geneid | 58528 |
---|---|
ensemblid | ENSG00000025039.15 |
hgncid | 19903 |
symbol | RRAGD |
name | Ras related GTP binding D |
refseq_nuc | NM_021244.5 |
refseq_prot | NP_067067.1 |
ensembl_nuc | ENST00000369415.9 |
ensembl_prot | ENSP00000358423.4 |
mane_status | MANE Select |
chr | chr6 |
start | 89364616 |
end | 89412273 |
strand | - |
ver | v1.2 |
region | chr6:89364616-89412273 |
region5000 | chr6:89359616-89417273 |
regionname0 | RRAGD_chr6_89364616_89412273 |
regionname5000 | RRAGD_chr6_89359616_89417273 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 400 | 370 | 93 | 66 | 154 | 17 | 38 | 120 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0002 | 0/0 | 400 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0003 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1203 | 360 | 86 | 66 | 154 | 16 | 36 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
c0002 | 0/0 | 1203 | 7 | 6 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
c0003 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
c0004 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
c0005 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
c0006 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
c0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3721 | 75 | 10 | 20 | 35 | 5 | 5 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0002 | 0/0 | 3722 | 51 | 0 | 6 | 44 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0003 | 0/1 | 3720 | 48 | 1 | 4 | 32 | 1 | 9 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0004 | 0/0 | 3725 | 31 | 15 | 5 | 7 | 2 | 2 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0005 | 0/0 | 3721 | 11 | 0 | 4 | 1 | 3 | 3 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0006 | 0/0 | 3721 | 10 | 3 | 2 | 0 | 1 | 4 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0007 | 0/0 | 3724 | 10 | 9 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0008 | 0/0 | 3724 | 10 | 2 | 3 | 5 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0009 | 0/0 | 3725 | 9 | 0 | 1 | 3 | 2 | 3 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0010 | 0/0 | 3718 | 7 | 0 | 0 | 7 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0011 | 0/0 | 3721 | 7 | 6 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0012 | 0/0 | 3726 | 7 | 7 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0013 | 1/0 | 3721 | 6 | 0 | 2 | 0 | 2 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0014 | 0/0 | 3720 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0015 | 0/0 | 3724 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0016 | 0/0 | 3722 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0017 | 0/0 | 3719 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0018 | 0/0 | 3721 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0019 | 0/0 | 3725 | 4 | 4 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0020 | 0/0 | 3720 | 3 | 0 | 2 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0021 | 0/0 | 3724 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0022 | 0/0 | 3723 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0023 | 0/0 | 3724 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0024 | 0/0 | 3725 | 3 | 0 | 3 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0025 | 0/0 | 3725 | 3 | 0 | 1 | 0 | 1 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0026 | 0/0 | 3722 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0027 | 0/0 | 3720 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0028 | 0/0 | 3720 | 2 | 0 | 1 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0029 | 0/0 | 3721 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0030 | 0/0 | 3725 | 2 | 0 | 1 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0031 | 0/0 | 3726 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0032 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0033 | 0/0 | 3722 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0034 | 0/0 | 3720 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0035 | 0/0 | 3721 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0036 | 0/0 | 3721 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0037 | 0/0 | 3720 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0038 | 0/0 | 3722 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0039 | 0/0 | 3720 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0040 | 0/0 | 3720 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0041 | 0/0 | 3720 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0042 | 0/0 | 3721 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0043 | 0/0 | 3719 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0044 | 0/0 | 3720 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0045 | 0/0 | 3720 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0046 | 0/0 | 3721 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0047 | 0/0 | 3722 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0048 | 0/0 | 3722 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0049 | 0/0 | 3722 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0050 | 0/0 | 3722 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0051 | 0/0 | 3722 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0052 | 0/0 | 3718 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0053 | 0/0 | 3720 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0054 | 0/0 | 3721 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0055 | 0/0 | 3725 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0056 | 0/0 | 3724 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0057 | 0/0 | 3724 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0058 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0059 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0060 | 0/0 | 3724 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0061 | 0/0 | 3725 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0062 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0063 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
t0064 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0002 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1203 | 360 | 86 | 66 | 154 | 16 | 36 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0002 | 0/0 | 1203 | 7 | 6 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0003 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0004 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0005 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0002c0006 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0003c0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4923 | 73 | 9 | 20 | 35 | 4 | 5 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0002 | 0/0 | 4924 | 51 | 0 | 6 | 44 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0003 | 0/1 | 4922 | 48 | 1 | 4 | 32 | 1 | 9 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0004 | 0/0 | 4927 | 30 | 15 | 5 | 7 | 2 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0005 | 0/0 | 4923 | 11 | 0 | 4 | 1 | 3 | 3 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0006 | 0/0 | 4923 | 10 | 3 | 2 | 0 | 1 | 4 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0007 | 0/0 | 4926 | 10 | 9 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0008 | 0/0 | 4926 | 10 | 2 | 3 | 5 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0009 | 0/0 | 4927 | 9 | 0 | 1 | 3 | 2 | 3 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0010 | 0/0 | 4920 | 7 | 0 | 0 | 7 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0011 | 0/0 | 4923 | 7 | 6 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0012 | 0/0 | 4928 | 7 | 7 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0013 | 1/0 | 4923 | 6 | 0 | 2 | 0 | 2 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0014 | 0/0 | 4922 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0015 | 0/0 | 4926 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0016 | 0/0 | 4924 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0017 | 0/0 | 4921 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0018 | 0/0 | 4923 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0019 | 0/0 | 4927 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0020 | 0/0 | 4922 | 3 | 0 | 2 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0022 | 0/0 | 4925 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0023 | 0/0 | 4926 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0024 | 0/0 | 4927 | 3 | 0 | 3 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0025 | 0/0 | 4927 | 3 | 0 | 1 | 0 | 1 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0026 | 0/0 | 4924 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0027 | 0/0 | 4922 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0028 | 0/0 | 4922 | 2 | 0 | 1 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0029 | 0/0 | 4923 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0030 | 0/0 | 4927 | 2 | 0 | 1 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0031 | 0/0 | 4928 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0032 | 0/0 | 4919 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0033 | 0/0 | 4924 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0034 | 0/0 | 4922 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0035 | 0/0 | 4923 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0037 | 0/0 | 4922 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0038 | 0/0 | 4924 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0041 | 0/0 | 4922 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0042 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0043 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0044 | 0/0 | 4922 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0045 | 0/0 | 4922 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0046 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0047 | 0/0 | 4924 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0048 | 0/0 | 4924 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0049 | 0/0 | 4924 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0050 | 0/0 | 4924 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0051 | 0/0 | 4924 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0052 | 0/0 | 4920 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0053 | 0/0 | 4922 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0054 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0055 | 0/0 | 4927 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0057 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0058 | 0/0 | 4927 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0059 | 0/0 | 4927 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0060 | 0/0 | 4926 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0061 | 0/0 | 4927 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0062 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0063 | 0/0 | 4925 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0001t0064 | 0/0 | 4927 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0002t0019 | 0/0 | 4927 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0002t0021 | 0/0 | 4926 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0002t0040 | 0/0 | 4922 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0002t0056 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0003t0004 | 0/0 | 4927 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0004t0039 | 0/0 | 4922 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0001c0005t0036 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0002c0006t0001 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
a0003c0007t0001 | 0/0 | 4923 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | copy fasta | chr6 | 89359616 | 89417273 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0005g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0005g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0006g0002 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0007g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0008g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0009g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0009g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0009g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0009g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0009g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0009g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0009g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0009g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0010g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0010g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0011g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0011g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0011g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0011g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0012g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0012g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0012g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0012g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0012g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0012g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0013g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0013g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0013g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0013g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0013g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0014g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0015g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0015g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0015g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0015g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0015g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0016g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0016g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0016g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0016g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0017g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0017g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0017g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0017g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0018g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0018g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0018g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0018g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0019g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0019g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0020g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0020g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0020g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0022g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0022g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0022g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0023g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0023g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0023g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0024g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0024g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0024g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0025g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0025g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0025g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0026g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0026g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0027g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0027g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0028g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0028g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0029g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0029g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0030g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0030g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0031g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0031g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0032g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0033g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0034g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0035g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0037g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0038g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0041g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0042g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0043g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0044g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0045g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0046g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0047g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0048g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0049g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0050g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0051g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0052g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0053g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0054g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0055g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0057g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0058g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0059g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0060g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0061g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0062g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0063g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0001t0064g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0002t0019g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0002t0019g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0002t0021g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0002t0021g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0002t0021g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0002t0040g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0002t0056g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0003t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0004t0039g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0001c0005t0036g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0002c0006t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
