geneid | 10325 |
---|---|
ensemblid | ENSG00000083750.13 |
hgncid | 19901 |
symbol | RRAGB |
name | Ras related GTP binding B |
refseq_nuc | NM_006064.5 |
refseq_prot | NP_006055.3 |
ensembl_nuc | ENST00000374941.9 |
ensembl_prot | ENSP00000364077.4 |
mane_status | MANE Select |
chr | chrX |
start | 55717749 |
end | 55758774 |
strand | + |
ver | v1.2 |
region | chrX:55717749-55758774 |
region5000 | chrX:55712749-55763774 |
regionname0 | RRAGB_chrX_55717749_55758774 |
regionname5000 | RRAGB_chrX_55712749_55763774 |
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 | 346 | 275 | 76 | 49 | 115 | 7 | 26 | 90 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
a0002 | 0/0 | 330 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
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 | 1041 | 275 | 76 | 49 | 115 | 7 | 26 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
c0002 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1011 | 167 | 41 | 25 | 78 | 5 | 16 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
t0002 | 0/0 | 1011 | 104 | 35 | 24 | 33 | 2 | 10 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
t0003 | 0/0 | 1011 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
t0004 | 0/0 | 1012 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
t0005 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
t0006 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
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 | 27 | 0 | 4 | 23 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0002 | 0/0 | 12 | 1 | 4 | 6 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0004 | 0/1 | 7 | 2 | 0 | 0 | 0 | 4 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0007 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0008 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0009 | 0/0 | 4 | 0 | 0 | 2 | 2 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0011 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0020 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
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 | 1041 | 275 | 76 | 49 | 115 | 7 | 26 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
a0002c0002 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2051 | 166 | 41 | 25 | 77 | 5 | 16 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
a0001c0001t0002 | 0/0 | 2051 | 104 | 35 | 24 | 33 | 2 | 10 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
a0001c0001t0003 | 0/0 | 2051 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
a0001c0001t0004 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
a0001c0001t0005 | 0/0 | 2051 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
a0001c0001t0006 | 0/0 | 2051 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
a0002c0002t0001 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | copy fasta | chrX | 55712749 | 55763774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 27 | 0 | 4 | 23 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0004 | 0/1 | 4 | 2 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 2 | 2 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0011 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0002 | 0/0 | 12 | 1 | 4 | 6 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0020 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | GBR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02155 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | CDX | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CDX | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18963 | hp1 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ASW | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ASW | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | GIH | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | USA | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0011 | REF | REF | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:55757327
|
C | CA | 1 | a0002 | 1 | NA19067.hp1 | frameshift_variant&splice_region_variant | HIGH | c.940dupA | p.Ile314fs | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/10 | 1520/2051 | 941/1041 | 314/346 | INFO_REALIGN_3_PRIME | chrX | 55757327 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:55717837
|
G | GC | 1 | a0001c0001t0004 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-486dupC | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/10 | 485 | INFO_REALIGN_3_PRIME | chrX | 55717837 | ||||
chrX:55717852
|
C | G | 3 | a0001c0001t0002a0001c0001t0003a0001c0001t0006 | 107 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
5_prime_UTR_variant | MODIFIER | c.-476C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/10 | 476 | chrX | 55717852 | |||||
chrX:55717872
|
G | C | 1 | a0001c0001t0003 | 2 | NA18946.hp1 NA18973.hp1 |
5_prime_UTR_variant | MODIFIER | c.-456G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/10 | 456 | chrX | 55717872 | |||||
chrX:55717877
|
C | G | 1 | a0001c0001t0005 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-451C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/10 | 451 | chrX | 55717877 | |||||
chrX:55718298
|
T | C | 1 | a0001c0001t0006 | 1 | NA18963.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/10 | 30 | chrX | 55718298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:55718450
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92+31G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/9 | chrX | 55718450 | ||||||
chrX:55718559
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.92+140T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/9 | chrX | 55718559 | ||||||
chrX:55718650
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.92+231G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/9 | chrX | 55718650 | ||||||
chrX:55719570
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.126+223G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55719570 | ||||||
chrX:55719828
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+481T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55719828 | ||||||
chrX:55719993
|
A | C | 77 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(74): Show | 99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.126+646A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55719993 | ||||||
chrX:55720212
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.126+865G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720212 | ||||||
chrX:55720559
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.126+1212G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720559 | ||||||
chrX:55720663
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.126+1316A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720663 | ||||||
chrX:55720687
|
CA | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(84): Show | 135 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.126+1356delA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 55720687 | |||||
chrX:55720687
|
CAA | C | 77 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0002g0002others(74): Show | 99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.126+1355_126+1356d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 55720687 | |||||
chrX:55720687
|
CAAA | C | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.126+1354_126+1356d others(5): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 55720687 | |||||
chrX:55720770
|
G | A | 1 | a0001c0001t0001g0014 | 2 | HG01243.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.127-1416G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720770 | ||||||
chrX:55720803
|
G | A | 9 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(6): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-1383G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720803 | ||||||
chrX:55720808
|
G | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(74): Show | 99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.127-1378G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720808 | ||||||
chrX:55721284
|
A | G | 77 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(74): Show | 99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.127-902A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721284 | ||||||
chrX:55721482
|
