr21:17552956
|
T | A | 16 | a0001c0002t0011g0107a0001c0003t0009g0021a0001c0003t0009g0022others(13): Show | 16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+1003T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552956 | ||||||
chr21:17553007
|
C | T | 16 | a0001c0002t0011g0107a0001c0003t0009g0021a0001c0003t0009g0022others(13): Show | 16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+1054C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553007 | ||||||
chr21:17553033
|
T | C | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1080T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553033 | ||||||
chr21:17553036
|
C | T | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1083C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553036 | ||||||
chr21:17553048
|
A | G | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1095A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553048 | ||||||
chr21:17553054
|
C | T | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1101C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553054 | ||||||
chr21:17553066
|
GCA | G | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1114_415+1115d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553066 | ||||||
chr21:17553071
|
C | CCT | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1118_415+1119i others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553071 | ||||||
chr21:17553072
|
A | G | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1119A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553072 | ||||||
chr21:17553081
|
C | A | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1128C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553081 | ||||||
chr21:17553174
|
C | T | 1 | a0001c0002t0061g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.415+1221C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553174 | ||||||
chr21:17553184
|
G | A | 270 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.415+1231G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553184 | ||||||
chr21:17553223
|
G | A | 10 | a0001c0002t0006g0001a0001c0002t0006g0101a0001c0002t0006g0102others(7): Show | 11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+1270G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553223 | ||||||
chr21:17553391
|
T | C | 3 | a0001c0002t0027g0016a0001c0002t0027g0144a0001c0002t0062g0164 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.415+1438T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553391 | ||||||
chr21:17553494
|
A | T | 1 | a0001c0001t0002g0127 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.415+1541A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553494 | ||||||
chr21:17553531
|
G | A | 1 | a0001c0001t0068g0027 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.415+1578G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553531 | ||||||
chr21:17553605
|
G | C | 8 | a0001c0002t0011g0107a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1652G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553605 | ||||||
chr21:17553614
|
C | CT | 6 | a0001c0002t0008g0160a0001c0003t0009g0021a0001c0003t0009g0024others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+1680dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | |||||
chr21:17553614
|
CT | C | 154 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.415+1680delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | |||||
chr21:17553614
|
CTT | C | 58 | a0001c0001t0001g0059a0001c0001t0001g0314a0001c0001t0002g0015others(55): Show | 59 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.415+1679_415+1680d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | |||||
chr21:17553614
|
CTTT | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0018others(76): Show | 81 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.415+1678_415+1680d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | |||||
chr21:17553614
|
CTTTTTTT others(4): Show |
C | 8 | a0001c0002t0011g0107a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1670_415+1680d others(13): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | |||||
chr21:17553652
|
C | T | 4 | a0001c0001t0001g0291a0001c0001t0025g0252a0001c0001t0026g0212others(1): Show | 4 | HG00423.hp1 NA18966.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+1699C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553652 | ||||||
chr21:17554023
|
T | C | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415+2070T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554023 | ||||||
chr21:17554116
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.415+2163C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554116 | ||||||
chr21:17554152
|
G | T | 1 | a0001c0001t0002g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.415+2199G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554152 | ||||||
chr21:17554263
|
T | C | 16 | a0001c0002t0011g0107a0001c0003t0009g0021a0001c0003t0009g0022others(13): Show | 16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+2310T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554263 | ||||||
chr21:17554291
|
AG | A | 188 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.415+2342delG | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17554291 | |||||
chr21:17554335
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.415+2382C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554335 | ||||||
chr21:17554425
|
A | G | 1 | a0001c0002t0010g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.415+2472A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554425 | ||||||
chr21:17554445
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.415+2492T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554445 | ||||||
chr21:17554488
|
G | C | 16 | a0001c0001t0002g0007a0001c0001t0002g0156a0001c0001t0002g0157others(13): Show | 17 | HG00544.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+2535G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554488 | ||||||
chr21:17554491
|
G | C | 56 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(53): Show | 57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.415+2538G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554491 | ||||||
