Item | Value |
---|---|
geneid | 5905 |
ensemblid | ENSG00000100401.21 |
hgncid | 9854 |
symbol | RANGAP1 |
name | Ran GTPase activating protein 1 |
refseq_nuc | NM_002883.4 |
refseq_prot | NP_002874.1 |
ensembl_nuc | ENST00000356244.8 |
ensembl_prot | ENSP00000348577.3 |
mane_status | MANE Select |
chr | chr22 |
start | 41244779 |
end | 41286187 |
strand | - |
ver | v1.2 |
region | chr22:41244779-41286187 |
region5000 | chr22:41239779-41291187 |
regionname0 | RANGAP1_chr22_41244779_41286187 |
regionname5000 | RANGAP1_chr22_41239779_41291187 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 587 | 340 | 78 | 56 | 152 | 14 | 38 | 112 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0002 | 0/0 | 587 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0003 | 0/0 | 587 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0004 | 0/0 | 587 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0005 | 0/0 | 587 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1764 | 185 | 28 | 35 | 95 | 6 | 20 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0002 | 1/0 | 1764 | 107 | 29 | 9 | 54 | 3 | 11 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0003 | 0/0 | 1764 | 44 | 20 | 12 | 1 | 4 | 7 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0004 | 0/0 | 1764 | 7 | 6 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0005 | 0/0 | 1764 | 3 | 2 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0006 | 0/0 | 1764 | 2 | 0 | 0 | 0 | 0 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0007 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0008 | 0/0 | 1764 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0009 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0010 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
c0011 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2065 | 151 | 41 | 9 | 93 | 1 | 6 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0002 | 0/1 | 2065 | 43 | 3 | 21 | 5 | 3 | 10 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0003 | 0/0 | 2065 | 38 | 1 | 2 | 29 | 2 | 4 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0004 | 0/0 | 2065 | 36 | 18 | 10 | 1 | 2 | 5 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0005 | 0/0 | 2065 | 28 | 4 | 3 | 14 | 2 | 5 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0006 | 0/0 | 2065 | 12 | 1 | 8 | 3 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0007 | 0/0 | 2065 | 7 | 6 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0008 | 0/0 | 2065 | 6 | 0 | 2 | 0 | 2 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0009 | 0/0 | 2065 | 5 | 0 | 1 | 0 | 1 | 3 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0010 | 0/0 | 2065 | 5 | 5 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0011 | 0/0 | 2065 | 5 | 4 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0012 | 0/0 | 2065 | 2 | 0 | 0 | 1 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0013 | 0/0 | 2065 | 2 | 0 | 0 | 0 | 0 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0014 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0015 | 0/0 | 2065 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0016 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0017 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0018 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0019 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0020 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0021 | 0/0 | 2065 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0022 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0023 | 0/0 | 2065 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0024 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0025 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0026 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
t0027 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0002 | 0/1 | 4 | 0 | 3 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1764 | 185 | 28 | 35 | 95 | 6 | 20 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0001c0002 | 1/0 | 1764 | 107 | 29 | 9 | 54 | 3 | 11 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0001c0003 | 0/0 | 1764 | 44 | 20 | 12 | 1 | 4 | 7 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0001c0008 | 0/0 | 1764 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0001c0009 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0001c0010 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0001c0011 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0002c0004 | 0/0 | 1764 | 7 | 6 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0003c0005 | 0/0 | 1764 | 3 | 2 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0004c0006 | 0/0 | 1764 | 2 | 0 | 0 | 0 | 0 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 | |
a0005c0007 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3828 | 60 | 12 | 2 | 45 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0002 | 0/1 | 3828 | 43 | 3 | 21 | 5 | 3 | 10 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0003 | 0/0 | 3828 | 37 | 1 | 2 | 28 | 2 | 4 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0005 | 0/0 | 3828 | 12 | 0 | 1 | 11 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0006 | 0/0 | 3828 | 11 | 0 | 8 | 3 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0009 | 0/0 | 3828 | 4 | 0 | 1 | 0 | 0 | 3 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0010 | 0/0 | 3828 | 5 | 5 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0011 | 0/0 | 3828 | 3 | 3 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0012 | 0/0 | 3828 | 2 | 0 | 0 | 1 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0014 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0015 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0017 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0018 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0019 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0020 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0021 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0001t0025 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0002t0001 | 1/0 | 3828 | 85 | 24 | 7 | 47 | 1 | 5 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0002t0005 | 0/0 | 3828 | 16 | 4 | 2 | 3 | 2 | 5 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0002t0016 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0002t0022 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0002t0023 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0002t0024 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0002t0026 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0002t0027 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0003t0001 | 0/0 | 3828 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0003t0004 | 0/0 | 3828 | 36 | 18 | 10 | 1 | 2 | 5 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0003t0008 | 0/0 | 3828 | 6 | 0 | 2 | 0 | 2 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0008t0009 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0009t0003 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0010t0001 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0001c0011t0001 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0002c0004t0007 | 0/0 | 3828 | 7 | 6 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0003c0005t0006 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0003c0005t0011 | 0/0 | 3828 | 2 | 1 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0004c0006t0013 | 0/0 | 3828 | 2 | 0 | 0 | 0 | 0 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
a0005c0007t0001 | 0/0 | 3828 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | copy fasta | chr22 | 41239779 | 41291187 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0002 | 0/1 | 4 | 0 | 3 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0006g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0006g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0009g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0010g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0011g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0011g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0012g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0012g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0014g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0017g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0018g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0019g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0021g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0001t0025g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0001 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0016g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0022g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0023g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0024g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0026g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0002t0027g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0008g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0008g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0008g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0003t0008g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0008t0009g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0009t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0001c0011t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0002c0004t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0002c0004t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0002c0004t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0002c0004t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0002c0004t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0002c0004t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0002c0004t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0003c0005t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0003c0005t0011g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0003c0005t0011g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0004c0006t0013g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0005c0007t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
a0005c0007t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0071 | EUR | GBR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00099 | hp2 | a0001 | c0001 | t0012 | g0242 | EUR | GBR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00140 | hp1 | a0001 | c0003 | t0004 | g0003 | EUR | GBR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00140 | hp2 | a0001 | c0002 | t0005 | g0165 | EUR | GBR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00280 | hp1 | a0001 | c0003 | t0004 | g0101 | EUR | FIN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | FIN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0273 | EUR | FIN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00323 | hp2 | a0001 | c0008 | t0009 | g0065 | EUR | FIN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00423 | hp2 | a0001 | c0001 | t0012 | g0263 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00621 | hp1 | a0001 | c0001 | t0019 | g0253 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00621 | hp2 | a0001 | c0002 | t0005 | g0021 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00639 | hp1 | a0002 | c0004 | t0007 | g0080 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00673 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00733 | hp2 | a0001 | c0003 | t0008 | g0119 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00735 | hp1 | a0001 | c0003 | t0004 | g0012 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00738 | hp2 | a0001 | c0003 | t0004 | g0102 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00741 | hp1 | a0001 | c0003 | t0004 | g0118 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0305 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01069 | hp1 | a0001 | c0003 | t0004 | g0114 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01070 | hp1 | a0001 | c0003 | t0004 | g0003 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01081 | hp1 | a0001 | c0003 | t0004 | g0015 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0298 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01109 | hp2 | a0003 | c0005 | t0011 | g0302 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01167 | hp2 | a0001 | c0003 | t0004 | g0123 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01169 | hp1 | a0001 | c0003 | t0004 | g0015 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01175 | hp2 | a0001 | c0002 | t0005 | g0137 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01243 | hp1 | a0001 | c0003 | t0004 | g0099 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01261 | hp1 | a0001 | c0001 | t0009 | g0059 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01361 | hp1 | a0001 | c0001 | t0006 | g0277 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0289 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0274 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01496 | hp1 | a0001 | c0003 | t0004 | g0094 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01517 | hp1 | a0001 | c0003 | t0008 | g0113 | EUR | IBS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0056 | EUR | IBS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01884 | hp1 | a0002 | c0004 | t0007 | g0083 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0282 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01943 | hp1 | a0001 | c0003 | t0008 | g0110 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0281 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01981 | hp1 | a0001 | c0002 | t0005 | g0127 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0280 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02055 | hp1 | a0002 | c0004 | t0007 | g0081 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02055 | hp2 | a0001 | c0003 | t0004 | g0105 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02135 | hp2 | a0001 | c0011 | t0001 | g0226 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02258 | hp1 | a0001 | c0001 | t0018 | g0299 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02258 | hp2 | a0002 | c0004 | t0007 | g0087 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02280 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0092 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0181 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02300 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02451 | hp2 | a0001 | c0002 | t0005 | g0132 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02523 | hp2 | a0001 | c0001 | t0014 | g0055 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02572 | hp1 | a0001 | c0003 | t0004 | g0121 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02572 | hp2 | a0001 | c0003 | t0004 | g0095 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02615 | hp1 | a0001 | c0003 | t0004 | g0098 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02622 | hp2 | a0001 | c0003 | t0004 | g0097 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0103 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02647 | hp1 | a0005 | c0007 | t0001 | g0234 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02647 | hp2 | a0001 | c0003 | t0004 | g0109 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02698 | hp1 | a0001 | c0003 | t0004 | g0126 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02717 | hp2 | a0001 | c0003 | t0004 | g0108 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02723 | hp2 | a0005 | c0007 | t0001 | g0237 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02735 | hp2 | a0001 | c0001 | t0015 | g0063 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02818 | hp1 | a0001 | c0001 | t0020 | g0088 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02818 | hp2 | a0002 | c0004 | t0007 | g0082 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0290 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02965 | hp1 | a0001 | c0003 | t0004 | g0122 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02965 | hp2 | a0001 | c0001 | t0011 | g0035 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02970 | hp2 | a0001 | c0002 | t0005 | g0304 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03017 | hp1 | a0001 | c0002 | t0005 | g0143 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0093 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03130 | hp2 | a0001 | c0003 | t0004 | g0013 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03139 | hp1 | a0002 | c0004 | t0007 | g0086 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0096 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03195 | hp2 | a0001 | c0003 | t0004 | g0112 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03209 | hp2 | a0001 | c0001 | t0025 | g0085 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03225 | hp2 | a0001 | c0010 | t0001 | g0227 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03453 | hp1 | a0003 | c0005 | t0011 | g0300 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03453 | hp2 | a0001 | c0002 | t0016 | g0078 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03486 | hp1 | a0001 | c0003 | t0004 | g0106 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03486 | hp2 | a0001 | c0002 | t0005 | g0188 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03490 | hp1 | a0001 | c0003 | t0004 | g0003 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03490 | hp2 | a0004 | c0006 | t0013 | g0031 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03491 | hp2 | a0001 | c0003 | t0008 | g0115 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03492 | hp1 | a0001 | c0003 | t0008 | g0120 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03492 | hp2 | a0004 | c0006 | t0013 | g0031 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03579 | hp2 | a0001 | c0003 | t0004 | g0288 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03669 | hp1 | a0001 | c0002 | t0005 | g0225 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03669 | hp2 | a0001 | c0003 | t0004 | g0124 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03688 | hp2 | a0001 | c0001 | t0009 | g0068 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03704 | hp2 | a0001 | c0001 | t0009 | g0064 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03710 | hp1 | a0001 | c0002 | t0023 | g0144 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03831 | hp1 | a0001 | c0003 | t0004 | g0012 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03834 | hp2 | a0001 | c0003 | t0004 | g0100 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03942 | hp2 | a0001 | c0002 | t0005 | g0142 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG04115 | hp2 | a0001 | c0001 | t0021 | g0297 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG04204 | hp1 | a0001 | c0001 | t0009 | g0073 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0228 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG04228 | hp1 | a0001 | c0002 | t0005 | g0140 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG04228 | hp2 | a0001 | c0002 | t0005 | g0229 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18522 | hp1 | a0003 | c0005 | t0006 | g0301 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18522 | hp2 | a0002 | c0004 | t0007 | g0089 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | CHB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18747 | hp1 | a0001 | c0002 | t0005 | g0175 | EAS | CHB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0248 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18944 | hp1 | a0001 | c0002 | t0027 | g0306 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18947 | hp2 | a0001 | c0009 | t0003 | g0050 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18956 | hp2 | a0001 | c0002 | t0005 | g0021 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18969 | hp2 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18973 | hp2 | a0001 | c0002 | t0022 | g0241 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18975 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18985 | hp2 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18992 | hp1 | a0001 | c0003 | t0004 | g0125 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19030 | hp2 | a0001 | c0003 | t0004 | g0117 | AFR | LWK | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | LWK | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19043 | hp2 | a0001 | c0003 | t0004 | g0111 | AFR | LWK | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19062 | hp2 | a0001 | c0002 | t0024 | g0145 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19088 | hp1 | a0001 | c0001 | t0006 | g0279 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19088 | hp2 | a0001 | c0002 | t0026 | g0185 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0035 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA19240 | hp2 | a0001 | c0001 | t0010 | g0077 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ASW | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | TSI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA20752 | hp2 | a0001 | c0002 | t0005 | g0190 | EUR | TSI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | TSI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA20805 | hp2 | a0001 | c0003 | t0008 | g0104 | EUR | TSI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02109 | hp1 | a0001 | c0003 | t0004 | g0116 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02486 | hp1 | a0001 | c0002 | t0005 | g0133 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02559 | hp1 | a0001 | c0001 | t0017 | g0275 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG03471 | hp2 | a0001 | c0003 | t0004 | g0107 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | USA | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
HG06807 | hp2 | a0001 | c0001 | t0010 | g0084 | AFR | USA | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0197 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | USA | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | USA | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0002 | REF | REF | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0224 | REF | REF | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41249805 | T | C | 1 | a0004 | 2 | HG03490.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.1496A>G | p.Gln499Arg | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/16 | 1736/3828 | 1496/1764 | 499/587 | chr22 | 41249805 | ||
chr22:41254367 | G | C | 1 | a0002 | 7 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(4): Show |
missense_variant | MODERATE | c.1201C>G | p.Arg401Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/16 | 1441/3828 | 1201/1764 | 401/587 | chr22 | 41254367 | ||
chr22:41256253 | G | C | 1 | a0005 | 2 | HG02647.hp1 HG02723.hp2 |
missense_variant | MODERATE | c.926C>G | p.Ala309Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 9/16 | 1166/3828 | 926/1764 | 309/587 | chr22 | 41256253 | ||
chr22:41264747 | C | G | 1 | a0003 | 3 | HG01109.hp2 HG03453.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.397G>C | p.Glu133Gln | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/16 | 637/3828 | 397/1764 | 133/587 | chr22 | 41264747 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41249753 | C | G | 8 | a0001c0001a0001c0003a0001c0008others(5): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
synonymous_variant | LOW | c.1548G>C | p.Leu516Leu | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/16 | 1788/3828 | 1548/1764 | 516/587 | chr22 | 41249753 | ||
chr22:41256729 | G | A | 1 | a0001c0003 | 44 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
synonymous_variant | LOW | c.870C>T | p.Gly290Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/16 | 1110/3828 | 870/1764 | 290/587 | chr22 | 41256729 | ||
chr22:41258026 | G | A | 1 | a0001c0008 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.696C>T | p.Phe232Phe | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/16 | 936/3828 | 696/1764 | 232/587 | chr22 | 41258026 | ||
chr22:41261473 | G | A | 1 | a0001c0009 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.588C>T | p.Gly196Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/16 | 828/3828 | 588/1764 | 196/587 | chr22 | 41261473 | ||
chr22:41264736 | G | C | 1 | a0001c0010 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.408C>G | p.Leu136Leu | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/16 | 648/3828 | 408/1764 | 136/587 | chr22 | 41264736 | ||
chr22:41280964 | G | C | 1 | a0001c0011 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.81C>G | p.Gly27Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/16 | 321/3828 | 81/1764 | 27/587 | chr22 | 41280964 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41244846 | T | C | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(11): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1757A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1757 | chr22 | 41244846 | |||||
chr22:41245265 | A | G | 1 | a0001c0002t0023 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1338T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1338 | chr22 | 41245265 | |||||
chr22:41245314 | T | C | 1 | a0001c0001t0021 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1289 | chr22 | 41245314 | |||||
chr22:41245520 | C | G | 1 | a0001c0002t0022 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1083G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1083 | chr22 | 41245520 | |||||
chr22:41245535 | A | C | 1 | a0001c0001t0015 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1068T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1068 | chr22 | 41245535 | |||||
chr22:41245566 | C | T | 7 | a0001c0001t0006a0001c0001t0011a0001c0001t0017others(4): Show | 20 | HG00673.hp1 HG00741.hp2 HG01099.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1037G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1037 | chr22 | 41245566 | |||||
chr22:41245800 | T | C | 1 | a0001c0002t0024 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*803A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 803 | chr22 | 41245800 | |||||
chr22:41245919 | C | T | 1 | a0001c0001t0020 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*684G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 684 | chr22 | 41245919 | |||||
chr22:41245920 | G | A | 3 | a0001c0001t0010a0001c0001t0025a0002c0004t0007 | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*683C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 683 | chr22 | 41245920 | |||||
chr22:41245980 | C | T | 2 | a0001c0003t0004a0001c0003t0008 | 42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*623G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 623 | chr22 | 41245980 | |||||
chr22:41245988 | G | A | 1 | a0004c0006t0013 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*615C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 615 | chr22 | 41245988 | |||||
chr22:41246020 | G | A | 1 | a0001c0002t0026 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*583C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 583 | chr22 | 41246020 | |||||
chr22:41246208 | C | T | 13 | a0001c0001t0002a0001c0001t0006a0001c0001t0011others(10): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*395G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 395 | chr22 | 41246208 | |||||
chr22:41246277 | C | T | 2 | a0001c0001t0010a0002c0004t0007 | 12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*326G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 326 | chr22 | 41246277 | |||||
chr22:41246320 | C | T | 1 | a0001c0001t0019 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*283G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 283 | chr22 | 41246320 | |||||