A | T | 1 | a0001c0001t0002g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.127-704A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721482 | ||||||
chrX:55721509
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-677C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721509 | ||||||
chrX:55721518
|
A | G | 77 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(74): Show | 99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.127-668A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721518 | ||||||
chrX:55721629
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.127-557G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721629 | ||||||
chrX:55721707
|
A | G | 4 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-479A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721707 | ||||||
chrX:55722082
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.127-104A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55722082 | ||||||
chrX:55722091
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127-95A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55722091 | ||||||
chrX:55722108
|
G | C | 1 | a0001c0001t0002g0130 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.127-78G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55722108 | ||||||
chrX:55722387
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.226+102A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722387 | ||||||
chrX:55722467
|
G | T | 77 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(74): Show | 99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.226+182G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722467 | ||||||
chrX:55722699
|
A | G | 9 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(6): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.226+414A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722699 | ||||||
chrX:55722700
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.226+415C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722700 | ||||||
chrX:55722705
|
G | A | 15 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0131others(12): Show | 18 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.226+420G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722705 | ||||||
chrX:55722845
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.226+560T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722845 | ||||||
chrX:55722973
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.226+688G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722973 | ||||||
chrX:55723025
|
A | C | 1 | a0001c0001t0002g0179 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.226+740A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723025 | ||||||
chrX:55723295
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.226+1010C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723295 | ||||||
chrX:55723447
|
C | CT | 1 | a0001c0001t0001g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.226+1175dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 55723447 | |||||
chrX:55723447
|
CT | C | 2 | a0001c0001t0001g0024a0001c0001t0002g0140 | 2 | NA18969.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.226+1175delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 55723447 | |||||
chrX:55723474
|
C | T | 68 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0017others(65): Show | 87 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.226+1189C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723474 | ||||||
chrX:55723570
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0112 | 2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.226+1285T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723570 | ||||||
chrX:55723601
|
A | G | 1 | a0001c0001t0002g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.226+1316A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723601 | ||||||
chrX:55723857
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.226+1572C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723857 | ||||||
chrX:55723914
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 127 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.226+1629A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723914 | ||||||
chrX:55724209
|
T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | HG01261.hp1 HG01496.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.226+1924T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55724209 | ||||||
chrX:55724741
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.226+2456T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55724741 | ||||||
chrX:55724920
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 273 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.226+2635G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55724920 | ||||||
chrX:55725419
|
A | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.226+3134A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55725419 | ||||||
chrX:55726106
|
A | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.227-3188A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726106 | ||||||
chrX:55726151
|
T | TA | 149 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(146): Show | 218 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.227-3132dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 55726151 | |||||
chrX:55726151
|
T | TAA | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0002g0018others(1): Show | 5 | HG01257.hp2 HG02523.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-3133_227-3132d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 55726151 | |||||
chrX:55726151
|
TA | T | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-3132delA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 55726151 | |||||
chrX:55726300
|
T | C | 15 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0131others(12): Show | 18 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.227-2994T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726300 | ||||||
chrX:55726419
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.227-2875T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726419 | ||||||
chrX:55726445
|
GTCTGTAA others(2): Show |
G | 1 | a0001c0001t0002g0177 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.227-2847_227-2839d others(11): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 55726445 | |||||
chrX:55726510
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.227-2784T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726510 | ||||||
chrX:55726696
|
T | G | 1 | a0001c0001t0002g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.227-2598T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726696 | ||||||
chrX:55726759
|
G | C | 1 | a0001c0001t0002g0143 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.227-2535G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726759 | ||||||
chrX:55726864
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 230 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.227-2430T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726864 | ||||||
chrX:55726865
|
C | G | 5 | a0001c0001t0001g0098a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG01255.hp1 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-2429C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726865 | ||||||
chrX:55728104
|
G | A | 4 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 7 | HG02818.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.227-1190G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728104 | ||||||
chrX:55728108
|
A | G | 1 | a0001c0001t0006g0176 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1186A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728108 | ||||||
chrX:55728148
|
A | T | 1 | a0001c0001t0002g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.227-1146A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728148 | ||||||
chrX:55728333
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.227-961C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728333 | ||||||
chrX:55728632
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.227-662G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728632 | ||||||
chrX:55728827
|
G | T | 1 | a0001c0001t0002g0179 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.227-467G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728827 | ||||||