a0003c0007t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0002 | EUR | GBR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00140 | hp1 | a0001 | c0001 | t0009 | g0303 | EUR | GBR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0239 | EUR | FIN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00280 | hp2 | a0002 | c0006 | t0001 | g0207 | EUR | FIN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0291 | EUR | FIN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00621 | hp2 | a0001 | c0001 | t0051 | g0135 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0308 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0297 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00738 | hp1 | a0001 | c0001 | t0011 | g0089 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00741 | hp1 | a0001 | c0001 | t0061 | g0325 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01069 | hp2 | a0001 | c0001 | t0034 | g0071 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01071 | hp2 | a0001 | c0001 | t0035 | g0070 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0290 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0274 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01099 | hp2 | a0001 | c0001 | t0041 | g0082 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01106 | hp1 | a0001 | c0001 | t0024 | g0338 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01106 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0326 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0101 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0240 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01168 | hp2 | a0001 | c0001 | t0024 | g0310 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01169 | hp1 | a0001 | c0001 | t0027 | g0243 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01192 | hp1 | a0001 | c0001 | t0008 | g0256 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01192 | hp2 | a0001 | c0001 | t0013 | g0076 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01243 | hp2 | a0001 | c0001 | t0055 | g0296 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01255 | hp2 | a0001 | c0001 | t0045 | g0077 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01257 | hp2 | a0001 | c0001 | t0027 | g0085 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01261 | hp1 | a0001 | c0001 | t0020 | g0083 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01346 | hp1 | a0001 | c0001 | t0009 | g0018 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01358 | hp1 | a0001 | c0001 | t0028 | g0221 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0242 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01433 | hp1 | a0001 | c0001 | t0020 | g0237 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01433 | hp2 | a0001 | c0001 | t0025 | g0343 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0017 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0289 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01516 | hp2 | a0001 | c0001 | t0013 | g0010 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0241 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01517 | hp2 | a0001 | c0001 | t0013 | g0010 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01884 | hp1 | a0001 | c0001 | t0059 | g0320 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0285 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01943 | hp2 | a0001 | c0001 | t0049 | g0225 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01978 | hp2 | a0001 | c0001 | t0024 | g0263 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01993 | hp2 | a0001 | c0001 | t0013 | g0078 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02040 | hp2 | a0001 | c0001 | t0050 | g0126 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02055 | hp1 | a0001 | c0001 | t0019 | g0337 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02056 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02071 | hp2 | a0001 | c0001 | t0008 | g0259 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02129 | hp1 | a0001 | c0001 | t0062 | g0286 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02129 | hp2 | a0001 | c0001 | t0008 | g0257 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02132 | hp2 | a0001 | c0001 | t0008 | g0258 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0251 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02145 | hp2 | a0001 | c0001 | t0064 | g0341 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | CDX | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0272 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02258 | hp2 | a0001 | c0002 | t0021 | g0335 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02293 | hp1 | a0001 | c0001 | t0030 | g0304 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02451 | hp1 | a0001 | c0001 | t0022 | g0311 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02451 | hp2 | a0001 | c0001 | t0015 | g0253 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02523 | hp2 | a0001 | c0001 | t0010 | g0022 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0312 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0306 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0017 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02615 | hp1 | a0001 | c0001 | t0011 | g0091 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02615 | hp2 | a0001 | c0001 | t0012 | g0270 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0284 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0093 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02647 | hp1 | a0001 | c0001 | t0011 | g0094 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02683 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02717 | hp1 | a0001 | c0001 | t0008 | g0264 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0268 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02723 | hp1 | a0001 | c0002 | t0021 | g0333 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0105 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0088 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02738 | hp1 | a0001 | c0001 | t0030 | g0262 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0271 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0323 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02886 | hp1 | a0001 | c0001 | t0063 | g0269 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02886 | hp2 | a0001 | c0001 | t0007 | g0336 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0315 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02895 | hp2 | a0001 | c0001 | t0016 | g0279 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02896 | hp2 | a0001 | c0001 | t0022 | g0250 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02897 | hp1 | a0001 | c0001 | t0016 | g0277 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02897 | hp2 | a0001 | c0001 | t0022 | g0249 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02922 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0265 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0329 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02965 | hp2 | a0001 | c0001 | t0015 | g0254 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02970 | hp2 | a0001 | c0001 | t0015 | g0252 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0328 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03041 | hp1 | a0001 | c0001 | t0016 | g0280 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03041 | hp2 | a0001 | c0001 | t0031 | g0267 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0327 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03130 | hp1 | a0001 | c0001 | t0023 | g0247 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0095 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03195 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03195 | hp2 | a0001 | c0002 | t0019 | g0332 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03209 | hp1 | a0001 | c0002 | t0021 | g0331 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03209 | hp2 | a0001 | c0001 | t0014 | g0035 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03225 | hp1 | a0001 | c0001 | t0026 | g0100 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03225 | hp2 | a0003 | c0007 | t0001 | g0218 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03239 | hp2 | a0001 | c0001 | t0042 | g0206 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0321 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03453 | hp2 | a0001 | c0001 | t0043 | g0032 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03486 | hp1 | a0001 | c0001 | t0052 | g0090 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0147 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0339 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0275 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0314 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03579 | hp1 | a0001 | c0004 | t0039 | g0235 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03579 | hp2 | a0001 | c0002 | t0019 | g0330 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03669 | hp1 | a0001 | c0001 | t0060 | g0309 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03688 | hp2 | a0001 | c0001 | t0038 | g0068 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03710 | hp2 | a0001 | c0001 | t0013 | g0079 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03831 | hp1 | a0001 | c0001 | t0046 | g0208 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03831 | hp2 | a0001 | c0001 | t0047 | g0086 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03834 | hp1 | a0001 | c0001 | t0009 | g0302 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03834 | hp2 | a0001 | c0001 | t0054 | g0244 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04115 | hp1 | a0001 | c0001 | t0009 | g0295 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0301 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04184 | hp2 | a0001 | c0001 | t0025 | g0342 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04199 | hp1 | a0001 | c0003 | t0004 | g0245 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0102 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04204 | hp1 | a0001 | c0005 | t0036 | g0069 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0087 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG04228 | hp2 | a0001 | c0001 | t0009 | g0299 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18522 | hp1 | a0001 | c0001 | t0023 | g0246 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0319 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18906 | hp2 | a0001 | c0001 | t0037 | g0097 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18944 | hp2 | a0001 | c0001 | t0028 | g0209 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18949 | hp2 | a0001 | c0001 | t0010 | g0026 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18951 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18959 | hp1 | a0001 | c0001 | t0017 | g0170 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18959 | hp2 | a0001 | c0001 | t0018 | g0142 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18963 | hp2 | a0001 | c0001 | t0010 | g0023 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18965 | hp1 | a0001 | c0001 | t0053 | g0226 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18967 | hp2 | a0001 | c0001 | t0018 | g0159 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18969 | hp1 | a0001 | c0001 | t0044 | g0198 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18974 | hp1 | a0001 | c0001 | t0048 | g0230 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18975 | hp1 | a0001 | c0001 | t0010 | g0024 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18982 | hp2 | a0001 | c0001 | t0009 | g0287 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18985 | hp1 | a0001 | c0001 | t0010 | g0028 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18993 | hp2 | a0001 | c0001 | t0057 | g0292 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA18995 | hp2 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19002 | hp1 | a0001 | c0001 | t0032 | g0025 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19002 | hp2 | a0001 | c0001 | t0009 | g0307 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19007 | hp1 | a0001 | c0001 | t0010 | g0029 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0324 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19030 | hp2 | a0001 | c0001 | t0015 | g0255 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19043 | hp2 | a0001 | c0001 | t0023 | g0248 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19054 | hp1 | a0001 | c0001 | t0017 | g0163 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19060 | hp1 | a0001 | c0001 | t0029 | g0190 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19065 | hp1 | a0001 | c0001 | t0018 | g0125 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19067 | hp1 | a0001 | c0001 | t0017 | g0167 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19068 | hp1 | a0001 | c0001 | t0018 | g0114 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19076 | hp1 | a0001 | c0001 | t0033 | g0030 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19083 | hp2 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19089 | hp1 | a0001 | c0001 | t0029 | g0184 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19089 | hp2 | a0001 | c0001 | t0017 | g0061 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0096 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA19240 | hp2 | a0001 | c0001 | t0026 | g0099 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20129 | hp1 | a0001 | c0001 | t0016 | g0276 | AFR | ASW | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20752 | hp1 | a0001 | c0001 | t0025 | g0340 | EUR | TSI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0294 | EUR | TSI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20805 | hp1 | a0001 | c0002 | t0040 | g0031 | EUR | TSI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20905 | hp1 | a0001 | c0001 | t0020 | g0081 | SAS | GIH | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | GIH | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0084 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0313 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02109 | hp2 | a0001 | c0001 | t0016 | g0278 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02486 | hp1 | a0001 | c0001 | t0058 | g0317 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02486 | hp2 | a0001 | c0001 | t0014 | g0037 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02559 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0092 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG03471 | hp2 | a0001 | c0001 | t0031 | g0266 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | USA | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | USA | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20300 | hp1 | a0001 | c0002 | t0056 | g0334 | AFR | USA | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | USA | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0146 | REF | REF | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0013 | g0080 | REF | REF | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:89368154
|
C | G | 1 | a0003 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1105G>C | p.Glu369Gln | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1385/4923 | 1105/1203 | 369/400 | chr6 | 89368154 | ||
chr6:89372512
|
C | T | 1 | a0002 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.976G>A | p.Val326Met | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/7 | 1256/4923 | 976/1203 | 326/400 | chr6 | 89372512 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:89377751
|
A | G | 1 | a0001c0005 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.822T>C | p.Asp274Asp | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/7 | 1102/4923 | 822/1203 | 274/400 | chr6 | 89377751 | ||
chr6:89380302
|
A | G | 1 | a0001c0004 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.510T>C | p.Thr170Thr | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/7 | 790/4923 | 510/1203 | 170/400 | chr6 | 89380302 | ||
chr6:89380305
|
A | G | 1 | a0001c0002 | 7 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(4): Show |
synonymous_variant | LOW | c.507T>C | p.Asn169Asn | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/7 | 787/4923 | 507/1203 | 169/400 | chr6 | 89380305 | ||
chr6:89411928
|
C | T | 1 | a0001c0003 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.66G>A | p.Glu22Glu | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 346/4923 | 66/1203 | 22/400 | chr6 | 89411928 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:89364805
|
C | A | 1 | a0001c0001t0046 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3251G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 3251 | chr6 | 89364805 | |||||
chr6:89365315
|
T | C | 1 | a0001c0004t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2741A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2741 | chr6 | 89365315 | |||||
chr6:89365564
|
T | A | 2 | a0001c0001t0029a0001c0001t0044 | 3 | NA18969.hp1 NA19060.hp1 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2492A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2492 | chr6 | 89365564 | |||||
chr6:89365640
|
A | G | 51 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(48): Show | 272 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*2416T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2416 | chr6 | 89365640 | |||||
chr6:89365928
|
G | C | 7 | a0001c0001t0002a0001c0001t0012a0001c0001t0018others(4): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2128C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2128 | chr6 | 89365928 | |||||
chr6:89365987
|
G | C | 8 | a0001c0001t0002a0001c0001t0012a0001c0001t0018others(5): Show | 70 | HG00438.hp1 HG01261.hp2 HG01891.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2069C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2069 | chr6 | 89365987 | |||||
chr6:89365987
|
G | T | 1 | a0001c0001t0051 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2069C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2069 | chr6 | 89365987 | |||||
chr6:89365994
|
G | A | 1 | a0001c0002t0040 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2062C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2062 | chr6 | 89365994 | |||||
chr6:89365998
|
TG | T | 1 | a0001c0001t0015 | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2057delC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2057 | chr6 | 89365998 | |||||
chr6:89366077
|
A | C | 8 | a0001c0001t0002a0001c0001t0012a0001c0001t0018others(5): Show | 68 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1979T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1979 | chr6 | 89366077 | |||||
chr6:89366112
|
A | C | 65 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(62): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*1944T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1944 | chr6 | 89366112 | |||||
chr6:89366246
|
G | A | 1 | a0001c0001t0058 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1810C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1810 | chr6 | 89366246 | |||||
chr6:89366388
|
C | T | 3 | a0001c0001t0007a0001c0001t0014a0001c0002t0040 | 16 | HG01109.hp1 HG02257.hp1 HG02486.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1668G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1668 | chr6 | 89366388 | |||||
chr6:89366400
|
T | G | 6 | a0001c0001t0007a0001c0001t0014a0001c0001t0020others(3): Show | 21 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1656A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1656 | chr6 | 89366400 | |||||
chr6:89366439
|