chr22:41246434 | C | T | 1 | a0001c0001t0018 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*169G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 169 | chr22 | 41246434 | |||||
chr22:41246441 | C | G | 1 | a0001c0001t0017 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 162 | chr22 | 41246441 | |||||
chr22:41246488 | C | T | 1 | a0001c0002t0016 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 115 | chr22 | 41246488 | |||||
chr22:41286010 | G | T | 6 | a0001c0001t0003a0001c0001t0009a0001c0001t0014others(3): Show | 45 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-63C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/16 | 4966 | chr22 | 41286010 | |||||
chr22:41286129 | G | A | 1 | a0001c0002t0027 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/16 | 5085 | chr22 | 41286129 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41246777 | G | T | 1 | a0001c0002t0005g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1695-105C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246777 | ||||||
chr22:41246825 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1695-153C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246825 | ||||||
chr22:41246845 | G | A | 4 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(1): Show | 5 | HG03130.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695-173C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246845 | ||||||
chr22:41246903 | C | A | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-231G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246903 | ||||||
chr22:41246992 | A | G | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-320T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246992 | ||||||
chr22:41247141 | C | T | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-469G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247141 | ||||||
chr22:41247207 | C | A | 1 | a0005c0007t0001g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1695-535G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247207 | ||||||
chr22:41247344 | C | T | 1 | a0001c0003t0004g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1695-672G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247344 | ||||||
chr22:41247347 | G | A | 1 | a0001c0002t0001g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1695-675C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247347 | ||||||
chr22:41247393 | C | T | 43 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(40): Show | 48 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1695-721G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247393 | ||||||
chr22:41247435 | T | C | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-763A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247435 | ||||||
chr22:41247591 | A | G | 1 | a0001c0001t0003g0008 | 2 | HG00558.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1695-919T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247591 | ||||||
chr22:41247664 | C | A | 1 | a0001c0002t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1695-992G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247664 | ||||||
chr22:41247728 | A | G | 5 | a0001c0001t0002g0006a0001c0001t0002g0249a0001c0001t0002g0264others(2): Show | 7 | HG00323.hp1 HG00733.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1695-1056T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247728 | ||||||
chr22:41247732 | C | T | 1 | a0001c0003t0001g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1695-1060G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247732 | ||||||
chr22:41247734 | G | T | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1695-1062C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247734 | ||||||
chr22:41247738 | G | A | 3 | a0001c0002t0001g0289a0001c0002t0001g0291a0001c0002t0001g0292 | 3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1695-1066C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247738 | ||||||
chr22:41247758 | C | G | 1 | a0001c0002t0027g0306 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1695-1086G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247758 | ||||||
chr22:41247779 | A | G | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-1107T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247779 | ||||||
chr22:41247780 | G | A | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-1108C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247780 | ||||||
chr22:41248011 | C | G | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1694+1319G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248011 | ||||||
chr22:41248070 | C | T | 77 | a0001c0001t0001g0246a0001c0001t0002g0002a0001c0001t0002g0006others(74): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1694+1260G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248070 | ||||||
chr22:41248128 | G | A | 1 | a0001c0001t0006g0281 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1694+1202C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248128 | ||||||
chr22:41248131 | A | T | 7 | a0001c0002t0001g0014a0001c0002t0001g0171a0001c0002t0001g0176others(4): Show | 8 | HG01243.hp2 HG01433.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1694+1199T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248131 | ||||||
chr22:41248191 | G | C | 1 | a0001c0003t0004g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1694+1139C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248191 | ||||||
chr22:41248230 | G | C | 96 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(93): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1694+1100C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248230 | ||||||
chr22:41248358 | G | GGCCT | 4 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(1): Show | 5 | HG03130.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694+968_1694+971d others(6): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248358 | ||||||
chr22:41248424 | G | A | 70 | a0001c0001t0001g0246a0001c0001t0002g0002a0001c0001t0002g0006others(67): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1694+906C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248424 | ||||||
chr22:41248708 | G | GCCT | 3 | a0001c0003t0004g0013a0001c0003t0004g0106a0001c0003t0004g0107 | 4 | HG02280.hp1 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1694+619_1694+621d others(5): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248708 | ||||||
chr22:41248816 | C | CACACATT others(12): Show |
1 | a0001c0001t0003g0076 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1694+495_1694+513d others(21): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248816 | ||||||
chr22:41248864 | G | A | 3 | a0001c0001t0001g0136a0001c0001t0001g0153a0001c0001t0001g0191 | 3 | HG00544.hp2 HG02056.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1694+466C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248864 | ||||||
chr22:41249081 | A | G | 171 | a0001c0001t0001g0079a0001c0001t0001g0246a0001c0001t0002g0002others(168): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1694+249T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41249081 | ||||||
chr22:41249253 | C | T | 2 | a0001c0001t0002g0283a0001c0001t0002g0294 | 2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1694+77G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41249253 | ||||||
chr22:41249299 | G | T | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1694+31C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41249299 | ||||||
chr22:41249305 | G | A | 1 | a0001c0002t0001g0186 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1694+25C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41249305 | ||||||
chr22:41249496 | TG | T | 245 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(242): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1573-46delC | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/15 | chr22 | 41249496 | ||||||
chr22:41249520 | T | A | 8 | a0001c0003t0004g0013a0001c0003t0004g0103a0001c0003t0004g0106others(5): Show | 9 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1573-69A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/15 | chr22 | 41249520 | ||||||
chr22:41249585 | G | A | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1573-134C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/15 | chr22 | 41249585 | ||||||
chr22:41249605 | C | T | 2 | a0005c0007t0001g0234a0005c0007t0001g0237 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1572+124G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/15 | chr22 | 41249605 | ||||||
chr22:41249867 | G | A | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1484-50C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41249867 | ||||||
chr22:41249903 | G | C | 3 | a0001c0002t0001g0147a0001c0002t0001g0172a0001c0002t0001g0187 | 3 | HG02080.hp2 NA18948.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1484-86C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41249903 | ||||||
chr22:41250039 | C | T | 2 | a0001c0003t0004g0116a0001c0003t0004g0117 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1484-222G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250039 | ||||||
chr22:41250266 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1484-449C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250266 | ||||||
chr22:41250333 | C | A | 1 | a0001c0002t0001g0168 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1484-516G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250333 | ||||||
chr22:41250450 | G | A | 1 | a0001c0001t0011g0035 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1483+557C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250450 | ||||||
chr22:41250488 | G | A | 1 | a0001c0002t0005g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1483+519C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250488 | ||||||
chr22:41250565 | G | T | 1 | a0002c0004t0007g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1483+442C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250565 | ||||||
chr22:41250566 | C | A | 1 | a0002c0004t0007g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1483+441G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250566 | ||||||
chr22:41250571 | G | A | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1483+436C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250571 | ||||||
chr22:41250583 | C | G | 4 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(1): Show | 5 | HG03130.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483+424G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250583 | ||||||
chr22:41250734 | A | G | 84 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(81): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1483+273T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250734 | ||||||
chr22:41250799 | G | A | 1 | a0001c0002t0001g0214 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1483+208C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250799 | ||||||
chr22:41250829 | G | A | 1 | a0001c0001t0025g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1483+178C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250829 | ||||||
chr22:41251121 | A | C | 1 | a0001c0002t0005g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1381-12T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251121 | ||||||
chr22:41251213 | G | A | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1381-104C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251213 | ||||||
chr22:41251232 | C | T | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1381-123G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251232 | ||||||
chr22:41251299 | G | A | 10 | a0001c0001t0001g0148a0001c0001t0001g0157a0001c0001t0001g0164others(7): Show | 10 | HG02083.hp1 HG02135.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.1381-190C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251299 | ||||||
chr22:41251443 | T | C | 1 | a0004c0006t0013g0031 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1381-334A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251443 | ||||||
chr22:41251487 | T | A | 239 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(236): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1381-378A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251487 | ||||||
chr22:41251627 | G | GA | 25 | a0001c0001t0001g0195a0001c0001t0001g0202a0001c0001t0001g0303others(22): Show | 28 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1381-519dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251627 | ||||||
chr22:41251684 | C | A | 1 | a0001c0002t0023g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1381-575G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251684 | ||||||
chr22:41251868 | C | T | 1 | a0001c0003t0004g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1381-759G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251868 | ||||||
chr22:41251991 | G | A | 8 | a0001c0001t0025g0085a0002c0004t0007g0080a0002c0004t0007g0081others(5): Show | 8 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1380+881C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251991 | ||||||
chr22:41251991 | G | GA | 4 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(1): Show | 5 | HG03130.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+880_1380+881i others(3): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251991 | ||||||
chr22:41252016 | C | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0156a0001c0001t0001g0192others(2): Show | 5 | NA18948.hp2 NA18949.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+856G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252016 | ||||||
chr22:41252054 | C | T | 2 | a0001c0001t0006g0298a0001c0001t0011g0035 | 3 | HG01099.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1380+818G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252054 | ||||||