chrX:55728921
|
CT | C | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.227-363delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 55728921 | |||||
chrX:55728962
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.227-332G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728962 | ||||||
chrX:55729112
|
G | T | 1 | a0001c0001t0004g0089 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.227-182G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55729112 | ||||||
chrX:55729261
|
A | T | 1 | a0001c0001t0001g0016 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.227-33A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55729261 | ||||||
chrX:55729604
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293+244T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55729604 | ||||||
chrX:55729679
|
C | G | 5 | a0001c0001t0001g0098a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG01255.hp1 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.293+319C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55729679 | ||||||
chrX:55729834
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.293+474A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55729834 | ||||||
chrX:55730015
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293+655C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55730015 | ||||||
chrX:55730424
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.294-940A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55730424 | ||||||
chrX:55730454
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.294-910C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55730454 | ||||||
chrX:55730574
|
C | A | 1 | a0001c0001t0002g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.294-790C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55730574 | ||||||
chrX:55730969
|
T | TG | 2 | a0001c0001t0002g0124a0002c0002t0001g0033 | 2 | HG03579.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.294-389dupG | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 55730969 | |||||
chrX:55731303
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.294-61G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55731303 | ||||||
chrX:55731311
|
T | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.294-53T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55731311 | ||||||
chrX:55731344
|
A | G | 18 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0076others(15): Show | 23 | HG01257.hp1 HG01258.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.294-20A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55731344 | ||||||
chrX:55731350
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.294-14A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55731350 | ||||||
chrX:55731697
|
A | G | 1 | a0001c0001t0005g0073 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.516+111A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731697 | ||||||
chrX:55731805
|
T | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+219T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731805 | ||||||
chrX:55731848
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(73): Show | 123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.516+262A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731848 | ||||||
chrX:55731935
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.516+349G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731935 | ||||||
chrX:55731975
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(73): Show | 123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.516+389C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731975 | ||||||
chrX:55731985
|
A | G | 3 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0174 | 3 | HG02155.hp2 NA18966.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.516+399A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731985 | ||||||
chrX:55732042
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+456A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732042 | ||||||
chrX:55732145
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+559A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732145 | ||||||
chrX:55732161
|
C | CA | 1 | a0001c0001t0001g0075 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+582dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55732161 | |||||
chrX:55732297
|
T | A | 1 | a0001c0001t0001g0029 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.516+711T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732297 | ||||||
chrX:55732489
|
C | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.516+903C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732489 | ||||||
chrX:55732729
|
C | T | 69 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0013others(66): Show | 89 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.516+1143C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732729 | ||||||
chrX:55732891
|
C | T | 1 | a0001c0001t0002g0012 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.516+1305C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732891 | ||||||
chrX:55732912
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.516+1326C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732912 | ||||||
chrX:55732949
|
G | GT | 1 | a0001c0001t0001g0030 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.516+1372dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55732949 | |||||
chrX:55732979
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.516+1393T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732979 | ||||||
chrX:55733043
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.516+1457G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733043 | ||||||
chrX:55733141
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.516+1555C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733141 | ||||||
chrX:55733180
|
C | G | 1 | a0001c0001t0002g0171 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.516+1594C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733180 | ||||||
chrX:55733497
|
GT | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+1918delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55733497 | |||||
chrX:55733706
|
A | G | 2 | a0001c0001t0003g0141a0001c0001t0003g0170 | 2 | NA18946.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.516+2120A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733706 | ||||||
chrX:55733931
|
GT | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(72): Show | 123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.516+2356delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55733931 | |||||
chrX:55733958
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+2372A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733958 | ||||||
chrX:55733963
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.516+2377T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733963 | ||||||
chrX:55733986
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.516+2400C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733986 | ||||||
chrX:55733994
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0112 | 2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.516+2408C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733994 | ||||||
chrX:55734032
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0107 | 9 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+2446C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734032 | ||||||
chrX:55734125
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+2539A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734125 | ||||||
chrX:55734206
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.516+2620G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734206 | ||||||
chrX:55734252
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.516+2666C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734252 | ||||||
chrX:55734265
|
G | GT | 11 | a0001c0001t0001g0023a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00544.hp1 HG02572.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.516+2694dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55734265 | |||||
chrX:55734265
|
