geneid | 64121 |
---|---|
ensemblid | ENSG00000116954.8 |
hgncid | 19902 |
symbol | RRAGC |
name | Ras related GTP binding C |
refseq_nuc | NM_022157.4 |
refseq_prot | NP_071440.1 |
ensembl_nuc | ENST00000373001.4 |
ensembl_prot | ENSP00000362092.3 |
mane_status | MANE Select |
chr | chr1 |
start | 38838198 |
end | 38859772 |
strand | - |
ver | v1.2 |
region | chr1:38838198-38859772 |
region5000 | chr1:38833198-38864772 |
regionname0 | RRAGC_chr1_38838198_38859772 |
regionname5000 | RRAGC_chr1_38833198_38864772 |
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 | 399 | 418 | 94 | 68 | 194 | 18 | 42 | 150 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
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 | 1/1 | 1200 | 403 | 87 | 65 | 192 | 18 | 39 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
c0002 | 0/0 | 1200 | 10 | 5 | 3 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
c0003 | 0/0 | 1200 | 3 | 2 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
c0004 | 0/0 | 1200 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
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 | 0/1 | 1482 | 265 | 71 | 46 | 117 | 11 | 19 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0002 | 0/0 | 1482 | 75 | 0 | 8 | 57 | 0 | 10 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0003 | 0/0 | 1483 | 16 | 1 | 4 | 8 | 1 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0004 | 0/0 | 1481 | 13 | 1 | 5 | 0 | 4 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0005 | 0/0 | 1484 | 11 | 5 | 3 | 1 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0006 | 0/0 | 1482 | 9 | 9 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0007 | 1/0 | 1482 | 6 | 0 | 0 | 0 | 2 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0008 | 0/0 | 1483 | 5 | 0 | 0 | 5 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0009 | 0/0 | 1482 | 4 | 3 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0010 | 0/0 | 1483 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0011 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0012 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0013 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0014 | 0/0 | 1483 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0015 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0016 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0017 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0018 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0019 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0020 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
t0021 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
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 | 37 | 0 | 6 | 29 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0002 | 0/0 | 35 | 2 | 7 | 24 | 1 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0003 | 0/0 | 25 | 4 | 7 | 10 | 3 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0004 | 0/0 | 16 | 0 | 2 | 7 | 4 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0005 | 0/0 | 13 | 0 | 1 | 12 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0006 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0007 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0008 | 0/0 | 8 | 0 | 3 | 0 | 4 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0011 | 0/0 | 7 | 0 | 2 | 2 | 1 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0013 | 1/0 | 6 | 0 | 0 | 0 | 2 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0014 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0027 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0028 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0029 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
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 | 1/1 | 1200 | 403 | 87 | 65 | 192 | 18 | 39 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0002 | 0/0 | 1200 | 10 | 5 | 3 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0003 | 0/0 | 1200 | 3 | 2 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0004 | 0/0 | 1200 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2681 | 265 | 71 | 46 | 117 | 11 | 19 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0002 | 0/0 | 2681 | 73 | 0 | 8 | 55 | 0 | 10 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0003 | 0/0 | 2682 | 16 | 1 | 4 | 8 | 1 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0004 | 0/0 | 2680 | 13 | 1 | 5 | 0 | 4 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0005 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0006 | 0/0 | 2681 | 9 | 9 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0007 | 1/0 | 2681 | 6 | 0 | 0 | 0 | 2 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0008 | 0/0 | 2682 | 5 | 0 | 0 | 5 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0009 | 0/0 | 2681 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0010 | 0/0 | 2682 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0011 | 0/0 | 2681 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0012 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0013 | 0/0 | 2681 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0014 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0015 | 0/0 | 2681 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0016 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0017 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0018 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0019 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0020 | 0/0 | 2681 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0001t0021 | 0/0 | 2661 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0002t0005 | 0/0 | 2683 | 10 | 5 | 3 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0003t0009 | 0/0 | 2681 | 3 | 2 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
a0001c0004t0002 | 0/0 | 2681 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | copy fasta | chr1 | 38833198 | 38864772 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 35 | 2 | 7 | 24 | 1 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0003 | 0/0 | 25 | 4 | 7 | 10 | 3 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0004 | 0/0 | 16 | 0 | 2 | 7 | 4 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0005 | 0/0 | 13 | 0 | 1 | 12 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0006 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0011 | 0/0 | 7 | 0 | 2 | 2 | 1 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0014 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0029 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0001 | 0/0 | 37 | 0 | 6 | 29 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0004g0008 | 0/0 | 8 | 0 | 3 | 0 | 4 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0006g0007 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0007g0013 | 1/0 | 6 | 0 | 0 | 0 | 2 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0008g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0010g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0011g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0012g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0014g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0015g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0016g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0017g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0018g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0019g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0020g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0001t0021g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0002t0005g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0002t0005g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0002t0005g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0002t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0002t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0002t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0003t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0003t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0003t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