G | A | 5 | a0001c0001t0016a0001c0001t0022a0001c0001t0043others(2): Show | 11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1617C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1617 | chr6 | 89366439 | |||||
chr6:89366525
|
T | TA | 10 | a0001c0001t0002a0001c0001t0012a0001c0001t0031others(7): Show | 67 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1530dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1530 | chr6 | 89366525 | |||||
chr6:89366525
|
TA | T | 33 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(30): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1530delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1530 | chr6 | 89366525 | |||||
chr6:89366525
|
TAA | T | 6 | a0001c0001t0017a0001c0001t0032a0001c0001t0034others(3): Show | 11 | HG01069.hp2 HG02258.hp2 HG02723.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1529_*1530delTT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1529 | chr6 | 89366525 | |||||
chr6:89366576
|
T | A | 5 | a0001c0001t0016a0001c0001t0022a0001c0001t0043others(2): Show | 11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1480A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1480 | chr6 | 89366576 | |||||
chr6:89366622
|
TA | T | 7 | a0001c0001t0016a0001c0001t0022a0001c0001t0023others(4): Show | 15 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1433delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1433 | chr6 | 89366622 | |||||
chr6:89366665
|
C | T | 20 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(17): Show | 78 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1391G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1391 | chr6 | 89366665 | |||||
chr6:89366851
|
G | A | 7 | a0001c0001t0006a0001c0001t0019a0001c0001t0026others(4): Show | 21 | HG00099.hp1 HG01109.hp2 HG01123.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1205C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1205 | chr6 | 89366851 | |||||
chr6:89366915
|
A | G | 8 | a0001c0001t0002a0001c0001t0012a0001c0001t0018others(5): Show | 68 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1141T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1141 | chr6 | 89366915 | |||||
chr6:89366935
|
G | A | 1 | a0001c0001t0059 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1121C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1121 | chr6 | 89366935 | |||||
chr6:89366951
|
A | T | 21 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(18): Show | 83 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1105T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1105 | chr6 | 89366951 | |||||
chr6:89366966
|
G | A | 5 | a0001c0001t0009a0001c0001t0030a0001c0001t0034others(2): Show | 14 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1090C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1090 | chr6 | 89366966 | |||||
chr6:89367022
|
C | T | 1 | a0001c0001t0011 | 7 | HG00738.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1034G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1034 | chr6 | 89367022 | |||||
chr6:89367040
|
A | G | 1 | a0001c0002t0056 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1016T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1016 | chr6 | 89367040 | |||||
chr6:89367135
|
A | G | 1 | a0001c0001t0050 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*921T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 921 | chr6 | 89367135 | |||||
chr6:89367174
|
A | G | 5 | a0001c0001t0016a0001c0001t0022a0001c0001t0043others(2): Show | 11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*882T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 882 | chr6 | 89367174 | |||||
chr6:89367265
|
C | T | 5 | a0001c0001t0009a0001c0001t0030a0001c0001t0034others(2): Show | 14 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*791G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 791 | chr6 | 89367265 | |||||
chr6:89367267
|
C | T | 5 | a0001c0001t0009a0001c0001t0030a0001c0001t0034others(2): Show | 14 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*789G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 789 | chr6 | 89367267 | |||||
chr6:89367269
|
C | T | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 787 | chr6 | 89367269 | |||||
chr6:89367274
|
G | T | 5 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(2): Show | 70 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*782C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 782 | chr6 | 89367274 | |||||
chr6:89367401
|
G | A | 1 | a0001c0001t0055 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*655C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 655 | chr6 | 89367401 | |||||
chr6:89367419
|
G | A | 1 | a0001c0001t0014 | 5 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*637C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 637 | chr6 | 89367419 | |||||
chr6:89367423
|
C | T | 2 | a0001c0001t0030a0001c0001t0055 | 3 | HG01243.hp2 HG02293.hp1 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*633G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 633 | chr6 | 89367423 | |||||
chr6:89367712
|
G | A | 7 | a0001c0001t0002a0001c0001t0018a0001c0001t0033others(4): Show | 60 | HG00438.hp1 HG00621.hp2 HG01099.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*344C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 344 | chr6 | 89367712 | |||||
chr6:89367837
|
A | G | 7 | a0001c0001t0007a0001c0001t0014a0001c0001t0020others(4): Show | 22 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*219T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 219 | chr6 | 89367837 | |||||
chr6:89367928
|
A | AT | 21 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(18): Show | 79 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*127dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 127 | chr6 | 89367928 | |||||
chr6:89367928
|
AT | A | 4 | a0001c0001t0016a0001c0001t0052a0001c0001t0053others(1): Show | 8 | HG02109.hp2 HG02886.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*127delA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 127 | chr6 | 89367928 | |||||
chr6:89412025
|
C | G | 1 | a0001c0001t0033 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 32 | chr6 | 89412025 | |||||
chr6:89412231
|
G | A | 2 | a0001c0001t0025a0001c0001t0064 | 4 | HG01433.hp2 HG02145.hp2 HG04184.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-238C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 238 | chr6 | 89412231 | |||||
chr6:89412235
|
G | A | 1 | a0001c0001t0054 | 1 | HG03834.hp2 | 5_prime_UTR_variant | MODIFIER | c.-242C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 242 | chr6 | 89412235 | |||||
chr6:89412257
|
G | GGAGA | 27 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(24): Show | 110 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-268_-265dupTCTC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 265 | chr6 | 89412257 | |||||
chr6:89412257
|
GGA | G | 2 | a0001c0001t0010a0001c0001t0032 | 8 | HG02056.hp2 HG02523.hp2 NA18949.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-266_-265delTC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 265 | chr6 | 89412257 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:89368242
|
C | T | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1052-35G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368242 | ||||||
chr6:89368320
|
G | A | 9 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0271others(6): Show | 10 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1052-113C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368320 | ||||||
chr6:89368330
|
G | T | 77 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(74): Show | 81 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(78): Show |
intron_variant | MODIFIER | c.1052-123C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368330 | ||||||
chr6:89368430
|
G | A | 11 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(8): Show | 11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1052-223C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368430 | ||||||
chr6:89368432
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1052-225A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368432 | ||||||
chr6:89368617
|
G | C | 11 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0052others(8): Show | 11 | HG00438.hp2 HG01515.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1052-410C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368617 | ||||||
chr6:89368683
|
T | C | 32 | a0001c0001t0005g0011a0001c0001t0005g0017a0001c0001t0005g0087others(29): Show | 36 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1052-476A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368683 | ||||||
chr6:89368735
|
G | T | 1 | a0001c0001t0024g0338 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1052-528C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368735 | ||||||
chr6:89368815
|
G | A | 78 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(75): Show | 82 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(79): Show |
intron_variant | MODIFIER | c.1052-608C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368815 | ||||||
chr6:89369021
|
T | G | 1 | a0001c0001t0019g0337 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1052-814A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369021 | ||||||
chr6:89369021
|
TTCTA | T | 18 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0271others(15): Show | 20 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1052-818_1052-815d others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369021 | ||||||
chr6:89369050
|
C | T | 4 | a0001c0001t0022g0249a0001c0001t0022g0250a0001c0001t0022g0311others(1): Show | 4 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1052-843G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369050 | ||||||
chr6:89369093
|
C | A | 11 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(8): Show | 11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1052-886G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369093 | ||||||
chr6:89369134
|
G | A | 2 | a0001c0001t0016g0278a0001c0001t0016g0280 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1052-927C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369134 | ||||||
chr6:89369495
|
C | T | 140 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(137): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1052-1288G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369495 | ||||||
chr6:89369508
|
G | T | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1052-1301C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369508 | ||||||
chr6:89369509
|
C | T | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1052-1302G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369509 | ||||||
chr6:89369827
|
T | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.1052-1620A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369827 | ||||||
chr6:89370039
|
C | T | 11 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(8): Show | 11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1052-1832G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370039 | ||||||
chr6:89370040
|
G | A | 6 | a0001c0001t0020g0081a0001c0001t0020g0083a0001c0001t0020g0237others(3): Show | 6 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1052-1833C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370040 | ||||||
chr6:89370204
|
A | C | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1052-1997T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370204 | ||||||
chr6:89370409
|
A | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.1051+2028T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370409 | ||||||
chr6:89370498
|
C | T | 1 | a0001c0001t0004g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1051+1939G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370498 | ||||||
chr6:89370578
|
A | G | 7 | a0001c0001t0011g0089a0001c0001t0011g0091a0001c0001t0011g0092others(4): Show | 7 | HG00738.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+1859T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370578 | ||||||
chr6:89370671
|
C | A | 65 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(62): Show | 69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.1051+1766G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370671 | ||||||
chr6:89370871
|
T | C | 1 | a0001c0001t0015g0253 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1051+1566A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370871 | ||||||
chr6:89370928
|
A | G | 1 | a0001c0001t0011g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1051+1509T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370928 | ||||||
chr6:89370966
|
TAAAC | T | 33 | a0001c0001t0004g0261a0001c0001t0004g0273a0001c0001t0004g0274others(30): Show | 34 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.1051+1467_1051+147 others(8): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370966 | ||||||
chr6:89371098
|
A | G | 1 | a0001c0001t0062g0286 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1051+1339T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371098 | ||||||
chr6:89371209
|
C | G | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(63): Show | 70 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.1051+1228G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371209 | ||||||
chr6:89371288
|
A | G | 1 | a0001c0001t0005g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1051+1149T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371288 | ||||||
chr6:89371411
|
C | T | 66 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(63): Show | 71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1051+1026G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371411 | ||||||
chr6:89371497
|
G | C | 1 | a0001c0001t0017g0061 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1051+940C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371497 | ||||||
chr6:89371653
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1051+784G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371653 | ||||||
chr6:89372068
|
C | T | 1 | a0001c0001t0003g0040 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1051+369G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89372068 | ||||||
chr6:89372242
|
C | G | 4 | a0001c0001t0001g0193a0001c0001t0001g0205a0001c0001t0024g0310others(1): Show | 4 | HG00741.hp2 HG01168.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051+195G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89372242 | ||||||
chr6:89372271
|
G | A | 51 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(48): Show | 53 | HG00438.hp2 HG00673.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.1051+166C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89372271 | ||||||
chr6:89372964
|
A | T | 2 | a0001c0001t0004g0261a0001c0001t0004g0273 | 2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.903-379T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89372964 | ||||||
chr6:89373024
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.903-439T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373024 | ||||||
chr6:89373026
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.903-441T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373026 | ||||||
chr6:89373441
|
C | G | 2 | a0001c0001t0031g0266a0001c0001t0031g0267 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.903-856G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373441 | ||||||
chr6:89373468
|
A | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.903-883T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373468 | ||||||
chr6:89373537
|
G | A | 6 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(3): Show | 6 | HG02109.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.903-952C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373537 | ||||||
chr6:89373568
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.903-983T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373568 | ||||||
chr6:89373617
|
C | CA | 12 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0271others(9): Show | 13 | HG00741.hp1 HG02257.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.903-1033dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373617 | ||||||
chr6:89373617
|
CA | C | 25 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0219others(22): Show | 25 | HG01255.hp2 HG01496.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.903-1033delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373617 | ||||||
chr6:89373617
|
CAA | C | 61 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(58): Show | 65 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(62): Show |
intron_variant | MODIFIER | c.903-1034_903-1033d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373617 | ||||||
chr6:89373672
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.903-1087G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373672 | ||||||
chr6:89373682
|
T | G | 1 | a0001c0001t0005g0239 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.903-1097A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373682 | ||||||
chr6:89373701
|
ATTTCT | A | 16 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(13): Show | 16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.903-1121_903-1117d others(7): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373701 | ||||||
chr6:89373739
|
C | T | 11 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0271others(8): Show | 12 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.903-1154G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373739 | ||||||
chr6:89373773
|
G | A | 1 | a0001c0001t0011g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.903-1188C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373773 | ||||||
chr6:89373782
|
CAG | C | 27 | a0001c0001t0005g0017a0001c0001t0005g0239a0001c0001t0005g0240others(24): Show | 30 | HG00280.hp1 HG01099.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.903-1199_903-1198d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373782 | ||||||
chr6:89374338
|
G | T | 1 | a0001c0001t0003g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.903-1753C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374338 | ||||||
chr6:89374375
|
T | G | 1 | a0001c0002t0019g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.903-1790A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374375 | ||||||
chr6:89374418
|
T | G | 2 | a0001c0001t0022g0249a0001c0001t0022g0250 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.903-1833A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374418 | ||||||
chr6:89374590
|
C | T | 67 | a0001c0001t0001g0014a0001c0001t0003g0007a0001c0001t0003g0008others(64): Show | 72 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.903-2005G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374590 | ||||||
chr6:89374607
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.903-2022C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374607 | ||||||
chr6:89374652
|
C | A | 1 | a0001c0001t0028g0209 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.903-2067G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374652 | ||||||