G | GTT | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.516+2693_516+2694d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55734265 | |||||
chrX:55734273
|
T | G | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.516+2687T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734273 | ||||||
chrX:55734344
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.516+2758T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734344 | ||||||
chrX:55734589
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+3003T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734589 | ||||||
chrX:55734778
|
G | T | 1 | a0001c0001t0002g0171 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.516+3192G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734778 | ||||||
chrX:55734799
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.516+3213A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734799 | ||||||
chrX:55735141
|
T | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+3555T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55735141 | ||||||
chrX:55735500
|
G | T | 1 | a0001c0001t0002g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.516+3914G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55735500 | ||||||
chrX:55735583
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.516+3997T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55735583 | ||||||
chrX:55736332
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.516+4746G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55736332 | ||||||
chrX:55736695
|
G | A | 1 | a0001c0001t0002g0127 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.516+5109G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55736695 | ||||||
chrX:55736890
|
C | T | 77 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(74): Show | 99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.516+5304C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55736890 | ||||||
chrX:55736977
|
A | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.516+5391A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55736977 | ||||||
chrX:55737215
|
C | G | 9 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(6): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+5629C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737215 | ||||||
chrX:55737652
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+6066C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737652 | ||||||
chrX:55737665
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.516+6079G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737665 | ||||||
chrX:55737913
|
G | A | 9 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(6): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+6327G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737913 | ||||||
chrX:55737937
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0123 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.516+6351G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737937 | ||||||
chrX:55738041
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.516+6455G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738041 | ||||||
chrX:55738136
|
T | TG | 1 | a0001c0001t0001g0035 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.516+6550_516+6551i others(3): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738136 | ||||||
chrX:55738191
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.516+6605C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738191 | ||||||
chrX:55738268
|
GCTT | G | 9 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(6): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+6686_516+6688d others(5): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55738268 | |||||
chrX:55738380
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+6794A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738380 | ||||||
chrX:55738546
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.516+6960A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738546 | ||||||
chrX:55738870
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.516+7284G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738870 | ||||||
chrX:55739402
|
CT | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+7818delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55739402 | |||||
chrX:55739591
|
T | C | 1 | a0001c0001t0002g0147 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.516+8005T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55739591 | ||||||
chrX:55739600
|
C | T | 79 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(76): Show | 102 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.516+8014C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55739600 | ||||||
chrX:55739864
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(73): Show | 123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.516+8278G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55739864 | ||||||
chrX:55740094
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8508G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740094 | ||||||
chrX:55740119
|
G | A | 1 | a0001c0001t0001g0016 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.516+8533G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740119 | ||||||
chrX:55740184
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.516+8598G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740184 | ||||||
chrX:55740304
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8718A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740304 | ||||||
chrX:55740310
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8724A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740310 | ||||||
chrX:55740318
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8732A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740318 | ||||||
chrX:55740322
|
C | CA | 4 | a0001c0001t0001g0008a0001c0001t0001g0071a0001c0001t0002g0148others(1): Show | 7 | HG03490.hp1 HG03831.hp1 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+8749dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55740322 | |||||
chrX:55740322
|
CA | C | 1 | a0001c0001t0001g0068 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.516+8749delA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55740322 | |||||
chrX:55740336
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8750T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740336 | ||||||
chrX:55740337
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8751C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740337 | ||||||
chrX:55740338
|
ATTGTGAT others(37): Show |
A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8753_516+8796d others(46): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740338 | ||||||
chrX:55740386
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8800C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740386 | ||||||
chrX:55740388
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8802C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740388 | ||||||
chrX:55740389
|
ATCTTTT | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8804_516+8809d others(8): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740389 | ||||||
chrX:55740396
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8810G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740396 | ||||||
chrX:55740397
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8811G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740397 | ||||||
chrX:55740400
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8814T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740400 | ||||||
chrX:55740478
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8892G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740478 | ||||||
chrX:55740531
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8945G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740531 | ||||||
chrX:55740853
|
C | CT | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.516+9274dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55740853 | |||||
chrX:55741014
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.516+9428A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55741014 | ||||||
chrX:55741025
|