chr21:17554492
|
G | C | 62 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0196others(59): Show | 62 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.415+2539G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554492 | ||||||
chr21:17554543
|
C | T | 44 | a0001c0001t0001g0226a0001c0001t0005g0163a0001c0002t0004g0322others(41): Show | 44 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.415+2590C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554543 | ||||||
chr21:17554567
|
A | G | 152 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.415+2614A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554567 | ||||||
chr21:17554616
|
T | C | 63 | a0001c0001t0002g0015a0001c0001t0005g0163a0001c0001t0030g0017others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.415+2663T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554616 | ||||||
chr21:17554819
|
TTGAC | T | 16 | a0001c0002t0011g0107a0001c0003t0009g0021a0001c0003t0009g0022others(13): Show | 16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+2870_415+2873d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17554819 | |||||
chr21:17554902
|
TG | T | 7 | a0001c0001t0002g0007a0001c0001t0002g0156a0001c0001t0002g0157others(4): Show | 8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+2951delG | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17554902 | |||||
chr21:17555085
|
A | G | 2 | a0001c0002t0059g0003a0001c0002t0060g0003 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.415+3132A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555085 | ||||||
chr21:17555300
|
T | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0232a0001c0001t0001g0278 | 3 | HG00735.hp2 HG01169.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.415+3347T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555300 | ||||||
chr21:17555421
|
A | G | 1 | a0001c0002t0057g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.415+3468A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555421 | ||||||
chr21:17555515
|
C | T | 16 | a0001c0002t0011g0107a0001c0003t0009g0021a0001c0003t0009g0022others(13): Show | 16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-3461C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555515 | ||||||
chr21:17555598
|
A | G | 50 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(47): Show | 50 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.416-3378A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555598 | ||||||
chr21:17555625
|
T | C | 5 | a0001c0001t0002g0015a0001c0001t0030g0017a0001c0006t0032g0011others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3351T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555625 | ||||||
chr21:17555632
|
TCTC | T | 25 | a0001c0002t0006g0001a0001c0002t0006g0101a0001c0002t0006g0102others(22): Show | 26 | HG00639.hp1 HG00642.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.416-3339_416-3337d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17555632 | |||||
chr21:17555658
|
A | G | 9 | a0001c0001t0005g0163a0001c0002t0013g0104a0001c0002t0013g0105others(6): Show | 9 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-3318A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555658 | ||||||
chr21:17555794
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.416-3182A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555794 | ||||||
chr21:17555831
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.416-3145G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555831 | ||||||
chr21:17555970
|
C | T | 8 | a0001c0002t0011g0107a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-3006C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555970 | ||||||
chr21:17556052
|
A | G | 49 | a0001c0001t0003g0004a0001c0001t0003g0025a0001c0001t0003g0028others(46): Show | 50 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.416-2924A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556052 | ||||||
chr21:17556326
|
A | G | 41 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(38): Show | 41 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.416-2650A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556326 | ||||||
chr21:17556414
|
T | A | 130 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.416-2562T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556414 | ||||||
chr21:17556432
|
G | A | 304 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(301): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.416-2544G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556432 | ||||||
chr21:17556468
|
GA | G | 56 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(53): Show | 57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.416-2504delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17556468 | |||||
chr21:17556741
|
T | A | 56 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(53): Show | 57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.416-2235T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556741 | ||||||
chr21:17556761
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.416-2215G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556761 | ||||||
chr21:17556778
|
A | T | 251 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.416-2198A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556778 | ||||||
chr21:17556806
|
G | A | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.416-2170G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556806 | ||||||
chr21:17556841
|
A | G | 130 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0015others(127): Show | 132 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.416-2135A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556841 | ||||||
chr21:17556899
|
A | G | 331 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(328): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.416-2077A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556899 | ||||||
chr21:17556924
|
T | C | 1 | a0001c0001t0003g0128 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.416-2052T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556924 | ||||||
chr21:17557001
|