chr6:89374654
|
C | T | 1 | a0001c0001t0009g0302 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.903-2069G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374654 | ||||||
chr6:89374706
|
G | T | 65 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(62): Show | 69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.903-2121C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374706 | ||||||
chr6:89374749
|
T | C | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.903-2164A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374749 | ||||||
chr6:89374770
|
G | GTT | 64 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(61): Show | 68 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(65): Show |
intron_variant | MODIFIER | c.903-2187_903-2186d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374770 | ||||||
chr6:89374798
|
A | C | 1 | a0001c0001t0003g0064 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.903-2213T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374798 | ||||||
chr6:89374896
|
C | T | 1 | a0001c0001t0002g0134 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.903-2311G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374896 | ||||||
chr6:89374905
|
T | G | 9 | a0001c0001t0014g0006a0001c0001t0014g0035a0001c0001t0014g0036others(6): Show | 10 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.903-2320A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374905 | ||||||
chr6:89374991
|
T | C | 1 | a0001c0001t0045g0077 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.903-2406A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374991 | ||||||
chr6:89375041
|
T | C | 5 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.903-2456A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375041 | ||||||
chr6:89375170
|
C | A | 4 | a0001c0001t0002g0149a0001c0001t0002g0151a0001c0001t0002g0153others(1): Show | 4 | HG02015.hp1 NA18953.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.902+2501G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375170 | ||||||
chr6:89375206
|
G | A | 1 | a0001c0001t0004g0293 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.902+2465C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375206 | ||||||
chr6:89375234
|
T | C | 3 | a0001c0001t0022g0249a0001c0001t0022g0250a0001c0001t0022g0311 | 3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.902+2437A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375234 | ||||||
chr6:89375384
|
C | T | 2 | a0001c0001t0010g0024a0001c0001t0010g0027 | 2 | HG02056.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.902+2287G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375384 | ||||||
chr6:89375432
|
C | T | 3 | a0001c0001t0004g0021a0001c0001t0004g0318a0001c0001t0004g0339 | 4 | HG02723.hp2 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.902+2239G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375432 | ||||||
chr6:89375472
|
CGTGTGCA others(3): Show |
C | 65 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(62): Show | 69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.902+2189_902+2198d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375472 | ||||||
chr6:89375557
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.902+2114G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375557 | ||||||
chr6:89375726
|
T | C | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.902+1945A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375726 | ||||||
chr6:89376175
|
A | G | 7 | a0001c0001t0005g0017a0001c0001t0005g0239a0001c0001t0005g0240others(4): Show | 8 | HG00280.hp1 HG00741.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.902+1496T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376175 | ||||||
chr6:89376193
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.902+1478A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376193 | ||||||
chr6:89376234
|
C | T | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.902+1437G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376234 | ||||||
chr6:89376290
|
A | G | 255 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(252): Show | 272 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.902+1381T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376290 | ||||||
chr6:89376300
|
G | GGT | 14 | a0001c0001t0001g0015a0001c0001t0001g0162a0001c0001t0001g0193others(11): Show | 15 | HG00741.hp2 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.902+1369_902+1370d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | ||||||
chr6:89376300
|
GGT | G | 64 | a0001c0001t0001g0220a0001c0001t0002g0003a0001c0001t0002g0009others(61): Show | 68 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(65): Show |
intron_variant | MODIFIER | c.902+1369_902+1370d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | ||||||
chr6:89376300
|
GGTGTGT | G | 12 | a0001c0001t0003g0060a0001c0001t0003g0072a0001c0001t0003g0073others(9): Show | 12 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.902+1365_902+1370d others(8): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | ||||||
chr6:89376300
|
GGTGTGTG others(1): Show |
G | 157 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(154): Show | 169 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.902+1363_902+1370d others(10): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | ||||||
chr6:89376300
|
GGTGTGTG others(3): Show |
G | 6 | a0001c0001t0004g0290a0001c0001t0015g0251a0001c0001t0015g0252others(3): Show | 6 | HG01081.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.902+1361_902+1370d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | ||||||
chr6:89376300
|
GGTGTGTG others(5): Show |
G | 17 | a0001c0001t0001g0004a0001c0001t0001g0175a0001c0001t0001g0182others(14): Show | 19 | HG00140.hp1 HG00423.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.902+1359_902+1370d others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | ||||||
chr6:89376302
|
T | G | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.902+1369A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376302 | ||||||
chr6:89376304
|
T | G | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.902+1367A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376304 | ||||||
chr6:89376308
|
T | G | 4 | a0001c0001t0022g0249a0001c0001t0022g0250a0001c0001t0022g0311others(1): Show | 4 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.902+1363A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376308 | ||||||
chr6:89376310
|
T | C | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.902+1361A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376310 | ||||||
chr6:89376310
|
T | G | 7 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(4): Show | 7 | HG02109.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.902+1361A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376310 | ||||||
chr6:89376312
|
T | C | 61 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(58): Show | 65 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(62): Show |
intron_variant | MODIFIER | c.902+1359A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376312 | ||||||
chr6:89376312
|
T | G | 5 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.902+1359A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376312 | ||||||
chr6:89376314
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.902+1357A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376314 | ||||||
chr6:89376705
|
GCT | G | 16 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(13): Show | 16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.902+964_902+965del others(2): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376705 | ||||||
chr6:89376736
|
A | AT | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.902+934dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376736 | ||||||
chr6:89376812
|
G | A | 1 | a0001c0001t0008g0258 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.902+859C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376812 | ||||||
chr6:89376895
|
T | C | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.902+776A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376895 | ||||||
chr6:89376935
|
C | T | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(63): Show | 70 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.902+736G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376935 | ||||||
chr6:89377098
|
T | A | 1 | a0001c0001t0023g0247 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.902+573A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377098 | ||||||
chr6:89377114
|
G | A | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.902+557C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377114 | ||||||
chr6:89377116
|
G | A | 2 | a0001c0001t0016g0278a0001c0001t0016g0280 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.902+555C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377116 | ||||||
chr6:89377217
|
G | T | 3 | a0001c0001t0004g0291a0001c0001t0004g0294a0001c0001t0004g0297 | 3 | HG00323.hp1 HG00735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.902+454C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377217 | ||||||
chr6:89377252
|
G | A | 1 | a0001c0001t0053g0226 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.902+419C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377252 | ||||||
chr6:89377371
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.902+300G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377371 | ||||||
chr6:89377447
|
A | G | 1 | a0001c0001t0002g0137 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.902+224T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377447 | ||||||
chr6:89377454
|
G | C | 67 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(64): Show | 71 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.902+217C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377454 | ||||||
chr6:89377495
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.902+176G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377495 | ||||||
chr6:89377535
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.902+136A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377535 | ||||||
chr6:89377625
|
G | A | 5 | a0001c0001t0020g0081a0001c0001t0020g0083a0001c0001t0020g0237others(2): Show | 5 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.902+46C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377625 | ||||||
chr6:89377822
|
T | A | 1 | a0001c0001t0052g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.760-9A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89377822 | ||||||
chr6:89377883
|
T | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.760-70A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89377883 | ||||||
chr6:89377931
|
T | C | 67 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(64): Show | 72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.760-118A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89377931 | ||||||
chr6:89377990
|
A | G | 1 | a0001c0001t0011g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.760-177T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89377990 | ||||||
chr6:89378058
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.760-245G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378058 | ||||||
chr6:89378074
|
C | T | 17 | a0001c0001t0001g0175a0001c0001t0015g0251a0001c0001t0015g0252others(14): Show | 17 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.760-261G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378074 | ||||||
chr6:89378092
|
C | T | 249 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(246): Show | 265 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.760-279G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378092 | ||||||
chr6:89378102
|
G | A | 1 | a0001c0001t0009g0299 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.760-289C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378102 | ||||||
chr6:89378116
|
C | G | 2 | a0001c0001t0034g0071a0001c0001t0035g0070 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.760-303G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378116 | ||||||
chr6:89378121
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.760-308C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378121 | ||||||
chr6:89378171
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0211 | 2 | HG01978.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.760-358C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378171 | ||||||
chr6:89378205
|
G | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.760-392C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378205 | ||||||
chr6:89378240
|
A | T | 133 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(130): Show | 142 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.760-427T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378240 | ||||||
chr6:89378243
|
G | A | 132 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(129): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.760-430C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378243 | ||||||
chr6:89378264
|
T | G | 4 | a0001c0001t0004g0261a0001c0001t0004g0273a0001c0001t0004g0274others(1): Show | 4 | HG01081.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-451A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378264 | ||||||
chr6:89378274
|
C | A | 67 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(64): Show | 71 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.760-461G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378274 | ||||||
chr6:89378302
|
C | CA | 43 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0271others(40): Show | 45 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.760-490dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378302 | ||||||
chr6:89378595
|
C | T | 11 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0271others(8): Show | 12 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+629G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378595 | ||||||
chr6:89378752
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.759+472G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378752 | ||||||
chr6:89378844
|
A | G | 67 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(64): Show | 71 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.759+380T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378844 | ||||||
chr6:89378856
|
CAAGT | C | 80 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(77): Show | 84 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(81): Show |
intron_variant | MODIFIER | c.759+364_759+367del others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378856 | ||||||
chr6:89378936
|
A | AT | 16 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(13): Show | 16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.759+287dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378936 | ||||||
chr6:89379145
|
G | A | 1 | a0001c0001t0016g0280 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.759+79C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89379145 | ||||||
chr6:89379352
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.645-14G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379352 | ||||||
chr6:89379456
|
C | T | 1 | a0001c0001t0037g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.645-118G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379456 | ||||||
chr6:89379589
|
G | A | 1 | a0001c0001t0011g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.645-251C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379589 | ||||||
chr6:89379632
|
C | T | 2 | a0001c0001t0020g0237a0001c0001t0041g0082 | 2 | HG01099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.645-294G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379632 | ||||||
chr6:89379793
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.644+375C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379793 | ||||||
chr6:89379850
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.644+318G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379850 | ||||||
chr6:89379903
|
T | C | 5 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+265A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379903 | ||||||
chr6:89379958
|
T | G | 141 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(138): Show | 150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.644+210A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379958 | ||||||
chr6:89379980
|
G | A | 15 | a0001c0001t0003g0038a0001c0001t0003g0143a0001c0001t0003g0144others(12): Show | 17 | HG00408.hp1 HG00735.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.644+188C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379980 | ||||||
chr6:89380506
|
A | G | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.445-139T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380506 | ||||||
chr6:89380539
|
CAA | C | 65 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(62): Show | 69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.445-174_445-173del others(2): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380539 | ||||||
chr6:89380562
|
A | T | 65 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(62): Show | 69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.445-195T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380562 | ||||||
chr6:89380645
|
A | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.445-278T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380645 | ||||||
chr6:89380703
|
T | C | 65 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(62): Show | 69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.445-336A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380703 | ||||||
chr6:89380767
|
C | T | 5 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-400G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380767 | ||||||
chr6:89380912
|
G | GA | 245 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(242): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.445-546dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380912 | ||||||
chr6:89380912
|
G | GAA | 9 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248others(6): Show | 9 | HG02258.hp2 HG02723.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-547_445-546dup others(2): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380912 | ||||||
chr6:89381075
|
G | A | 1 | a0001c0001t0062g0286 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.445-708C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381075 | ||||||
chr6:89381320
|
A | G | 1 | a0001c0001t0012g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445-953T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381320 | ||||||
chr6:89381371
|
T | A | 3 | a0001c0001t0022g0249a0001c0001t0022g0250a0001c0001t0022g0311 | 3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-1004A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381371 | ||||||
chr6:89381402
|
G | C | 134 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(131): Show | 143 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.445-1035C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381402 | ||||||