chr22:41252087 | C | T | 83 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(80): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1380+785G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252087 | ||||||
chr22:41252309 | T | A | 2 | a0005c0007t0001g0234a0005c0007t0001g0237 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1380+563A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252309 | ||||||
chr22:41252427 | G | A | 1 | a0001c0002t0005g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1380+445C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252427 | ||||||
chr22:41252498 | T | C | 121 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(118): Show | 142 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1380+374A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252498 | ||||||
chr22:41252583 | G | C | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1380+289C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252583 | ||||||
chr22:41252586 | G | C | 2 | a0001c0003t0004g0116a0001c0003t0004g0117 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1380+286C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252586 | ||||||
chr22:41252644 | C | T | 3 | a0001c0003t0004g0094a0001c0003t0004g0095a0001c0003t0004g0097 | 3 | HG01496.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1380+228G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252644 | ||||||
chr22:41252695 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1380+177G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252695 | ||||||
chr22:41252726 | C | T | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1380+146G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252726 | ||||||
chr22:41252779 | G | A | 1 | a0001c0001t0011g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1380+93C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252779 | ||||||
chr22:41252804 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG00609.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1380+68C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252804 | ||||||
chr22:41253043 | C | A | 1 | a0001c0002t0005g0140 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1261-52G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253043 | ||||||
chr22:41253256 | G | A | 1 | a0001c0003t0004g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1261-265C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253256 | ||||||
chr22:41253305 | C | T | 7 | a0001c0001t0006g0298a0001c0001t0011g0035a0001c0001t0017g0275others(4): Show | 8 | HG01099.hp2 HG01109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1261-314G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253305 | ||||||
chr22:41253321 | G | C | 1 | a0001c0001t0002g0258 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1261-330C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253321 | ||||||
chr22:41253322 | G | C | 1 | a0001c0001t0002g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1261-331C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253322 | ||||||
chr22:41253498 | G | A | 1 | a0001c0001t0019g0253 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1261-507C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253498 | ||||||
chr22:41253746 | T | C | 3 | a0001c0002t0005g0021a0001c0002t0005g0175a0001c0002t0024g0145 | 4 | HG00621.hp2 NA18747.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+562A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253746 | ||||||
chr22:41253831 | G | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1260+477C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253831 | ||||||
chr22:41253928 | C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0211 | 3 | HG00423.hp1 NA19068.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1260+380G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253928 | ||||||
chr22:41253937 | G | A | 84 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(81): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1260+371C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253937 | ||||||
chr22:41254186 | C | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0030others(53): Show | 69 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1260+122G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41254186 | ||||||
chr22:41254237 | T | A | 1 | a0001c0001t0011g0035 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1260+71A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41254237 | ||||||
chr22:41254579 | C | G | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1074-85G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254579 | ||||||
chr22:41254695 | C | G | 171 | a0001c0001t0001g0079a0001c0001t0001g0246a0001c0001t0002g0002others(168): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1074-201G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254695 | ||||||
chr22:41254739 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1074-245C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254739 | ||||||
chr22:41254826 | G | T | 1 | a0001c0002t0027g0306 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1074-332C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254826 | ||||||
chr22:41254844 | C | T | 5 | a0001c0001t0002g0006a0001c0001t0002g0249a0001c0001t0002g0264others(2): Show | 7 | HG00323.hp1 HG00733.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-350G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254844 | ||||||
chr22:41254879 | G | A | 3 | a0003c0005t0006g0301a0003c0005t0011g0300a0003c0005t0011g0302 | 3 | HG01109.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1074-385C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254879 | ||||||
chr22:41254959 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1074-465C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254959 | ||||||
chr22:41254964 | T | C | 2 | a0005c0007t0001g0234a0005c0007t0001g0237 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1074-470A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254964 | ||||||
chr22:41254983 | C | CA | 69 | a0001c0001t0001g0198a0001c0001t0001g0246a0001c0001t0002g0002others(66): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1074-490dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254983 | ||||||
chr22:41254996 | C | A | 1 | a0001c0001t0005g0247 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1074-502G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254996 | ||||||
chr22:41254997 | A | C | 1 | a0001c0001t0003g0076 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1074-503T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254997 | ||||||
chr22:41255022 | T | C | 39 | a0001c0003t0001g0092a0001c0003t0001g0093a0001c0003t0004g0003others(36): Show | 44 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1074-528A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255022 | ||||||
chr22:41255030 | G | A | 83 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(80): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1074-536C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255030 | ||||||
chr22:41255207 | T | C | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1074-713A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255207 | ||||||
chr22:41255343 | G | A | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1073+678C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255343 | ||||||
chr22:41255356 | G | A | 1 | a0002c0004t0007g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1073+665C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255356 | ||||||
chr22:41255436 | A | G | 97 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(94): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1073+585T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255436 | ||||||
chr22:41255463 | T | C | 76 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(73): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1073+558A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255463 | ||||||
chr22:41255589 | C | T | 1 | a0001c0001t0017g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1073+432G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255589 | ||||||
chr22:41255700 | G | A | 160 | a0001c0001t0001g0079a0001c0001t0001g0246a0001c0001t0002g0002others(157): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1073+321C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255700 | ||||||
chr22:41255774 | T | A | 1 | a0001c0002t0001g0290 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1073+247A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255774 | ||||||
chr22:41255816 | T | A | 1 | a0001c0001t0001g0191 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1073+205A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255816 | ||||||
chr22:41255818 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1073+203C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255818 | ||||||
chr22:41256328 | C | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0030a0001c0001t0002g0033others(9): Show | 17 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.889-38G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256328 | ||||||
chr22:41256341 | C | G | 84 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(81): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.889-51G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256341 | ||||||
chr22:41256373 | G | A | 1 | a0001c0002t0005g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.889-83C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256373 | ||||||
chr22:41256425 | A | G | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.889-135T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256425 | ||||||
chr22:41256475 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.889-185G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256475 | ||||||
chr22:41256517 | C | G | 7 | a0001c0002t0001g0014a0001c0002t0001g0171a0001c0002t0001g0176others(4): Show | 8 | HG01243.hp2 HG01433.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.888+194G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256517 | ||||||
chr22:41256615 | A | G | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.888+96T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256615 | ||||||
chr22:41256842 | G | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0030others(46): Show | 61 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.775-18C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41256842 | ||||||
chr22:41256856 | G | A | 1 | a0002c0004t0007g0086 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.775-32C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41256856 | ||||||
chr22:41257013 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.775-189G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257013 | ||||||
chr22:41257464 | G | A | 7 | a0001c0002t0001g0014a0001c0002t0001g0171a0001c0002t0001g0176others(4): Show | 8 | HG01243.hp2 HG01433.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+484C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257464 | ||||||
chr22:41257536 | T | G | 133 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(130): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.774+412A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257536 | ||||||
chr22:41257744 | A | G | 61 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(58): Show | 67 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.774+204T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257744 | ||||||
chr22:41257868 | C | T | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.774+80G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257868 | ||||||
chr22:41258119 | G | A | 1 | a0001c0002t0005g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.616-13C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258119 | ||||||
chr22:41258197 | A | G | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-91T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258197 | ||||||
chr22:41258452 | T | C | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-346A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258452 | ||||||
chr22:41258564 | G | A | 84 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(81): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.616-458C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258564 | ||||||
chr22:41258565 | A | G | 84 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(81): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.616-459T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258565 | ||||||
chr22:41258666 | CTTT | C | 3 | a0001c0002t0001g0236a0001c0002t0001g0238a0001c0002t0001g0239 | 3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.616-563_616-561del others(3): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258666 | ||||||
chr22:41258710 | G | C | 1 | a0001c0001t0014g0055 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.616-604C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258710 | ||||||
chr22:41258892 | C | T | 2 | a0001c0002t0005g0140a0001c0002t0005g0142 | 2 | HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.616-786G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258892 | ||||||
chr22:41258950 | C | T | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-844G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258950 | ||||||
chr22:41258951 | A | G | 224 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(221): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.616-845T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258951 | ||||||
chr22:41259053 | G | A | 1 | a0001c0001t0006g0277 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.616-947C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259053 | ||||||