C | T | 3 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0011t0063g0162 | 3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.416-1975C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557001 | ||||||
chr21:17557002
|
G | T | 2 | a0001c0001t0001g0201a0001c0001t0015g0268 | 2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.416-1974G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557002 | ||||||
chr21:17557016
|
G | A | 233 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.416-1960G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557016 | ||||||
chr21:17557227
|
GGTTATAG others(3): Show |
G | 2 | a0001c0001t0002g0193a0001c0001t0002g0225 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.416-1748_416-1739d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557227 | ||||||
chr21:17557281
|
G | C | 24 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0001t0003g0299others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-1695G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557281 | ||||||
chr21:17557355
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.416-1621C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557355 | ||||||
chr21:17557409
|
T | G | 1 | a0001c0002t0004g0342 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.416-1567T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557409 | ||||||
chr21:17557426
|
C | A | 235 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(232): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.416-1550C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557426 | ||||||
chr21:17557499
|
C | T | 3 | a0001c0002t0021g0333a0001c0002t0021g0334a0001c0002t0034g0332 | 3 | HG02015.hp2 HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.416-1477C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557499 | ||||||
chr21:17557522
|
G | A | 236 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.416-1454G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557522 | ||||||
chr21:17557542
|
T | A | 1 | a0001c0001t0019g0331 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.416-1434T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557542 | ||||||
chr21:17557637
|
T | C | 15 | a0001c0002t0008g0039a0001c0002t0008g0060a0001c0002t0008g0061others(12): Show | 15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.416-1339T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557637 | ||||||
chr21:17557671
|
G | A | 8 | a0001c0002t0011g0107a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-1305G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557671 | ||||||
chr21:17557752
|
GAA | G | 236 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.416-1223_416-1222d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557752 | ||||||
chr21:17557851
|
G | A | 1 | a0001c0002t0057g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.416-1125G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557851 | ||||||
chr21:17557911
|
G | A | 236 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.416-1065G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557911 | ||||||
chr21:17558068
|
A | G | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.416-908A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558068 | ||||||
chr21:17558081
|
C | CT | 7 | a0001c0002t0013g0104a0001c0002t0013g0105a0001c0002t0013g0106others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-882dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17558081 | |||||
chr21:17558081
|
CT | C | 94 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(91): Show | 95 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.416-882delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17558081 | |||||
chr21:17558081
|
CTT | C | 203 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.416-883_416-882del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17558081 | |||||
chr21:17558093
|
T | A | 1 | a0001c0001t0001g0009 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.416-883T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558093 | ||||||
chr21:17558094
|
T | A | 203 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.416-882T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558094 | ||||||
chr21:17558115
|
A | G | 203 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.416-861A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558115 | ||||||
chr21:17558118
|
T | C | 1 | a0001c0002t0061g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.416-858T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558118 | ||||||
chr21:17558247
|
G | C | 3 | a0001c0001t0002g0196a0001c0001t0002g0304a0001c0001t0017g0297 | 3 | HG02451.hp1 HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.416-729G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558247 | ||||||
chr21:17558247
|
GC | G | 12 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(9): Show | 12 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-727delC | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17558247 | |||||
chr21:17558335
|
A | G | 1 | a0001c0001t0003g0047 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.416-641A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558335 | ||||||
chr21:17558597
|
A | T | 2 | a0001c0001t0003g0302a0001c0001t0067g0013 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.416-379A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558597 | ||||||
chr21:17558614
|
G | A | 12 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(9): Show | 12 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-362G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558614 | ||||||
chr21:17558685
|
ATT | A | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-290_416-289del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558685 | ||||||
chr21:17558747
|
T | G | 8 | a0001c0002t0011g0107a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-229T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558747 | ||||||
chr21:17558943
|
T | C | 7 | a0001c0001t0002g0007a0001c0001t0002g0156a0001c0001t0002g0157others(4): Show | 8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-33T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558943 | ||||||
chr21:17559164
|