chr6:89381442
|
A | C | 5 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-1075T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381442 | ||||||
chr6:89381543
|
T | C | 13 | a0001c0001t0006g0002a0001c0001t0006g0084a0001c0001t0006g0098others(10): Show | 15 | HG00099.hp1 HG01109.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.445-1176A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381543 | ||||||
chr6:89381677
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.445-1310C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381677 | ||||||
chr6:89381728
|
G | C | 52 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(49): Show | 54 | HG00438.hp2 HG00673.hp2 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.445-1361C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381728 | ||||||
chr6:89381731
|
C | T | 1 | a0001c0001t0005g0239 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.445-1364G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381731 | ||||||
chr6:89382017
|
C | CA | 80 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(77): Show | 84 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(81): Show |
intron_variant | MODIFIER | c.445-1651dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382017 | ||||||
chr6:89382079
|
G | A | 7 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0326others(4): Show | 8 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-1712C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382079 | ||||||
chr6:89382284
|
T | A | 1 | a0001c0001t0002g0127 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.445-1917A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382284 | ||||||
chr6:89382329
|
C | T | 1 | a0001c0001t0002g0112 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.445-1962G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382329 | ||||||
chr6:89382400
|
A | AAT | 12 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(9): Show | 12 | HG01106.hp1 HG01433.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-2035_445-2034d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATAT | 5 | a0001c0001t0003g0063a0001c0001t0009g0289a0001c0001t0009g0295others(2): Show | 5 | HG00438.hp2 HG00741.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2037_445-2034d others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATAT | 94 | a0001c0001t0002g0160a0001c0001t0003g0034a0001c0001t0003g0039others(91): Show | 99 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.445-2039_445-2034d others(8): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(1): Show |
25 | a0001c0001t0002g0137a0001c0001t0003g0038a0001c0001t0003g0046others(22): Show | 26 | HG00408.hp1 HG00423.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.445-2041_445-2034d others(10): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(3): Show |
9 | a0001c0001t0003g0008a0001c0001t0003g0143a0001c0001t0004g0291others(6): Show | 10 | HG00323.hp1 HG00673.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.445-2043_445-2034d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(5): Show |
6 | a0001c0001t0004g0021a0001c0001t0004g0339a0001c0001t0016g0278others(3): Show | 7 | HG02109.hp2 HG02723.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-2045_445-2034d others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(7): Show |
10 | a0001c0001t0003g0007a0001c0001t0003g0042a0001c0001t0003g0045others(7): Show | 13 | HG00099.hp1 HG01123.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-2047_445-2034d others(16): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(9): Show |
5 | a0001c0001t0003g0043a0001c0001t0010g0023a0001c0001t0012g0270others(2): Show | 5 | HG02040.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2049_445-2034d others(18): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(11): Show |
6 | a0001c0001t0002g0133a0001c0001t0012g0312a0001c0001t0012g0313others(3): Show | 6 | HG01993.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-2051_445-2034d others(20): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(13): Show |
5 | a0001c0001t0002g0132a0001c0001t0006g0098a0001c0001t0016g0277others(2): Show | 5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2053_445-2034d others(22): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(15): Show |
3 | a0001c0001t0002g0124a0001c0001t0012g0285a0001c0001t0050g0126 | 3 | HG01891.hp2 HG02040.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.445-2055_445-2034d others(24): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(17): Show |
7 | a0001c0001t0002g0110a0001c0001t0002g0113a0001c0001t0002g0119others(4): Show | 7 | HG01261.hp2 HG02148.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(26): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(19): Show |
9 | a0001c0001t0002g0003a0001c0001t0002g0106a0001c0001t0002g0118others(6): Show | 11 | HG00438.hp1 HG01952.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(28): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(21): Show |
6 | a0001c0001t0002g0012a0001c0001t0002g0115a0001c0001t0002g0149others(3): Show | 7 | HG00621.hp2 HG02015.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(30): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(23): Show |
11 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0112others(8): Show | 11 | HG01109.hp2 HG02080.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(32): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(25): Show |
6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0006g0103others(3): Show | 6 | HG02055.hp1 HG03139.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(34): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(27): Show |
3 | a0001c0001t0002g0140a0001c0001t0002g0150a0001c0001t0033g0030 | 3 | HG02132.hp1 NA18964.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.445-2034_445-2033i others(36): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(29): Show |
4 | a0001c0001t0002g0107a0001c0001t0002g0127a0001c0001t0002g0131others(1): Show | 4 | NA18942.hp1 NA18943.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(38): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(31): Show |
5 | a0001c0001t0002g0117a0001c0001t0002g0130a0001c0001t0002g0148others(2): Show | 5 | HG02451.hp1 NA18949.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(40): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(33): Show |
3 | a0001c0001t0002g0111a0001c0001t0002g0116a0001c0001t0002g0141 | 3 | HG02056.hp1 NA18965.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.445-2034_445-2033i others(42): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(35): Show |
4 | a0001c0001t0002g0009a0001c0001t0002g0129a0001c0001t0022g0249others(1): Show | 5 | HG02896.hp2 HG02897.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(44): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(37): Show |
1 | a0001c0001t0002g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.445-2034_445-2033i others(46): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | AATATATA others(39): Show |
1 | a0001c0001t0062g0286 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.445-2034_445-2033i others(48): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0134 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.445-2034_445-2033i others(27): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382400
|
AAT | A | 5 | a0001c0001t0020g0081a0001c0001t0020g0083a0001c0001t0020g0237others(2): Show | 5 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2035_445-2034d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | ||||||
chr6:89382468
|
C | T | 1 | a0001c0001t0004g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.445-2101G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382468 | ||||||
chr6:89382498
|
T | C | 255 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(252): Show | 272 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.445-2131A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382498 | ||||||
chr6:89382602
|
G | A | 3 | a0001c0001t0003g0034a0001c0001t0003g0049a0001c0001t0003g0169 | 3 | HG02155.hp1 NA18945.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.445-2235C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382602 | ||||||
chr6:89382679
|
G | A | 1 | a0001c0005t0036g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.445-2312C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382679 | ||||||
chr6:89382685
|
C | T | 1 | a0001c0001t0004g0288 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.445-2318G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382685 | ||||||
chr6:89382884
|
T | TA | 8 | a0001c0001t0011g0091a0001c0002t0019g0330a0001c0002t0019g0332others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.445-2518dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382884 | ||||||
chr6:89382978
|
C | T | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.445-2611G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382978 | ||||||
chr6:89382980
|
T | A | 16 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(13): Show | 16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-2613A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382980 | ||||||
chr6:89383083
|
T | C | 34 | a0001c0001t0004g0261a0001c0001t0004g0273a0001c0001t0004g0274others(31): Show | 35 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-2716A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383083 | ||||||
chr6:89383113
|
A | G | 2 | a0001c0001t0009g0289a0001c0001t0009g0295 | 2 | HG01516.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.445-2746T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383113 | ||||||
chr6:89383257
|
T | G | 1 | a0001c0001t0038g0068 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.445-2890A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383257 | ||||||
chr6:89383403
|
A | AG | 11 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248others(8): Show | 11 | HG02258.hp2 HG02723.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-3037dupC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383403 | ||||||
chr6:89383417
|
T | C | 1 | a0001c0001t0004g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.445-3050A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383417 | ||||||
chr6:89383644
|
G | A | 1 | a0001c0001t0009g0299 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.445-3277C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383644 | ||||||
chr6:89383708
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.445-3341G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383708 | ||||||
chr6:89383750
|
C | T | 63 | a0001c0001t0001g0205a0001c0001t0002g0003a0001c0001t0002g0009others(60): Show | 67 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(64): Show |
intron_variant | MODIFIER | c.445-3383G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383750 | ||||||
chr6:89383787
|
A | T | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.445-3420T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383787 | ||||||
chr6:89383983
|
G | A | 1 | a0001c0001t0001g0015 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.444+3312C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383983 | ||||||
chr6:89384100
|
T | TA | 19 | a0001c0001t0001g0183a0001c0001t0003g0066a0001c0001t0007g0020others(16): Show | 20 | HG01109.hp1 HG01433.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.444+3194dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384100 | ||||||
chr6:89384310
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.444+2985G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384310 | ||||||
chr6:89384341
|
G | A | 7 | a0001c0001t0005g0017a0001c0001t0005g0239a0001c0001t0005g0240others(4): Show | 8 | HG00280.hp1 HG00741.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+2954C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384341 | ||||||
chr6:89384374
|
T | C | 15 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+2921A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384374 | ||||||
chr6:89384554
|
C | T | 1 | a0001c0001t0008g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.444+2741G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384554 | ||||||
chr6:89384658
|
T | C | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.444+2637A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384658 | ||||||
chr6:89384687
|
C | T | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.444+2608G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384687 | ||||||
chr6:89384713
|
G | A | 6 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(3): Show | 6 | HG02109.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+2582C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384713 | ||||||
chr6:89384732
|
G | A | 1 | a0001c0001t0020g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.444+2563C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384732 | ||||||
chr6:89384771
|
G | A | 1 | a0001c0001t0002g0127 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.444+2524C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384771 | ||||||
chr6:89384813
|
CA | C | 92 | a0001c0001t0001g0199a0001c0001t0001g0203a0001c0001t0002g0109others(89): Show | 98 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.444+2481delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384813 | ||||||
chr6:89384813
|
CAA | C | 80 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(77): Show | 85 | HG00438.hp1 HG00621.hp2 HG01109.hp1 others(82): Show |
intron_variant | MODIFIER | c.444+2480_444+2481d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384813 | ||||||
chr6:89384813
|
CAAA | C | 12 | a0001c0001t0002g0134a0001c0001t0002g0154a0001c0001t0012g0315others(9): Show | 12 | HG02109.hp2 HG02451.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+2479_444+2481d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384813 | ||||||
chr6:89385125
|
T | C | 72 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(69): Show | 77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.444+2170A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385125 | ||||||
chr6:89385404
|
A | G | 1 | a0001c0001t0001g0013 | 2 | NA18948.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.444+1891T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385404 | ||||||
chr6:89385638
|
G | A | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.444+1657C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385638 | ||||||
chr6:89385679
|
G | A | 5 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(2): Show | 5 | HG02109.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+1616C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385679 | ||||||
chr6:89385890
|
G | A | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.444+1405C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385890 | ||||||
chr6:89385903
|
A | G | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.444+1392T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385903 | ||||||
chr6:89385971
|
G | A | 1 | a0001c0001t0003g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.444+1324C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385971 | ||||||
chr6:89386026
|
C | T | 15 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+1269G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386026 | ||||||
chr6:89386063
|
A | G | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.444+1232T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386063 | ||||||
chr6:89386115
|
T | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0189a0001c0001t0029g0184others(2): Show | 5 | HG00621.hp1 NA18964.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+1180A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386115 | ||||||
chr6:89386121
|
G | A | 1 | a0001c0001t0006g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.444+1174C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386121 | ||||||
chr6:89386132
|
A | C | 1 | a0001c0001t0009g0307 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.444+1163T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386132 | ||||||
chr6:89386202
|
T | A | 15 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+1093A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386202 | ||||||
chr6:89386224
|
C | T | 1 | a0001c0001t0005g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.444+1071G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386224 | ||||||
chr6:89386237
|
T | G | 15 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+1058A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386237 | ||||||
chr6:89386254
|
A | G | 21 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0271others(18): Show | 23 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.444+1041T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386254 | ||||||
chr6:89386351
|
C | T | 1 | a0001c0001t0045g0077 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.444+944G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386351 | ||||||
chr6:89386794
|
G | C | 1 | a0001c0001t0003g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.444+501C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386794 | ||||||
chr6:89386814
|
C | A | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+481G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386814 | ||||||
chr6:89386964
|
T | C | 15 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+331A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386964 | ||||||
chr6:89387085
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.444+210C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89387085 | ||||||
chr6:89387707
|
A | G | 6 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(3): Show | 6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-117T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89387707 | ||||||
chr6:89387824
|
C | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149-234G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89387824 | ||||||
chr6:89387877
|
A | G | 3 | a0001c0001t0015g0252a0001c0001t0015g0253a0001c0001t0015g0254 | 3 | HG02451.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-287T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89387877 | ||||||
chr6:89388149
|
G | A | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.149-559C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388149 | ||||||
chr6:89388440
|
T | G | 2 | a0001c0001t0011g0089a0001c0001t0011g0093 | 2 | HG00738.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.149-850A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388440 | ||||||
chr6:89388510
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.149-920G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388510 | ||||||
chr6:89388593
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.149-1003G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388593 | ||||||
chr6:89388666
|
G | C | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-1076C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388666 | ||||||
chr6:89388893
|