chr22:41259054 | A | G | 217 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(214): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.616-948T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259054 | ||||||
chr22:41259080 | C | T | 1 | a0001c0001t0017g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.616-974G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259080 | ||||||
chr22:41259146 | G | A | 1 | a0001c0002t0001g0147 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.616-1040C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259146 | ||||||
chr22:41259327 | C | A | 3 | a0002c0004t0007g0080a0002c0004t0007g0081a0002c0004t0007g0089 | 3 | HG00639.hp1 HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.616-1221G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259327 | ||||||
chr22:41259336 | G | A | 9 | a0001c0001t0011g0035a0001c0001t0017g0275a0001c0002t0001g0177others(6): Show | 10 | HG00639.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.616-1230C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259336 | ||||||
chr22:41259428 | T | G | 1 | a0001c0002t0001g0236 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.616-1322A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259428 | ||||||
chr22:41259435 | A | T | 2 | a0001c0001t0009g0068a0001c0001t0009g0073 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.616-1329T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259435 | ||||||
chr22:41259436 | A | G | 1 | a0001c0001t0002g0268 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.616-1330T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259436 | ||||||
chr22:41259560 | C | A | 1 | a0001c0001t0001g0303 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.616-1454G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259560 | ||||||
chr22:41259627 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.616-1521T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259627 | ||||||
chr22:41259673 | C | T | 12 | a0001c0002t0001g0011a0001c0002t0001g0020a0001c0002t0001g0090others(9): Show | 14 | NA18956.hp1 NA18982.hp1 NA18986.hp2 others(11): Show |
intron_variant | MODIFIER | c.616-1567G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259673 | ||||||
chr22:41259747 | A | T | 1 | a0001c0001t0001g0303 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.616-1641T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259747 | ||||||
chr22:41259754 | G | A | 1 | a0001c0002t0005g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.616-1648C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259754 | ||||||
chr22:41259966 | G | A | 11 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(8): Show | 12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.615+1480C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259966 | ||||||
chr22:41259993 | G | A | 1 | a0002c0004t0007g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.615+1453C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259993 | ||||||
chr22:41260012 | A | AT | 97 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(94): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.615+1433dupA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260012 | ||||||
chr22:41260129 | A | G | 96 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(93): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.615+1317T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260129 | ||||||
chr22:41260290 | T | C | 1 | a0001c0002t0027g0306 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.615+1156A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260290 | ||||||
chr22:41260328 | G | A | 118 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(115): Show | 139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.615+1118C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260328 | ||||||
chr22:41260370 | G | A | 7 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.615+1076C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260370 | ||||||
chr22:41260474 | G | A | 1 | a0001c0011t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.615+972C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260474 | ||||||
chr22:41260505 | G | A | 119 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(116): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.615+941C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260505 | ||||||
chr22:41260566 | G | A | 2 | a0001c0002t0001g0236a0001c0002t0001g0239 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.615+880C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260566 | ||||||
chr22:41260567 | G | A | 2 | a0001c0002t0001g0236a0001c0002t0001g0239 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.615+879C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260567 | ||||||
chr22:41260574 | G | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.615+872C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260574 | ||||||
chr22:41260674 | C | T | 1 | a0001c0002t0005g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.615+772G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260674 | ||||||
chr22:41261071 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.615+375A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41261071 | ||||||
chr22:41261168 | C | T | 1 | a0001c0003t0004g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.615+278G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41261168 | ||||||
chr22:41261604 | T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0195 | 3 | NA19010.hp1 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.481-24A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261604 | ||||||
chr22:41261622 | C | T | 119 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(116): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.481-42G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261622 | ||||||
chr22:41261634 | G | A | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-54C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261634 | ||||||
chr22:41261694 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.481-114T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261694 | ||||||
chr22:41261701 | G | A | 85 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(82): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.481-121C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261701 | ||||||
chr22:41261774 | T | TG | 3 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084 | 4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-195_481-194ins others(1): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261774 | ||||||
chr22:41261776 | A | T | 3 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084 | 4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-196T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261776 | ||||||
chr22:41261840 | T | G | 1 | a0001c0001t0003g0066 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.481-260A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261840 | ||||||
chr22:41261996 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481-416C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261996 | ||||||
chr22:41262071 | T | C | 11 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(8): Show | 12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.481-491A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262071 | ||||||
chr22:41262166 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.481-586C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262166 | ||||||
chr22:41262167 | A | G | 1 | a0001c0001t0001g0303 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.481-587T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262167 | ||||||
chr22:41262217 | G | A | 4 | a0001c0003t0004g0013a0001c0003t0004g0106a0001c0003t0004g0107others(1): Show | 5 | HG02280.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-637C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262217 | ||||||
chr22:41262242 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.481-662G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262242 | ||||||
chr22:41262277 | G | A | 4 | a0001c0002t0001g0004a0001c0002t0001g0146a0001c0002t0001g0293others(1): Show | 6 | HG00558.hp2 HG02056.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-697C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262277 | ||||||
chr22:41262316 | G | A | 4 | a0001c0003t0001g0092a0001c0003t0001g0093a0001c0003t0004g0098others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-736C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262316 | ||||||
chr22:41262333 | A | C | 2 | a0001c0001t0006g0278a0001c0001t0006g0279 | 2 | NA19000.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.481-753T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262333 | ||||||
chr22:41262370 | C | G | 3 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084 | 4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-790G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262370 | ||||||
chr22:41262597 | A | G | 215 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(212): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.481-1017T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262597 | ||||||
chr22:41262600 | C | CT | 55 | a0001c0001t0001g0246a0001c0001t0002g0002a0001c0001t0002g0006others(52): Show | 69 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.481-1021dupA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262600 | ||||||
chr22:41262628 | C | T | 119 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(116): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.481-1048G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262628 | ||||||
chr22:41262650 | GGATCACG others(7): Show |
G | 6 | a0001c0002t0001g0014a0001c0002t0001g0171a0001c0002t0001g0289others(3): Show | 7 | HG01243.hp2 HG01433.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-1084_481-1071d others(16): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262650 | ||||||
chr22:41262655 | A | T | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-1075T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262655 | ||||||
chr22:41262685 | T | C | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-1105A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262685 | ||||||
chr22:41262705 | C | T | 1 | a0001c0002t0001g0022 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.481-1125G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262705 | ||||||
chr22:41263010 | C | T | 1 | a0001c0002t0005g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.481-1430G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263010 | ||||||
chr22:41263094 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.481-1514A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263094 | ||||||
chr22:41263322 | G | T | 11 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(8): Show | 12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.480+1342C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263322 | ||||||
chr22:41263372 | CTGTT | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0211a0001c0001t0020g0088others(1): Show | 4 | HG02818.hp1 HG04184.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1288_480+1291d others(6): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263372 | ||||||
chr22:41263576 | G | A | 119 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(116): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.480+1088C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263576 | ||||||
chr22:41263646 | A | C | 3 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084 | 4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1018T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263646 | ||||||
chr22:41263962 | G | A | 11 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(8): Show | 12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.480+702C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263962 | ||||||
chr22:41264141 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.480+523G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264141 | ||||||
chr22:41264285 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.480+379C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264285 | ||||||
chr22:41264288 | GC | G | 235 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(232): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.480+375delG | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264288 | ||||||
chr22:41264297 | G | A | 119 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(116): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.480+367C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264297 | ||||||
chr22:41264360 | G | A | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.480+304C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264360 | ||||||
chr22:41264406 | C | G | 85 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(82): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.480+258G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264406 | ||||||
chr22:41264431 | T | C | 11 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(8): Show | 12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.480+233A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264431 | ||||||
chr22:41264586 | G | C | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.480+78C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264586 | ||||||
chr22:41264641 | G | A | 45 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(42): Show | 47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.480+23C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264641 | ||||||
chr22:41264875 | T | C | 1 | a0001c0001t0010g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.301-32A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41264875 | ||||||