C | T | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.571+33C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559164 | ||||||
chr21:17559176
|
C | T | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.571+45C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559176 | ||||||
chr21:17559346
|
AT | A | 47 | a0001c0001t0001g0214a0001c0001t0001g0279a0001c0001t0001g0280others(44): Show | 47 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.571+225delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559346 | |||||
chr21:17559356
|
T | A | 20 | a0001c0001t0003g0069a0001c0002t0008g0039a0001c0002t0008g0060others(17): Show | 20 | HG01884.hp2 HG01978.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.571+225T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559356 | ||||||
chr21:17559356
|
TA | T | 197 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.571+231delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559356 | |||||
chr21:17559358
|
A | T | 3 | a0001c0001t0002g0196a0001c0001t0002g0304a0001c0001t0017g0297 | 3 | HG02451.hp1 HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.571+227A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559358 | ||||||
chr21:17559387
|
G | A | 1 | a0001c0004t0011g0080 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.571+256G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559387 | ||||||
chr21:17559419
|
A | G | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.571+288A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559419 | ||||||
chr21:17559432
|
T | C | 1 | a0001c0002t0062g0164 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571+301T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559432 | ||||||
chr21:17559611
|
G | C | 1 | a0001c0001t0001g0306 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.571+480G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559611 | ||||||
chr21:17559641
|
T | A | 236 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.571+510T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559641 | ||||||
chr21:17559666
|
TG | T | 70 | a0001c0001t0001g0009a0001c0001t0001g0040a0001c0001t0001g0112others(67): Show | 70 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.571+538delG | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559666 | |||||
chr21:17559666
|
TGG | T | 52 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0025others(49): Show | 53 | HG00438.hp1 HG00733.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.571+537_571+538del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559666 | |||||
chr21:17559667
|
GGGT | G | 7 | a0001c0003t0009g0021a0001c0003t0009g0023a0001c0003t0009g0024others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+537_571+539del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559667 | ||||||
chr21:17559668
|
G | GT | 7 | a0001c0002t0006g0102a0001c0002t0006g0103a0001c0002t0010g0183others(4): Show | 7 | HG00642.hp1 HG01175.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.571+537_571+538ins others(1): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559668 | ||||||
chr21:17559668
|
G | T | 1 | a0001c0002t0006g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.571+537G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559668 | ||||||
chr21:17559668
|
GGT | G | 173 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0050others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.571+538_571+539del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559668 | ||||||
chr21:17559669
|
G | T | 52 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0046others(49): Show | 53 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.571+538G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559669 | ||||||
chr21:17559674
|
T | G | 7 | a0001c0001t0002g0095a0001c0001t0002g0116a0001c0001t0002g0176others(4): Show | 7 | HG00621.hp2 HG01109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+543T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559674 | ||||||
chr21:17559675
|
T | G | 75 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0015others(72): Show | 77 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.571+544T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559675 | ||||||
chr21:17559677
|
T | G | 5 | a0001c0001t0003g0028a0001c0001t0003g0046a0001c0001t0003g0057others(2): Show | 5 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.571+546T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559677 | ||||||
chr21:17559678
|
T | G | 45 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0025others(42): Show | 46 | HG00438.hp1 HG00733.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.571+547T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559678 | ||||||
chr21:17559691
|
T | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.571+560T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559691 | ||||||
chr21:17559747
|
C | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.571+616C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559747 | ||||||
chr21:17559865
|
C | G | 321 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(318): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.571+734C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559865 | ||||||
chr21:17559869
|
G | C | 1 | a0001c0002t0062g0164 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571+738G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559869 | ||||||
chr21:17559918
|
C | G | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.572-784C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559918 | ||||||
chr21:17559968
|
C | T | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.572-734C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559968 | ||||||
chr21:17559971
|
AT | A | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.572-719delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559971 | |||||
chr21:17560012
|
C | T | 7 | a0001c0001t0002g0007a0001c0001t0002g0156a0001c0001t0002g0157others(4): Show | 8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.572-690C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560012 | ||||||
chr21:17560034
|