A | AT | 5 | a0001c0001t0001g0110a0001c0001t0002g0126a0001c0001t0002g0166others(2): Show | 5 | HG01175.hp1 HG02071.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+9457dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55741025 | |||||
chrX:55741025
|
AT | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG03516.hp2 HG03688.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.516+9457delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55741025 | |||||
chrX:55741025
|
ATT | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(67): Show | 117 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.516+9456_516+9457d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55741025 | |||||
chrX:55741063
|
CT | C | 1 | a0001c0001t0002g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.516+9481delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55741063 | |||||
chrX:55741125
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+9539G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55741125 | ||||||
chrX:55741290
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG01255.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.516+9704G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55741290 | ||||||
chrX:55741483
|
A | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0112 | 2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.517-9618A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55741483 | ||||||
chrX:55742059
|
C | T | 1 | a0001c0001t0002g0177 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.517-9042C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742059 | ||||||
chrX:55742112
|
T | C | 1 | a0001c0001t0002g0189 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.517-8989T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742112 | ||||||
chrX:55742205
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.517-8896A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742205 | ||||||
chrX:55742275
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.517-8826A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742275 | ||||||
chrX:55742513
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.517-8588C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742513 | ||||||
chrX:55742979
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.517-8122G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742979 | ||||||
chrX:55743166
|
G | A | 1 | a0001c0001t0001g0016 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.517-7935G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743166 | ||||||
chrX:55743313
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.517-7788T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743313 | ||||||
chrX:55743677
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.517-7424A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743677 | ||||||
chrX:55743814
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(158): Show | 231 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.517-7287A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743814 | ||||||
chrX:55743911
|
A | AACTTTCT others(19): Show |
1 | a0001c0001t0002g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.517-7181_517-7156d others(28): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55743911 | |||||
chrX:55743921
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.517-7180C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743921 | ||||||
chrX:55744088
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.517-7013A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744088 | ||||||
chrX:55744321
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.517-6780G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744321 | ||||||
chrX:55744387
|
C | CAAAAA | 1 | a0001c0001t0002g0179 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517-6701_517-6697d others(7): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(5): Show |
7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0085others(4): Show | 7 | HG02647.hp1 NA18939.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-6708_517-6697d others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(6): Show |
100 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 159 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.517-6709_517-6697d others(15): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(7): Show |
37 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0028others(34): Show | 48 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.517-6710_517-6697d others(16): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0002g0125a0001c0001t0002g0138a0001c0001t0002g0186 | 3 | HG02258.hp1 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.517-6711_517-6697d others(17): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.517-6712_517-6697d others(18): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0002g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.517-6697_517-6696i others(22): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0002g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.517-6697_517-6696i others(25): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0002g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.517-6697_517-6696i others(26): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0002g0183 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.517-6697_517-6696i others(27): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744387
|
C | CAAAAAAA others(29): Show |
2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-6697_517-6696i others(38): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | |||||
chrX:55744408
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(73): Show | 123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.517-6693G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744408 | ||||||
chrX:55744701
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0113 | 2 | HG00735.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.517-6400A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744701 | ||||||
chrX:55744902
|
A | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-6199A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744902 | ||||||
chrX:55745056
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517-6045C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745056 | ||||||
chrX:55745285
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.517-5816T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745285 | ||||||
chrX:55745352
|
A | G | 1 | a0001c0001t0002g0152 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.517-5749A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745352 | ||||||
chrX:55745577
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.517-5524T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745577 | ||||||
chrX:55745767
|
A | G | 6 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0113others(3): Show | 6 | HG00735.hp1 HG01255.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-5334A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745767 | ||||||
chrX:55745959
|
A | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 272 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.517-5142A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745959 | ||||||
chrX:55746221
|
T | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(76): Show | 102 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.517-4880T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746221 | ||||||
chrX:55746620
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517-4481C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746620 | ||||||
chrX:55746657
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.517-4444A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746657 | ||||||
chrX:55746752
|
G | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-4349G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746752 | ||||||
chrX:55746982
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.517-4119G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746982 | ||||||
chrX:55747198
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-3903T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747198 | ||||||
chrX:55747213