a0001c0004t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | GBR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0137 | EUR | GBR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00438 | hp2 | a0001 | c0001 | t0018 | g0114 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00597 | hp1 | a0001 | c0001 | t0016 | g0159 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01081 | hp2 | a0001 | c0001 | t0011 | g0053 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0094 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01175 | hp1 | a0001 | c0002 | t0005 | g0020 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01255 | hp1 | a0001 | c0001 | t0013 | g0093 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0013 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01517 | hp1 | a0001 | c0001 | t0007 | g0013 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01981 | hp2 | a0001 | c0002 | t0005 | g0020 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02027 | hp1 | a0001 | c0001 | t0008 | g0024 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0023 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02165 | hp1 | a0001 | c0001 | t0012 | g0071 | EAS | CDX | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02257 | hp2 | a0001 | c0002 | t0005 | g0063 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02602 | hp2 | a0001 | c0001 | t0020 | g0115 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02647 | hp2 | a0001 | c0002 | t0005 | g0064 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02698 | hp1 | a0001 | c0001 | t0015 | g0143 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02738 | hp1 | a0001 | c0001 | t0007 | g0013 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02809 | hp2 | a0001 | c0001 | t0010 | g0023 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02896 | hp1 | a0001 | c0002 | t0005 | g0052 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0104 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02897 | hp2 | a0001 | c0002 | t0005 | g0052 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0070 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03209 | hp2 | a0001 | c0003 | t0009 | g0056 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0092 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03540 | hp2 | a0001 | c0002 | t0005 | g0062 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03579 | hp1 | a0001 | c0001 | t0014 | g0105 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03669 | hp1 | a0001 | c0002 | t0005 | g0031 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0013 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03927 | hp2 | a0001 | c0003 | t0009 | g0054 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG04115 | hp1 | a0001 | c0002 | t0005 | g0031 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0013 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0101 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18747 | hp1 | a0001 | c0001 | t0017 | g0149 | EAS | CHB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18946 | hp1 | a0001 | c0001 | t0008 | g0024 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18949 | hp2 | a0001 | c0001 | t0008 | g0118 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18953 | hp2 | a0001 | c0004 | t0002 | g0030 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18967 | hp2 | a0001 | c0001 | t0019 | g0100 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19006 | hp1 | a0001 | c0001 | t0008 | g0024 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | LWK | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19059 | hp1 | a0001 | c0001 | t0021 | g0145 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19059 | hp2 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19065 | hp2 | a0001 | c0004 | t0002 | g0030 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA19240 | hp2 | a0001 | c0003 | t0009 | g0055 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0008 | EUR | TSI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | TSI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | GIH | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG01123 | hp2 | a0001 | c0002 | t0005 | g0020 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0023 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | USA | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | USA | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0013 | REF | REF | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:38845945
|
T | G | 1 | a0001c0002 | 10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
synonymous_variant | LOW | c.1042A>C | p.Arg348Arg | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/7 | 1168/2681 | 1042/1200 | 348/399 | chr1 | 38845945 | ||
chr1:38859464
|
C | T | 1 | a0001c0003 | 3 | HG03209.hp2 HG03927.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.183G>A | p.Lys61Lys | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/7 | 309/2681 | 183/1200 | 61/399 | chr1 | 38859464 | ||
chr1:38859527
|
C | T | 1 | a0001c0004 | 2 | NA18953.hp2 NA19065.hp2 |
synonymous_variant | LOW | c.120G>A | p.Ala40Ala | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/7 | 246/2681 | 120/1200 | 40/399 | chr1 | 38859527 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:38838227
|
A | G | 1 | a0001c0001t0018 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1326T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 1326 | chr1 | 38838227 | |||||
chr1:38838323
|
C | T | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*1230G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 1230 | chr1 | 38838323 | |||||
chr1:38838543
|
G | A | 1 | a0001c0001t0017 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1010C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 1010 | chr1 | 38838543 | |||||
chr1:38838575
|
A | G | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | 412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
3_prime_UTR_variant | MODIFIER | c.*978T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 978 | chr1 | 38838575 | |||||
chr1:38838630
|
C | T | 1 | a0001c0001t0016 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*923G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 923 | chr1 | 38838630 | |||||
chr1:38838736
|
T | C | 1 | a0001c0001t0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*817A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 817 | chr1 | 38838736 | |||||
chr1:38838875
|
CA | C | 2 | a0001c0001t0004a0001c0001t0013 | 14 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*677delT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 677 | chr1 | 38838875 | |||||
chr1:38839040
|
G | C | 1 | a0001c0001t0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*513C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 513 | chr1 | 38839040 | |||||
chr1:38839056
|
A | G | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
3_prime_UTR_variant | MODIFIER | c.*497T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 497 | chr1 | 38839056 | |||||
chr1:38839077
|
C | A | 1 | a0001c0001t0014 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 476 | chr1 | 38839077 | |||||
chr1:38839215
|
A | G | 1 | a0001c0001t0015 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 338 | chr1 | 38839215 | |||||
chr1:38839304
|
C | A | 1 | a0001c0001t0019 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 249 | chr1 | 38839304 | |||||
chr1:38839330
|
A | AT | 5 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(2): Show | 26 | HG00140.hp2 HG00423.hp2 HG00738.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*222dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 222 | chr1 | 38839330 | |||||
chr1:38839330
|
A | ATT | 2 | a0001c0001t0005a0001c0002t0005 | 11 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*221_*222dupAA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 222 | chr1 | 38839330 | |||||
chr1:38839407
|