C | A | 1 | a0001c0001t0009g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.149-1303G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388893 | ||||||
chr6:89389026
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.149-1436G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389026 | ||||||
chr6:89389104
|
AGGTCTGT others(12): Show |
A | 2 | a0001c0001t0001g0214a0001c0001t0001g0232 | 2 | NA18945.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.149-1533_149-1515d others(21): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389104 | ||||||
chr6:89389326
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.149-1736G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389326 | ||||||
chr6:89389395
|
A | T | 71 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(68): Show | 76 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.149-1805T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389395 | ||||||
chr6:89389487
|
C | T | 6 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(3): Show | 6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-1897G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389487 | ||||||
chr6:89389488
|
G | A | 9 | a0001c0001t0014g0006a0001c0001t0014g0035a0001c0001t0014g0036others(6): Show | 10 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-1898C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389488 | ||||||
chr6:89389496
|
C | T | 16 | a0001c0001t0004g0281a0001c0001t0004g0283a0001c0001t0004g0288others(13): Show | 16 | HG00323.hp1 HG00423.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.149-1906G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389496 | ||||||
chr6:89389555
|
C | CA | 92 | a0001c0001t0001g0186a0001c0001t0001g0220a0001c0001t0001g0228others(89): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.149-1966dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389555 | ||||||
chr6:89389555
|
C | CAA | 11 | a0001c0001t0001g0199a0001c0001t0002g0120a0001c0001t0002g0158others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.149-1967_149-1966d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389555 | ||||||
chr6:89389745
|
T | C | 2 | a0001c0001t0003g0072a0001c0001t0003g0073 | 2 | NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.149-2155A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389745 | ||||||
chr6:89390180
|
G | GA | 18 | a0001c0001t0001g0215a0001c0001t0001g0232a0001c0001t0002g0136others(15): Show | 18 | HG01069.hp1 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.149-2591dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390180 | ||||||
chr6:89390195
|
A | G | 1 | a0001c0001t0006g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.149-2605T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390195 | ||||||
chr6:89390577
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.149-2987A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390577 | ||||||
chr6:89390796
|
G | A | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-3206C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390796 | ||||||
chr6:89390867
|
C | T | 1 | a0001c0001t0055g0296 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.149-3277G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390867 | ||||||
chr6:89390924
|
A | G | 20 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0271others(17): Show | 22 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.149-3334T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390924 | ||||||
chr6:89391168
|
T | G | 1 | a0001c0001t0060g0309 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.149-3578A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391168 | ||||||
chr6:89391293
|
A | G | 250 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(247): Show | 266 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.149-3703T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391293 | ||||||
chr6:89391294
|
A | G | 1 | a0001c0001t0003g0046 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.149-3704T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391294 | ||||||
chr6:89391384
|
C | CA | 79 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(76): Show | 83 | HG00438.hp1 HG00621.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.149-3795dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391384 | ||||||
chr6:89391415
|
T | C | 73 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(70): Show | 78 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.149-3825A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391415 | ||||||
chr6:89391453
|
C | T | 2 | a0001c0001t0003g0058a0001c0001t0003g0065 | 2 | NA18981.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.149-3863G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391453 | ||||||
chr6:89391472
|
A | G | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.149-3882T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391472 | ||||||
chr6:89391683
|
T | C | 3 | a0001c0001t0022g0249a0001c0001t0022g0250a0001c0001t0022g0311 | 3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.149-4093A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391683 | ||||||
chr6:89391798
|
A | G | 1 | a0001c0001t0011g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.149-4208T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391798 | ||||||
chr6:89391948
|
C | A | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.149-4358G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391948 | ||||||
chr6:89391956
|
C | CA | 26 | a0001c0001t0001g0179a0001c0001t0001g0185a0001c0001t0001g0200others(23): Show | 28 | HG00280.hp1 HG00408.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.149-4367dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | ||||||
chr6:89391956
|
C | CAA | 43 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0316others(40): Show | 47 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.149-4368_149-4367d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | ||||||
chr6:89391956
|
C | CAAA | 41 | a0001c0001t0004g0261a0001c0001t0004g0273a0001c0001t0004g0281others(38): Show | 43 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.149-4369_149-4367d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | ||||||
chr6:89391956
|
C | CAAAA | 12 | a0001c0001t0004g0274a0001c0001t0004g0282a0001c0001t0004g0308others(9): Show | 13 | HG00733.hp2 HG01081.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.149-4370_149-4367d others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | ||||||
chr6:89391956
|
CA | C | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0229others(3): Show | 6 | HG01169.hp2 HG01258.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-4367delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | ||||||
chr6:89391969
|
A | AAAAAG | 72 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0106others(69): Show | 75 | HG00438.hp1 HG01261.hp2 HG01891.hp2 others(72): Show |
intron_variant | MODIFIER | c.149-4380_149-4379i others(7): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391969 | ||||||
chr6:89392047
|
T | C | 4 | a0001c0001t0003g0161a0001c0001t0003g0165a0001c0001t0003g0166others(1): Show | 4 | NA18944.hp1 NA18947.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-4457A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392047 | ||||||
chr6:89392151
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.149-4561T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392151 | ||||||
chr6:89392231
|
T | C | 7 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0052others(4): Show | 7 | HG01515.hp2 HG01934.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-4641A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392231 | ||||||
chr6:89392255
|
C | T | 1 | a0001c0001t0003g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.149-4665G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392255 | ||||||
chr6:89392346
|
G | A | 3 | a0001c0001t0002g0121a0001c0001t0002g0136a0001c0001t0002g0152 | 3 | NA18974.hp2 NA18981.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.149-4756C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392346 | ||||||
chr6:89392372
|
T | C | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.149-4782A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392372 | ||||||
chr6:89392387
|
G | A | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-4797C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392387 | ||||||
chr6:89392444
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.149-4854G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392444 | ||||||
chr6:89392445
|
A | G | 3 | a0001c0001t0011g0091a0001c0001t0011g0092a0001c0001t0011g0094 | 3 | HG02559.hp2 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.149-4855T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392445 | ||||||
chr6:89392479
|
C | CA | 181 | a0001c0001t0002g0156a0001c0001t0003g0007a0001c0001t0003g0008others(178): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.149-4890_149-4889i others(3): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392479 | ||||||
chr6:89392479
|
C | CAA | 66 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(63): Show | 70 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(67): Show |
intron_variant | MODIFIER | c.149-4890_149-4889i others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392479 | ||||||
chr6:89392480
|
G | A | 255 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(252): Show | 272 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.149-4890C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392480 | ||||||
chr6:89392756
|
G | A | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.149-5166C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392756 | ||||||
chr6:89392782
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.149-5192A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392782 | ||||||
chr6:89392797
|
A | T | 1 | a0001c0001t0010g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.149-5207T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392797 | ||||||
chr6:89392904
|
G | A | 77 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(74): Show | 81 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(78): Show |
intron_variant | MODIFIER | c.149-5314C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392904 | ||||||
chr6:89393032
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.149-5442T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393032 | ||||||
chr6:89393095
|
C | T | 1 | a0001c0001t0060g0309 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.149-5505G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393095 | ||||||
chr6:89393151
|
T | G | 256 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(253): Show | 273 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.149-5561A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393151 | ||||||
chr6:89393191
|
T | C | 1 | a0001c0001t0007g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.149-5601A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393191 | ||||||
chr6:89393285
|
C | T | 1 | a0001c0001t0004g0300 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.149-5695G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393285 | ||||||
chr6:89393467
|
T | A | 2 | a0001c0001t0003g0057a0001c0001t0003g0060 | 2 | NA18946.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.149-5877A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393467 | ||||||
chr6:89393636
|
G | C | 15 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.149-6046C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393636 | ||||||
chr6:89394047
|
G | T | 11 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.149-6457C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394047 | ||||||
chr6:89394085
|
T | G | 3 | a0001c0001t0022g0249a0001c0001t0022g0250a0001c0001t0022g0311 | 3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.149-6495A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394085 | ||||||
chr6:89394164
|
A | T | 2 | a0001c0001t0005g0011a0001c0001t0027g0085 | 3 | HG00738.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.149-6574T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394164 | ||||||
chr6:89394167
|
G | C | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-6577C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394167 | ||||||
chr6:89394231
|
T | TA | 11 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.149-6642dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394231 | ||||||
chr6:89394311
|
A | T | 5 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-6721T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394311 | ||||||
chr6:89394359
|
G | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149-6769C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394359 | ||||||
chr6:89394398
|
A | G | 255 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(252): Show | 272 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.149-6808T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394398 | ||||||
chr6:89394676
|
C | T | 65 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(62): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.149-7086G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394676 | ||||||
chr6:89395368
|
T | C | 2 | a0001c0001t0003g0045a0001c0001t0009g0299 | 2 | HG04228.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.149-7778A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395368 | ||||||
chr6:89395378
|
C | T | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.149-7788G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395378 | ||||||
chr6:89395553
|
T | C | 12 | a0001c0001t0005g0011a0001c0001t0005g0017a0001c0001t0005g0087others(9): Show | 14 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.149-7963A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395553 | ||||||
chr6:89395620
|
G | C | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.149-8030C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395620 | ||||||
chr6:89395762
|
T | C | 10 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(7): Show | 10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-8172A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395762 | ||||||
chr6:89395969
|
C | CA | 254 | a0001c0001t0001g0222a0001c0001t0002g0003a0001c0001t0002g0009others(251): Show | 271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.149-8380dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395969 | ||||||
chr6:89396404
|
G | GAAAAC | 255 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(252): Show | 272 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.149-8815_149-8814i others(7): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396404 | ||||||
chr6:89396421
|
T | TTTTA | 74 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(71): Show | 78 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(75): Show |
intron_variant | MODIFIER | c.149-8835_149-8832d others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396421 | ||||||
chr6:89396616
|
G | A | 7 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(4): Show | 7 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-9026C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396616 | ||||||
chr6:89396643
|
T | G | 1 | a0001c0001t0019g0275 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.149-9053A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396643 | ||||||
chr6:89396649
|
G | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149-9059C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396649 | ||||||
chr6:89396728
|
A | AT | 39 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0001g0177others(36): Show | 40 | HG00423.hp2 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.149-9139dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | ||||||
chr6:89396728
|
AT | A | 59 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0185others(56): Show | 65 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.149-9139delA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | ||||||
chr6:89396728
|
ATT | A | 11 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(8): Show | 11 | HG00438.hp1 HG01952.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.149-9140_149-9139d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | ||||||
chr6:89396728
|
ATTT | A | 50 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(47): Show | 54 | HG00621.hp2 HG01261.hp2 HG01891.hp2 others(51): Show |
intron_variant | MODIFIER | c.149-9141_149-9139d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | ||||||
chr6:89396728
|
ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0145others(3): Show | 6 | HG00438.hp2 HG02055.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-9146_149-9139d others(10): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | ||||||
chr6:89396728
|
ATTTTTTT others(2): Show |
A | 57 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(54): Show | 61 | HG00408.hp1 HG00673.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.149-9147_149-9139d others(11): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | ||||||
chr6:89396728
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0003g0045a0001c0001t0017g0167a0001c0001t0017g0170 | 3 | NA18951.hp2 NA18959.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.149-9148_149-9139d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | ||||||
chr6:89396737
|
T | A | 1 | a0001c0001t0003g0056 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.149-9147A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396737 | ||||||
chr6:89396744
|
T | A | 1 | a0001c0001t0003g0168 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149-9154A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396744 | ||||||
chr6:89396945
|
C | T | 65 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(62): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.149-9355G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396945 | ||||||
chr6:89397000
|
C | T | 1 | a0001c0001t0024g0263 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.149-9410G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397000 | ||||||
chr6:89397001
|
G | A | 68 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(65): Show | 72 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.149-9411C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397001 | ||||||
chr6:89397228
|
A | AG | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-9639dupC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397228 | ||||||
chr6:89397521
|
G | A | 10 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(7): Show | 10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-9931C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397521 | ||||||
chr6:89397603
|
C | CA | 19 | a0001c0001t0001g0232a0001c0001t0002g0137a0001c0001t0002g0153others(16): Show | 19 | HG00438.hp2 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.149-10014dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397603 | ||||||
chr6:89397604
|
AAAAAAAA others(3): Show |