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(72): Show | 122 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.517-3888G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747213 | ||||||
chrX:55747293
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.517-3808A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747293 | ||||||
chrX:55747592
|
G | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-3509G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747592 | ||||||
chrX:55747654
|
G | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.517-3447G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747654 | ||||||
chrX:55747707
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-3394C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747707 | ||||||
chrX:55747812
|
G | GCTCCCT | 18 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0040others(15): Show | 21 | HG00735.hp1 HG00738.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.517-3259_517-3254d others(8): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55747812 | |||||
chrX:55747812
|
G | GCTCCCTC others(5): Show |
67 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(64): Show | 115 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(112): Show |
intron_variant | MODIFIER | c.517-3265_517-3254d others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55747812 | |||||
chrX:55747812
|
G | GCTCCCTC others(11): Show |
5 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0001g0085others(2): Show | 5 | HG00609.hp1 HG01255.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-3271_517-3254d others(20): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55747812 | |||||
chrX:55747812
|
GCTCCCT | G | 1 | a0001c0001t0001g0016 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.517-3259_517-3254d others(8): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55747812 | |||||
chrX:55747812
|
GCTCCCTC others(5): Show |
G | 68 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0017others(65): Show | 87 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.517-3265_517-3254d others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55747812 | |||||
chrX:55747836
|
TCTCCCTC others(5): Show |
T | 3 | a0001c0001t0001g0101a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG00642.hp1 HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.517-3264_517-3253d others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747836 | ||||||
chrX:55747967
|
G | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 7 | HG01257.hp1 HG01258.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-3134G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747967 | ||||||
chrX:55748066
|
C | T | 77 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(74): Show | 99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.517-3035C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748066 | ||||||
chrX:55748112
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.517-2989C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748112 | ||||||
chrX:55748137
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.517-2964C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748137 | ||||||
chrX:55748138
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.517-2963G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748138 | ||||||
chrX:55748179
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.517-2922G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748179 | ||||||
chrX:55748236
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.517-2865T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748236 | ||||||
chrX:55748288
|
A | AC | 3 | a0001c0001t0001g0093a0001c0001t0002g0102a0001c0001t0002g0168 | 3 | HG01109.hp1 NA18956.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.517-2809dupC | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748288 | |||||
chrX:55748311
|
G | A | 1 | a0001c0001t0002g0189 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.517-2790G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748311 | ||||||
chrX:55748347
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 126 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.517-2754A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748347 | ||||||
chrX:55748441
|
G | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(74): Show | 99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.517-2660G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748441 | ||||||
chrX:55748480
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.517-2621C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748480 | ||||||
chrX:55748520
|
A | AC | 3 | a0001c0001t0001g0030a0001c0001t0001g0047a0001c0001t0001g0090 | 3 | NA19055.hp1 NA19072.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.517-2577dupC | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748520 | |||||
chrX:55748520
|
A | ACC | 1 | a0001c0001t0002g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.517-2578_517-2577d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748520 | |||||
chrX:55748528
|
T | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0168 | 2 | NA18956.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.517-2573T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748528 | ||||||
chrX:55748542
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-2559C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748542 | ||||||
chrX:55748564
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.517-2537C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748564 | ||||||
chrX:55748625
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.517-2476C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748625 | ||||||
chrX:55748636
|
C | A | 1 | a0001c0001t0001g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-2465C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748636 | ||||||
chrX:55748641
|
C | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 7 | HG02818.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-2460C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748641 | ||||||
chrX:55748707
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0048 | 2 | HG02135.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.517-2394G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748707 | ||||||
chrX:55748711
|
G | A | 1 | a0001c0001t0002g0189 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.517-2390G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748711 | ||||||
chrX:55748783
|
T | TG | 1 | a0001c0001t0001g0062 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.517-2311dupG | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748783 | |||||
chrX:55748794
|
G | GC | 1 | a0001c0001t0001g0047 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.517-2301dupC | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748794 | |||||
chrX:55748855
|
C | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-2246C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748855 | ||||||
chrX:55748878
|
TGCCCGGC others(42): Show |
T | 1 | a0001c0001t0002g0022 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.517-2211_517-2163d others(51): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748878 | |||||
chrX:55748889
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.517-2212C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748889 | ||||||
chrX:55748890
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.517-2211C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748890 | ||||||
chrX:55748891
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.517-2210G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748891 | ||||||
chrX:55748896
|
ATCCGGGA others(42): Show |
A | 1 | a0001c0001t0002g0154 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.517-2185_517-2137d others(51): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748896 | |||||
chrX:55748910
|
T | TG | 2 | a0001c0001t0001g0076a0001c0001t0001g0117 | 2 | HG02809.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.517-2184dupG | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748910 | |||||
chrX:55748916
|
GGTCAGCC others(42): Show |
G | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517-2173_517-2125d others(51): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748916 | |||||