C | T | 1 | a0001c0001t0012 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 146 | chr1 | 38839407 | |||||
chr1:38839441
|
T | C | 1 | a0001c0001t0020 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 112 | chr1 | 38839441 | |||||
chr1:38839462
|
ACAAGCAG others(13): Show |
A | 1 | a0001c0001t0021 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*71_*90delGACATGGG others(12): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 71 | chr1 | 38839462 | |||||
chr1:38839491
|
C | T | 1 | a0001c0001t0010 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 62 | chr1 | 38839491 | |||||
chr1:38859725
|
C | T | 1 | a0001c0001t0011 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/7 | 79 | chr1 | 38859725 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:38839731
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028others(16): Show | 37 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1049-27G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38839731 | ||||||
chr1:38840147
|
C | CA | 6 | a0001c0001t0001g0086a0001c0001t0002g0025a0001c0001t0002g0116others(3): Show | 15 | HG02055.hp1 HG02559.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1049-444dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840147 | ||||||
chr1:38840401
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1049-697T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840401 | ||||||
chr1:38840402
|
C | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1049-698G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840402 | ||||||
chr1:38840409
|
C | G | 3 | a0001c0001t0006g0007a0001c0001t0006g0070a0001c0001t0014g0105 | 10 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-705G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840409 | ||||||
chr1:38840410
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0036others(6): Show | 22 | HG01069.hp2 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1049-706C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840410 | ||||||
chr1:38840482
|
G | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0132others(4): Show | 9 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1049-778C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840482 | ||||||
chr1:38840800
|
G | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0034others(9): Show | 30 | HG00323.hp1 HG00741.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1049-1096C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840800 | ||||||
chr1:38840816
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1049-1112T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840816 | ||||||
chr1:38840973
|
A | G | 5 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0062others(2): Show | 8 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1269T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840973 | ||||||
chr1:38841367
|
A | T | 1 | a0001c0001t0005g0178 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1049-1663T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841367 | ||||||
chr1:38841368
|
A | AT | 10 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 13 | HG02109.hp2 HG02738.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1049-1665dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841368 | ||||||
chr1:38841368
|
A | ATT | 35 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(32): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1049-1666_1049-166 others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841368 | ||||||
chr1:38841368
|
A | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028others(17): Show | 38 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1049-1664T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841368 | ||||||
chr1:38841368
|
AT | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0037 | 7 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-1665delA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841368 | ||||||
chr1:38841476
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0132others(4): Show | 9 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1049-1772C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841476 | ||||||
chr1:38841603
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(34): Show | 98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1049-1899C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841603 | ||||||
chr1:38841675
|
A | T | 4 | a0001c0001t0009g0104a0001c0003t0009g0054a0001c0003t0009g0055others(1): Show | 4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049-1971T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841675 | ||||||
chr1:38841676
|
T | A | 5 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0062others(2): Show | 8 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1972A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841676 | ||||||
chr1:38841677
|
T | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0138 | 8 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1973A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841677 | ||||||
chr1:38841865
|
G | A | 1 | a0001c0001t0004g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1049-2161C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841865 | ||||||
chr1:38842000
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1049-2296A>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842000 | ||||||
chr1:38842055
|
G | A | 9 | a0001c0001t0001g0057a0001c0001t0004g0008a0001c0001t0004g0092others(6): Show | 17 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1049-2351C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842055 | ||||||
chr1:38842205
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1049-2501C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842205 | ||||||
chr1:38842287
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1049-2583G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842287 | ||||||
chr1:38842612
|
G | C | 1 | a0001c0001t0014g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1049-2908C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842612 | ||||||
chr1:38842628
|
T | A | 5 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 5 | HG02818.hp2 HG03098.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049-2924A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842628 | ||||||
chr1:38842976
|
A | G | 9 | a0001c0001t0001g0057a0001c0001t0004g0008a0001c0001t0004g0092others(6): Show | 17 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1048+2963T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842976 | ||||||
chr1:38843366
|
C | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061 | 7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+2573G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843366 | ||||||
chr1:38843435
|
T | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(45): Show | 112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1048+2504A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843435 | ||||||
chr1:38843443
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1048+2496C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843443 | ||||||
chr1:38843492
|
A | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(40): Show | 104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1048+2447T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843492 | ||||||
chr1:38843545
|
C | T | 1 | a0001c0001t0009g0104 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1048+2394G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843545 | ||||||
chr1:38843562
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028others(16): Show | 37 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1048+2377A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843562 | ||||||
chr1:38843645
|
G | A | 5 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0062others(2): Show | 8 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+2294C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843645 | ||||||
chr1:38843693
|