chr22:41264960 | A | G | 215 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(212): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.301-117T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41264960 | ||||||
chr22:41265040 | G | T | 1 | a0001c0002t0001g0022 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.301-197C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265040 | ||||||
chr22:41265150 | G | T | 119 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(116): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.301-307C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265150 | ||||||
chr22:41265225 | C | T | 4 | a0001c0001t0001g0155a0001c0001t0001g0193a0001c0001t0001g0303others(1): Show | 4 | HG02027.hp2 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-382G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265225 | ||||||
chr22:41265764 | G | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.301-921C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265764 | ||||||
chr22:41265854 | A | G | 11 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(8): Show | 12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.301-1011T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265854 | ||||||
chr22:41265887 | C | T | 2 | a0005c0007t0001g0234a0005c0007t0001g0237 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.301-1044G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265887 | ||||||
chr22:41265973 | T | C | 225 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(222): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.301-1130A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265973 | ||||||
chr22:41265980 | A | G | 9 | a0001c0002t0001g0011a0001c0002t0001g0020a0001c0002t0001g0090others(6): Show | 11 | NA18956.hp1 NA18982.hp1 NA18986.hp2 others(8): Show |
intron_variant | MODIFIER | c.301-1137T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265980 | ||||||
chr22:41265998 | C | T | 1 | a0001c0002t0001g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.301-1155G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265998 | ||||||
chr22:41266022 | G | A | 8 | a0001c0001t0006g0007a0001c0001t0006g0277a0001c0001t0006g0278others(5): Show | 10 | HG00673.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-1179C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266022 | ||||||
chr22:41266074 | C | T | 1 | a0001c0001t0011g0035 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.301-1231G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266074 | ||||||
chr22:41266134 | G | A | 8 | a0001c0001t0001g0148a0001c0001t0001g0164a0001c0001t0001g0196others(5): Show | 8 | HG02083.hp1 HG02135.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-1291C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266134 | ||||||
chr22:41266201 | CA | C | 117 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(114): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.301-1359delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266201 | ||||||
chr22:41266252 | T | TAGCCCTG others(10): Show |
226 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(223): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.301-1410_301-1409i others(19): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266252 | ||||||
chr22:41266396 | A | G | 1 | a0001c0002t0005g0165 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.301-1553T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266396 | ||||||
chr22:41266692 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.300+1405C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266692 | ||||||
chr22:41266792 | C | A | 1 | a0001c0002t0005g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.300+1305G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266792 | ||||||
chr22:41266792 | C | T | 1 | a0001c0002t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.300+1305G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266792 | ||||||
chr22:41266888 | C | CTTTTTTT others(1): Show |
214 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(211): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.300+1201_300+1208d others(10): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266888 | ||||||
chr22:41266888 | C | CTTTTTTT others(3): Show |
2 | a0001c0002t0001g0230a0001c0002t0001g0231 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.300+1199_300+1208d others(12): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266888 | ||||||
chr22:41267095 | A | T | 226 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(223): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.300+1002T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267095 | ||||||
chr22:41267161 | G | A | 44 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(41): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.300+936C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267161 | ||||||
chr22:41267589 | G | A | 7 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+508C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267589 | ||||||
chr22:41267742 | G | C | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.300+355C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267742 | ||||||
chr22:41267763 | G | A | 3 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084 | 4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+334C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267763 | ||||||
chr22:41268067 | G | A | 5 | a0001c0003t0004g0015a0001c0003t0004g0101a0001c0003t0004g0102others(2): Show | 6 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+30C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41268067 | ||||||
chr22:41268181 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.241-25A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268181 | ||||||
chr22:41268406 | C | T | 44 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(41): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.241-250G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268406 | ||||||
chr22:41268509 | T | C | 227 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(224): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.241-353A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268509 | ||||||
chr22:41268535 | A | G | 143 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.241-379T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268535 | ||||||
chr22:41268739 | G | C | 2 | a0001c0001t0003g0038a0001c0001t0003g0045 | 2 | HG00408.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.241-583C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268739 | ||||||
chr22:41268826 | G | A | 1 | a0001c0001t0025g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.241-670C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268826 | ||||||
chr22:41268874 | G | C | 11 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.241-718C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268874 | ||||||
chr22:41268874 | G | T | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-718C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268874 | ||||||
chr22:41268934 | A | C | 8 | a0001c0001t0010g0096a0001c0003t0004g0094a0001c0003t0004g0095others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-778T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268934 | ||||||
chr22:41268938 | G | A | 85 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(82): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.241-782C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268938 | ||||||
chr22:41269086 | C | T | 1 | a0001c0001t0011g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.241-930G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269086 | ||||||
chr22:41269329 | T | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.241-1173A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269329 | ||||||
chr22:41269428 | T | A | 1 | a0001c0001t0002g0268 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.241-1272A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269428 | ||||||
chr22:41269718 | G | A | 118 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(115): Show | 139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.241-1562C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269718 | ||||||
chr22:41269739 | C | CA | 48 | a0001c0001t0001g0079a0001c0001t0001g0138a0001c0001t0001g0204others(45): Show | 50 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.241-1584dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269739 | ||||||
chr22:41269739 | CA | C | 10 | a0001c0001t0001g0192a0001c0001t0002g0272a0001c0001t0005g0245others(7): Show | 10 | HG01943.hp1 HG02293.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.241-1584delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269739 | ||||||
chr22:41269961 | G | T | 1 | a0002c0004t0007g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.241-1805C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269961 | ||||||
chr22:41269991 | G | A | 3 | a0001c0002t0001g0178a0001c0002t0001g0189a0001c0002t0005g0190 | 3 | HG01081.hp2 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.241-1835C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269991 | ||||||
chr22:41270025 | G | C | 8 | a0001c0003t0004g0013a0001c0003t0004g0103a0001c0003t0004g0106others(5): Show | 9 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.241-1869C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270025 | ||||||
chr22:41270165 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.241-2009C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270165 | ||||||
chr22:41270181 | C | A | 2 | a0001c0001t0002g0283a0001c0001t0002g0294 | 2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.241-2025G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270181 | ||||||
chr22:41270273 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.241-2117A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270273 | ||||||
chr22:41270298 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.241-2142C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270298 | ||||||
chr22:41270591 | G | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.241-2435C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270591 | ||||||
chr22:41270757 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.241-2601T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270757 | ||||||
chr22:41270939 | TG | T | 54 | a0001c0001t0001g0246a0001c0001t0002g0002a0001c0001t0002g0006others(51): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.241-2784delC | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270939 | ||||||
chr22:41270971 | G | A | 1 | a0001c0002t0005g0304 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.241-2815C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270971 | ||||||
chr22:41270983 | A | G | 5 | a0001c0002t0001g0017a0001c0002t0001g0129a0001c0002t0001g0179others(2): Show | 6 | NA18943.hp2 NA18967.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-2827T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270983 | ||||||
chr22:41271224 | TA | T | 7 | a0001c0001t0001g0208a0001c0001t0001g0219a0001c0001t0005g0245others(4): Show | 7 | HG01433.hp1 HG02109.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.241-3069delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271224 | ||||||
chr22:41271386 | T | TA | 100 | a0001c0001t0001g0026a0001c0001t0001g0148a0001c0001t0001g0155others(97): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.240+3213dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271386 | ||||||
chr22:41271386 | T | TAA | 18 | a0001c0001t0001g0079a0001c0001t0003g0042a0001c0001t0003g0046others(15): Show | 19 | HG00423.hp2 HG00735.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.240+3212_240+3213d others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271386 | ||||||
chr22:41271395 | AC | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0191a0001c0002t0001g0214 | 3 | HG04184.hp1 NA19074.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.240+3204delG | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271395 | ||||||
chr22:41271396 | C | A | 213 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(210): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.240+3204G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271396 | ||||||
chr22:41271402 | A | C | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.240+3198T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271402 | ||||||
chr22:41271409 | C | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240+3191G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271409 | ||||||
chr22:41271489 | G | C | 117 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(114): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.240+3111C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271489 | ||||||
chr22:41271610 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.240+2990G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271610 | ||||||
chr22:41271625 | C | T | 1 | a0001c0001t0017g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.240+2975G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271625 | ||||||
chr22:41271687 | C | T | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240+2913G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271687 | ||||||
chr22:41271692 | C | CA | 16 | a0001c0001t0001g0206a0001c0001t0002g0262a0001c0001t0002g0267others(13): Show | 17 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.240+2907dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271692 | ||||||
chr22:41271692 | CA | C | 10 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+2907delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271692 | ||||||