A | 5 | a0001c0001t0005g0011a0001c0001t0005g0087a0001c0001t0005g0088others(2): Show | 6 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-10024_149-1001 others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397604 | ||||||
chr6:89397614
|
C | A | 6 | a0001c0001t0001g0186a0001c0002t0019g0332a0001c0002t0021g0331others(3): Show | 6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-10024G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397614 | ||||||
chr6:89397614
|
C | CA | 5 | a0001c0001t0002g0110a0001c0001t0002g0138a0001c0001t0004g0322others(2): Show | 5 | HG01261.hp2 HG02258.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-10025dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397614 | ||||||
chr6:89397623
|
ACAAAAAA others(3): Show |
A | 6 | a0001c0001t0005g0017a0001c0001t0005g0239a0001c0001t0005g0240others(3): Show | 7 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-10043_149-1003 others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397623 | ||||||
chr6:89397633
|
C | A | 242 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(239): Show | 257 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.149-10043G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397633 | ||||||
chr6:89397674
|
C | T | 3 | a0001c0001t0022g0249a0001c0001t0022g0250a0001c0001t0022g0311 | 3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.149-10084G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397674 | ||||||
chr6:89397818
|
A | T | 1 | a0001c0001t0002g0122 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.149-10228T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397818 | ||||||
chr6:89397885
|
A | T | 1 | a0001c0001t0008g0256 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.149-10295T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397885 | ||||||
chr6:89398207
|
G | C | 4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(1): Show | 4 | HG00438.hp2 NA18953.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.149-10617C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398207 | ||||||
chr6:89398221
|
A | G | 17 | a0001c0001t0005g0011a0001c0001t0005g0017a0001c0001t0005g0087others(14): Show | 19 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.149-10631T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398221 | ||||||
chr6:89398226
|
G | A | 65 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(62): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.149-10636C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398226 | ||||||
chr6:89398298
|
C | T | 1 | a0001c0001t0011g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.149-10708G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398298 | ||||||
chr6:89398329
|
T | C | 6 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(3): Show | 6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-10739A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398329 | ||||||
chr6:89398552
|
G | C | 1 | a0001c0001t0011g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.149-10962C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398552 | ||||||
chr6:89398570
|
C | T | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.149-10980G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398570 | ||||||
chr6:89398859
|
C | G | 68 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(65): Show | 72 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.149-11269G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398859 | ||||||
chr6:89399103
|
G | A | 10 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(7): Show | 10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-11513C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399103 | ||||||
chr6:89399174
|
T | C | 1 | a0001c0001t0004g0283 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.149-11584A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399174 | ||||||
chr6:89399192
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0139 | 2 | NA19005.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.149-11602G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399192 | ||||||
chr6:89399349
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | NA19054.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.149-11759T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399349 | ||||||
chr6:89399567
|
T | C | 1 | a0001c0001t0028g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.149-11977A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399567 | ||||||
chr6:89399622
|
T | A | 2 | a0001c0001t0026g0099a0001c0001t0026g0100 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.149-12032A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399622 | ||||||
chr6:89399622
|
T | G | 2 | a0001c0001t0034g0071a0001c0001t0035g0070 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.149-12032A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399622 | ||||||
chr6:89399651
|
G | A | 1 | a0001c0001t0063g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.149-12061C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399651 | ||||||
chr6:89399655
|
C | T | 71 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(68): Show | 76 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.149-12065G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399655 | ||||||
chr6:89399767
|
A | AT | 185 | a0001c0001t0001g0176a0001c0001t0001g0189a0001c0001t0002g0003others(182): Show | 196 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.148+12078dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399767 | ||||||
chr6:89399767
|
A | ATT | 50 | a0001c0001t0001g0175a0001c0001t0002g0121a0001c0001t0002g0150others(47): Show | 54 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.148+12077_148+1207 others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399767 | ||||||
chr6:89399767
|
A | ATTT | 11 | a0001c0001t0007g0329a0001c0001t0014g0006a0001c0001t0014g0035others(8): Show | 12 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.148+12076_148+1207 others(7): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399767 | ||||||
chr6:89399767
|
A | ATTTT | 10 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0271others(7): Show | 11 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+12075_148+1207 others(8): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399767 | ||||||
chr6:89399835
|
C | T | 1 | a0001c0001t0003g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.148+12011G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399835 | ||||||
chr6:89399858
|
C | T | 1 | a0001c0001t0064g0341 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.148+11988G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399858 | ||||||
chr6:89399977
|
G | A | 3 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0003g0147 | 3 | HG02055.hp2 HG03491.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148+11869C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399977 | ||||||
chr6:89400129
|
C | T | 1 | a0001c0001t0054g0244 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.148+11717G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400129 | ||||||
chr6:89400409
|
A | T | 341 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(338): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.148+11437T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400409 | ||||||
chr6:89400595
|
T | TA | 157 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(154): Show | 166 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.148+11250dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400595 | ||||||
chr6:89400698
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0222 | 3 | NA19006.hp1 NA19065.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.148+11148C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400698 | ||||||
chr6:89400749
|
C | T | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.148+11097G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400749 | ||||||
chr6:89400765
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.148+11081G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400765 | ||||||
chr6:89400948
|
T | C | 1 | a0001c0001t0030g0304 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.148+10898A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400948 | ||||||
chr6:89401059
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.148+10787G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401059 | ||||||
chr6:89401246
|
G | A | 1 | a0001c0001t0045g0077 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.148+10600C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401246 | ||||||
chr6:89401261
|
TA | T | 62 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(59): Show | 66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.148+10584delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401261 | ||||||
chr6:89401262
|
A | AT | 72 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(69): Show | 76 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.148+10583dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401262 | ||||||
chr6:89401262
|
A | T | 10 | a0001c0001t0002g0110a0001c0001t0016g0276a0001c0001t0016g0277others(7): Show | 10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+10584T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401262 | ||||||
chr6:89401356
|
C | G | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.148+10490G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401356 | ||||||
chr6:89401452
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.148+10394G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401452 | ||||||
chr6:89401461
|
G | A | 1 | a0001c0001t0030g0304 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.148+10385C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401461 | ||||||
chr6:89401464
|
C | T | 12 | a0001c0001t0005g0017a0001c0001t0005g0239a0001c0001t0005g0240others(9): Show | 13 | HG00280.hp1 HG00741.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.148+10382G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401464 | ||||||
chr6:89401628
|
TTGTTCCC | T | 10 | a0001c0001t0016g0276a0001c0001t0016g0277a0001c0001t0016g0278others(7): Show | 10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+10211_148+1021 others(11): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401628 | ||||||
chr6:89401681
|
A | C | 4 | a0001c0001t0014g0006a0001c0001t0014g0035a0001c0001t0014g0036others(1): Show | 5 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+10165T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401681 | ||||||
chr6:89401760
|
A | G | 3 | a0001c0001t0006g0098a0001c0001t0006g0101a0001c0001t0037g0097 | 3 | HG01109.hp2 HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.148+10086T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401760 | ||||||
chr6:89402038
|
A | AT | 27 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0174others(24): Show | 30 | HG00621.hp1 HG00735.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.148+9807dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATT | 12 | a0001c0001t0005g0011a0001c0001t0005g0017a0001c0001t0005g0087others(9): Show | 14 | HG00280.hp1 HG00738.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.148+9806_148+9807d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(1): Show |
18 | a0001c0001t0006g0002a0001c0001t0006g0101a0001c0001t0006g0102others(15): Show | 20 | HG00099.hp1 HG01109.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.148+9800_148+9807d others(10): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(2): Show |
22 | a0001c0001t0004g0305a0001c0001t0004g0308a0001c0001t0006g0084others(19): Show | 22 | HG00733.hp2 HG00738.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.148+9799_148+9807d others(11): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(3): Show |
23 | a0001c0001t0004g0274a0001c0001t0004g0282a0001c0001t0004g0283others(20): Show | 23 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.148+9798_148+9807d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(4): Show |
54 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(51): Show | 61 | HG00423.hp1 HG00621.hp2 HG01261.hp2 others(58): Show |
intron_variant | MODIFIER | c.148+9797_148+9807d others(13): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(5): Show |
25 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0115others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.148+9796_148+9807d others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(10): Show |
7 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0272others(4): Show | 8 | HG02257.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+9807_148+9808i others(19): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0007g0326 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.148+9807_148+9808i others(20): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(6): Show |
29 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0154others(26): Show | 29 | HG00408.hp1 HG00438.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.148+9795_148+9807d others(15): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(7): Show |
28 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(25): Show | 30 | HG00673.hp2 HG01255.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.148+9794_148+9807d others(16): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(8): Show |
10 | a0001c0001t0003g0046a0001c0001t0003g0066a0001c0001t0003g0072others(7): Show | 10 | HG01069.hp2 HG02523.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+9793_148+9807d others(17): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(9): Show |
3 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0035g0070 | 3 | HG01071.hp2 HG01934.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.148+9792_148+9807d others(18): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402038
|
A | ATTTTTTT others(11): Show |
3 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109 | 3 | HG02080.hp1 NA18943.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.148+9790_148+9807d others(20): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | ||||||
chr6:89402046
|
T | TTTTTCTT others(10): Show |
1 | a0001c0001t0007g0271 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.148+9799_148+9800i others(19): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402046 | ||||||
chr6:89402127
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.148+9719T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402127 | ||||||
chr6:89402237
|
G | A | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(63): Show | 70 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.148+9609C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402237 | ||||||
chr6:89402289
|
G | A | 2 | a0001c0001t0002g0139a0001c0002t0040g0031 | 2 | NA19056.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.148+9557C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402289 | ||||||
chr6:89402561
|
G | C | 6 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(3): Show | 6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+9285C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402561 | ||||||
chr6:89402639
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.148+9207C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402639 | ||||||
chr6:89402729
|
A | T | 1 | a0001c0001t0010g0023 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.148+9117T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402729 | ||||||
chr6:89402809
|
T | C | 1 | a0001c0002t0021g0335 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.148+9037A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402809 | ||||||
chr6:89402910
|
T | G | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.148+8936A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402910 | ||||||
chr6:89403164
|
G | A | 5 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+8682C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403164 | ||||||
chr6:89403167
|
C | A | 6 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(3): Show | 6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+8679G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403167 | ||||||
chr6:89403170
|
G | A | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.148+8676C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403170 | ||||||
chr6:89403180
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0049g0225others(1): Show | 4 | HG01943.hp2 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.148+8666C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403180 | ||||||
chr6:89403231
|
G | A | 1 | a0001c0001t0012g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.148+8615C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403231 | ||||||
chr6:89403242
|
G | A | 1 | a0001c0001t0004g0288 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.148+8604C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403242 | ||||||
chr6:89403264
|
T | C | 1 | a0001c0001t0004g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.148+8582A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403264 | ||||||
chr6:89403306
|
A | G | 78 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(75): Show | 82 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.148+8540T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403306 | ||||||
chr6:89403308
|
G | A | 65 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(62): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.148+8538C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403308 | ||||||
chr6:89403311
|
G | A | 76 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0034others(73): Show | 80 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.148+8535C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403311 | ||||||
chr6:89403317
|
C | T | 1 | a0001c0001t0037g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.148+8529G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403317 | ||||||
chr6:89403362
|
G | A | 4 | a0001c0001t0014g0006a0001c0001t0014g0035a0001c0001t0014g0036others(1): Show | 5 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+8484C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403362 | ||||||
chr6:89403423
|
C | T | 2 | a0001c0001t0003g0050a0001c0001t0003g0051 | 2 | HG01934.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.148+8423G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403423 | ||||||
chr6:89403453
|
A | C | 1 | a0001c0001t0004g0290 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.148+8393T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403453 | ||||||
chr6:89403538
|
C | T | 248 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(245): Show | 264 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.148+8308G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403538 | ||||||
chr6:89403556
|
T | G | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 86 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+8290A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403556 | ||||||
chr6:89403627
|
CT | C | 96 | a0001c0001t0002g0106a0001c0001t0003g0007a0001c0001t0003g0008others(93): Show | 102 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(99): Show |