C | A | 1 | a0001c0001t0001g0027 | 3 | HG00621.hp1 HG02683.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1048+2246G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843693 | ||||||
chr1:38843717
|
C | CA | 8 | a0001c0001t0001g0019a0001c0001t0001g0133a0001c0001t0001g0153others(5): Show | 12 | HG00741.hp2 HG01952.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048+2221dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843717 | ||||||
chr1:38843738
|
G | C | 1 | a0001c0002t0005g0031 | 2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1048+2201C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843738 | ||||||
chr1:38843817
|
T | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+2122A>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843817 | ||||||
chr1:38843938
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1048+2001A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843938 | ||||||
chr1:38843970
|
A | C | 1 | a0001c0001t0002g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1048+1969T>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843970 | ||||||
chr1:38844012
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061 | 7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+1927A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844012 | ||||||
chr1:38844031
|
A | G | 1 | a0001c0001t0001g0034 | 2 | HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1048+1908T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844031 | ||||||
chr1:38844269
|
T | C | 1 | a0001c0001t0002g0111 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1048+1670A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844269 | ||||||
chr1:38844309
|
C | T | 1 | a0001c0001t0001g0048 | 2 | HG01099.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1048+1630G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844309 | ||||||
chr1:38844409
|
C | T | 7 | a0001c0001t0004g0008a0001c0001t0004g0092a0001c0001t0004g0094others(4): Show | 14 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1048+1530G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844409 | ||||||
chr1:38844447
|
G | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+1492C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844447 | ||||||
chr1:38844448
|
G | A | 1 | a0001c0001t0001g0044 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1048+1491C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844448 | ||||||
chr1:38844448
|
G | GA | 10 | a0001c0001t0001g0083a0001c0001t0001g0148a0001c0001t0002g0128others(7): Show | 17 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1048+1490dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844448 | ||||||
chr1:38844448
|
GA | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0061a0001c0001t0001g0084others(2): Show | 11 | HG02071.hp1 HG02155.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1048+1490delT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844448 | ||||||
chr1:38844487
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0132others(4): Show | 9 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+1452G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844487 | ||||||
chr1:38844539
|
G | C | 1 | a0001c0001t0002g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1048+1400C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844539 | ||||||
chr1:38844593
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0082 | 8 | HG02109.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048+1346A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844593 | ||||||
chr1:38844728
|
A | G | 3 | a0001c0001t0003g0047a0001c0001t0003g0140a0001c0001t0003g0141 | 4 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+1211T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844728 | ||||||
chr1:38844730
|
C | G | 2 | a0001c0001t0001g0072a0001c0001t0012g0071 | 2 | HG00408.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1048+1209G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844730 | ||||||
chr1:38844758
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1048+1181G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844758 | ||||||
chr1:38844807
|
G | A | 1 | a0001c0001t0002g0120 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1048+1132C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844807 | ||||||
chr1:38844833
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1048+1106A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844833 | ||||||
chr1:38844967
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(50): Show | 130 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1048+972T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844967 | ||||||
chr1:38845137
|
G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1048+802C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845137 | ||||||
chr1:38845178
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0068a0001c0001t0001g0083others(2): Show | 7 | HG00639.hp2 HG01243.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+761T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845178 | ||||||
chr1:38845185
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061 | 7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+754A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845185 | ||||||
chr1:38845214
|
C | T | 1 | a0001c0001t0001g0033 | 2 | NA18941.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1048+725G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845214 | ||||||
chr1:38845419
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0002g0109a0001c0001t0002g0122 | 4 | HG03491.hp2 HG03831.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+520A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845419 | ||||||
chr1:38845437
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1048+502C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845437 | ||||||
chr1:38845627
|
AT | A | 1 | a0001c0001t0001g0026 | 3 | NA18950.hp2 NA18984.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1048+311delA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845627 | ||||||
chr1:38845698
|
A | T | 3 | a0001c0001t0003g0047a0001c0001t0003g0140a0001c0001t0003g0141 | 4 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+241T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845698 | ||||||
chr1:38845709
|
T | C | 1 | a0001c0001t0001g0049 | 2 | HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1048+230A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845709 | ||||||
chr1:38845765
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1048+174C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845765 | ||||||
chr1:38845853
|
C | T | 6 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0052others(3): Show | 10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048+86G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845853 | ||||||
chr1:38845862
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0153 | 5 | HG00741.hp2 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+77A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845862 | ||||||
chr1:38846119
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061 | 7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.900-32C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846119 | ||||||
chr1:38846196
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.900-109T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846196 | ||||||
chr1:38846326
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(34): Show | 98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.900-239C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846326 | ||||||
chr1:38846472
|
A | AC | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.900-386dupG | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846472 | ||||||
chr1:38846487
|
C | T | 1 | a0001c0001t0001g0027 | 3 | HG00621.hp1 HG02683.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.900-400G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846487 | ||||||
chr1:38846488