chr22:41271723 | A | G | 85 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(82): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.240+2877T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271723 | ||||||
chr22:41271993 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.240+2607T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271993 | ||||||
chr22:41272004 | C | T | 1 | a0001c0002t0005g0140 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.240+2596G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272004 | ||||||
chr22:41272110 | G | T | 2 | a0001c0001t0003g0054a0001c0001t0003g0057 | 2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.240+2490C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272110 | ||||||
chr22:41272245 | G | C | 1 | a0001c0001t0018g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.240+2355C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272245 | ||||||
chr22:41272521 | A | C | 2 | a0005c0007t0001g0234a0005c0007t0001g0237 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.240+2079T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272521 | ||||||
chr22:41272715 | C | T | 2 | a0001c0002t0001g0168a0001c0002t0022g0241 | 2 | NA18969.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.240+1885G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272715 | ||||||
chr22:41272798 | C | G | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240+1802G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272798 | ||||||
chr22:41273214 | C | T | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.240+1386G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273214 | ||||||
chr22:41273338 | T | C | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240+1262A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273338 | ||||||
chr22:41273406 | C | T | 1 | a0001c0001t0006g0298 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.240+1194G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273406 | ||||||
chr22:41273467 | A | C | 1 | a0001c0001t0011g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.240+1133T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273467 | ||||||
chr22:41273494 | G | A | 13 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(10): Show | 16 | HG00609.hp1 HG00673.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.240+1106C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273494 | ||||||
chr22:41273766 | C | CA | 106 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(103): Show | 130 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.240+833dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAA | 43 | a0001c0001t0001g0026a0001c0001t0001g0136a0001c0001t0001g0161others(40): Show | 45 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.240+832_240+833dup others(2): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAA | 7 | a0001c0001t0003g0053a0001c0001t0010g0010a0001c0001t0010g0077others(4): Show | 8 | HG00639.hp1 HG01884.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+830_240+833dup others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(1): Show |
5 | a0001c0003t0004g0013a0001c0003t0004g0106a0001c0003t0004g0109others(2): Show | 6 | HG01167.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+826_240+833dup others(8): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(2): Show |
18 | a0001c0001t0010g0096a0001c0003t0004g0003a0001c0003t0004g0015others(15): Show | 21 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.240+825_240+833dup others(9): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(3): Show |
11 | a0001c0003t0004g0012a0001c0003t0004g0095a0001c0003t0004g0097others(8): Show | 12 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+824_240+833dup others(10): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0003g0009a0001c0001t0003g0039a0001c0001t0003g0040others(3): Show | 7 | HG00733.hp2 HG03492.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+823_240+833dup others(11): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(5): Show |
12 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0003g0043others(9): Show | 12 | HG00408.hp2 HG00544.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+822_240+833dup others(12): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(6): Show |
9 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0069others(6): Show | 9 | HG00099.hp1 HG02055.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+821_240+833dup others(13): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0003g0060a0001c0001t0003g0072a0001c0001t0005g0274others(1): Show | 4 | HG01106.hp2 HG01261.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+820_240+833dup others(14): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0047 | 4 | HG00558.hp1 NA18949.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+819_240+833dup others(15): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0003g0037a0001c0001t0003g0061a0001c0001t0003g0076 | 3 | NA18946.hp2 NA19077.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.240+818_240+833dup others(16): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0003g0062 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.240+817_240+833dup others(17): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273766 | CA | C | 7 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0048others(4): Show | 7 | NA18947.hp2 NA18964.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+833delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | ||||||
chr22:41273824 | C | T | 3 | a0001c0001t0001g0128a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG00673.hp2 HG02015.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.240+776G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273824 | ||||||
chr22:41274265 | C | T | 1 | a0001c0001t0017g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.240+335G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41274265 | ||||||
chr22:41274366 | G | A | 1 | a0001c0003t0004g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.240+234C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41274366 | ||||||
chr22:41275048 | C | G | 1 | a0002c0004t0007g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113-321G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275048 | ||||||
chr22:41275395 | G | A | 3 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084 | 4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-668C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275395 | ||||||
chr22:41275405 | T | C | 1 | a0001c0002t0001g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.113-678A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275405 | ||||||
chr22:41275447 | A | G | 304 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(301): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.113-720T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275447 | ||||||
chr22:41275728 | G | A | 84 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(81): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.113-1001C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275728 | ||||||
chr22:41275758 | G | A | 4 | a0001c0003t0004g0013a0001c0003t0004g0106a0001c0003t0004g0107others(1): Show | 5 | HG02280.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1031C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275758 | ||||||
chr22:41275781 | G | GA | 56 | a0001c0001t0001g0215a0001c0001t0001g0246a0001c0001t0002g0002others(53): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.113-1055dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275781 | ||||||
chr22:41275804 | G | A | 8 | a0001c0001t0006g0007a0001c0001t0006g0277a0001c0001t0006g0278others(5): Show | 10 | HG00673.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-1077C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275804 | ||||||
chr22:41275904 | C | T | 1 | a0001c0001t0009g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.113-1177G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275904 | ||||||
chr22:41276236 | C | T | 1 | a0002c0004t0007g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.113-1509G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276236 | ||||||
chr22:41276267 | A | C | 161 | a0001c0001t0001g0079a0001c0001t0001g0246a0001c0001t0002g0002others(158): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.113-1540T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276267 | ||||||
chr22:41276510 | A | G | 162 | a0001c0001t0001g0079a0001c0001t0001g0246a0001c0001t0002g0002others(159): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.113-1783T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276510 | ||||||
chr22:41276626 | C | T | 1 | a0001c0001t0011g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.113-1899G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276626 | ||||||
chr22:41276812 | G | A | 2 | a0001c0003t0004g0015a0001c0003t0004g0123 | 3 | HG01081.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.113-2085C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276812 | ||||||
chr22:41276913 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.113-2186C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276913 | ||||||
chr22:41276922 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.113-2195C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276922 | ||||||
chr22:41276986 | G | GA | 10 | a0001c0001t0002g0269a0001c0001t0003g0040a0001c0002t0001g0130others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-2260dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276986 | ||||||
chr22:41277071 | A | AT | 109 | a0001c0001t0001g0019a0001c0001t0001g0079a0001c0001t0001g0136others(106): Show | 120 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.113-2345dupA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277071 | ||||||
chr22:41277071 | A | ATT | 12 | a0001c0001t0003g0008a0001c0001t0003g0041a0001c0001t0003g0042others(9): Show | 13 | HG00544.hp1 HG00558.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.113-2346_113-2345d others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277071 | ||||||
chr22:41277071 | AT | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0138a0001c0001t0001g0218others(8): Show | 12 | HG01884.hp2 HG01934.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.113-2345delA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277071 | ||||||
chr22:41277170 | C | T | 1 | a0002c0004t0007g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.113-2443G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277170 | ||||||
chr22:41277227 | G | T | 13 | a0001c0001t0001g0246a0001c0001t0002g0250a0001c0001t0002g0251others(10): Show | 15 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.113-2500C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277227 | ||||||
chr22:41277300 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.113-2573C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277300 | ||||||
chr22:41277321 | G | A | 8 | a0001c0001t0006g0007a0001c0001t0006g0277a0001c0001t0006g0278others(5): Show | 10 | HG00673.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-2594C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277321 | ||||||
chr22:41277324 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.113-2597G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277324 | ||||||
chr22:41277325 | G | A | 1 | a0001c0002t0001g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.113-2598C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277325 | ||||||
chr22:41277348 | G | A | 1 | a0001c0002t0001g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.113-2621C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277348 | ||||||
chr22:41277399 | C | G | 1 | a0001c0002t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.113-2672G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277399 | ||||||
chr22:41277413 | T | A | 1 | a0001c0003t0004g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.113-2686A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277413 | ||||||
chr22:41277588 | A | T | 46 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(43): Show | 48 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.113-2861T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277588 | ||||||
chr22:41277611 | A | G | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.113-2884T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277611 | ||||||
chr22:41277983 | G | C | 1 | a0001c0003t0004g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.112+2950C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277983 | ||||||
chr22:41278038 | G | GT | 72 | a0001c0001t0001g0138a0001c0001t0001g0223a0001c0001t0001g0246others(69): Show | 87 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.112+2894dupA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278038 | ||||||
chr22:41278160 | C | T | 4 | a0001c0001t0010g0096a0001c0003t0004g0094a0001c0003t0004g0095others(1): Show | 4 | HG01496.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+2773G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278160 | ||||||
chr22:41278183 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.112+2750A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278183 | ||||||
chr22:41278199 | C | T | 61 | a0001c0001t0001g0246a0001c0001t0002g0002a0001c0001t0002g0006others(58): Show | 76 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.112+2734G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278199 | ||||||
chr22:41278259 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.112+2674C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278259 | ||||||
chr22:41278444 | A | G | 1 | a0001c0001t0011g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112+2489T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278444 | ||||||