chrX:55748970
|
G | GC | 72 | a0001c0001t0001g0025a0001c0001t0001g0049a0001c0001t0001g0062others(69): Show | 91 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.517-2124dupC | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748970 | |||||
chrX:55748970
|
G | GCC | 2 | a0001c0001t0002g0153a0001c0001t0002g0154 | 2 | HG01192.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.517-2125_517-2124d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748970 | |||||
chrX:55748981
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.517-2120C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748981 | ||||||
chrX:55748998
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.517-2103C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748998 | ||||||
chrX:55749009
|
T | TG | 4 | a0001c0001t0001g0028a0001c0001t0001g0050a0001c0001t0001g0091others(1): Show | 4 | HG01884.hp1 HG02738.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-2085dupG | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749009 | |||||
chrX:55749062
|
G | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0123 | 3 | HG00735.hp1 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.517-2039G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749062 | ||||||
chrX:55749069
|
G | GC | 1 | a0001c0001t0002g0155 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.517-2026dupC | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749069 | |||||
chrX:55749069
|
G | GT | 1 | a0001c0001t0001g0030 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.517-2032_517-2031i others(3): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749069 | ||||||
chrX:55749070
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(72): Show | 123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.517-2031C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749070 | ||||||
chrX:55749076
|
G | A | 6 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-2025G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749076 | ||||||
chrX:55749183
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(158): Show | 231 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.517-1918A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749183 | ||||||
chrX:55749185
|
T | TG | 9 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0064others(6): Show | 9 | HG01175.hp2 HG01928.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-1908dupG | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749185 | |||||
chrX:55749266
|
AG | A | 1 | a0001c0001t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.517-1834delG | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749266 | ||||||
chrX:55749288
|
C | CCAGCCGC others(91): Show |
1 | a0001c0001t0002g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.517-1723_517-1722i others(100): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749288 | |||||
chrX:55749302
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.517-1799C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749302 | ||||||
chrX:55749313
|
T | TG | 1 | a0001c0001t0002g0179 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517-1781dupG | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749313 | |||||
chrX:55749337
|
CCAGCCGC others(41): Show |
C | 1 | a0001c0001t0002g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.517-1753_517-1706d others(50): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749337 | |||||
chrX:55749410
|
T | TG | 2 | a0001c0001t0001g0051a0001c0001t0001g0090 | 2 | HG02056.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.517-1684dupG | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749410 | |||||
chrX:55749449
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-1652G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749449 | ||||||
chrX:55749473
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517-1628G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749473 | ||||||
chrX:55749490
|
A | AGTGAGGA others(34): Show |
1 | a0001c0001t0001g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.517-1587_517-1586i others(43): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749490 | |||||
chrX:55749511
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.517-1590G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749511 | ||||||
chrX:55749514
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.517-1587A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749514 | ||||||
chrX:55749635
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 126 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.517-1466T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749635 | ||||||
chrX:55749740
|
AAC | A | 1 | a0001c0001t0001g0029 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.517-1360_517-1359d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749740 | ||||||
chrX:55749788
|
A | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 126 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.517-1313A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749788 | ||||||
chrX:55749884
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.517-1217G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749884 | ||||||
chrX:55749980
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-1121T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749980 | ||||||
chrX:55750048
|
T | TA | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0032others(7): Show | 14 | HG01106.hp1 HG01255.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-1023dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750048 | |||||
chrX:55750048
|
T | TAA | 3 | a0001c0001t0001g0024a0001c0001t0001g0067a0001c0001t0001g0112 | 3 | HG02615.hp2 NA19062.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.517-1024_517-1023d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750048 | |||||
chrX:55750048
|
TA | T | 70 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0027others(67): Show | 91 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.517-1023delA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750048 | |||||
chrX:55750048
|
TAA | T | 15 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0021others(12): Show | 19 | HG00738.hp1 HG01081.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.517-1024_517-1023d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750048 | |||||
chrX:55750048
|
TAAA | T | 1 | a0001c0001t0002g0139 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.517-1025_517-1023d others(5): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750048 | |||||
chrX:55750050
|
A | T | 1 | a0001c0001t0001g0027 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.517-1051A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750050 | ||||||
chrX:55750184
|
A | ATG | 5 | a0001c0001t0001g0015a0001c0001t0001g0096a0001c0001t0001g0107others(2): Show | 6 | HG02055.hp1 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-881_517-880dup others(2): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | |||||
chrX:55750184
|
A | ATGTG | 1 | a0001c0001t0001g0113 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.517-883_517-880dup others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | |||||
chrX:55750184
|
ATG | A | 63 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0072others(60): Show | 79 | HG00140.hp1 HG00544.hp1 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.517-881_517-880del others(2): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | |||||
chrX:55750184
|
ATGTG | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(81): Show | 135 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.517-883_517-880del others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | |||||
chrX:55750184
|
ATGTGTG | A | 1 | a0001c0001t0002g0020 | 2 | HG03041.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.517-885_517-880del others(6): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | |||||
chrX:55750184
|
ATGTGTGT others(1): Show |
A | 1 | a0001c0001t0001g0056 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.517-887_517-880del others(8): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | |||||
chrX:55750184