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(49): Show | 132 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.900-401C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846488 | ||||||
chr1:38846569
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.900-482G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846569 | ||||||
chr1:38846667
|
C | T | 1 | a0001c0001t0010g0023 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.900-580G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846667 | ||||||
chr1:38846668
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.900-581C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846668 | ||||||
chr1:38846747
|
T | C | 6 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0052others(3): Show | 10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.900-660A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846747 | ||||||
chr1:38846873
|
C | T | 4 | a0001c0001t0009g0104a0001c0003t0009g0054a0001c0003t0009g0055others(1): Show | 4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-786G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846873 | ||||||
chr1:38846948
|
T | C | 1 | a0001c0001t0003g0140 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.900-861A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846948 | ||||||
chr1:38846962
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.900-875A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846962 | ||||||
chr1:38847003
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(39): Show | 103 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.900-916C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847003 | ||||||
chr1:38847178
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.900-1091G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847178 | ||||||
chr1:38847215
|
T | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(34): Show | 98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.900-1128A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847215 | ||||||
chr1:38847359
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-1272G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847359 | ||||||
chr1:38847410
|
G | C | 2 | a0001c0001t0006g0007a0001c0001t0006g0070 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-1323C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847410 | ||||||
chr1:38847413
|
C | A | 2 | a0001c0001t0006g0007a0001c0001t0006g0070 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-1326G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847413 | ||||||
chr1:38847415
|
GCCTAGGC | G | 2 | a0001c0001t0006g0007a0001c0001t0006g0070 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-1335_900-1329d others(9): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847415 | ||||||
chr1:38847427
|
CAAGA | C | 1 | a0001c0001t0006g0007 | 8 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.900-1344_900-1341d others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847427 | ||||||
chr1:38847431
|
A | AAC | 18 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0032others(15): Show | 27 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.900-1346_900-1345d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | ||||||
chr1:38847431
|
A | AACAC | 4 | a0001c0001t0003g0047a0001c0001t0003g0140a0001c0001t0010g0023others(1): Show | 8 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.900-1348_900-1345d others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | ||||||
chr1:38847431
|
A | AACACAC | 7 | a0001c0001t0001g0044a0001c0001t0001g0132a0001c0001t0001g0134others(4): Show | 15 | HG00099.hp1 HG00639.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.900-1350_900-1345d others(8): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | ||||||
chr1:38847431
|
A | AACACACA others(1): Show |
4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0004g0094others(1): Show | 4 | HG01167.hp1 HG01346.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-1352_900-1345d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | ||||||
chr1:38847431
|
A | AACACACA others(3): Show |
2 | a0001c0001t0001g0057a0001c0001t0004g0092 | 2 | HG02280.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.900-1354_900-1345d others(12): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | ||||||
chr1:38847431
|
A | AACACACA others(5): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0133 | 3 | HG02257.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.900-1356_900-1345d others(14): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | ||||||
chr1:38847431
|
AAC | A | 3 | a0001c0002t0005g0062a0001c0002t0005g0063a0001c0002t0005g0064 | 3 | HG02257.hp2 HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.900-1346_900-1345d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | ||||||
chr1:38847431
|
AACACACA others(1): Show |
A | 2 | a0001c0002t0005g0020a0001c0002t0005g0031 | 5 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.900-1352_900-1345d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | ||||||
chr1:38847503
|
G | A | 3 | a0001c0001t0006g0007a0001c0001t0006g0070a0001c0001t0014g0105 | 10 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.900-1416C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847503 | ||||||
chr1:38847556
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(39): Show | 103 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.900-1469C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847556 | ||||||
chr1:38847560
|
A | AT | 5 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.900-1474dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847560 | ||||||
chr1:38847577
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0076others(3): Show | 12 | HG01069.hp2 HG02572.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.900-1490C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847577 | ||||||
chr1:38847626
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028others(13): Show | 33 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.900-1539G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847626 | ||||||
chr1:38847915
|
C | T | 1 | a0001c0001t0004g0094 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.900-1828G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847915 | ||||||
chr1:38847928
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.900-1841C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847928 | ||||||
chr1:38848027
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.900-1940G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848027 | ||||||
chr1:38848033
|
C | CA | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.900-1947dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848033 | ||||||
chr1:38848033
|
C | CAA | 5 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 9 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.900-1948_900-1947d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848033 | ||||||
chr1:38848033
|
C | CAAA | 10 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(7): Show | 19 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.900-1949_900-1947d others(5): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848033 | ||||||
chr1:38848377
|
C | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0091 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.900-2290G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848377 | ||||||
chr1:38848525
|
T | C | 6 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0052others(3): Show | 10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.900-2438A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848525 | ||||||
chr1:38848613
|
A | G | 1 | a0001c0001t0003g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.900-2526T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848613 | ||||||
chr1:38848672
|
T | C | 1 | a0001c0003t0009g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.900-2585A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848672 | ||||||
chr1:38848796
|
G | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061 | 7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.900-2709C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848796 | ||||||