chr22:41278517 | G | A | 155 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0006others(152): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.112+2416C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278517 | ||||||
chr22:41278521 | T | A | 1 | a0001c0002t0001g0091 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.112+2412A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278521 | ||||||
chr22:41278523 | C | A | 1 | a0001c0002t0001g0091 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.112+2410G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278523 | ||||||
chr22:41278653 | C | G | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+2280G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278653 | ||||||
chr22:41278776 | G | T | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.112+2157C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278776 | ||||||
chr22:41278832 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.112+2101G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278832 | ||||||
chr22:41278956 | C | G | 2 | a0001c0002t0001g0230a0001c0002t0001g0231 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.112+1977G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278956 | ||||||
chr22:41278979 | A | T | 1 | a0001c0001t0003g0038 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.112+1954T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278979 | ||||||
chr22:41279011 | C | T | 143 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.112+1922G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279011 | ||||||
chr22:41279035 | C | T | 1 | a0001c0001t0003g0037 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.112+1898G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279035 | ||||||
chr22:41279104 | G | A | 162 | a0001c0001t0001g0079a0001c0001t0001g0246a0001c0001t0002g0002others(159): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.112+1829C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279104 | ||||||
chr22:41279122 | A | G | 74 | a0001c0001t0001g0246a0001c0001t0002g0002a0001c0001t0002g0006others(71): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.112+1811T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279122 | ||||||
chr22:41279325 | C | T | 1 | a0001c0001t0017g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112+1608G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279325 | ||||||
chr22:41279373 | G | A | 1 | a0001c0002t0005g0225 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.112+1560C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279373 | ||||||
chr22:41279558 | T | C | 3 | a0001c0002t0001g0134a0001c0002t0001g0135a0001c0002t0005g0133 | 3 | HG02486.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.112+1375A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279558 | ||||||
chr22:41279698 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.112+1235T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279698 | ||||||
chr22:41279699 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.112+1234C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279699 | ||||||
chr22:41279800 | CA | C | 164 | a0001c0001t0001g0246a0001c0001t0002g0002a0001c0001t0002g0006others(161): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.112+1132delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279800 | ||||||
chr22:41279954 | C | T | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+979G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279954 | ||||||
chr22:41279990 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.112+943G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279990 | ||||||
chr22:41280172 | A | G | 41 | a0001c0001t0010g0096a0001c0002t0001g0014a0001c0003t0001g0092others(38): Show | 47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.112+761T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41280172 | ||||||
chr22:41280484 | C | G | 1 | a0001c0011t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.112+449G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41280484 | ||||||
chr22:41280555 | C | CAGCT | 86 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(83): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.112+374_112+377dup others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41280555 | ||||||
chr22:41280595 | GCAAGGGT others(5): Show |
G | 1 | a0001c0001t0017g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112+326_112+337del others(12): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41280595 | ||||||
chr22:41281149 | G | C | 3 | a0003c0005t0006g0301a0003c0005t0011g0300a0003c0005t0011g0302 | 3 | HG01109.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-38-67C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281149 | ||||||
chr22:41281210 | T | C | 161 | a0001c0001t0001g0079a0001c0001t0001g0246a0001c0001t0002g0002others(158): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.-38-128A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281210 | ||||||
chr22:41281237 | GA | G | 85 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(82): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.-38-156delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281237 | ||||||
chr22:41281313 | C | T | 56 | a0001c0001t0001g0246a0001c0001t0002g0002a0001c0001t0002g0006others(53): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-38-231G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281313 | ||||||
chr22:41281735 | T | C | 1 | a0002c0004t0007g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-38-653A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281735 | ||||||
chr22:41282347 | T | C | 97 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(94): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-38-1265A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282347 | ||||||
chr22:41282634 | T | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38-1552A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282634 | ||||||
chr22:41282691 | T | C | 1 | a0001c0002t0001g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-38-1609A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282691 | ||||||
chr22:41282812 | G | A | 1 | a0001c0002t0005g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-38-1730C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282812 | ||||||
chr22:41282892 | G | A | 12 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38-1810C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282892 | ||||||
chr22:41283222 | GTT | G | 41 | a0001c0001t0010g0096a0001c0002t0001g0014a0001c0003t0001g0092others(38): Show | 47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-38-2142_-38-2141d others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283222 | ||||||
chr22:41283224 | TGGG | T | 43 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0036others(40): Show | 45 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-38-2145_-38-2143d others(5): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283224 | ||||||
chr22:41283226 | G | T | 41 | a0001c0001t0010g0096a0001c0002t0001g0014a0001c0003t0001g0092others(38): Show | 47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-38-2144C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283226 | ||||||
chr22:41283227 | G | T | 41 | a0001c0001t0010g0096a0001c0002t0001g0014a0001c0003t0001g0092others(38): Show | 47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-38-2145C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283227 | ||||||
chr22:41283230 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-38-2148C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283230 | ||||||
chr22:41283232 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-38-2150G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283232 | ||||||
chr22:41283279 | G | A | 1 | a0001c0002t0022g0241 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-38-2197C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283279 | ||||||
chr22:41283381 | C | T | 2 | a0001c0003t0001g0092a0001c0003t0001g0093 | 2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-38-2299G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283381 | ||||||
chr22:41283408 | T | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-38-2326A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283408 | ||||||
chr22:41283516 | C | T | 1 | a0001c0001t0012g0242 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-38-2434G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283516 | ||||||
chr22:41283520 | T | C | 2 | a0001c0001t0002g0283a0001c0001t0002g0294 | 2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-38-2438A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283520 | ||||||
chr22:41283520 | T | TAAC | 9 | a0001c0001t0002g0276a0001c0001t0006g0007a0001c0001t0006g0277others(6): Show | 11 | HG00673.hp1 HG00741.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38-2441_-38-2439d others(5): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283520 | ||||||
chr22:41283832 | G | T | 3 | a0001c0002t0001g0011a0001c0002t0001g0090a0001c0002t0001g0091 | 4 | NA18956.hp1 NA18982.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+2154C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283832 | ||||||
chr22:41283896 | CAT | C | 63 | a0001c0001t0001g0246a0001c0001t0002g0002a0001c0001t0002g0006others(60): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-39+2088_-39+2089d others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283896 | ||||||
chr22:41283923 | C | CAAGAAAC others(22): Show |
1 | a0001c0001t0001g0303 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+2034_-39+2062d others(31): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283923 | ||||||
chr22:41283975 | G | A | 2 | a0001c0001t0002g0283a0001c0001t0002g0294 | 2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-39+2011C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283975 | ||||||
chr22:41284044 | C | G | 1 | a0001c0001t0003g0036 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-39+1942G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284044 | ||||||
chr22:41284045 | G | A | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(1): Show | 4 | NA19054.hp2 NA19070.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+1941C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284045 | ||||||
chr22:41284125 | T | C | 1 | a0001c0003t0004g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-39+1861A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284125 | ||||||
chr22:41284290 | G | A | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-39+1696C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284290 | ||||||
chr22:41284296 | G | A | 4 | a0001c0002t0001g0289a0001c0002t0001g0290a0001c0002t0001g0291others(1): Show | 4 | HG01433.hp1 HG02895.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+1690C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284296 | ||||||
chr22:41284634 | G | A | 1 | a0001c0002t0001g0293 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-39+1352C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284634 | ||||||
chr22:41284647 | G | A | 1 | a0002c0004t0007g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-39+1339C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284647 | ||||||
chr22:41284651 | C | G | 12 | a0001c0001t0010g0010a0001c0001t0010g0077a0001c0001t0010g0084others(9): Show | 13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-39+1335G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284651 | ||||||
chr22:41284894 | C | T | 44 | a0001c0001t0001g0079a0001c0001t0003g0008a0001c0001t0003g0009others(41): Show | 46 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.-39+1092G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284894 | ||||||
chr22:41284975 | A | T | 1 | a0001c0001t0001g0303 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+1011T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284975 | ||||||
chr22:41285003 | T | G | 1 | a0001c0001t0001g0303 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+983A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285003 | ||||||
chr22:41285043 | T | A | 1 | a0001c0001t0002g0294 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-39+943A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285043 | ||||||
chr22:41285105 | G | A | 3 | a0001c0001t0002g0295a0001c0001t0002g0296a0001c0001t0021g0297 | 3 | HG01346.hp2 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-39+881C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285105 | ||||||
chr22:41285367 | T | G | 6 | a0001c0001t0006g0298a0001c0001t0011g0035a0001c0001t0018g0299others(3): Show | 7 | HG01099.hp2 HG01109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39+619A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285367 | ||||||
chr22:41285368 | A | T | 1 | a0001c0001t0001g0303 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+618T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285368 | ||||||
chr22:41285371 | C | A | 1 | a0001c0001t0001g0303 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+615G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285371 | ||||||
chr22:41285443 | C | A | 1 | a0001c0002t0005g0304 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-39+543G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285443 | ||||||
chr22:41285479 | G | T | 1 | a0001c0002t0016g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-39+507C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285479 | ||||||
chr22:41285617 | A | C | 1 | a0001c0001t0010g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-39+369T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285617 | ||||||
chr22:41285699 | T | C | 1 | a0001c0001t0006g0305 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-39+287A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285699 |