G | A | 236 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.572-668G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560034 | ||||||
chr21:17560038
|
G | A | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.572-664G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560038 | ||||||
chr21:17560117
|
C | T | 1 | a0001c0001t0003g0308 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.572-585C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560117 | ||||||
chr21:17560125
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.572-577A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560125 | ||||||
chr21:17560187
|
G | A | 4 | a0001c0001t0002g0167a0001c0001t0002g0170a0001c0001t0002g0174others(1): Show | 4 | NA18964.hp2 NA18971.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.572-515G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560187 | ||||||
chr21:17560222
|
A | G | 1 | a0001c0001t0005g0035 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.572-480A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560222 | ||||||
chr21:17560291
|
A | C | 77 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0018others(74): Show | 79 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.572-411A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560291 | ||||||
chr21:17560332
|
G | T | 60 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(57): Show | 61 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.572-370G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560332 | ||||||
chr21:17560414
|
G | A | 3 | a0001c0006t0032g0011a0001c0006t0032g0012a0001c0006t0078g0010 | 3 | HG01109.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.572-288G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560414 | ||||||
chr21:17560437
|
G | C | 321 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(318): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.572-265G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560437 | ||||||
chr21:17560510
|
A | T | 1 | a0001c0001t0068g0027 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.572-192A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560510 | ||||||
chr21:17560616
|
T | A | 236 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.572-86T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560616 | ||||||
chr21:17560654
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.572-48A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560654 | ||||||
chr21:17560658
|
C | T | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.572-44C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560658 | ||||||
chr21:17560678
|
G | C | 8 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(5): Show | 8 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.572-24G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560678 | ||||||
chr21:17560918
|
G | T | 8 | a0001c0002t0011g0107a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.694+94G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17560918 | ||||||
chr21:17560989
|
A | G | 1 | a0003c0010t0004g0343 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.694+165A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17560989 | ||||||
chr21:17561018
|
G | T | 1 | a0001c0001t0002g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.694+194G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561018 | ||||||
chr21:17561062
|
T | G | 1 | a0001c0001t0002g0094 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.694+238T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561062 | ||||||
chr21:17561217
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.695-121C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561217 | ||||||
chr21:17561243
|
C | CAT | 330 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(327): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.695-95_695-94insAT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561243 | ||||||
chr21:17561246
|
G | C | 17 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(14): Show | 17 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.695-92G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561246 | ||||||
chr21:17561250
|
A | G | 2 | a0001c0001t0003g0142a0001c0001t0003g0143 | 2 | NA18991.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.695-88A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561250 | ||||||
chr21:17561306
|
A | G | 2 | a0001c0007t0002g0092a0001c0007t0002g0093 | 2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.695-32A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561306 | ||||||
chr21:17561307
|
TA | T | 6 | a0001c0001t0003g0020a0001c0001t0003g0086a0001c0001t0003g0299others(3): Show | 6 | HG01109.hp1 HG01361.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-30delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561307 | ||||||
chr21:17561510
|
A | G | 56 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(53): Show | 57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.833+34A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561510 | ||||||
chr21:17561520
|
T | A | 1 | a0001c0001t0001g0315 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.833+44T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561520 | ||||||
chr21:17561540
|
C | T | 1 | a0001c0001t0003g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.833+64C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561540 | ||||||
chr21:17561554
|
C | A | 1 | a0001c0001t0048g0231 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.833+78C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561554 | ||||||
chr21:17561586
|
A | G | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+110A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561586 | ||||||
chr21:17561598
|
C | T | 3 | a0001c0002t0027g0016a0001c0002t0027g0144a0001c0002t0062g0164 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.833+122C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561598 | ||||||
chr21:17561668
|
G | T | 15 | a0001c0002t0008g0039a0001c0002t0008g0060a0001c0002t0008g0061others(12): Show | 15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.833+192G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561668 | ||||||
chr21:17561672
|