chr1:38848909
|
A | G | 2 | a0001c0001t0002g0113a0001c0004t0002g0030 | 3 | NA18953.hp2 NA19065.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.899+2706T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848909 | ||||||
chr1:38848965
|
C | G | 1 | a0001c0001t0002g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.899+2650G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848965 | ||||||
chr1:38849029
|
C | T | 2 | a0001c0001t0006g0007a0001c0001t0006g0070 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.899+2586G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849029 | ||||||
chr1:38849286
|
T | C | 6 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0052others(3): Show | 10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.899+2329A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849286 | ||||||
chr1:38849422
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.899+2193G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849422 | ||||||
chr1:38849612
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(47): Show | 123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.899+2003G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849612 | ||||||
chr1:38849613
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.899+2002C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849613 | ||||||
chr1:38849666
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.899+1949G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849666 | ||||||
chr1:38849752
|
A | G | 3 | a0001c0001t0003g0047a0001c0001t0003g0140a0001c0001t0003g0141 | 4 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+1863T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849752 | ||||||
chr1:38849763
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.899+1852C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849763 | ||||||
chr1:38849824
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.899+1791T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849824 | ||||||
chr1:38849936
|
G | A | 1 | a0001c0002t0005g0052 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.899+1679C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849936 | ||||||
chr1:38849955
|
C | T | 2 | a0001c0003t0009g0055a0001c0003t0009g0056 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.899+1660G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849955 | ||||||
chr1:38849959
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0170 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.899+1656G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849959 | ||||||
chr1:38849971
|
C | T | 1 | a0001c0001t0010g0023 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1644G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849971 | ||||||
chr1:38849972
|
C | T | 1 | a0001c0001t0010g0023 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1643G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849972 | ||||||
chr1:38849973
|
A | G | 1 | a0001c0001t0010g0023 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1642T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849973 | ||||||
chr1:38849974
|
C | A | 1 | a0001c0001t0010g0023 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1641G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849974 | ||||||
chr1:38849977
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.899+1638G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849977 | ||||||
chr1:38849980
|
G | GCCACC | 1 | a0001c0001t0010g0023 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1634_899+1635i others(7): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849980 | ||||||
chr1:38849982
|
GGA | G | 1 | a0001c0001t0010g0023 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1631_899+1632d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849982 | ||||||
chr1:38849987
|
A | T | 1 | a0001c0001t0010g0023 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1628T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849987 | ||||||
chr1:38849988
|
C | T | 1 | a0001c0001t0010g0023 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1627G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849988 | ||||||
chr1:38850092
|
G | A | 2 | a0001c0001t0004g0094a0001c0001t0004g0095 | 2 | HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.899+1523C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850092 | ||||||
chr1:38850121
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.899+1494C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850121 | ||||||
chr1:38850133
|
G | C | 1 | a0001c0001t0004g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.899+1482C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850133 | ||||||
chr1:38850138
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.899+1477C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850138 | ||||||
chr1:38850143
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.899+1472A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850143 | ||||||
chr1:38850203
|
T | A | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.899+1412A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850203 | ||||||
chr1:38850276
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.899+1339G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850276 | ||||||
chr1:38850307
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0142others(8): Show | 21 | HG00408.hp1 HG00597.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.899+1308C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850307 | ||||||
chr1:38850329
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028others(13): Show | 33 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.899+1286T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850329 | ||||||
chr1:38850383
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.899+1232C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850383 | ||||||
chr1:38850390
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028others(16): Show | 37 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.899+1225A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850390 | ||||||
chr1:38850427
|
T | C | 1 | a0001c0001t0001g0044 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.899+1188A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850427 | ||||||
chr1:38850436
|
C | G | 1 | a0001c0002t0005g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.899+1179G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850436 | ||||||
chr1:38850440
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.899+1175C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850440 | ||||||
chr1:38850493
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.899+1122C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850493 | ||||||
chr1:38850512
|
T | TAATA | 39 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(36): Show | 78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.899+1099_899+1102d others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850512 | ||||||
chr1:38850512
|
T | TAATAAAT others(1): Show |
12 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0142others(9): Show | 19 | HG02055.hp2 HG02109.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.899+1095_899+1102d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850512 | ||||||
chr1:38850512
|
TAATA | T | 16 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(13): Show | 37 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.899+1099_899+1102d others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850512 | ||||||
chr1:38850512
|
TAATAAAT others(1): Show |
T | 6 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0076others(3): Show | 12 | HG01069.hp2 HG02572.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.899+1095_899+1102d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850512 | ||||||
chr1:38850581
|
T | G | 2 | a0001c0001t0006g0007a0001c0001t0006g0070 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.899+1034A>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850581 | ||||||