intron_variant | MODIFIER | c.148+8218delA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403627 | ||||||
chr6:89403627
|
CTT | C | 85 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(82): Show | 91 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.148+8217_148+8218d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403627 | ||||||
chr6:89403627
|
CTTT | C | 64 | a0001c0001t0002g0141a0001c0001t0004g0019a0001c0001t0004g0261others(61): Show | 68 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.148+8216_148+8218d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403627 | ||||||
chr6:89403700
|
T | C | 7 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(4): Show | 7 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+8146A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403700 | ||||||
chr6:89403795
|
C | G | 6 | a0001c0001t0005g0017a0001c0001t0005g0239a0001c0001t0005g0240others(3): Show | 7 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+8051G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403795 | ||||||
chr6:89403854
|
C | T | 1 | a0001c0001t0025g0340 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.148+7992G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403854 | ||||||
chr6:89404082
|
T | A | 1 | a0001c0001t0010g0023 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.148+7764A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404082 | ||||||
chr6:89404290
|
A | C | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.148+7556T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404290 | ||||||
chr6:89404311
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.148+7535A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404311 | ||||||
chr6:89404409
|
C | T | 6 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(3): Show | 6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+7437G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404409 | ||||||
chr6:89404422
|
G | T | 72 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(69): Show | 77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.148+7424C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404422 | ||||||
chr6:89404650
|
G | A | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+7196C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404650 | ||||||
chr6:89404710
|
C | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.148+7136G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404710 | ||||||
chr6:89404897
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(79): Show | 88 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.148+6949G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404897 | ||||||
chr6:89404904
|
A | T | 1 | a0001c0001t0010g0023 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.148+6942T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404904 | ||||||
chr6:89404941
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0162a0001c0001t0001g0228others(1): Show | 4 | HG00140.hp2 HG01257.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+6905A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404941 | ||||||
chr6:89404955
|
G | C | 41 | a0001c0001t0003g0038a0001c0001t0003g0143a0001c0001t0003g0144others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.148+6891C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404955 | ||||||
chr6:89404959
|
T | C | 33 | a0001c0001t0003g0038a0001c0001t0003g0143a0001c0001t0003g0144others(30): Show | 37 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.148+6887A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404959 | ||||||
chr6:89405022
|
A | G | 5 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(2): Show | 5 | NA18968.hp1 NA18979.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+6824T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405022 | ||||||
chr6:89405083
|
G | C | 44 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0261others(41): Show | 47 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.148+6763C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405083 | ||||||
chr6:89405151
|
T | C | 1 | a0001c0001t0011g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.148+6695A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405151 | ||||||
chr6:89405166
|
C | A | 7 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0326others(4): Show | 8 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+6680G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405166 | ||||||
chr6:89405167
|
G | A | 2 | a0001c0001t0031g0266a0001c0001t0031g0267 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.148+6679C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405167 | ||||||
chr6:89405169
|
T | A | 3 | a0001c0001t0022g0249a0001c0001t0022g0250a0001c0001t0022g0311 | 3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.148+6677A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405169 | ||||||
chr6:89405224
|
T | G | 1 | a0001c0001t0059g0320 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.148+6622A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405224 | ||||||
chr6:89405328
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.148+6518A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405328 | ||||||
chr6:89405353
|
C | CA | 120 | a0001c0001t0001g0172a0001c0001t0001g0231a0001c0001t0001g0232others(117): Show | 126 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.148+6492dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405353 | ||||||
chr6:89405353
|
C | CAA | 37 | a0001c0001t0002g0154a0001c0001t0003g0038a0001c0001t0003g0046others(34): Show | 40 | HG00280.hp1 HG00408.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.148+6491_148+6492d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405353 | ||||||
chr6:89405353
|
C | CAAA | 9 | a0001c0001t0005g0017a0001c0001t0005g0241a0001c0001t0005g0242others(6): Show | 10 | HG01169.hp1 HG01358.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+6490_148+6492d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405353 | ||||||
chr6:89405374
|
A | G | 8 | a0001c0001t0011g0089a0001c0001t0011g0091a0001c0001t0011g0092others(5): Show | 8 | HG00738.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.148+6472T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405374 | ||||||
chr6:89405591
|
G | A | 18 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0326others(15): Show | 20 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.148+6255C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405591 | ||||||
chr6:89405752
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(78): Show | 87 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.148+6094G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405752 | ||||||
chr6:89405842
|
G | A | 2 | a0001c0001t0004g0322a0001c0001t0004g0323 | 2 | HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.148+6004C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405842 | ||||||
chr6:89405972
|
G | C | 2 | a0001c0001t0008g0264a0001c0001t0008g0265 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.148+5874C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405972 | ||||||
chr6:89406071
|
G | A | 2 | a0001c0001t0034g0071a0001c0001t0035g0070 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.148+5775C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406071 | ||||||
chr6:89406100
|
CAA | C | 15 | a0001c0001t0003g0007a0001c0001t0003g0039a0001c0001t0003g0040others(12): Show | 16 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.148+5744_148+5745d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406100 | ||||||
chr6:89406174
|
TA | T | 6 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(3): Show | 6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+5671delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406174 | ||||||
chr6:89406180
|
T | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0156others(3): Show | 7 | HG00438.hp1 NA18967.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+5666A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406180 | ||||||
chr6:89406189
|
T | C | 28 | a0001c0001t0003g0038a0001c0001t0005g0011a0001c0001t0005g0017others(25): Show | 32 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.148+5657A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406189 | ||||||
chr6:89406199
|
G | T | 7 | a0001c0002t0019g0330a0001c0002t0019g0332a0001c0002t0021g0331others(4): Show | 7 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+5647C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406199 | ||||||
chr6:89406204
|
G | C | 19 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0326others(16): Show | 21 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.148+5642C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406204 | ||||||
chr6:89406267
|
A | G | 42 | a0001c0001t0003g0038a0001c0001t0005g0011a0001c0001t0005g0017others(39): Show | 46 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.148+5579T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406267 | ||||||
chr6:89406383
|
G | A | 248 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0009others(245): Show | 264 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.148+5463C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406383 | ||||||
chr6:89406425
|
C | T | 80 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0012others(77): Show | 86 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+5421G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406425 | ||||||
chr6:89406455
|
C | A | 1 | a0001c0001t0003g0066 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.148+5391G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406455 | ||||||
chr6:89406536
|
A | G | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+5310T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406536 | ||||||
chr6:89406673
|
C | T | 3 | a0001c0001t0004g0261a0001c0001t0004g0273a0001c0001t0004g0274 | 3 | HG01081.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.148+5173G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406673 | ||||||
chr6:89406683
|
G | A | 8 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(5): Show | 8 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.148+5163C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406683 | ||||||
chr6:89406858
|
TG | T | 7 | a0001c0001t0012g0270a0001c0001t0012g0284a0001c0001t0012g0285others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+4987delC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406858 | ||||||
chr6:89406911
|
C | G | 33 | a0001c0001t0003g0038a0001c0001t0005g0011a0001c0001t0005g0017others(30): Show | 37 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.148+4935G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406911 | ||||||
chr6:89407301
|
T | A | 56 | a0001c0001t0001g0162a0001c0001t0003g0007a0001c0001t0003g0008others(53): Show | 58 | HG00438.hp2 HG00673.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.148+4545A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407301 | ||||||
chr6:89407308
|
T | A | 1 | a0001c0001t0004g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.148+4538A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407308 | ||||||
chr6:89407437
|
A | C | 1 | a0001c0001t0001g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.148+4409T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407437 | ||||||
chr6:89407448
|
G | A | 3 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248 | 3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.148+4398C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407448 | ||||||
chr6:89407499
|
A | G | 255 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0009others(252): Show | 272 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.148+4347T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407499 | ||||||
chr6:89407591
|
G | A | 2 | a0001c0001t0012g0284a0001c0001t0012g0285 | 2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.148+4255C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407591 | ||||||
chr6:89407678
|
G | A | 3 | a0001c0001t0008g0264a0001c0001t0008g0265a0001c0004t0039g0235 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.148+4168C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407678 | ||||||
chr6:89407821
|
C | T | 1 | a0001c0001t0063g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.148+4025G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407821 | ||||||
chr6:89407855
|
C | T | 1 | a0001c0001t0006g0084 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.148+3991G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407855 | ||||||
chr6:89407868
|
C | T | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+3978G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407868 | ||||||
chr6:89408064
|
CATCTGTT others(30): Show |
C | 1 | a0001c0001t0027g0243 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.148+3745_148+3781d others(39): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408064 | ||||||
chr6:89408087
|
T | A | 1 | a0001c0001t0001g0236 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.148+3759A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408087 | ||||||
chr6:89408225
|
A | AT | 6 | a0001c0001t0007g0020a0001c0001t0007g0268a0001c0001t0007g0326others(3): Show | 7 | HG01109.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3620dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408225 | ||||||
chr6:89408328
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.148+3518C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408328 | ||||||
chr6:89408617
|
A | G | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.148+3229T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408617 | ||||||
chr6:89408733
|
T | G | 13 | a0001c0001t0007g0020a0001c0001t0007g0326a0001c0001t0007g0327others(10): Show | 14 | HG01109.hp1 HG02258.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.148+3113A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408733 | ||||||
chr6:89408852
|
A | C | 9 | a0001c0001t0004g0339a0001c0001t0014g0006a0001c0001t0014g0035others(6): Show | 10 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+2994T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408852 | ||||||
chr6:89409045
|
G | A | 39 | a0001c0001t0004g0019a0001c0001t0004g0288a0001c0001t0004g0290others(36): Show | 41 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.148+2801C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409045 | ||||||
chr6:89409135
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(333): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.148+2711A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409135 | ||||||
chr6:89409188
|
T | C | 2 | a0001c0001t0034g0071a0001c0001t0035g0070 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.148+2658A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409188 | ||||||
chr6:89409317
|
C | T | 1 | a0001c0001t0003g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.148+2529G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409317 | ||||||
chr6:89409324
|
A | G | 151 | a0001c0001t0001g0067a0001c0001t0002g0009a0001c0001t0003g0007others(148): Show | 161 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.148+2522T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409324 | ||||||
chr6:89409418
|
G | A | 5 | a0001c0001t0024g0338a0001c0001t0025g0340a0001c0001t0025g0342others(2): Show | 5 | HG01106.hp1 HG01433.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+2428C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409418 | ||||||
chr6:89409477
|
T | G | 2 | a0001c0001t0003g0072a0001c0001t0003g0073 | 2 | NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.148+2369A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409477 | ||||||
chr6:89409795
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.148+2051G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409795 | ||||||
chr6:89409848
|
C | T | 2 | a0001c0001t0031g0266a0001c0001t0031g0267 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.148+1998G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409848 | ||||||
chr6:89410295
|
A | T | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+1551T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89410295 | ||||||
chr6:89410428
|
G | A | 4 | a0001c0001t0012g0312a0001c0001t0012g0313a0001c0001t0012g0314others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.148+1418C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89410428 | ||||||
chr6:89410519
|
C | T | 5 | a0001c0001t0015g0251a0001c0001t0015g0252a0001c0001t0015g0253others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+1327G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89410519 | ||||||
chr6:89410627
|
T | C | 1 | a0001c0001t0020g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.148+1219A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89410627 | ||||||
chr6:89411164
|
G | C | 10 | a0001c0001t0004g0019a0001c0001t0004g0316a0001c0001t0004g0318others(7): Show | 11 | HG01496.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+682C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411164 | ||||||
chr6:89411174
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.148+672C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411174 | ||||||
chr6:89411196
|
G | C | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.148+650C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411196 | ||||||
chr6:89411272
|
A | C | 139 | a0001c0001t0001g0067a0001c0001t0003g0007a0001c0001t0003g0008others(136): Show | 147 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.148+574T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411272 | ||||||
chr6:89411343
|
C | T | 1 | a0001c0001t0010g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.148+503G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411343 | ||||||
chr6:89411370
|
C | T | 18 | a0001c0001t0004g0021a0001c0001t0004g0261a0001c0001t0004g0339others(15): Show | 21 | HG00735.hp1 HG01106.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.148+476G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411370 | ||||||
chr6:89411414
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.148+432G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411414 | ||||||
chr6:89411428
|
T | A | 2 | a0001c0001t0004g0021a0001c0001t0004g0339 | 3 | HG02723.hp2 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.148+418A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411428 | ||||||
chr6:89411560
|
C | T | 2 | a0001c0001t0022g0249a0001c0001t0022g0250 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.148+286G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411560 | ||||||
chr6:89411685
|
G | A | 6 | a0001c0001t0005g0017a0001c0001t0005g0239a0001c0001t0005g0240others(3): Show | 7 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+161C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411685 | ||||||
chr6:89411718
|
C | T | 5 | a0001c0001t0023g0246a0001c0001t0023g0247a0001c0001t0023g0248others(2): Show | 5 | HG03130.hp1 HG03453.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+128G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411718 |