C | T | 2 | a0001c0001t0002g0292a0001c0001t0002g0293 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.833+196C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561672 | ||||||
chr21:17561678
|
C | G | 10 | a0001c0002t0006g0001a0001c0002t0006g0101a0001c0002t0006g0102others(7): Show | 11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.833+202C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561678 | ||||||
chr21:17561761
|
G | A | 8 | a0001c0002t0011g0107a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+285G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561761 | ||||||
chr21:17561767
|
G | A | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.833+291G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561767 | ||||||
chr21:17562051
|
G | T | 331 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(328): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.833+575G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562051 | ||||||
chr21:17562061
|
T | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0306 | 3 | HG00408.hp2 NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.833+585T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562061 | ||||||
chr21:17562133
|
A | C | 22 | a0001c0001t0002g0002a0001c0001t0002g0109a0001c0001t0002g0111others(19): Show | 23 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.833+657A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562133 | ||||||
chr21:17562142
|
A | T | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.833+666A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562142 | ||||||
chr21:17562152
|
T | TA | 321 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(318): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.833+682dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17562152 | |||||
chr21:17562194
|
CAGTG | C | 59 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(56): Show | 60 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.833+722_833+725del others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17562194 | |||||
chr21:17562221
|
G | A | 237 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(234): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.833+745G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562221 | ||||||
chr21:17562230
|
G | T | 59 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(56): Show | 60 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.833+754G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562230 | ||||||
chr21:17562335
|
TC | T | 82 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0015others(79): Show | 84 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.833+860delC | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562335 | ||||||
chr21:17562351
|
G | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.833+875G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562351 | ||||||
chr21:17562815
|
A | G | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.833+1339A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562815 | ||||||
chr21:17562912
|
T | C | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.833+1436T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562912 | ||||||
chr21:17562965
|
C | T | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+1489C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562965 | ||||||
chr21:17562981
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.833+1505C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562981 | ||||||
chr21:17563079
|
C | T | 82 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0015others(79): Show | 84 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.833+1603C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563079 | ||||||
chr21:17563107
|
T | A | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.833+1631T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563107 | ||||||
chr21:17563155
|
GTTAA | G | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+1683_833+1686d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563155 | |||||
chr21:17563258
|
C | G | 338 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(335): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.833+1782C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563258 | ||||||
chr21:17563260
|
G | C | 321 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(318): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.833+1784G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563260 | ||||||
chr21:17563353
|
G | C | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+1877G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563353 | ||||||
chr21:17563360
|
T | C | 1 | a0001c0002t0006g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.833+1884T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563360 | ||||||
chr21:17563440
|
G | C | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+1964G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563440 | ||||||
chr21:17563484
|
C | T | 2 | a0001c0002t0059g0003a0001c0002t0060g0003 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.834-1944C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563484 | ||||||
chr21:17563576
|
G | A | 15 | a0001c0002t0008g0039a0001c0002t0008g0060a0001c0002t0008g0061others(12): Show | 15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.834-1852G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563576 | ||||||
chr21:17563663
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.834-1765C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563663 | ||||||
chr21:17563664
|
G | A | 67 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(64): Show | 68 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.834-1764G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563664 | ||||||
chr21:17563668
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.834-1760A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563668 | ||||||
chr21:17563757
|
C | T | 8 | a0001c0003t0009g0021a0001c0003t0009g0022a0001c0003t0009g0023others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-1671C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563757 | ||||||