chr1:38850591
|
T | C | 1 | a0001c0001t0002g0124 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.899+1024A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850591 | ||||||
chr1:38850637
|
GA | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0133 | 3 | HG02257.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.899+977delT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850637 | ||||||
chr1:38850639
|
A | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0133 | 3 | HG02257.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.899+976T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850639 | ||||||
chr1:38850667
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.899+948T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850667 | ||||||
chr1:38850783
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.899+832A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850783 | ||||||
chr1:38850843
|
TG | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(47): Show | 123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.899+771delC | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850843 | ||||||
chr1:38850844
|
G | GT | 7 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 13 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.899+770dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850844 | ||||||
chr1:38850845
|
T | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(47): Show | 123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.899+770A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850845 | ||||||
chr1:38850971
|
T | A | 2 | a0001c0001t0002g0025a0001c0001t0002g0126 | 4 | NA18953.hp1 NA18954.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.899+644A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850971 | ||||||
chr1:38851244
|
C | T | 1 | a0001c0001t0017g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.899+371G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38851244 | ||||||
chr1:38851279
|
T | TTAAA | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.899+332_899+335dup others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38851279 | ||||||
chr1:38851429
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.899+186G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38851429 | ||||||
chr1:38851491
|
G | C | 4 | a0001c0001t0009g0104a0001c0003t0009g0054a0001c0003t0009g0055others(1): Show | 4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+124C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38851491 | ||||||
chr1:38851897
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.757-140G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 4/6 | chr1 | 38851897 | ||||||
chr1:38852038
|
A | T | 1 | a0001c0001t0014g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.757-281T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 4/6 | chr1 | 38852038 | ||||||
chr1:38852131
|
A | T | 1 | a0001c0001t0001g0074 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.756+243T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 4/6 | chr1 | 38852131 | ||||||
chr1:38852332
|
A | G | 4 | a0001c0001t0009g0104a0001c0003t0009g0054a0001c0003t0009g0055others(1): Show | 4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+42T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 4/6 | chr1 | 38852332 | ||||||
chr1:38852752
|
G | T | 1 | a0001c0001t0001g0174 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.642-264C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852752 | ||||||
chr1:38852803
|
C | T | 1 | a0001c0001t0001g0021 | 3 | NA18939.hp2 NA18977.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.642-315G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852803 | ||||||
chr1:38852935
|
C | G | 1 | a0001c0001t0003g0140 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.642-447G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852935 | ||||||
chr1:38852942
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.642-454G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852942 | ||||||
chr1:38852967
|
A | G | 6 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0052others(3): Show | 10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.642-479T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852967 | ||||||
chr1:38853106
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0012g0071 | 2 | HG00408.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.642-618T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853106 | ||||||
chr1:38853299
|
G | A | 1 | a0001c0001t0019g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.642-811C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853299 | ||||||
chr1:38853321
|
A | C | 6 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0052others(3): Show | 10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.642-833T>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853321 | ||||||
chr1:38853337
|
C | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(40): Show | 104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.642-849G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853337 | ||||||
chr1:38853366
|
G | T | 7 | a0001c0001t0004g0008a0001c0001t0004g0092a0001c0001t0004g0094others(4): Show | 14 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.642-878C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853366 | ||||||
chr1:38853545
|
A | C | 2 | a0001c0001t0006g0007a0001c0001t0006g0070 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.642-1057T>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853545 | ||||||
chr1:38853571
|
C | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0045 | 7 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.642-1083G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853571 | ||||||
chr1:38853575
|
A | G | 68 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.642-1087T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853575 | ||||||
chr1:38853578
|
T | A | 1 | a0001c0002t0005g0052 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.642-1090A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853578 | ||||||
chr1:38853688
|
G | A | 8 | a0001c0001t0001g0057a0001c0001t0004g0008a0001c0001t0004g0092others(5): Show | 15 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.642-1200C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853688 | ||||||
chr1:38853708
|
T | C | 2 | a0001c0001t0002g0025a0001c0001t0002g0126 | 4 | NA18953.hp1 NA18954.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-1220A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853708 | ||||||
chr1:38853747
|
C | CA | 9 | a0001c0001t0001g0069a0001c0001t0001g0097a0001c0001t0001g0098others(6): Show | 9 | HG02572.hp1 HG02602.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.642-1260dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853747 | ||||||
chr1:38853753
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.642-1265T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853753 | ||||||
chr1:38853806
|
A | G | 4 | a0001c0001t0009g0104a0001c0003t0009g0054a0001c0003t0009g0055others(1): Show | 4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-1318T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853806 | ||||||
chr1:38853932
|
G | A | 1 | a0001c0002t0005g0052 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.642-1444C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853932 | ||||||
chr1:38853953
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.642-1465T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853953 | ||||||
chr1:38854039
|
T | A | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.642-1551A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854039 | ||||||
chr1:38854065
|
C | CT | 5 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0002g0040others(2): Show | 6 | HG02622.hp2 HG04184.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-1578dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854065 | ||||||