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0002g0165 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.517-893_517-880del others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | |||||
chrX:55750218
|
GTGT | G | 1 | a0001c0001t0001g0041 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.517-881_517-879del others(3): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750218 | |||||
chrX:55750307
|
G | T | 3 | a0001c0001t0002g0161a0001c0001t0002g0167a0001c0001t0002g0169 | 3 | NA18964.hp2 NA18975.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.517-794G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750307 | ||||||
chrX:55750347
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(73): Show | 124 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.517-754A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750347 | ||||||
chrX:55750369
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.517-732C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750369 | ||||||
chrX:55750907
|
G | T | 1 | a0001c0001t0002g0163 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.517-194G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750907 | ||||||
chrX:55751209
|
C | T | 1 | a0001c0001t0002g0160 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.612+13C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | chrX | 55751209 | ||||||
chrX:55751236
|
G | GA | 1 | a0001c0001t0001g0090 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.612+48dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 55751236 | |||||
chrX:55751248
|
A | G | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.612+52A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | chrX | 55751248 | ||||||
chrX:55751706
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(72): Show | 122 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.612+510T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | chrX | 55751706 | ||||||
chrX:55752094
|
C | CT | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 266 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.612+911dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 55752094 | |||||
chrX:55752094
|
C | CTT | 2 | a0001c0001t0001g0076a0001c0001t0002g0179 | 2 | HG01099.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.612+910_612+911dup others(2): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 55752094 | |||||
chrX:55752799
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0113 | 2 | HG00735.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.613-593A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | chrX | 55752799 | ||||||
chrX:55753550
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.735+36T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55753550 | ||||||
chrX:55753882
|
CA | C | 1 | a0001c0001t0002g0160 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.735+374delA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 55753882 | |||||
chrX:55753955
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG01255.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.735+441G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55753955 | ||||||
chrX:55754105
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.735+591C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754105 | ||||||
chrX:55754540
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.735+1026C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754540 | ||||||
chrX:55754624
|
T | A | 4 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+1110T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754624 | ||||||
chrX:55754639
|
C | G | 9 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(6): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.735+1125C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754639 | ||||||
chrX:55754799
|
G | A | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.736-1042G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754799 | ||||||
chrX:55754806
|
A | G | 1 | a0001c0001t0002g0159 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.736-1035A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754806 | ||||||
chrX:55754882
|
G | GT | 1 | a0001c0001t0001g0055 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.736-954dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 55754882 | |||||
chrX:55754900
|
AGTAACAA others(51): Show |
A | 1 | a0001c0001t0001g0076 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.736-940_736-883del others(58): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754900 | ||||||
chrX:55755495
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0123 | 3 | HG00735.hp1 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.736-346T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755495 | ||||||
chrX:55755501
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.736-340T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755501 | ||||||
chrX:55755621
|
A | C | 1 | a0001c0001t0002g0128 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.736-220A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755621 | ||||||
chrX:55755643
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.736-198A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755643 | ||||||
chrX:55755790
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.736-51G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755790 | ||||||
chrX:55756093
|
C | CAG | 1 | a0001c0001t0001g0076 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.827+162_827+163dup others(2): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 55756093 | |||||
chrX:55756098
|
C | CGTTGTCC others(49): Show |
1 | a0001c0001t0001g0076 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.827+176_827+177ins others(56): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 55756098 | |||||
chrX:55756381
|
A | G | 4 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 7 | HG02818.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.827+449A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | chrX | 55756381 | ||||||
chrX:55756855
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | NA18951.hp2 NA18970.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.828-361C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | chrX | 55756855 | ||||||
chrX:55757049
|
T | TA | 1 | a0002c0002t0001g0033 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.828-165dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 55757049 | |||||
chrX:55757135
|
CAA | C | 9 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(6): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.828-78_828-77delAA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 55757135 | |||||
chrX:55757189
|
T | TA | 1 | a0002c0002t0001g0033 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.828-25dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 55757189 | |||||
chrX:55757208
|
T | TC | 1 | a0002c0002t0001g0033 | 1 | NA19067.hp1 | splice_region_variant&intron_variant | LOW | c.828-6dupC | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 55757208 | |||||
chrX:55757576
|
T | G | 1 | a0001c0001t0004g0089 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.943+245T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757576 | ||||||
chrX:55757600
|
T | TA | 1 | a0002c0002t0001g0033 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.943+274dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 55757600 | |||||
chrX:55757621
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(70): Show | 120 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.943+290G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757621 | ||||||
chrX:55757699
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A | G | 1 | a0001c0001t0001g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.943+368A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757699 | ||||||
chrX:55757747
|
A | G | 6 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.943+416A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757747 | ||||||
chrX:55757783
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.943+452G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757783 | ||||||
chrX:55757962
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.944-284C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757962 |