chr21:17563801
|
T | C | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.834-1627T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563801 | ||||||
chr21:17563813
|
C | T | 1 | a0001c0001t0015g0254 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.834-1615C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563813 | ||||||
chr21:17563829
|
C | T | 237 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(234): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.834-1599C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563829 | ||||||
chr21:17563834
|
G | A | 1 | a0001c0002t0070g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.834-1594G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563834 | ||||||
chr21:17563897
|
C | T | 1 | a0001c0004t0011g0080 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.834-1531C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563897 | ||||||
chr21:17563940
|
C | CA | 9 | a0001c0001t0002g0215a0001c0001t0030g0017a0001c0002t0057g0019others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.834-1467dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAA | 48 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0081others(45): Show | 49 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.834-1468_834-1467d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAA | 40 | a0001c0001t0002g0007a0001c0001t0002g0094a0001c0001t0002g0095others(37): Show | 41 | HG00544.hp1 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.834-1469_834-1467d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAA | 33 | a0001c0001t0005g0033a0001c0001t0005g0179a0001c0001t0017g0297others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.834-1470_834-1467d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA | 8 | a0001c0002t0011g0107a0001c0004t0011g0038a0001c0004t0011g0080others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-1473_834-1467d others(9): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0023g0248a0001c0001t0050g0219a0001c0001t0055g0307 | 3 | NA18941.hp2 NA18975.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.834-1480_834-1467d others(16): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0023g0242a0001c0001t0041g0260a0001c0002t0062g0164 | 3 | HG03471.hp2 NA18940.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.834-1481_834-1467d others(17): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0266 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.834-1482_834-1467d others(18): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(10): Show |
6 | a0001c0001t0001g0224a0001c0001t0001g0234a0001c0001t0001g0245others(3): Show | 6 | HG00140.hp2 HG01884.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.834-1483_834-1467d others(19): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(11): Show |
21 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0067others(18): Show | 21 | HG00140.hp1 HG00408.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.834-1484_834-1467d others(20): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(12): Show |
34 | a0001c0001t0001g0006a0001c0001t0001g0113a0001c0001t0001g0126others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.834-1485_834-1467d others(21): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(13): Show |
27 | a0001c0001t0001g0005a0001c0001t0001g0112a0001c0001t0001g0114others(24): Show | 28 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.834-1486_834-1467d others(22): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(14): Show |
8 | a0001c0001t0001g0226a0001c0001t0001g0251a0001c0001t0001g0263others(5): Show | 8 | HG00621.hp1 HG01975.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-1487_834-1467d others(23): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0283a0001c0001t0001g0289a0001c0001t0049g0281others(1): Show | 4 | HG01975.hp1 NA19010.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.834-1467_834-1466i others(24): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0043g0119 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.834-1467_834-1466i others(25): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0007g0237a0001c0001t0007g0261 | 2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.834-1467_834-1466i others(26): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0044g0210 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834-1467_834-1466i others(27): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0007g0008 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.834-1467_834-1466i others(29): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(22): Show |
1 | a0005c0012t0001g0282 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.834-1467_834-1466i others(31): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.834-1467_834-1466i others(32): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563940
|
CA | C | 55 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(52): Show | 56 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.834-1467delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | |||||
chr21:17563963
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.834-1465G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563963 | ||||||
chr21:17564066
|
A | C | 2 | a0001c0001t0002g0015a0001c0001t0030g0017 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.834-1362A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564066 | ||||||
chr21:17564141
|
T | A | 5 | a0001c0002t0006g0001a0001c0002t0006g0117a0001c0002t0006g0152others(2): Show | 6 | HG01099.hp1 HG01192.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.834-1287T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564141 | ||||||
chr21:17564169
|
T | TA | 7 | a0001c0001t0002g0007a0001c0001t0002g0156a0001c0001t0002g0157others(4): Show | 8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-1258dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17564169 | |||||
chr21:17564194
|
C | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0295 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.834-1234C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564194 | ||||||
chr21:17564216
|