chr1:38854065
|
CT | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.642-1578delA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854065 | ||||||
chr1:38854065
|
CTT | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0102others(9): Show | 25 | HG01069.hp2 HG01070.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.642-1579_642-1578d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854065 | ||||||
chr1:38854194
|
A | G | 1 | a0001c0001t0002g0107 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.641+1514T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854194 | ||||||
chr1:38854257
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0138a0001c0001t0001g0139 | 4 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+1451G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854257 | ||||||
chr1:38854344
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+1364A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854344 | ||||||
chr1:38854358
|
T | C | 1 | a0001c0001t0001g0038 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.641+1350A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854358 | ||||||
chr1:38854394
|
T | C | 1 | a0001c0001t0003g0050 | 2 | NA18952.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.641+1314A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854394 | ||||||
chr1:38854421
|
T | TTGTTA | 6 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0052others(3): Show | 10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.641+1286_641+1287i others(7): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854421 | ||||||
chr1:38854637
|
C | T | 1 | a0001c0001t0015g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.641+1071G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854637 | ||||||
chr1:38854733
|
C | T | 1 | a0001c0001t0001g0018 | 4 | HG02630.hp1 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+975G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854733 | ||||||
chr1:38854843
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.641+865G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854843 | ||||||
chr1:38854846
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0138a0001c0001t0001g0139 | 4 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+862C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854846 | ||||||
chr1:38854920
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.641+788G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854920 | ||||||
chr1:38855318
|
TAAGACTC others(6): Show |
T | 4 | a0001c0001t0001g0043a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 5 | HG02257.hp1 HG02922.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+377_641+389del others(13): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38855318 | ||||||
chr1:38855456
|
CTT | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061 | 7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.641+250_641+251del others(2): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38855456 | ||||||
chr1:38856041
|
A | G | 1 | a0001c0001t0002g0039 | 2 | NA19007.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.442-134T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856041 | ||||||
chr1:38856250
|
T | G | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.442-343A>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856250 | ||||||
chr1:38856334
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.442-427G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856334 | ||||||
chr1:38856651
|
C | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.441+228G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856651 | ||||||
chr1:38856798
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.441+81A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856798 | ||||||
chr1:38857301
|
C | A | 1 | a0001c0001t0001g0103 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.238-219G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857301 | ||||||
chr1:38857555
|
G | A | 1 | a0001c0001t0002g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.238-473C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857555 | ||||||
chr1:38857683
|
G | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028others(17): Show | 37 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.238-601C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857683 | ||||||
chr1:38857758
|
G | A | 1 | a0001c0001t0014g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.238-676C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857758 | ||||||
chr1:38857841
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.238-759A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857841 | ||||||
chr1:38858126
|
CGTACCCA others(1): Show |
C | 5 | a0001c0002t0005g0020a0001c0002t0005g0031a0001c0002t0005g0062others(2): Show | 8 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-1052_238-1045d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858126 | ||||||
chr1:38858197
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.238-1115T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858197 | ||||||
chr1:38858312
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.237+1098C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858312 | ||||||
chr1:38858372
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237+1038C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858372 | ||||||
chr1:38858381
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061 | 7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.237+1029G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858381 | ||||||
chr1:38858469
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0045 | 7 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.237+941G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858469 | ||||||
chr1:38858613
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.237+797T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858613 | ||||||
chr1:38858721
|
C | A | 1 | a0001c0001t0002g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.237+689G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858721 | ||||||
chr1:38858827
|
G | T | 1 | a0001c0001t0001g0059 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.237+583C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858827 | ||||||
chr1:38858878
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.237+532C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858878 | ||||||
chr1:38858940
|
A | C | 1 | a0001c0001t0002g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.237+470T>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858940 | ||||||
chr1:38859051
|
G | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0132others(4): Show | 9 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.237+359C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859051 | ||||||
chr1:38859141
|
G | T | 3 | a0001c0001t0003g0047a0001c0001t0003g0140a0001c0001t0003g0141 | 4 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+269C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859141 | ||||||
chr1:38859143
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.237+267C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859143 | ||||||
chr1:38859187
|
C | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.237+223G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859187 | ||||||
chr1:38859220
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.237+190C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859220 | ||||||
chr1:38859342
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0183 | 4 | HG01070.hp2 HG02683.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+68C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859342 | ||||||
chr1:38859345
|
C | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.237+65G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859345 | ||||||
chr1:38859391
|
T | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.237+19A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859391 |