G | A | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.834-1212G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564216 | ||||||
chr21:17564224
|
G | A | 38 | a0001c0001t0028g0090a0001c0001t0028g0091a0001c0002t0006g0001others(35): Show | 39 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.834-1204G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564224 | ||||||
chr21:17564251
|
G | T | 1 | a0001c0001t0003g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.834-1177G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564251 | ||||||
chr21:17564321
|
T | TA | 57 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(54): Show | 58 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.834-1094dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17564321 | |||||
chr21:17564321
|
TA | T | 10 | a0001c0001t0002g0007a0001c0001t0002g0156a0001c0001t0002g0157others(7): Show | 11 | HG00544.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.834-1094delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17564321 | |||||
chr21:17564418
|
T | G | 1 | a0001c0001t0005g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.834-1010T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564418 | ||||||
chr21:17564529
|
T | C | 2 | a0001c0001t0003g0142a0001c0001t0003g0143 | 2 | NA18991.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.834-899T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564529 | ||||||
chr21:17564536
|
A | G | 110 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(107): Show | 112 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.834-892A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564536 | ||||||
chr21:17564543
|
G | T | 1 | a0001c0001t0003g0025 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.834-885G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564543 | ||||||
chr21:17564566
|
C | T | 1 | a0001c0009t0075g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.834-862C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564566 | ||||||
chr21:17564596
|
G | C | 77 | a0001c0001t0001g0059a0001c0001t0003g0004a0001c0001t0003g0020others(74): Show | 78 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.834-832G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564596 | ||||||
chr21:17564633
|
C | A | 2 | a0001c0001t0007g0237a0001c0001t0007g0261 | 2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.834-795C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564633 | ||||||
chr21:17564796
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.834-632G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564796 | ||||||
chr21:17564957
|
A | G | 10 | a0001c0002t0006g0001a0001c0002t0006g0101a0001c0002t0006g0102others(7): Show | 11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.834-471A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564957 | ||||||
chr21:17564994
|
C | G | 75 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0025others(72): Show | 76 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.834-434C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564994 | ||||||
chr21:17565003
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.834-425G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565003 | ||||||
chr21:17565015
|
G | T | 2 | a0001c0002t0059g0003a0001c0002t0060g0003 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.834-413G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565015 | ||||||
chr21:17565057
|
C | G | 1 | a0001c0001t0002g0196 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.834-371C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565057 | ||||||
chr21:17565163
|
C | A | 5 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(2): Show | 5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.834-265C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565163 | ||||||
chr21:17565239
|
A | G | 7 | a0001c0002t0011g0107a0001c0004t0011g0038a0001c0004t0011g0080others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.834-189A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565239 | ||||||
chr21:17565262
|
T | A | 2 | a0001c0001t0002g0276a0001c0001t0002g0295 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.834-166T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565262 | ||||||
chr21:17565264
|
T | C | 33 | a0001c0002t0004g0322a0001c0002t0004g0324a0001c0002t0004g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.834-164T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565264 | ||||||
chr21:17565282
|
GAC | G | 10 | a0001c0001t0003g0048a0001c0002t0013g0104a0001c0002t0013g0105others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.834-115_834-114del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | |||||
chr21:17565282
|
GACAC | G | 61 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0042others(58): Show | 63 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.834-117_834-114del others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | |||||
chr21:17565282
|
GACACAC | G | 10 | a0001c0001t0003g0025a0001c0001t0003g0028a0001c0001t0003g0049others(7): Show | 10 | HG00438.hp1 HG00544.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.834-119_834-114del others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | |||||
chr21:17565282
|
GACACACA others(1): Show |
G | 3 | a0001c0002t0027g0016a0001c0002t0027g0144a0001c0002t0062g0164 | 3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.834-121_834-114del others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | |||||
chr21:17565282
|
GACACACA others(3): Show |
G | 10 | a0001c0001t0002g0015a0001c0001t0002g0018a0001c0001t0030g0017others(7): Show | 10 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.834-123_834-114del others(10): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | |||||
chr21:17565282
|
GACACACA others(5): Show |
G | 84 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0007others(81): Show | 86 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.834-125_834-114del others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | |||||
chr21:17565282
|
GACACACA others(7): Show |
G | 149 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.834-127_834-114del others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 |